Section |
Name |
Details |
A5.02.08 |
|
Consider first line dressings appropriate to wound bed type and exudate level |
A5.04.01 |
|
Before using active products, ensure all potential reasons for non-healing have been explored. |
A5.05.02 |
|
Consider standard interactive dressings first. |
A5.06.01 |
|
Consider standard interactive dressings first as advised by Tissue Viability Nurse. |
A5.10 |
|
Consider standard dressings first |
06.04.01.01 |
Evorel Sequi® |
|
05.03 |
Molnupiravir |
|
05.01.09 |
Rifampicin Rimactane® |
Hospital use only under microbiological and Tuberculosis specialist advice |
01.06.04 |
Sodium Citrate |
Micro-enema
Microlette®, Relaxit® and Micralax® |
20 |
3% acetic acid for Barrett’s oesophagus surveillance |
For use by endoscopy speciality at Sandwell and West Birmingham NHS Trust |
10.02.01 |
3,4-diaminopyridine (3,4-DAP) |
Hospital use only |
A5.15 |
3M Cavilon Durable Barrier Cream |
Preferred local option Skin protectant Type of wound product is suitable for Intact skin As a barrier against bodily fluids, prevention of skin damage associated with incontinence Can be used alongside containment products Can be used to prevent friction to vulnerable areas of skin Frequency of use Reapply sparingly twice daily Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Do not use on infected skin Not be used as an emollient Not to be used around the peri wound Can increase adherence of some dressing products and therefore care should be taken when adhesive products are being used in conjunction with the cream on people with fragile skin Rationale for inclusion in formulary The only barrier cream that can be used in conjunction with containment products without blocking the absorption of the pad Cost effective, does not require reapplication at every episode of hygiene |
A5.15 |
3M Cavilon No Sting Barrier Film Pump Spray and Applicators |
Preferred local option Protective transparent barrier film Type of wound product is suitable for Superficial broken skin and abrasions As a barrier against bodily fluids, prevention of skin damage associated with incontinence Can be used: -alongside containment products, -to prevent friction to vulnerable areas of skin -on superficial abrasions caused by incontinence -to protect peri wound from exudate -to protect against aggressive adhesive products -to protect the skin surrounding stoma sites Frequency of use Every 72 hours Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Do not use on infected skin Allow product to dry before applying the containment products, dressings or clothing (30 seconds) Too many layers can make the area of skin feel stiff Can affect electrode readings in the treated area Rationale for inclusion in formulary Available in a foam applicator and spray to aid application Non sticky after use Can be used on broken areas of skin Cost effective, does not require reapplication at every episode of hygiene |
05.03.01 |
Abacavir |
|
05.03.01 |
Abacavir and Lamivudine |
|
05.03.01 |
Abacavir with dolutegravir and lamivudine Triumeq ® |
|
10.01.03 |
Abatacept Orencia® |
Hospital ONLY
£££££
Available via home Care
NHSE commissioned for Juvenile Arthritis and paediatric indications where adult TA available |
08.01.05 |
Abemaciclib Verzenios® |
In line with NICE
Providers are NHS hospital trusts |
08.03.04.02 |
Abiraterone Zytiga® |
Commissioned by NHSE or via Cancer Drug Fund |
08.01.05 |
Acalabrutinib Calquence® |
In line with NICE |
04.10.01 |
Acamprosate Campral EC® |
For initiation by specialists in substance misuse |
02.08 |
Acenocoumarol Sinthrome® |
Use on the advice of a specialist only |
02.02.07 |
Acetazolamide |
|
11.06 |
Acetazolamide |
Hospital only |
11.06 |
Acetazolamide |
Used alone for short term post op only. Can be used with beta-blocker or other ocular hypotensive Systemic absorption can give rise to sulphonamide associated side effects On Specialist Ophthalmologist Recommendation |
11.06 |
Acetazolamide SR |
Used alone for short term post op only. Can be used with beta-blocker or other ocular hypotensive Systemic absorption can give rise to sulphonamide associated side effects On Specialist Ophthalmologist Recommendation |
12.01.01 |
Acetic Acid 2% Earcalm ® |
|
20 |
Acetic Acid Solution 3% |
Restricted for use by endoscopy only |
03.07 |
Acetylcysteine |
Brand: Parvolex |
03.07 |
Acetylcysteine oral presentations |
- Brands (NACSYS and Nexus)
- See brands -Prescribe as Acetylcyteine S/f tabs
|
11.08.01 |
Acetylcysteine 10% Ilube® |
|
11.08.01 |
Acetylcysteine 5% with Hypromellose 0.35% Ilube® |
|
03.07 |
Acetylcysteine effervescent tablet Aceteff® |
Acetylcysteine SF effervescent tabs most cost effective |
05.03.02.01 |
Aciclovir |
Tablets most cost effective choice
Dispersible tablets £
Suspension ££ |
05.03.02.01 |
Aciclovir |
|
11.03.03 |
Aciclovir |
|
13.10.03 |
Aciclovir 5% cream |
|
05.03.02 |
Aciclovir lauriad Sitavig |
|
01.01.02 |
Acidex |
|
13.05.02 |
Acitretin Neotigason® |
Prescribed only by or under the supervision of a Consultant Dermatologist. not licensed for GP's to prescribe |
03.01.02 |
Aclidinium Eklira Genuair® |
For COPD only
How to use a Genuair Inhaler |
03.01.04 |
Aclidinium & formoterol inhaler Duaklir Genuair® |
How to use a Genuair Inhaler |
A5.08.07 |
Actico® |
Preferred local option Cohesive inelastic high compression bandage. Short stretch bandage Type of wound product is suitable for Venous leg ulceration Lymphoedema Management of chronic oedema Duration dressing remains on wound before changing Daily to 7 days Frequency of dressing change Dependant on exudate levels if wound present or oedema management. Caution/contraindications (when not to use the dressing, patient groups to avoid etc. Not recommended on those patients with an ABPI lower than 0.8. Caution in diabetic patients Caution when cardiac overload or renal failure present or suspected. Rationale for inclusion in formulary Only cohesive short stretch bandage. Nurses competent in its usage. |
19.08 |
ActiFormCool® |
Type of wound product is suitable for
Necrotic or sloughy wounds that require hydration and cooling pain relief
Can be used on dry wounds with the backing left in place
Cut to shape of the wound
Requires a secondary dressing
Duration dressing remains on wound before changing
1-3 days if dressings become discoloured or opaque or at first signs of exudate strike through
Frequency of dressing change
If dressing becomes discoloured or opaque or at first signs of exudate strike through. Do not allow to dry out
Caution/contraindications (when not to use the dressing, patient groups to avoid etc.)
Should not be used as a covering for deep narrow cavities or sinuses. Do not use on infected wounds.
Not suitable for heavily exuding wounds, known product or component sensitivity. Not for application on ischaemic wounds.
Rationale for inclusion in formulary
Dry necrotic, sloughy or painful wounds
For ease of application - sheet gel rather than liquid
Can be used prior to larval therapy to maintain moisture levels
Primary dressing-see below for secondary:
EXUDATE SECONDARY DRESSING WITH HYDROGEL
None/dry wound Semi-permeable film to reduce moisture loss
Light Non-adherent dressing + tape or Mepore
Moderate Surgical absorbent + tape |
A5.02.01 |
ActiFormCool® |
Preferred local option Type of wound product is suitable for Necrotic or sloughy wounds that require hydration and cooling pain relief Can be used on dry wounds with the backing left in place Cut to shape of the wound Requires a secondary dressing Duration dressing remains on wound before changing 1-3 days if dressings become discoloured or opaque or at first signs of exudate strike through Frequency of dressing change If dressing becomes discoloured or opaque or at first signs of exudate strike through. Do not allow to dry out Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Should not be used as a covering for deep narrow cavities or sinuses. Do not use on infected wounds. Not suitable for heavily exuding wounds, known product or component sensitivity. Not for application on ischaemic wounds. Rationale for inclusion in formulary Dry necrotic, sloughy or painful wounds For ease of application - sheet gel rather than liquid Can be used prior to larval therapy to maintain moisture levels Primary dressing |
A5.03.01 |
Actilite |
Specialist recommendation only Non-adherent viscose net dressing 99% Manuka honey and 1% Manuka oil. Type of wound product is suitable for A primary dressing for low to moderate shallow exuding wound with light slough. Granulating or epithelialising wounds with clinical signs of infection. Requires a secondary dressing. Max Duration dressing remains on wound before changing 3-7 Days Frequency of dressing change 3 to 7 days depending on exudate Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Known allergy to Bee Venom and Honey products Blood sugars should be monitored in patients with diabetes Stinging sensation may be experienced. If unacceptable for patient then discontinue. Rationale for inclusion in formulary For antimicrobial and de-sloughing properties Ease of application Can be cut to size Easy removal in one piece Availability of different sizes Not found to be harmful to peri-wound skin Malodour Cost effective |
A5.02.05 |
ActivHeal® |
PODIATRY ONLY Two layer dressing consisting of a polyurethane bacterial barrier membrane with a centrally located hydrophilic pad +/- acrylic adhesive border. Type of wound product is suitable for Moderately exuding wounds with signs of granulation, epithelialisation or slough. Can be used as primary or secondary Duration dressing remains on wound before changing 1-7 days Frequency of dressing change Up to 7 days dependent on exudate levels Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Full thickness burns Surgical implantations Rationale for inclusion in formulary Cost effective Simple to use on the foot and digits Can be cut to shape |
A5.02.05 |
ActivHeal® Foam Tracheostomy |
Specialist recommendation only Preferred local option Tracheostomy foam dressing Type of wound product is suitable for ActivHeal® Foam Tracheostomy dressing has a fenestration, which allows the dressing to fit neatly around a tracheostomy tube. The dressing can also be used around intubation and cannula insertion procedures, external bone fixators and appropriately-sized wound drainage tubes. Duration dressing remains on wound before changing Dependant on clinical need and soiling Frequency of dressing change Up to 7 days, dependant on clinical need and soiling Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Do not use if reaction to any of its components Rationale for inclusion in formulary Specific dressing shaped and able to cut for tracheostomies. Cost effective |
A5.03.01 |
Activon Tube |
Specialist recommendation only Preferred local option 100% medical grade Manuka Honey. Type of wound product is suitable for Use as topical treatment for infected sloughy shallow or cavity wounds. Primary or addition to other Activon products. Requires secondary dressing. Max Duration dressing remains on wound before changing Up to 4 days Frequency of dressing change Daily in acute infection Up to 4 days in chronic infection dependant on exudate Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Wounds with active blood loss Known allergies to bee Venom and Honey products Blood sugars should be monitored in diabetic patients Stinging sensation may be experienced – discontinue if not tolerant. Rationale for inclusion in formulary Anti-microbial and de-sloughing properties Control of odours Benefit of adding to other action products and increasing honey Suitable for use in cavities Cost effective |
A5.03.01 |
Activon Tulle |
Specialist recommendation only Preferred local option Knitted viscose mesh impregnated with 100% Manuka Honey. Type of wound product is suitable for Creates a moist healing environment effectively eliminates odour. Provides anti-microbial action. Debrides and de-sloughs shallow wounds where the exudate level has started to decrease. Requires secondary dressing Max Duration dressing remains on wound before changing Up to 4 days Frequency of dressing change Daily in acute infection Up to 4 days for chronic infection depending on exudate Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Wounds with active blood loss Known allergies to bee Venom and Honey products Blood sugars should be monitored in diabetic patients Stinging sensation may be experienced – discontinue if not tolerant. Rationale for inclusion in formulary Anti-microbial and de-sloughing properties for wounds with reduced levels of exudate. Control of odours Ease of application and removal in one piece Can be cut to size Available to various size Cost effective |
01.05.03 |
Adalimumab Humira® |
For specialist use only in line with NICE guidance
£££££ |
10.01.03 |
Adalimumab |
Specialist/hospital use only
£££££
Biosimilar brands of Humira® available:
- Amgevita®
- Hulio®
- Hyrimoz®
- Imraldi®
NHSE commissioned for paediatric indications where adult TA available |
11.99.99.99 |
Adalimumab Humira® |
|
13.05.03 |
Adalimumab |
Initiated by hospital consultant only
In line with NICE |
13.06.01 |
Adapalene |
Avoid in pregnancy Use topical retinoids at all stages of acne to help minimise formation of comedones. May cause irritation, build upfrequency or duration of application over 2-3 weeks. |
13.06.01 |
Adapalene with benzyl peroxide Epiduo® |
May be used in preference to antimicrobial -containing agents. |
09.05.02.01 |
Addiphos® |
|
05.03.03 |
Adefovir Dipivoxil Hepsera® |
|
02.03.02 |
Adenosine Adenocor® |
Hospital use only |
02.06 |
Adrenaline / Epinephrine |
|
03.04.03 |
Adrenaline / epinephrine EpiPen® |
|
03.04.03 |
Adrenaline / Epinephrine Jext® |
|
03.04.03 |
Adrenaline / Epinephrine Emerade® |
There has been a patient-level recall of Emerade 500 micrograms pens. This follows earlier recalls for Emerade 150 and 300 microgram pens. (18 May 2020)
Supplies of Emerade will therefore no longer be available in the UK until technical issues with the pen are resolved.
MHRA - Advice for patients with an Emerade 500 microgram auto-injector letter
|
21 |
Adrenaline / Epinephrine |
- The risk of bleeding can be affected by other factors such as the presence of fungating or infected wounds. Smaller bleeds can be palliated using topical adrenaline.
|
03.04.03 |
Adrenaline / Epinephrine 1 in 1,000 Minijet ® Adrenaline 1 in 1000 |
|
03.04.03 |
Adrenaline / Epinephrine 1 in 10,000 Minijet ® Adrenaline 1 in 10000 |
|
03.01.05 |
AeroChamber Plus® |
|
08.01.05 |
Afatinib Giotrif® |
Commissioned by NHSE
In line with NICE |
11.08.02 |
Aflibercept Eylea® |
Use in line with NICE |
04.03.04 |
Agomelatine Valdoxan® |
Supported by a RICaD (in development) |
05.05 |
Albendazole |
Unlicensed |
09.02.02.02 |
Albumin human solution |
Hospital use only |
08.01.05 |
Alectinib Alecensa® |
In line with NICE |
08.02.03 |
Alemtuzumab Lemtrada® |
Hospital only
In line with NICE |
06.06 |
Alendronic Acid |
|
06.06.02 |
Alendronic acid Binosto® |
|
09.06.04 |
Alfacalcidol |
Oral preparations Injection-hospital only |
15.01.04.03 |
Alfentanil |
Hospital only. Palliative care team only for end of life care. |
15.01.04.03 |
Alfentanil Rapifen® |
Hospital only |
21 |
Alfentanil |
|
15.01.04.03 |
Alfentanil intensive care |
Hospital only. Palliative care team recommendation during end of life care only. |
07.04.01 |
Alfuzosin Hydrochloride |
Reduce BP - care with other antihypertensives Caution in elderly Care with hepatic and severe renal impairment Contraindicated in postural hypotension or micturition syncope. Caution in patients with a history of QT prolongation or concomitant use with other drugs known to prolong QT interval. |
01.03 |
Alginic acid |
|
A5.03.01 |
Algivon |
Specialist recommendation only Preferred local option Alginate dressing impregnated with 100% Manuka Honey. Type of wound product is suitable for Primary dressing for infected, shallow cavity wounds, particularly if necrotic or malodorous with moderate exudate. Requires secondary dressing. Max Duration dressing remains on wound before changing Up to 4 days for chronic infection Frequency of dressing change Daily for acute infection Up to 4 days for chronic infection/depending upon exudate Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Wounds with active blood loss Known allergy to be venom and honey products Blood sugars should be monitored in diabetic patients Stinging sensation may be experienced – discontinue if not tolerated Rationale for inclusion in formulary Antimicrobial and de sloughing properties Absorbent Malodour Ease of application and removal in one piece Can be cut to size Available in various sizes Can be shaped to wound size and depth Cost effective |
09.08.01 |
Alglucosidase alfa Myozyme® |
NHSE commissioned |
02.12 |
Alirocumab Praluent® |
In line with NICE. |
02.05.05.03 |
Aliskiren Rasilez® |
Guidance for CCGs: Items which should not be routinely prescribed in primary care |
13.05.01 |
Alitretinoin Toctino® |
Dermatologist use only in line with NICE. |
19.22 |
ALL SILVER DRESSINGS |
There is insufficient evidence to make recommendations on the routine use of silver dressings. Current literature states that the content and type of silver manufactured in such dressings varies widely making it difficult to ascertain the true benefits in terms of clinical effectiveness and cost. In addition recent comparative studies of silver with more conventional antimicrobials such as iodines and honey have shown poor performance indicators favouring more conventional antimicrobials (Thorn et al, 2009 and Du Toit & Page, 2009). With these findings in mind it is advocated that silver dressings be considered as a last dressing choice. However, where a clinician considers a silver dressing is appropriate, the dressing with the lowest acquisition cost appropriate to the clinical indication should be selected. This decision must be discussed with and agreed by the Prescriber. The clinician must then complete the Formulary Exceptions Monitoring Form and Authorisation Form for Silver Dressings and return to Tissue Viability Service for approval. If approved, the wound should be reassessed at 10-14 days and if: • Wound progressing normally – stop silver • Signs of reduced bacterial load – continue with silver to a maximum of another 2 weeks • No improvements – consider another antimicrobial and seek medical or tissue viability advice as appropriate. The use of silver dressings will be monitored and may be the subject of future clinical audit.
|
A5.03.03 |
ALLEVYN®Ag |
Hospital use only for pin sites A non adherent foam dressing impregnated with silver sulphadiazine that can be cut to suit the patient Type of wound product is suitable for For use around infected pin sites Duration dressing remains on wound before changing Daily or as directed Frequency of dressing change Daily Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Patients who have a known sensitivity to Silver Sulphadiazine or Sulphonamides Females who are at or near full term pregnancy or lactating Not for use on neonates or new born infants during the first month of life Rationale for inclusion in formulary Used around infected pin sites in patients with external metalwork to help reduce bacterial load |
A5.02.05 |
ALLEVYN® |
Available in adhesive, non adhesive and gentle Type of wound product is suitable for Wound management by secondary intention on acute, chronic, full thickness or partial thickness or shallow granulating wounds including pressure ulcers, leg ulcers, diabetic foot ulcers, malignant wounds surgical wounds, malignant wounds donor sites and fungating ulcers Can be used as a primary or secondary dressing Duration dressing remains on wound before changing Can stay in place up to 3-7 days Frequency of dressing change Dependent on exudate levels Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) In common with all adhesive products, some cases of irritation and/or maceration of the skin may occur. It should be noted that inappropriate use or too frequent dressing changes, particularly in patients with fragile skin, can result in skin stripping. If this occurs change to the ALLEVYN® gentle border range. If redness or sensitisation occur, discontinue use Caution under compression when exudate levels are moderate to high. Rationale for inclusion in formulary Can be used for low to moderate exudate levels Different sizes and shapes available Cost effective |
A5.02.05 |
ALLEVYN® cavity |
Specialist recommendation only Type of wound product is suitable for Wound management by secondary intention on acute, chronic, full thickness or partial thickness or shallow granulating wounds including pressure ulcers, leg ulcers, diabetic foot ulcers, malignant wounds surgical wounds, malignant wounds donor sites and fungating ulcers. Can be used as a primary or secondary dressing Duration dressing remains on wound before changing Can stay in place up to 3-7 days Frequency of dressing change Dependent on exudate levels Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) In common with all adhesive products, some cases of irritation and/or maceration of the skin may occur.It should be noted that inappropriate use or too frequent dressing changes, particularly in patients with fragile skin, can result in skin stripping. If this occurs change to the ALLEVYN® gentle border range.If redness or sensitisation occur, discontinue use. Caution under compression when exudate levels are moderate to high. Rationale for inclusion in formulary Can be used for low to moderate exudate levels. Different sizes and shapes available. Cost effective |
A5.02.03 |
Allevyn® Life |
Specialist recommendation only Hydrocellular foam dressing Type of wound product is suitable for Shallow granulating wounds, acute and chronic exuding wounds, full and partial thickness wounds such as leg ulcer, malignant wound, surgical wound. Primary dressing Silicone adhesive Duration dressing remains on wound before changing Up to 7 days dependent on dressing indicators Frequency of dressing change Up to 3 times a week maximum Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Do not use with oxidising agents such as hypochlorite solutions or hydrogen peroxide Discontinue if reddening or sensitivity occurs. Do not cut Caution under compression where exudate levels are moderate to high Rationale for inclusion in formulary Fragile skin with absorbency and conformability, problematic healing wounds. Odour control. |
A5.02.05 |
Allevyn® Non-Adhesive |
Type of wound product is suitable for Wound management by secondary intention on acute, chronic, full thickness or partial thickness or shallow granulating wounds including pressure ulcers, leg ulcers, diabetic foot ulcers, malignant wounds surgical wounds, malignant wounds donor sites and fungating ulcers Can be used as a primary or secondary dressing Duration dressing remains on wound before changing Can stay in place up to 3-7 days Frequency of dressing change Dependent on exudate levels Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) In common with all adhesive products, some cases of irritation and/or maceration of the skin may occur. It should be noted that inappropriate use or too frequent dressing changes, particularly in patients with fragile skin, can result in skin stripping. If this occurs change to the Allevyn® gentle border range. If redness or sensitisation occur, discontinue use Caution under compression when exudate levels are moderate to high. Rationale for inclusion in formulary Can be used for low to moderate exudate levels Different sizes and shapes available Cost effective |
09.05.01.01 |
Alliance calcium syrup |
Replacement for Calcium Sandoz® (Discontinued) |
10.01.04 |
Allopurinol |
|
06.01.02.03 |
Alogliptin Vipidia® |
In line with NICE No significant clinical benefit when used in combination with Insulin – avoid using together |
06.01.02.03 |
Alogliptin with Metformin Vipdomet® |
A variety of combinations tablets (dual therapies) of oral diabetes medication can be prescribed and are available in the Drug Tariff.
Overall, they may improve compliance in patients, however some combinations would then not allow the flexibility in dosing that is required for diabetes management and in some cases increase the tablet burden. There are specific sick-day rules related to stopping certain medication which would be further complicated where they are not prescribed in their separate formulations.
Furthermore, for the overall health economy not all combination therapies are cost-effective and this will be increasingly so as the patents expire over the near future.
There are some combination therapies that are not recommended in the oral guidance and clinicians are guided to review and discuss these with patients as part of shared -care decision making.
There are complexities also around the lack of licensing of dual therapies in specific cohorts of patients, related to prescribing for the indication of heart failure or renal disease, making this a complex area for prescribing in primary care. |
02.14 |
Alprostadil |
|
07.01.01.01 |
Alprostadil Prostin VR® |
|
07.04.05 |
Alprostadil Vitaros® |
Specialist initiation only
For patients who would otherwise use alprostadil injection |
07.04.05 |
Alprostadil Intracavernosal injection Caverject® |
Not prescribable under the NHS except to treat erectile dysfunction in men who: Have diabetes, multiple sclerosis, Parkinson's Diseas, poliomyelitis, prostate cancer, severe pelvic injury, single gene neurological disease, spina bifda or psinal cord injury. Are receiving renal dialysis for renal failure Have had radical pelvic surgery, prostatectomy (including transurethral resection of the prostate), or kidney transplant Were receiving Caverject®, Erecnos®, MUSE®, Viagra®, or Viridal® for erectile dysfunction at the expense of the NHS on 14th September 1998 Are suffering severe distress as a result og impotence (prescribed in specialist centres only) |
02.10 |
Alteplase |
Hospital only drug |
09.04 |
AltraJuce |
|
09.04 |
Altraplen Compact® (formally know as Nutriplen® |
- More than 1.5 kcal/mL and 5g (or more) protein/100 mL
- Alternative to second line supplement choice
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula
- Not suitable for child under 3 years; use with caution in child 3–6 years.
|
09.04 |
Altraplen® Protein (formally known as Nutriplen® Protein) |
- More than 1.5 kcal/mL and 5g (or more) protein/100 mL
- Used in cases where increased protein is required
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula
- Not suitable for child under 3 years; use with caution in child 3–6 years
|
09.04 |
Altrashot |
|
13.12 |
Aluminimum Salts |
|
09.05.02.02 |
Aluminium Hydroxide |
Specialist Recommendation |
04.09.01 |
Amantadine Hydrochloride |
Capsules
Syrup - for patients with swallowing difficulties |
05.03.04 |
Amantadine Hydrochloride |
|
02.05 |
Ambrisentan |
|
05.01.04 |
Amikacin |
Hospital use only under microbiological advice |
05.01.04 |
Amikacin Amikin® |
Hospital use only under microbiological advice |
02.02.03 |
Amiloride Hydrochloride |
|
03.01.03 |
Aminophylline IV |
|
05.01 |
Aminosalicylic Acid Granupas 4 g gastro-resistant granules |
Hospital use only under microbiological advice |
05.01 |
Aminosalicylic Acid |
Hospital use only under microbiological advice |
02.03.02 |
Amiodarone |
Use current status at Place/Trust
Sandwell
Specialist intiation supported by a RICaD
Amiodarone RICaD-Sandwell only
Atrial fibrillation : Rhythm control should be used when: symptomatic; under 65's; first time -lone AF; secondary to treated or corrected precipitant with congestive heart failure. Beta-blockers are first line, amiodarone should be used second line where structural heart disease is present Check thyroid function and liver function every 6 months Phototoxicity reactions possible - advise use of wide spectrum sunscreen. Suspect pneumonitis if new or preogressive shortness of breath or cough develops
Following the policy - Items which should not routinely be prescribed in Primary Care. Patients who are established on Amiodarone should continue their prescriptions as normal
The guidance applies to new patients only
Wolverhampton
Walsall
Dudley
|
02.03.02 |
Amiodarone |
|
04.02.01 |
Amisulpride |
Supported by ESCA |
04.03.01 |
Amitriptyline |
Tablets more cost effective than SF solution
Sugar Free solution £££££ |
04.07.03 |
Amitriptyline |
1st line
Low abuse potential, low cost
Off label use |
04.07.04.02 |
Amitriptyline |
|
02.06.02 |
Amlodipine |
|
13.10.02 |
Amorolfine 5% |
|
03.13 |
Amoxicillin |
Hospital only |
03.13 |
Amoxicillin |
|
03.13 |
Amoxicillin |
|
05.01.01.03 |
Amoxicillin |
|
05.01.01.03 |
Amoxicillin |
|
03.13 |
Amphotericin Fungizone® |
Hospital only |
03.13 |
Amphotericin Fungizone® |
|
05.02 |
Amphotericin Fungizone ® |
|
05.02 |
Amphotericin |
|
05.02 |
Amphotericin AmBisome ® |
|
05.02 |
Amphotericin |
|
11.03.02 |
Amphotericin (eye) |
|
09.01.04 |
Anagrelide Xagrid® |
|
10.01.03 |
Anakinra Kineret® |
Specialist/hospital use only
In line with NICE |
04.07.04.01 |
Analgesics Migraleve Pink® |
|
08.03.04.01 |
Anastrozole |
|
02.08 |
Andexanet |
|
18 |
Andexanet alfa Ondexxya® |
Use in line with NICE |
05.02.04 |
Anidulafungin |
|
01.01.01 |
Antacid and oxetacaine suspension 150 ml |
Suspension
Specialist Use Only |
14.05.03 |
Anti-D (Rh0) Immunoglobulin |
This is commissioned by NHS England not CCG |
14.05 |
Anti-D (Rh0) Immunoglobulin |
This is commissioned by NHS England not CCG |
08.02.02 |
Anti-human thymocyte immunoglobulin (rabbit) Thymoglobuline® |
Commissioned by NHSE
Hospital only |
01.07 |
Anusol® |
Anusol® - other brands also available |
01.07.02 |
Anusol-HC® |
|
08.03.04.02 |
Apalutamide Erleada® |
Use in line with NICE |
02.08 |
Apixaban |
|
04.09.01 |
Apomorphine APO-Go® |
|
04.09.01 |
Apomorphine Dacepton® |
- solution for injection in cartridge
- solution for infusion (accepted July 2020)
|
A5.16 |
Appeel ® |
Available in 4 different applications Preferred local option-5ml sachets & wipes pack of 30 Type of wound product is suitable for Adhesive dressing or appliance removal where skin stripping, loss of skin integrity and pain is a concern •Sachet– suitable for larger dressing removal •Wipes – ideal for adhesive around tubes •Foam applicator – ideal for infants or use of the face •Spray, single patient, multiple use product for all dressings and/or urinary sheath removal Frequency of use Use at each dressing change Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Should not be used when there is a known sensitivity to any of the ingredients If in doubt, patch test a small area, prior to use The product is flammable and should be used in a well ventilated area Avoid use around, flames and sources of ignition Rationale for inclusion in formulary For pain free removal of dressings where fragile skin is a concern |
11.08.02 |
Apraclonidine 0.5% eye drops |
For use on advice of specialist |
11.08.02 |
Apraclonidine 1% SDU eye drops |
The only preservative free sympathomimetic |
13.05.03 |
Apremilast |
In line with NICE Use in adults is commissioned by CCGs |
04.06 |
Aprepitant Emend® |
For use with chemotherapy only
For chemo-related nausea and vomiting
Second-line agent in patients who have failed with 5HT3 antagonist
Hospital use only |
02.11 |
Aprotinin Trasylol® |
|
09.04 |
Aptamil Pepti® Junior |
|
19.12 |
Aquacel ® |
Second choice to formulary alginate dressings. Indications: sloughy, granulating wounds, moderate to heavy exudate. Fibrous sterile sheet made of hydrocolloid fibers which changes to a soft gel when in contact with exudate. Ensure dressing is1cm larger than the wound as it reduces in size on gelling, and cover with moisture retentive dressing |
19.12 |
Aquacel ® Ribbon |
Second line to formulary alginate dressings Indications: sloughy, granulating wounds, moderate to heavy exudate. Fibrous sterile sheet made of hydrocolloid fibers which changes to a soft gel when in contact with exudate. Ensure dressing is1cm larger than the wound as it reduces in size on gelling, and cover with moisture retentive dressing |
A5.02.04 |
Aquacel® |
Preferred local option Type of wound product is suitable for Moderate to heavy exudate, sloughy, necrotic or granulating wounds. Available in rope for cavities Duration dressing remains on wound before changing Maximum 7 days Frequency of dressing change 1-7 days depends on clinical need Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Not suitable for dry wounds. Non dissolvable. Known product or component sensitivity Do not cut Rationale for inclusion in formulary Aids debridement of slough or necrotic tissue Remains intact so easily removed in one piece Absorbs exudate which aids most wound healing facilitating atraumatic dressing change, Cost effective |
A5.03.03 |
Aquacel® Ag Extra |
Specialist recommendation only Hydrofibre with silver Type of wound product is suitable for Management of clinically infected, sloughy, necrotic or granulating wounds with moderate to heavy exudate. Moderate to highly exuding wounds. Aquacel® Ag Extra can be used to break down biofilms Requires a secondary dressing Duration dressing remains on wound before changing Dependent upon exudate 1 - 7 days Frequency of dressing change Dependent upon level of exudate and clinical presentation Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Should not be used on individuals who are sensitive to or have had an allergic reaction to the dressing or its components. Not suitable for dry wounds. No haemostatic properties. Rationale for inclusion in formulary Specialist antimicrobial product Moderate to high exudate levels Can be used to break down biofilms Remains intact on wound bed and easily removable in one piece (non dispersible) |
13.02.01 |
Aquadrate® Urea 10% |
Over the counter preparation suitable for self-care/purchase if appropriate |
19.08 |
Aquaform |
Alternative to GranuGEL®
Hydrogel: Clear viscose sterile gel
Aids autolytic debridement and removal of devitalised tissue.
Type of wound product is suitable for
Low exuding, necrotic or sloughy wounds
Duration dressing remains on wound before changing
Up to 3 days
Frequency of dressing change
1-3 days
Caution/contraindications (when not to use the dressing, patient groups to avoid etc.)
Not suitable for heavily exuding wounds. Caution known product or component sensitivity.
Full thickness burns or infected wounds
Not for application to ischaemic wounds
Rationale for inclusion in formulary
Required for wound beds that need donation of moisture to rehydrate the wound bed and debride. Cost effective
Apply 5mm depth to prevent drying out. Single Use Only
Require secondary dressing – see below
EXUDATE SECONDARY DRESSING WITH HYDROGEL
None/dry wound Semi-permeable film to reduce moisture loss
Light Non-adherent dressing + tape or Mepore
Moderate Surgical absorbent + tape |
06.02.02 |
Aqueous iodine |
Hospital use only. |
01.06 |
Arachis Oil |
|
07.03.04 |
Arcing spring diaphragm |
Sizes 60-95mm (rising in 5mm) |
02.08 |
Argatroban Exembol® |
|
04.02.01 |
Aripiprazole |
- Supported by ESCA
- Use in Tourette's syndrome approved
|
04.02.02 |
Aripiprazole Abilify Maintena® |
The APC's view is that, on clinical grounds, the status of antipsychotic depot injections should be amber with a framework in place in Primary Care before transfer
HOWEVER, until the commissioning arrangements have been agreed to allow safe transfer of patient care, the status will remain RED |
08.01.05 |
Arsenic Trioxide Trisenox® |
In line with NICE |
05.04 |
Artemether > Riamet |
|
05.04.01 |
Artemether with Lumefantrine Riamet® |
|
05.04 |
Artesunate |
|
15.02 |
Articaine Hydrochloride with Adrenaline Septanest® |
Dental use only |
09.06.03 |
Ascorbic Acid |
|
09.08.01 |
Asfotase alfa |
In line with NICE Highly Specialised Technology guidance |
04.07.01 |
Aspirin |
For gargling - topical analgesia |
02.09 |
Aspirin (antiplatelet) |
|
02.09 |
Aspirin e/c |
|
05.03.01 |
Atazanavir |
|
05.03.01 |
Atazanavir with cobicistat Evotaz® |
Blueteq /prior approval form |
02.04 |
Atenolol |
|
08.02.03 |
Atezolizumab Tecentriq® |
In line with NICE
Providers are NHS Trusts |
04.04 |
Atomoxetine Strattera® |
Please note that commissioning discussion is underway. However the present status is as follows:-
Age 6 and over - Solihull practices. Supported with ESCA
Age 16 and over - Birmingham practices. Supported with ESCA
Age under 16 - Birmingham practices
Supported with an ESCA - Sandwell & West Birmingham CCG for patients seen by the Black Country ADHD Services |
02.12 |
Atorvastatin |
|
07.01.03 |
Atosiban Tractocile® |
For Specialist/ Hospital Use Only |
05.04 |
Atovaquone |
|
15.01.05 |
Atracurium |
Hospital only |
19.01 |
ATRAUMAN® |
Type of wound product is suitable for
For flat granulating and epithelising wound for non to heavy exudate where adherence may occur. To be used as a primary dressing with a secondary for absorption.
Duration dressing remains on wound before changing
Up to 7 days
Frequency of dressing change
1-7 days, depending on levels of exudate
Caution/contraindications (when not to use the dressing, patient groups to avoid etc.)
Known product or component sensitivity
Rationale for inclusion in formulary
Used to reduce adherence to wound bed. Most cost effective non adherent dressing.
Dressing impregnated with neutraltriglycerides to prevent penetration of granulation tissue.
Petroleum free. |
A5.01.01 |
Atrauman® |
Preferred local option Type of wound product is suitable for For flat granulating and epithelising wound for non to heavy exudate where adherence may occur. To be used as a primary dressing with a secondary for absorption. Duration dressing remains on wound before changing Up to 7 days Frequency of dressing change 1-7 days, depending on levels of exudate Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Known product or component sensitivity Rationale for inclusion in formulary Used to reduce adherence to wound bed. Most cost effective non adherent dressing. Dressing impregnated with neutraltriglycerides to prevent penetration of granulation tissue. Petroleum free. |
A5.03.03 |
Atrauman® Ag |
Specialist recommendation only Non adherent Primary Dressing containing metallic silver Type of wound product is suitable for For clinically infected shallow, granulating wounds with low exudate. To be used as a primary dressing with a secondary for absorption. Duration dressing remains on wound before changing Up to 7 days Frequency of dressing change 1-7 days, depending on levels of exudate Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Known product or component sensitivity Must be removed prior to x-ray, ultrasound, diathermy and MRI Rationale for inclusion in formulary Used to reduce adherence to wound bed with clinical signs of infection Most cost effective non adherent dressing containing silver. Dressing impregnated with neutral triglycerides to prevent penetration of granulation tissue. Petroleum free. |
02.06 |
Atropine |
|
15.01.03 |
Atropine |
For Myaesthenia Gravis only |
15.01.03 |
Atropine |
HOSPITAL ONLY |
15.01.03 |
Atropine minijet® |
HOSPITAL ONLY |
15.01.03 |
Atropine |
|
21 |
Atropine 1% |
- Oral use for drooling/secretions in neurological disease.
|
11.05 |
Atropine Sulphate |
|
11.05 |
Atropine Sulphate |
|
15.01.03 |
Atropine sulphate |
|
11.05 |
Atropine Sulphate Single Use |
Branded preservative free drops i.e. single use drops should be prescribed where available as manufactured 'specials' cost significantly more and don't have a product license
Restricted to patients needing preservative free On specialist ophthalmologist recommendation
Used by glaucoma surgeons for neovascular glaucoma |
08.01.05 |
Autologous anti-CD19-transduced CD3+ cells |
In line with NICE |
09.01.04 |
Avatrombopag Doptelet® |
In line with NICE |
13.02.01 |
Aveeno cream® |
£££- Paediatrics only
£££- Recommended by specialist for oncology use only
|
08.02.03 |
Avelumab Bavencio® |
In line with NICE
Hospital ONLY |
10.01.03 |
Avelumab Bavencio® |
In line with NICE |
07.04.05 |
Aviptadil 25 micrograms/Phentolamine 2mg Invicorp® |
•Approved on formulary December 2017 •Specialist initiation •3rd line after oral PDE-5 inhibitors failed and patient not responding to or intolerant of alprostadil •To be reviewed within 12 months to assess alprostadil supply issues and patent expiry |
08.02.04 |
Axicabtagene ciloleucel Yescarta® |
In line with NICE |
09.04.02 |
Aymes ActaSolve High Energy Powder sachets |
- Energy 195Kcal/ 100ml, Protein 4.1g/ 100ml
- ACBS approved: for adults with short-bowel syndrome, intractable malabsorption, pre-operative preparation of undernourished patients, inflammatory bowel disease, total gastrectomy, bowel fistulae and disease-related malnutrition.
|
09.04.02 |
AYMES ActaSolve Smoothie Powder sachets |
- Powder 66 g reconstituted with 150ml water provides: protein 10.7 g, carbohydrate 41.5 g, fat 9.7 g, energy 1249 kJ (297 kcal)
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula except dysphagia.
|
09.04 |
Aymes Shake |
Patient to be assessed using the malnutrition universal screening tool (MUST) before initiation of nutritional supplements. |
09.04 |
Aymes® Complete |
- 1.5 kcal/mL and 5g (or more) protein/100 mL
- Second line choice for 200ml ready-made. If powder is not tolerated or contraindicated
Patient to be assessed using the malnutrition universal screening tool (MUST) before initiation of nutritional supplements. |
09.04 |
Aymes® creme |
Dessert style
Patient to be assessed using the malnutrition universal screening tool (MUST) before initiation of nutritional supplements
|
09.04 |
Aymes® Savoury |
- More than 1kcal/ml and less than 5g protein/100mL
- In line with food first
- Not suitable for CKD 4-5, renal pts
- Not suitable for lactose intolerance
- Not suitable for bile acid malabsorption or fat maldigestion associated with biliary diseases/conditions
- To be made up with whole milk
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula . Use with caution in child 1–6 years
|
08.01.03 |
Azacitidine Vidaza® |
Commissioned by NHSE Hospital only |
01.05.03 |
Azathioprine |
Walsall
Amber Initiation Walsall only
Wolverhampton
Amber Shared Care Wolverhampton only
ESCA Azathioprine (Wolverhampton only)
Sandwell
Amber Shared Care Sandwell only
For use in Inflammatory Bowel Disease (IBD) as per effective shared care agreement
ESCA Azathioprine (Sandwell only)
Dudley
Amber Shared Care Dudley only
ESCA Azathioprine (Dudley only) |
03.12 |
Azathioprine |
Sandwell
Amber Shared Care Supported by an ESCA
ESCA Sandwell only
Dudley
Amber Shared Care Supported by an ESCA
ESCA Dudley only
Walsall
Not on formulary
Wolverhampton
Amber Shared Care Supported by an ESCA
ESCA for Wolverhampton only |
04.13 |
Azathioprine |
Specialist use only for neurological conditions |
08.02.01 |
Azathioprine |
Commissioned by NHSE for post transplant patients. Prescribing to remain with the specialist for this patient group Injection-hospital only Tablets/suspension for oncology/haematology |
09.01.03 |
Azathioprine |
For the treatment of Auto immune haemolytic anaemia
Supported by an ESCA |
10.01.03 |
Azathioprine |
Cytotoxic - do not crush or disperse in water. Supported by an ESCA |
13.05.03 |
Azathioprine Dermatology |
Supported by an ESCA |
13.06.01 |
Azelaic acid 15% Finacea® |
|
13.06.01 |
Azelaic Acid 20% cream Skinoren® |
Use 2nd line to retinoids if benzoyl peroxide is not tolerated |
12.02.01 |
Azelastine and fluticasone Dymista |
Third line option for adults and children over 12 years with moderate to severe allergic rhinitis who have failed to respond to a steroid nasal spray with the addition of an oral antihistamine. Follow treatment algorithm |
11.04.02 |
Azelastine hydrochloride Optilast® |
|
05.01.05 |
Azithromycin Azyter® |
|
05.01.05 |
Azithromycin |
Tablets/ suspension -For Sexual Health (GUM Clinics) in Primary care only
IV-For Respiratory Indications |
11.03.01 |
Azithromycin Azyter® |
First line for ophthalmic chlamydia |
05.01.02.03 |
Aztreonam |
Hospital use only under microbiological advice |
10.02.02 |
Baclofen |
Hospital use only |
10.02.02 |
Baclofen |
|
21 |
Baclofen |
- Hiccup
- Off-label use according to West Midlands Palliative Care Physicians Guidelines.
|
13.02.01 |
Balneum Plus® |
Contains urea 5%, lauromacrogols 3%
Over the counter preparation suitable for self-care/purchase if appropriate |
13.02.01.01 |
Balneum Plus® Bath Additive |
Over the counter preparation suitable for self-care/purchase if appropriate |
05.03.01 |
Baloxavir marboxil |
|
01.05.01 |
Balsalazide Sodium Colazide ® |
Sandwell
Amber Recommended -Sandwell only
Walsall
Green -Walsall only
Wolverhampton
Amber Specialist Initiation continued in Primary Care -Wolverhampton only
Dudley
Amber SC-Dudley only
ESCA Balsalazide (Dudley only) |
10.01.03 |
Baricitinib Olumiant® |
In line with NICE |
13.05.03 |
Baricitinib Olumiant® |
In line with NICE |
09.04 |
Basecal® |
- Over one year of age. Metabolic disorder pts
- Also these are the only protein free (containing fat, carbohydrate, vitamins and minerals) powders aimed at children ≥1-year-old and adults with inborn errors of protein metabolism (particularly patients with urea cycle disorders and organic acidaemias). Basecal 100 and Basecal 200 are commonly added as an energy source in low protein module tube feeds. The dose will depend on energy requirements and tolerance to natural protein. It is commonly used in combination with a controlled amount of natural protein e.g. measured dose of standard enteral tube feed. It will help meet essential energy and nutrient requirements. The dose and type of product should always be advised by the specialist dietitian according to the needs of the patient
|
08.02.02 |
Basiliximab Simulect® |
Commissioned by NHSE for renal transplant patients Hospital only |
14.04 |
BCG intradermal vaccine |
|
14.04 |
BCG vaccine diagnostic agent |
|
03.02 |
Beclometasone and formoterol Fostair® NEXThaler® |
How to use a NEXThaler Inhaler |
03.02 |
Beclometasone and formoterol Fostair® |
Licensed for both asthma and COPD Asthma - use lowest effective dose. Consider step down at each review. Consider switch if appropriate
Alternative to Seretide Evohaler / Seretide 250 Accuhaler
Note: when switching patients already using Beclometasone 250mcg CFC inhaler (e.g. Clenil), Fostair 100/6 can be prescribed and dose adjusted according to response
How to use a Metered Dose Inhaler How to use a Metered Dose Inhaler with a Large Volume Spacer Device How to use a Metered Dose Inhaler with a Small Volume Spacer Device
|
03.02 |
Beclometasone Dipropionate Clenil Modulite® |
May 2020 - see Clenil® Modulite® 100mcg (beclometasone): release of batch specific variation
How to use a Metered Dose Inhaler How to use a Metered Dose Inhaler with a Large Volume Spacer Device How to use a Metered Dose Inhaler with a Small Volume Spacer Device
|
12.02.01 |
Beclometasone Dipropionate |
|
03.02.03 |
Beclometasone/formoterol/glycopyrronium Trimbow NEXThaler® |
How to use a NEXThaler Inhaler |
03.02.03 |
Beclometasone/formoterol/glycopyrronium |
|
03.02.03 |
Beclometasone/formoterol/glycopyrronium Trimbow 172/5/9 ® |
Note:
-Two strengths of Trimbow available
* Trimbow 172/5/9
* Trimbow 87/5/9
-Trimbow 172/5/9 is licensed for Asthma maintenance therapy only |
03.02.03 |
Beclometasone/formoterol/glycopyrronium Trimbow 87/5/9 ® |
Trimbow 87/5/9 is licensed for Moderate-to-severe chronic obstructive pulmonary disease and Asthma maintenance therapy |
05.01.07 |
Bedaquiline |
Hospital use only under microbiological and Tuberculosis specialist advice |
03.04 |
Bee and Wasp Allergen Extracts Pharmalgen® |
|
03.04.02 |
Bee venom extract |
|
08.02.02 |
Belatacept Nulojix® |
Not routinely commissioned by NHSE. NICE TA in progress
Hospital only |
08.01.05 |
Belimumab Benlysta® |
In line with NICE |
02.12 |
Bempedoic acid |
|
02.12 |
Bempedoic acid with ezetimibe Nustendi® |
In line with NICE
|
08.01.01 |
Bendamustine |
Commissioned by NHSE |
02.02.01 |
Bendroflumethiazide |
2.5mg dose (higher doses are not indicated in hypertension) |
A5.02.04 |
BeneHold TASA® |
Approved by APC April 2019
Hydrocolloid Range with film border
Type of wound product is suitable for Lightly to moderately exuding wounds
Duration dressing remains on wound before changing Up to 7 days
Frequency of dressing change Only when necessary - up to 7 days
Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Do not use on third-degree burns. Should not be used on individuals who are sensitive to or have had an allergic reaction to the dressing or its components
Rationale for inclusion in formulary Reduced dressing changes. More cost effective. Reduce use of more expensive foam dressings |
03.04.02 |
Benralizumab |
|
03.14 |
Benralizumab Fasenra® |
|
15.02 |
Benzocaine 20% Ultracare® Bubble Gum |
Hospital only |
13.06.01 |
Benzoyl Peroxide |
Starting with 2.5% and increasing to 5 % or 10%. Titrating the strength reduces irritancy with Benzoyl Peroxide . May bleach clothing. Avoid in pregnancy. |
13.06.01 |
Benzoyl Peroxide 3% with Clindamycin 1% Duac® Once Daily |
|
13.06.01 |
Benzoyl Peroxide 5% with Clindamycin 1% Duac® Once Daily |
Maybe more effective and aid compliance compared to twice daily products. |
12.03.01 |
Benzydamine 0.15% |
|
01.07 |
Benzyl benzoate with bismuth oxide, bismuth subgallate, hydrocortisone acetate, peru balsam and zinc oxide |
|
05.01.01.01 |
Benzylpenicillin Benzathine |
For use by GUM & STD services only |
05.01.01.01 |
Benzylpenicillin Sodium |
Injectable for suspected Meningitis in Primary Care
In secondary care for related indications |
03.04.03 |
Berotralstat Orladeyo® |
Use in line with NICE TA |
04.06 |
Betahistine Dihydrochloride |
Ménière's disease, vertigo |
09.08.01 |
Betaine Cystadane® |
NHSE commissioned |
06.03.02 |
Betamethasone |
|
11.04.01 |
Betamethasone |
For use on the advice of a specialist |
11.04.01 |
Betamethasone |
For use on the advice of a specialist |
12.01.01 |
Betamethasone ear drops |
|
13.04 |
Betamethasone (as Dipropionate) 0.05% with Salicylic Acid Diprosalic® |
Potency - Potent
Ointment contains 3% salicylic acid Scalp application contains 2% salicylic acid |
13.04 |
Betamethasone (as Valerate) 0.025% Betnovate-RD® |
Potency - Moderate Cream Ointment |
13.04 |
Betamethasone (as Valerate) 0.1% Betnovate® |
Potency - Potent Cream Ointment Scalp application |
13.04 |
Betamethasone (as Valerate) 0.1% with Fucidic Acid 2% Fucibet® |
Potency - Potent
Restricted to use in inflammatory conditions associated with an infection with confirmed susceptibility to the antimicrobial component. Use for short periods - typically no more than one week |
12.01.01 |
Betamethasone 0.1% with Neomycin 0.5% ear drops |
|
11.04.01 |
Betamethasone 0.1% with Neomycin 0.5% eye drops |
Short term use only |
13.04 |
Betamethasone Dipropionate 0.064% with Clotrimazole 1% Lotriderm® |
Potency - Potent
Specialist initiation by Dermatology only Restricted to use in inflammatory conditions associated with an infection with confirmed susceptibility to the antimicrobial component. Use for short periods - typically no more than one week |
12.02.01 |
Betamethasone Sodium Phosphate |
|
13.04 |
Betamethasone valerate medicated plaster Betesil® |
Potency - Potent
Maximum treatment period 30 days
Available as a box of 4, size 7.5cm x 10cm medicated plaster |
09.04 |
Betaquick® |
- High-energy supplements: fat
- 21% MCT emulsion, used orally and in cooking as an energy source for children and adults on a ketogenic diet
|
11.06 |
Betaxolol |
On Specialist Ophthalmologist Recommendation |
11.06 |
Betaxolol |
On Specialist Ophthalmologist Recommendation |
11.06 |
Betaxolol Unit Dose |
On Specialist Ophthalmologist Recommendation |
07.04.01 |
Bethanechol Chloride Myotonine® |
For Specialist / Hospital Use Only |
08.01.05 |
Bevacizumab |
Funding available through Cancer Drugs Fund (CDF) for indications listed in CDF list |
11.08.02 |
Bevacizumab intravitreal injection Avastin® |
|
08.01.05 |
Bexarotene |
|
02.12 |
Bezafibrate |
Immediate release formulation
Modified release formulation |
A5.02.05 |
Biatain® |
PODIATRY ONLY Polyurethane foam dressing with bevelled edges Type of wound product is suitable for Moderately exuding wounds with signs of granulation, epithelialisation or slough. Can be used as primary or secondary Duration dressing remains on wound before changing 1-7 days Frequency of dressing change Up to 7 days dependent on exudate levels Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Do not use with oxidising solutions such as hydrogen peroxide Full thickness burns Surgical implantations Rationale for inclusion in formulary Simple to use on the foot and digits Can be cut to shape |
08.03.04.02 |
Bicalutamide |
|
05.03.01 |
Bictegravir with emtricitabine and tenofovir alafenamide Biktarvy® |
|
11.06 |
Bimatoprost |
2nd line
On Specialist Ophthalmologist Recommendation |
11.06 |
Bimatoprost with Timolol Ganfort® |
On Specialist Ophthalmologist Recommendation
|
13.05.02 |
Bimekizumab Bimzelx® |
Use in line with NICE |
12.03.05 |
Biotene Oralbalance® |
Approved for ACBS conditions i.e. patients suffering from xerostomia (dry mouth) as a result of having or having undergone radiotherapy or sicca syndrome Palliative care Dental Practitioners |
06.01.01.02 |
Biphasic Insulin Aspart |
BRANDS
- NovoMix 30 FlexPen
- NovoMix 30 Penfill
|
06.01.01.02 |
Biphasic Insulin Lispro |
BRANDS
- Humalog Mix25
- Humalog Mix25 KwikPen
- Humalog Mix50
- Humalog Mix50 KwikPen
|
06.01.01.02 |
Biphasic Isophane Insulin Insuman Comb® |
Insuman comb 25
Insuman comb 50
|
06.01.01.02 |
Biphasic Isophane Insulin |
BRANDS
- Humulin M3
- Humulin M3 KwikPen
|
01.06.02 |
Bisacodyl |
5mg E/C tablets
10mg Suppository |
12.04 |
Bismuth Iodine Paraffin Paste BIPP® |
|
12.04 |
Bismuth Subnitrate and Iodoform Paste for Gauze |
|
01.03.03 |
Bismuth subsalicylate Pepto Bismol® |
|
02.04 |
Bisoprolol |
|
02.06 |
Bivalirudin Angiox® |
|
02.08 |
Bivalirudin Angiox® |
|
08.01.02 |
Bleomycin |
Commissioned by NHSE Hospital only |
13.07 |
Bleomycin intra-lesiona |
|
08.02.03 |
Blinatumomab Blincyto® |
In line with NICE |
12.03.01 |
Bonjela Junior® |
From 3 month of age |
08.01.05 |
Bortezomib Velcade® |
In line with NICE |
02.05.01 |
Bosentan |
|
08.01.05 |
Bosutinib Bosulif® |
In line with NICE Hospital only-NHSE commissioned |
20 |
Botulinium toxin 100 units for achalasia |
For use by endoscopy speciality at Sandwell and West Birmingham NHS Trust |
01.02 |
Botulinium Toxin A |
|
04.12 |
Botulinum neurotoxin type A Xeomin® |
In line with NICE |
04.07.04.02 |
Botulinum Toxin Type A |
For hospital use only
Use in line with NICE |
13.12 |
Botulinum toxin type A |
For hyperhidrosis (commissioning discussion to take place). |
14.04 |
Botulism antitoxin |
Hospital only |
09.04.01 |
Bread |
Low-protein foods
These products are not available to purchase in supermarkets
They are important to provide essential energy and variety to aid the palatability of low protein diets. They are important for good metabolic control of the patient. Poor access to these products could lead to poor dietary adherence. This will cause poor metabolic control which may lead to irreversible brain damage
The NSPKU guidelines for prescription of low protein foods can be used for other amino acid disorderssuch as MSUD, homocystinuria, tyrosinaemia and pyridoxine response epilepsy
Protein free - necessary for children and adults with inborn errors of protein metabolism who do not tolerate very little natural protein
The specialist dietician will make individual reccomendations based on diagnosis,protein recommendations, weight etc.
- Essential protein-free basic products. Necessary for children and adults with inborn errors of protein metabolism who tolerate very little natural protein. 1 slice ordinary bread = 4g protein and is not allowed in low protein diets
|
08.01.05 |
Brentuximab vedotin Adcetris® |
In line with NICE |
08.01.05 |
Brigatinib Alunbrig® |
In line with NICE
Providers - NHS hospital trusts |
13.06 |
Brimonidine 3mg/g Mirvaso® |
For facial erythema in rosacea |
11.06 |
Brimonidine Tartrate |
On Specialist Ophthalmologist Recommendation |
11.06 |
Brimonidine Tartrate 0.2% with Timolol 0.5% Combigan® |
Avoid in patients receiving verapamil and in those with bradycardia, heart block, uncontrolled heart failure, asthma or COPD On Specialist Ophthalmologist Recommendation |
11.06 |
Brinzolamide 1% with Timolol 0.5% Azarga® |
On Specialist Ophthalmologist Recommendation |
11.06 |
Brinzolamide 10mg/ml |
On Specialist Ophthalmologist Recommendation |
11.06 |
Brinzolamide 10mg/ml and brimonidine tartrate 2mg/ml Simbrinza® |
On Specialist Ophthalmologist Recommendation
Third line option, after prostaglandin analogues (1st line) and beta-blocker/ prostaglandin analogue plus beta-blocker (2nd line)
For patients in whom monotherapy provides insufficient IOP reduction. |
11.06 |
Brinzolamide 10mg/ml with Timolol 5mg/ml |
2nd/3rd line
On Specilaist Ophthalmologist Recommendation |
04.08.01 |
Brivaracetam Briviact® |
•Initiation by Tertiary Epilepsy Specialist only. •For adjunctive therapy in the treatment of partial-onset seizures with or without secondary generalisation in adult and adolescent patients from 16 years of age with severe refractory epilepsy warranting tertiary specialist input for patients who have tried three or more AEDs. The patient has used levetiracetam and has documentation of intolerance and patient is using a third line agent (perampanel, zonisamide, lacosamide, eslicarbazepine) which would be replaced by brivaracetam
Supported by an ESCA
|
04.08.01 |
Brivaracetam Briviact ® |
|
10.01.03 |
Brodalumab Kyntheum® |
In line with NICE |
13.05.02 |
Brodalumab Kyntheum® |
Hospital use only
In line with NICE |
11.08.02 |
Brolucizumab Beovu® |
In line with NICE |
06.07 |
Bromocriptine |
|
01.05.02 |
Budesonide Jorveza® |
In line with NICE |
01.05.02 |
Budesonide Cortiment® |
|
01.05.02 |
Budesonide Entocort® |
|
01.05.02 |
Budesonide Budenofalk® |
- Rectal foam Enema
- Gastro-resistant Capsules
- Granules
|
03.02 |
Budesonide Easyhaler® |
How to use an Easyhaler Inhaler |
03.02 |
Budesonide Pulmicort Turbohaler® |
How to use a Turbohaler Inhaler
|
03.02 |
Budesonide |
|
03.02 |
Budesonide Pulmicort Respules® |
|
03.02 |
Budesonide |
- Dry powder Inhaler
- Easyhaler
- Prescribe by brand
How to use a Turbohaler Inhaler
How to use an Easyhaler Inhaler |
03.02 |
Budesonide and Formoterol Fobumix Easyhaler® |
How to use an Easyhaler Inhaler |
03.02 |
Budesonide and Formoterol 100/6 Symbicort Turbohaler® |
- For treatment of asthma only
- Use lowest effective dose. Consider step down at each review.
- Prescribe by brand to ensure patient receives the device they are used to.
How to use a Turbohaler Inhaler
|
03.02 |
Budesonide and Formoterol 200/6 Symbicort Turbohaler® |
For Asthma, maintenance and reliever therapy in adults and adolescents (12 years and older) with mild asthma
How to use a Turbohaler Inhaler
|
02.02.02 |
Bumetanide |
|
15.02 |
Bupivacaine |
Hospital only |
15.02 |
Bupivacaine and Adrenaline |
Hospital only |
15.02 |
Bupivacaine hydrochloride Marcain® |
Hospital only |
15.02 |
Bupivacaine Hydrochloride with Glucose Marcain Heavy® |
Hospital only |
15.02 |
Bupivacaine with Fentanyl |
Hospital only |
04.10.03 |
Buprenorphine |
For use under specialist addiction services |
21 |
Buprenorphine |
- Recommend 7-day patch.
- With specialist recommendation, first line choice if renal failure and patient requires a strong opioid.
|
04.07.02 |
Buprenorphine Patch |
ONCE A WEEK patch (7-day patch)
For specialist initiation: specialist pain clinics, palliative care and for patients with swallowing difficulties
Patches should be prescribed by BRAND
|
04.07.02 |
Buprenorphine Patch Transtec® |
TWICE WEEKLY patch
For specialist initiation: specialist pain clinics, palliative care and for patients with swallowing difficulties
Patches should be prescribed by BRAND
|
04.07.02 |
Buprenorphine sublingual tablet |
Specialist use only
For use in opioid dependence, see section 4.10.3
|
04.03.04 |
Bupropion |
Hospital use only |
04.10.02 |
Bupropion Hydrochloride Zyban® |
|
08.03.04.02 |
Buserelin |
Hospital only
Listed in Chapter 6 for other indications
|
04.01.02 |
Buspirone Hydrochloride |
£££££
Second line |
08.01.01 |
Busulfan |
Commissioned by NHSE Concentrate for infusion-hospital only |
03.04.03 |
C1- esterase Inhibitor Berinert® |
|
03.04.03 |
C1- esterase Inhibitor Cinryze® |
|
08.01.05 |
Cabazitaxel Jevtana® |
In line with NICE |
06.07 |
Cabergoline |
Amber Recommended - Cabaser
Amber Recommended - Dostinex |
05.03.01 |
Cabotegravir Vocabria® |
In line with NICE |
08.01.05 |
Cabozantinib Cabometyx® |
In line with NICE |
13.14.03 |
Cade oil 12% w/w & salicylic acid 6% w/w in emulsifying ointment |
|
03.05.01 |
Caffeine citrate |
|
09.04.01 |
Cake, biscuits and snacks |
Low-protein foods
These products are not available to purchase in supermarkets
They are important to provide essential energy and variety to aid the palatability of low protein diets. They are important for good metabolic control of the patient. Poor access to these products could lead to poor dietary adherence. This will cause poor metabolic control which may lead to irreversible brain damage
The NSPKU guidelines for prescription of low protein foods can be used for other amino acid disorderssuch as MSUD, homocystinuria, tyrosinaemia and pyridoxine response epilepsy
Protein free - necessary for children and adults with inborn errors of protein metabolism who do not tolerate very little natural protein
The specialist dietician will make individual reccomendations based on diagnosis,protein recommendations, weight etc.
- Important protein-free foods to provide important energy, assist dietary adherence and provide variety when natural protein tolerance is very limited. Necessary for children and adults with inborn errors of protein metabolism who tolerate very little natural protein
|
13.03 |
Calamine aqueous cream |
Over the counter preparation suitable for self-care/purchase if appropriate |
13.03 |
Calamine lotion |
Over the counter preparation suitable for self-care/purchase if appropriate |
09.05.01.01 |
Calcichew® (calcium salts) |
|
13.05.02 |
Calcipotriol 50mcg/g |
Ointment Scalp solution £££ |
13.05.02 |
Calcipotriol 50mcg/g with betamethasone 0.5mg/g Enstilar® |
•The recommended treatment period is 4 weeks •Maximum 15g per day •Excipients include liquid paraffin and butane Extremely flammable aerosol |
13.05.02 |
Calcipotriol 50micrograms/g with Betamethasone 0.05% Dovobet® |
•4 weeks therapy then assess Maximum 15g per day or 100g per week. Step down to calcipotrol oint as per NICE CG153 |
13.05.02 |
Calcipotriol 50micrograms/g with betamethasone 0.05% Dovobet® |
Scalp psoriasis: usual duration of treatment is 4 weeks Mild to moderate plaque psoriasis, apply once daily to max. 30% of body surface (max. 15 g daily) for 8 weeks |
06.06 |
CALCITONIN |
CALCITONIN (SALMON)/SALCATONIN - Red
CALCITONIN SALMON/ CALCITONIN - Red |
06.06.01 |
Calcitonin (salmon) / Salcatonin |
Injection
Nasal spray
For hospital use only |
06.06 |
Calcitriol |
|
09.06.04 |
Calcitriol |
|
13.05.02 |
Calcitriol 3micrograms/g Silkis® |
Specialist recommendation only. For delicate areas, face & flexures. |
09.06.04 |
Calcium and vitamin D preparations |
Please follow Optimise Rx for most cost effective brand |
09.05.01.01 |
Calcium Chloride (parenteral) |
Hospital only |
09.05.01.01 |
Calcium Gluconate |
Hospital only |
08.01 |
Calcium Levofolinate Isovorin® |
For hospital use only in chemotherapy induced mucositis and myelosuppression |
09.05.02.02 |
Calcium salts |
Specialist Recomendation |
09.04 |
Calogen® |
- High-energy supplements: fat
- Used as a source of LCT, as an energy supplement and additive to feed to enhance energy density
- Does not contain protein
- Also this is the only LCT fat source that can be used as a fat energy source in patients with organic acidaemias e.g. propionic acidaemia and methyl malonic acidaemia and urea cycle disorders. It may also be used as part of a modular feed or protein-free energy source. The dose and type of product should always be advised by the specialist dietitian according to the needs of the patient
- Disease-related malnutrition, malabsorption states, or other conditions requiring fortification with a high fat (or fat and carbohydrate) supplement. Liquid supplements
|
06.01.02.03 |
Canagliflozin |
For treating Type 2 diabetes in line with NICE, and chronic kidney disease.
Do not use SGLT2-inhibitors in patients with T1DM, regardless of CKD and/or heart failure status due to risk of DKA (diabetic ketoacidosis) |
06.01.02.03 |
Canagliflozin/Metformin Vokanamet® |
|
02.05.05.02 |
Candesartan cilexetil |
|
02.06 |
Cangrelor |
|
04.08.01 |
Cannabidiol Epidyolex® |
In line with NICE |
13.09 |
Capasal® |
Over the counter preparation suitable for self-care/purchase if appropriate |
08.01.03 |
Capecitabine |
Commissioned by NHSE |
12.03.01 |
Caphosol® |
Oncology and Haematology use only |
09.01.04 |
Caplacizumab Cablivi® |
In ine with NICE
Providers are NHS Specialist Centres
|
05.01.09 |
Capreomycin |
Hospital use only under Microbiological/Tuberculosis advice only |
04.07.03 |
Capsaicin |
For local neuropthic pain
ONLY strength licensed for post-herpetic neualgia and diabetic peripheral polyneuropathy
For other strength, see section 10.3.2
Please note that capsaicin 8% patches are non-formulary |
06.01.02.03 |
Capsaicin |
|
10.03.02 |
Capsaicin cream 0.025% |
Tier 2
Topical capsaicin 0.025% cream(Zacin) should be considered as an adjunct to core treatments for knee or hand osteoarthritis. [NICE 2008] |
10.03.02 |
Capsaicin cream 0.075% |
See Chapter 7.4.3 for neuropathic pain
|
02.05.05.01 |
Captopril |
For existing patients and Paediatric use |
04.02.03 |
Carbamazepine |
On specialist advice
|
04.07.03 |
Carbamazepine |
For the treatment of trigeminal neuralgia only
Baseline LFTs,FBC and U & Es- then 6 monthly |
04.08.01 |
Carbamazepine |
Tablets
M/R tablets
SF liquid
Suppositories
Tegretol is the preferred brand for new patients however please ensure that existing patients are maintained on a specific manufacturers brand
MHRA Advice Patients being treated for epilepsy should be maintained on a specific manufacturer's product |
06.02.02 |
Carbimazole |
Counselling: warn patient to tell doctor immediately if sore throat, mouth ulcers, bruising, fever, malaise or non-specific illness develops
|
03.07 |
Carbocisteine |
Prescribe as 375 mg caps. Avoid prescribing 750 mg caps
|
A5.02.08 |
CarboFlex® |
Specialist recommendation only Preferred local option Odour absorbent wound contact dressings containing activated charcoal Type of wound product is suitable for For the management of moderate to heavily exuding malodorous wounds including fungating Duration dressing remains on wound before changing Up to 7 days Frequency of dressing change As exudate level determines Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Known sensitivity to the dressing or its components As soon as CarboFlex® becomes contaminated with exudate, odour control diminishes The underlying cause of wound odour should be identified prior to commencement of product Rationale for inclusion in formulary CarboFlex® is a layered dressing to provide higher levels of fluid handling On shallow or cavity wounds with moderate to heavy levels of exudate |
11.08.01 |
Carbomers Clinitas Gel® |
Clinitas Gel does not have benzalkonium chloride (BAK) as a preservative. It is preserved with cetrimide. |
07.01.01 |
Carboprost Hemabate® |
For Specialist/ Hospital Use Only |
09.04 |
Carbzero® |
- High-energy supplements: fat
- 20% LCT emulsion, used as an energy source for children and adults on a ketogenic diet, may be used orally or in cooking
- For use in ketogenic diets. Long chain triglyceride liquid emulsion used as a milk replacement (when diluted) for some patients with PKU on very low protein diets who cannot tolerate other low protein milk replacements. It will help meet essential energy requirements. The dose and type of product should always be advised by the specialist dietitian according to the needs of the patient
|
09.04 |
Carbzero® |
- High-energy supplements: fat
- 20% LCT emulsion, used as an energy source for children and adults on a ketogenic diet, may be used orally or in cooking
- For use in ketogenic diets. Long chain triglyceride liquid emulsion used as a milk replacement (when diluted) for some patients with PKU on very low protein diets who cannot tolerate other low protein milk replacements. It will help meet essential energy requirements. The dose and type of product should always be advised by the specialist dietitian according to the needs of the patient
|
08.01.05 |
Carfilzomib Kyprolis® |
In line with NICE |
11.08.01 |
Carmellose 0.5% SDU |
Reserve single use eye drops for patients who have known hypersensitivity to preservatives |
11.08.01 |
Carmellose 1% multi (Moorfields) |
|
08.01.01 |
Carmustine Gliadel® |
Commissioned by NHSE Hospital only |
09.09 |
Carobel, Instant® |
- Used as a feed thickener for infants with GORD and in children with swallowing issues who require thickened fluids
- Used in dysphagic patients or those requiring thickened feeds
- For thickening feeds in the treatment of vomiting
|
02.04 |
Carvedilol |
|
05.02.04 |
Caspofungin |
|
05.01.02.01 |
Cefalexin |
|
05.01.02.01 |
Cefazolin |
Hospital use only under microbiological advice |
05.01.02.01 |
Cefepime |
Hospital use only under microbiological advice |
05.01.02.01 |
Cefiderocol Fetcroja® |
Hospital use only under microbiological advice. Blueteq applications required |
05.01.02.01 |
Cefixime Suprax® |
Hospital use only under microbiological advice |
05.01.02.01 |
Cefotaxime |
Hospital use only under microbiological advice |
03.13 |
Ceftazidime |
Hospital only |
05.01.02.01 |
Ceftazidime |
Hospital use only under microbiological advice
Under OPAT sheme |
05.01.02.01 |
Ceftazidime with avibactam |
Hospital use only under microbiological advice |
05.01.02.01 |
Ceftobiprole Zevtera® |
Hospital use only under microbiological advice |
05.01.02.01 |
Ceftolozane with tazobactam |
Hospital use only under microbiological advice |
05.01.02.01 |
Ceftriaxone |
Injectable - Green under OPAT scheme in Primary Care
Secondary care - for specific indications |
03.13 |
Cefuroxime |
Hospital only |
05.01.02.01 |
Cefuroxime Oral and IV |
|
11.03.01 |
Cefuroxime |
Hospital only |
11.08.02 |
Cefuroxime |
Hospital only |
10.01.01 |
Celecoxib Celebrex® |
COX-2 inhibitor Not routinely recommended as first or second-line treatment choice. Consider the use of a standard NSAID and a PPI (choose the agent with the lowest acquisition cost) ahead of a COX-2 inhibitor. CVD risk assessment Supported by RICaD-in development |
A5.08.07 |
Cellona |
Preferred local option Specialist recommendation only Sub compression wadding bandage to pad and shape a limb prior to compression therapy Type of wound product is suitable for Provides padding for larger limbs under compression. Duration dressing remains on wound before changing Up to 7 days Frequency of dressing change Daily up to weekly dependant on exudate and oedema management. Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Advised not to apply directly to skin as can cause irritation. Rationale for inclusion in formulary Cost effective for use in larger quantities when used in lymphoedema management. |
08.01.05 |
Cemiplimab Libtayo® |
In line with NICE |
08.01.05 |
Cenegermin Oxervate® |
In line with NICE |
04.08.01 |
Cenobamate Ontozry® |
In line with NICE |
09.04.01 |
Cereals |
Low-protein foods
These products are not available to purchase in supermarkets
They are important to provide essential energy and variety to aid the palatability of low protein diets. They are important for good metabolic control of the patient. Poor access to these products could lead to poor dietary adherence. This will cause poor metabolic control which may lead to irreversible brain damage
The NSPKU guidelines for prescription of low protein foods can be used for other amino acid disorderssuch as MSUD, homocystinuria, tyrosinaemia and pyridoxine response epilepsy
Protein free - necessary for children and adults with inborn errors of protein metabolism who do not tolerate very little natural protein
The specialist dietician will make individual reccomendations based on diagnosis,protein recommendations, weight etc.
- Essential protein-free basic products. Necessary for children and adults with inborn errors of protein metabolism who tolerate very little natural protein. 2 regular Weetabix = 4.5g protein and this protein amount is more than the amount of protein that may be tolerated
|
08.01.05 |
Ceritinib Zykadia® |
In line with NICE |
10.01.03 |
Certolizumab Pegol Cimzia® |
Specialist/hospital use only
Available via Home Care
|
12.01.03 |
Cerumol® |
|
03.04.01 |
Cetirizine Hydrochloride |
OTC preparation suitable for self-care/purchase if appropriate
- Capsules
- Oral Solution- Green for children and those unable to swallow
|
A5.13 |
Cetraben pump cream |
Emollient containing white soft paraffin and light liquid paraffin Type of wound product is suitable for For inflamed, dry, chapped skin Frequency of use Daily Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Allergy or hypersensitivity to any of the ingredients Rationale for inclusion in formulary Treatment of dry skin Dermatology approved |
13.02.01 |
Cetraben® |
More greasy option
Over the counter preparation suitable for self-care/purchase if appropriate |
08.01.05 |
Cetuximab Erbitux® |
In line with NICE |
04.01.01 |
Chloral Hydrate 500mg in 5mL |
For hospital use only.
Unlicensed special.
|
08.01.01 |
Chlorambucil |
Commissioned by NHSE |
05.01.07 |
Chloramphenicol |
For specialist use only |
11.03.01 |
Chloramphenicol |
- 0.5% eye drops - First line
- 0.5% Minims (SDU) for patients who require preservative free
- 1% eye ointment
|
12.01.01 |
Chloramphenicol |
Only with positive culture/sensitivity data |
04.01.02 |
Chlordiazepoxide |
Adjunct in acute alcohol withdrawal |
04.10.01 |
Chlordiazepoxide |
Adjunct in acute alcohol withdrawal |
13.11.02 |
Chlorhexidine gluconate 0.015% with cetrimide 0.15% Tisept® |
|
13.11.02 |
Chlorhexidine gluconate 0.05% Unisept® |
|
12.03.04 |
Chlorhexidine gluconate 0.2% |
|
12.03.04 |
Chlorhexidine gluconate 1% |
|
13.11.02 |
Chlorhexidine gluconate 4% |
|
13.11.02 |
Chlorhexidine gluconate 4% |
|
13.11.02 |
Chlorhexidine gluconate preparations |
|
12.02.03 |
Chlorhexidine Hydrochloride 0.1%, Neomycin Suphate 0.5% Naseptin® |
- Contains arachis (peanut) oil, not siutable for patients with allergy to peanuts
- Patients with soya allergy should also avoid Naseptin®
|
08.01.05 |
Chlormethine gel Ledaga® |
Use in line with NICE |
05.04 |
Chloroquine |
Green for treatments NHS funded |
03.04.01 |
Chlorphenamine |
OTC preparation suitable for self-care/purchase if appropriate
- Oral Solution- for children and those unable to swallow
|
03.04.01 |
Chlorphenamine maleate |
|
04.02.01 |
Chlorpromazine |
Not to be used for psychiatric / anxiolytic purposes in Primary Care |
04.02.01 |
Chlorpromazine |
Supported by an ESCA |
04.06 |
Chlorpromazine hydrochloride |
For nausea
Hyperemesis in pregnancy (off label use) |
02.02.01 |
Chlortalidone |
|
14.04 |
Cholera vaccine Dukoral® |
Via travel vaccine service |
12.03.01 |
Choline Salicylate |
Provides short term analgesic effects. Avoid excessive use or use under dentures as may itself cause ulceration
For patients over 16 years only
|
06.05 |
Choriogonadotropin Alfa Ovitrelle® |
|
A5.04.02 |
CICA-CARE |
Specialist recommendation only Silicone sheet for scar treatment Type of wound product is suitable for Not for use on open wounds- to be applied on healed scar only. This is not a dressing but a scar treatment Duration dressing remains on wound before changing 23 hours Frequency of dressing change Daily Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Do not use on open or infected wounds. Do not use on skin affected by acne. Discontinue use if a rash or itching occur. Rationale for inclusion in formulary Scar therapy Silicone sheets have been shown to soften, flatten scarring aiding movement, nerve sensations and function. Self adherent, Re-usable |
01.05.03 |
Ciclosporin |
Treatment of ulcerative colitis - for specialist use only
MHRA specify the ciclosporin must be prescribed and dispensed by brand as bioavailabilty differences exist between brands
|
04.13 |
Ciclosporin |
Specialist use only for neurological conditions |
08.02.02 |
Ciclosporin Neoral®,Sandimmun® |
Prescribe by brand Post-transplant immunosuppression is comissioned by NHSE and all prescribing should remain with the specialist
Post transplant- if prescribing is NOT established with GP before 1st April 2013
Post transplant - if prescribing IS established with GP before 1st April 2013
|
08.02.02 |
Ciclosporin |
Hospital only |
10.01.03 |
Ciclosporin |
Prescribe and dispense by brand Supported by an ESCA |
13.05.03 |
Ciclosporin |
Supported by an ESCA |
11.99.99.99 |
Ciclosporin 1mg/mL Ikervis® |
- Specialist Opthalmologist Initiation
- Treatment of severe keratitis in adult patients with dry eye disease, which has not improved despite treatment with tear substitutes
- In line with NICE
|
11.99.99.99 |
Ciclosporin 1mg/ml eye drops, emulsion Verkazia® |
- Specialist Opthalmologist Initiation
- Treatment of severe vernal keratoconjunctivitis (VKC) in children from 4 years of age and adolescents
|
11.99.99.99 |
Ciclosporin 2mg/g Optimmune® |
|
05.03.02.02 |
Cidofovir |
|
01.03.01 |
Cimetidine |
|
09.05.01.02 |
Cinacalcet Mimpara® |
NHSE funded for dialysis only
All prescribing retained by secondary care
In line with NICE TA117 |
04.06 |
Cinnarizine |
|
05.01.12 |
Ciprofloxacin |
|
05.01.12 |
Ciprofloxacin |
|
11.03.01 |
Ciprofloxacin |
Specialist Ophthalmologist recommendation (Corneal consultant)
For existing patients only on consultant ophthalmologist advice |
12.01.01 |
Ciprofloxacin 0.3% drops |
Off label use of eye drops Specialist recommendation only |
12.01.01 |
Ciprofloxacin 2mg/ml (0.2%) Ear Drops Cetraxal® |
Licensed product for topical treatment of acute otitis externa (AOE) |
15.01.05 |
Cisatracurium Nimbex® |
Hospital only |
08.01.05 |
Cisplatin |
Commissioned by NHSE
Hospital only |
04.03.03 |
Citalopram |
4 drops (8 mg) is equivalent in therapeutic effect to 10mg tablet
Risk of QT prolongation |
04.03.03 |
Citalopram |
Risk of QT prolongation |
03.09 |
Citric acid oral presentations |
|
08.01.03 |
Cladribine |
NHSE does not routinely commission this drug
Hospital only |
08.02.04 |
Cladribine Mavenclad® |
In line with NICE
Hospital only |
05.01.05 |
Clarithromycin |
|
05.01.05 |
Clarithromycin |
|
06.04.01.01 |
Climanor® |
|
05.01.06 |
Clindamycin |
Use 150mg capsules
300mg capsules are Non-formulary |
05.01.06 |
Clindamycin 300mg/2ml |
|
07.02.02 |
Clindamycin Dalacin® |
|
13.06.02 |
Clindamycin |
Specialist initiation-12 week course. |
13.06.01 |
Clindamycin 1% Dalacin T® |
|
A5.08.03 |
CliniFast |
Preferred local option Elasticated Sub bandage lining Type of wound product is suitable for To be used under retention and compression bandages when conformity is required Can be used for wet/dry wrapping. Duration dressing remains on wound before changing As required Frequency of dressing change As required Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Ensure the correct size for a limb is selected Rationale for inclusion in formulary Cost effective choice when conformity to a limb is required |
19.32 |
CLINIPORE® |
|
A5.07.03 |
Clinipore® |
Preferred local option Permeable non woven, synthetic adhesive tape for securing bandages Frequency of dressing change Determined by wound type and dressing change Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) None listed Rationale for inclusion in formulary Available on drug tariff, cost effective and evaluated as meeting the requirements of a tape including adherence. |
A5.02.08 |
CliniSorb® |
Specialist recommendation only Preferred local option Odour absorbent charcoal dressing Type of wound product is suitable for Malodourous wounds such as fungating wounds Duration dressing remains on wound before changing Up to 7 days Frequency of dressing change 1-7 days dependent on exudate levels Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Not indicated as a primary dressing in dry wounds Store at room temperature Exudate levels will reduce the effectiveness of the charcoal Rationale for inclusion in formulary CliniSorb® is an activated charcoal dressing which adsorb toxins removing malodour from the wound Can be cut to size Cost effective |
06.04.01.01 |
Clinorette® |
|
04.08.01 |
Clobazam |
On specialist advice
MHRA Advice Care should be taken when switching between oral formulations. The need for continued supply of a particluar manufacturer's product should be based on clinical judgement and consultation with patient and/or carer, taking into account factors such as seizure frequency and treatment history |
13.04 |
Clobetasol Propionate 0.05% Dermovate® |
Potency - very potent Short term use only unless under supervision of a dermatologist Cream Ointment Scalp application |
13.04 |
Clobetasone Butyrate 0.05% Eumovate® |
Potency - moderate Cream Ointment |
08.01.03 |
Clofarabine Evoltra® |
Funding may be available from cancer drugs fund
Hospital only |
05.01.10 |
Clofazimine |
Hospital use only under microbiological and Tuberculosis specialist advice |
06.05 |
Clomifene citrate |
|
04.03.01 |
Clomipramine |
An alternative to SSRIs in obsessive-compulsive disorder (OCD) |
04.08.01 |
Clonazepam |
On specialist advice
MHRA Advice Care should be taken when switching between oral formulations. The need for continued supply of a particluar manufacturer's product should be based on clinical judgement and consultation with patient and/or carer, taking into account factors such as seizure frequency and treatment history |
21 |
Clonazepam |
- Off-label use according to West Midlands Palliative Care Physcians Guidelines.
|
02.05.02 |
Clonidine Hydrochloride Catapres® |
Use only on advice of specialist
|
06.04 |
Clonidine Hydrochloride |
|
02.05.02 |
Clonidine Liqiud |
|
02.09 |
Clopidogrel |
|
07.02.02 |
Clotrimazole |
|
13.10.02 |
Clotrimazole 1% cream |
|
12.01.01 |
Clotrimazole solution Canesten® |
Only with positive culture/sensitivity data |
04.02.01 |
Clozapine |
Specialist initiation and maintenance only |
02.08.02 |
CoaguChek XS PT Test PST |
Sandwell only - |
13.14.03 |
Coal tar BP 10% w/w in YSP |
|
13.14.03 |
Coal tar BP 2% w/w in YSP |
|
13.14.03 |
Coal tar BP 5% w/w in YSP |
|
13.09 |
Coal Tar Extract 5% (Alcoholic) Alphosyl 2 in 1® |
Over the counter preparation suitable for self-care/purchase if appropriate |
13.05.02 |
Coal tar lotion 5% Exorex® |
|
13.05.02 |
Coal Tar Solution 2.5%, Arachis (peanut) Oil extract of Coal Tar 7.5%, Tar 7.5%, Cade Oil 7.5%, Liqiud Paraffin 35% Polytar Emollient® |
Contains peanut oil |
13.14.02 |
Coal tar solution BP 3.3% w/w and propylene glycol 20% w/w in Synalar® gel |
|
13.14.02 |
Coal tar solution BP 5% w/w in betamethasone valerate 0.025% w/w ointment |
|
13.14.03 |
Coal tar solution BP 6% w/w & salicylic acid 6% w/w in Ung. Merck |
|
13.14.03 |
coal tar solution BP 6% w/w / salicylic acid 2% w/w in emulsifying ointment |
|
05.01.01.03 |
Co-amoxiclav |
|
05.01.01.03 |
Co-amoxiclav |
|
19.48 |
COBAN 2 LITE® |
Indications: venous leg ulceration. Doppler assessment (ABPI) and/or specialist assessment are required before use. Only to be applied by trained individuals – refer to manufacturer’s application guidelines for details. System used is dependent upon ankle circumference which should be re-measured at each dressing change to ensure that the system used is still safe and effective. Provide compression equivalent to multi-layer bandaging yet have the advantage of only two layers allowing patients to wear shoes increasing patient comfort and concordance. |
19.48 |
COBAN 2® |
Indications: venous leg ulceration. Doppler assessment (ABPI) and/or specialist assessment are required before use. Only to be applied by trained individuals – refer to manufacturer’s application guidelines for details. System used is dependent upon ankle circumference which should be re-measured at each dressing change to ensure that the system used is still safe and effective. Provide compression equivalent to multi-layer bandaging yet have the advantage of only two layers allowing patients to wear shoes increasing patient comfort and concordance. |
A5.08.08 |
Coban® & Coban® Lite |
Preferred local option Two layer compression system available in full and reduced compression (Coban® Lite). Comprises of a latex free foam padding and cohesive bandage. Type of wound product is suitable for Treatment of venous and mixed aetiology leg ulcers Duration dressing remains on wound before changing 1 to 7 days Frequency of dressing change Daily up to weekly dependant on exudate and oedema management. Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Arterial disease Not to be used with other padding or wadding Rationale for inclusion in formulary Two layer compression kit, Once applied the two layers form a band to become a single layer bandage. Bandage technique can be adapted to reduce forefoot oedema (Extra training required) |
04.09.01 |
Co-beneldopa |
Capsules
M/R capsules
Dispersible tablets |
05.03.01 |
Cobicistat Tybost ® |
|
15.02 |
Cocaine |
Hospital only: 10% solution 25% paste 5% nasal solution |
15.02 |
Cocaine with Adrenaline |
Hospital only |
04.09.01 |
Co-careldopa |
Tablets
M/R tablets |
04.09.01 |
Co-Careldopa and Entacapone Stalevo |
|
12.01.01 |
Cochlear implants |
In line with NICE
Providers - NHS hospital trusts |
13.14.06 |
Coconut oil 25% w/w in emulsifying ointment |
|
13.06.02 |
Co-Cyprindiol 2000/35 |
Prescribe as GENERIC |
01.06.02 |
Co-danthramer |
Capsules 25/200, 75/1000
Co-danthramer strong preferred as per palliative care formulary guidance
|
01.06.02 |
Co-danthrusate |
Capsules 50/60
|
21 |
Co-danthrusate / Co-danthramer / Danthron |
- Specialist initiation ONLY due to risk of severe side-effects
|
01.04.02 |
Codeine |
Avoid long term use due to possible dependence |
04.07.02 |
Codeine phosphate |
|
04.07.02 |
Codeine Phosphate |
Tablets
25mg/5ml syrup
Use with caution in patients aged over 65
Contraindicated in children below the age of 12 |
10.01.04 |
Colchicine |
acute gout |
09.06.04 |
Colecalciferol oral |
Please follow Optimise Rx for most cost effective brand
Please see guidance below to support prescribing Please prescribe generically as listed below Oral Capsules or Tablets Colecalciferol 800unit capsules Colecalciferol 800unit tablets Colecalciferol 1,000unit capsules Colecalciferol 1,000unit tablets Colecalciferol 3,200unit capsules Colecalciferol 4,000unit tablets Colecalciferol 20,000unit capsules Colecalciferol 25,000unit tablets Colecalciferol 40,000unit capsules Oral Solution Colecalciferol 2,740units/ml oral drops sugar free Colecalciferol 10,000units/ml oral drops sugar free Colecalciferol 10,000units/ml oral solution sugar free Colecalciferol 15,000units/5ml oral solution Colecalciferol 25,000units/1ml oral solution unit dose ampoules sugar free Colecalciferol 50,000units/1ml oral solution unit dose ampoules sugar free Licensed brands currently available (updated March 2017) Aviticol 800 IU Capsules Aviticol 1,000 IU Capsules (Listed in the Drug Tariff) Aviticol 20,000 IU Capsules Desunin 800 IU Tablets (Listed in the Drug Tariff) Desunin 4,000 IU Tablets (Listed in the Drug Tariff) Fultium-D3 800 IU Capsules (Listed in the Drug Tariff) Fultium-D3 3,200 IU Capsules (Listed in the Drug Tariff) Fultium-D3 20,000 IU Capsules (Listed in the Drug Tariff) Fultium-D3 2740 IU/ml oral drops, solution (Listed in the Drug Tariff) InVita D3 800 IU Capsules InVita D3 2,400 IU/ml oral drops, solution InVita D3 25,000 IU oral solution (Listed in the Drug Tariff) InVitaD3 50,000 IU oral solution (Listed in the Drug Tariff) Plenachol 20,000 IU Capsules Plenachol 40,000 IU Capsules (Listed in the Drug Tariff) Stexerol-D3 1,000 IU Tablets (Listed in the Drug Tariff) Stexerol-D3 25,000 IU Tablets (Listed in the Drug Tariff) STRIVIT-D3 800 IU Capsules THORENS 10 000 IU/ml oral drops, solution (Listed in the Drug Tariff) THORENS 25 000 IU/2.5 ml oral solution |
01.09 |
Colesevelam Cholestagel® |
Supported by a RICaD (in development) |
02.12 |
Colesevelam Cholestagel® |
|
02.12 |
Colestipol Colestid® |
|
01.09 |
Colestyramine |
Supported by a RICaD (In development)
|
02.12 |
Colestyramine |
|
05.01.07 |
Colistimethate |
Hospital use only under microbiological advice |
05.01.07 |
Colistimethate Promixin® |
|
05.01.07 |
Colistimethate for nebulisation Colomycin® |
|
05.01.07 |
Colistimethate for nebulisation |
|
05.01.07 |
Colistimethate inhaler Colobreathe® |
|
03.13 |
Colistimethate sodium |
Commissioned by NHS England for Cystic Fibrosis only
|
10.03.01 |
Collagenase clostridium histolyticum Xiapex® |
In line with NICE |
01.01.01 |
Co-magaldrox |
Sugar free suspension
Mucogel is the most cost-effective brand
Low sodium content
Use with caution in patients with renal impairment as aluminium and magnesium accumulate
|
06.04.01.01 |
COMBINED CYCLICAL HRT |
BRANDS
|
19.38 |
COMFIFAST® |
Red (small limb) Green (medium limb) Blue (large limb) Yellow (child’s trunk or very large limbs) Beige (adults trunk) Elasticated viscose stockinette indicated for retention of dressings on difficult parts of the body or covering wet wraps such as paste bandages. NOT to be used under bandages as a comfort measure or to secure primary dressings unless patients has known sensitivity to wool. |
09.02.02.01 |
Compound Sodium Lactate Intravenous Infusion |
Hospital use only |
A5.08.07 |
Comprilan® |
Preferred local option Specialist recommendation only 100 % cotton short stretch compression bandage Type of wound product is suitable for Venous leg ulceration Varicosis Management of chronic oedema Management of primary and secondary lymphoedema Deep venous thrombosis Thrombophlebitis Duration dressing remains on wound before changing 1 to 7 days Frequency of dressing change Dependant on exudate levels if wound present or oedema management. Caution/contraindications (when not to use the dressing, patient groups to avoid etc. Advanced Peripheral arterial occlusive disease Decompensated cardiac insufficiency Septic phlebitis Phlegmasia coerula doleris Rationale for inclusion in formulary Cotton short stretch bandage. Used by lymphoedema nurse specialists |
03.04.03 |
Conestat Alfa Ruconest® |
Hospital only- NHSE Commissioned |
A5.15 |
Conotrane cream |
Barrier cream Type of wound product is suitable for Intact skin, not to be applied to a wound. To protect the skin from moisture, irritation and chafing. Frequency of use Application at every episode of hygiene. Apply a thin layer sparingly Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Not to be used in conjunction with containment products for incontinence due to the inclusion of liquid paraffin in the ingredients, which will repel urine/faeces back onto the skin. Any allergy to the listed ingredients Rationale for inclusion in formulary Dermatology approved |
13.02.02 |
Conotrane® |
Over the counter preparation suitable for self-care/purchase if appropriate |
06.01.06 |
Continuous Glucose Monitoring Dexcom One Sensor ® |
In line with NHSE criteria, see annex A in the following link: https://www.blackcountryformulary.nhs.uk/docs/files/National-arrangements-for-funding-of-relevant-diabetes-patients-June-2020-Updated-final.pdf
|
09.06.07 |
Copper (chelated) |
|
07.03.05 |
Copper intra-uterine devices |
Various |
09.04 |
Corn flour and corn starch |
- Slow release CHO to prevent hypoglycaemia in GSD
- Slow release carbohydrate to prevent hypoglycaemia in all types of GSD. Cheaper than glycosade and easier to mix. Used in less severe forms of GSD. Between 1 to 2g/kg body weight is prescribed dependent on age, weight and clinical symptoms of hypoglycaemia. Doses may be given at regular intervals during the day and night or at bedtime only. The dose and frequency of dose should always be advised by the specialist dietitian according to the needs of the patient
- For glycogen storage disease
|
05.01.08 |
Co-trimoxazole |
|
05.01.08 |
Co-trimoxazole |
|
A5.08.03 |
Cotton Stockinette BP |
Sub bandage lining Type of wound product is suitable for To be used under retention and compression bandages Duration dressing remains on wound before changing As required Frequency of dressing change As required Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Not to be used under Coban compression therapy Not to be used under compression hosiery Does not conform to a limb shape. If conformity is required, choose CliniFast Rationale for inclusion in formulary Cost effective choice when conformity to a limb is not required |
09.04 |
Cow & Gate Pepti-Junior® |
- Infant and child: Hydrolysate formula
- Whey hydrolysate. Use in infants who have malabsorption problems and require a peptide and MCT containing feed. Eg after gut surgery
- Use as tube or oral feed
- Disaccharide and/or whole protein intolerance, or where amino acids and peptides are indicated in conjunction with medium chain triglycerides
|
08.01.05 |
Crisantaspase Erwinase® |
Commissioned by NHSE |
08.01.05 |
Crizanlizumab Adakveo® |
In line with NICE |
08.01.05 |
Crizotinib Xalkori® |
Hospital Only
In line with NICE |
13.03 |
Crotamiton Eurax® |
Over the counter preparation suitable for self-care/purchase if appropriate |
A5.03.04 |
Cutimed® Sorbact® |
Specialist recommendation only DACC coated dressings providing antimicrobial properties, available in a pad, gel, gel sheet, ribbon, round swab and rectangular swab Type of wound product is suitable for Colonised or clinically infected moist wound, suitable for any wound type Duration dressing remains on wound before changing 1-3 days Frequency of dressing change 1-3 days dependent on exudate levels Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Do not use in combination with oils and creams Known hypersensitivity to ingredients Not for dry wound Not for heavily exuding wounds Rationale for inclusion in formulary Alternative to available antimicrobials |
A5.02.02 |
C-View |
Vapour-permeable adhesive film Type of wound product is suitable for Dry non infected wounds, retention of lines, fixation of secondary dressings, protection of intact skin, protection of skin against friction, protection of newly epithelialized wounds Duration dressing remains on wound before changing Up to 7 days Frequency of dressing change Up to 7 days Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Clinically infected wounds, bleeding or exuding wounds Rationale for inclusion in formulary Retention of lines, protection of intact skin, fixation of other dressings. Waterproof |
A5.02.02 |
C-View Post-Op |
Vapour-permeable adhesive film with absorbent pad Type of wound product is suitable for Dry non infected wounds, low exuding wounds, minor burns, protection of intact skin, protection of newly epithelialized wounds Duration dressing remains on wound before changing Up to 7 days Frequency of dressing change Up to 7 days Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Clinically infected wounds, bleeding or exuding wounds Rationale for inclusion in formulary Protection of intact skin, low exuding wounds. Waterproof |
04.06 |
Cyclizine |
Tablets
Injection - for use in palliative care only |
04.06 |
Cyclizine |
For use in palliative care only |
11.05 |
Cyclopentolate Hydrochloride |
|
11.05 |
Cyclopentolate Hydrochloride |
|
11.05 |
Cyclopentolate Hydrochloride Single Use |
Branded preservative free drops i.e. single use drops should be prescribed where available as manufactured 'specials' cost significantly more and don't have a product license. Restricted to patients needing preservative free. On specialist ophthalmologist recommendation |
08.01.01 |
Cyclophosphamide |
Commissioned by NHSE Injection-hospital only Tablets-for oncology |
05.01.09 |
Cycloserine |
Hospital use only under microbiological and Tuberculosis specialist advice |
06.04.02 |
Cyproterone acetate |
BRANDS
|
08.03.04.02 |
Cyproterone Acetate |
|
09.04 |
Cystine500® |
- To correct cysteine deficiency in homocystinuria
- The only pre-measured sachet of cysteine to correct cysteine deficiency in homocystinuria. The dose and frequency of administration will be determined by the specialist dietitian
- Nutritional supplement for the dietary management of inborn errors of amino acid metabolism in adults and children from birth
|
08.01.03 |
Cytarabine |
Commissioned by NHSE
Hospital only |
08.01.03 |
Cytarabine-Daunorubicin Liposomal Vyxeus® |
In line with NICE |
02.08 |
Dabigatran |
|
08.01.05 |
Dabrafenib with trametinib |
In line with NICE |
08.01.05 |
Dacarbazine |
|
08.01.05 |
Dacomitinib Vizimpro® |
In line with NICE |
08.01.02 |
Dactinomycin |
Commissioned by NHSE Hospital only |
05.01.07 |
Dalbavancin |
Hospital use only under microbiological advice |
09.04 |
Dalia |
- Low protein milk for children and adults with phenylketonuria and other disorders of protein metabolism
- Low protein milk (similar energy content to cow’s milk) for children and adults with phenylketonuria and other disorders of protein metabolism
|
02.08.01 |
Dalteparin |
Use current Place/Trust Status and local guidelines
Sandwell
Non formulary
Wolverhampton
Walsall
Non formulary
Dudley
|
02.08 |
Danaparoid Orgaran® |
|
06.07 |
Danazol |
Off label use for hereditary angiodema |
01.06.02 |
Danthron |
|
10.02.02 |
Dantrolene |
|
15.01.08 |
Dantrolene Sodium Dantrium Intravenous® |
Hospital only |
06.01.02.03 |
Dapagliflozin |
for treating Type 2 diabetes and chronic kidney disease in line with NICE
Do not use SGLT2-inhibitors in patients with T1DM, regardless of CKD and/or heart failure status due to risk of DKA (diabetic ketoacidosis)
Treatment of all grades of symptomatic heart failure
SGLT2 inhibitors: updated advice on the risk of diabetic ketoacidosis
MHRA: SGLT2 inhibitors: updated advice on increased risk of lower-limb amputation (mainly toes) |
06.01.02.03 |
Dapagliflozin / Metformin Xigduo® |
|
05.01.10 |
Dapsone |
Hospital use only under microbiological advice |
05.01.07 |
Daptomycin |
Hospital use only under microbiological advice |
08.01.05 |
Daratumumab Darzalex® |
In line with NICE |
09.01.03 |
Darbepoetin Alfa Aranesp® |
•NHSE commissioned for use in renal dialysis
•Primary Care commissioned for use in cancer- in line with NICE TA323
|
08.03.04.02 |
Darolutamide Nubeqa® |
In line with NICE |
05.03.01 |
Darunavir |
|
05.03.01 |
Darunavir with cobicistat Rezolsta® |
Blueteq /prior approval form |
05.03.01 |
Darunavir with cobicistat, emtricitabine and tenofovir alafenamide Symtuza® |
Blueteq /prior approval form |
08.01.05 |
Dasatinib Sprycel® |
In line with NICE |
08.01.02 |
Daunorubicin |
Commissioned by NHSE Hospital only |
A5.05.03 |
Debrisoft® |
Preferred local option Debridement pad to cleanse and debride wounds. Type of wound product is suitable for Acute or chronic wounds with surface debris eg pressure ulcers, leg ulcers, diabetic foot ulcers Hyperkeratosis Duration dressing remains on wound before changing Not applicable Frequency of dressing change At each dressing change or as required Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Known sensitivity to polyester Heavy slough and necrotic tissue may require autolytic debridement to soften prior to use Thick hyperkeratosis may take more than one treatment Must be wet with clean warm water prior to use Do not get an emollient on the pad as this blocks the monofilaments Rationale for inclusion in formulary Lifts debris, superficial slough and exudate without damaging new granulation or epithelial cells Removes biofilms Lifts hyperkeratosis and dry flaking skin peri-wound Recommended by NICE Treatment well tolerated Convenient, easy to use, disposable single use pad |
08.01.03 |
Decitabine Dacogen® |
NHSE do not routinely commission this
Hospital only |
09.01.03 |
Deferasirox Exjade® |
NHSE commissioned |
09.01.03 |
Deferiprone Ferriprox® |
NHSE commissioned |
08.03.04.02 |
Degarelix |
•Commissioned by CCGs, in line with NICE •Transfer to Primary Care supported by an ESCA. ESCA: Degarelix |
05.01.09 |
Delamanid Deltyba ® |
Hospital use only under microbiological and Tuberculosis specialist advice |
05.01.03 |
Demeclocycline |
For Antimicrobial use by Microbiologist and Hyponatraemia indications |
06.05 |
Demeclocycline |
Treatment of hyponatraemia resulting from inappropriate secretion of antidiuretic hormone, if fluid restriction alone does not restore sodium concentration or is not tolerable |
16.01 |
Demo Drug nelDemo |
Area 1
Area 2
Area 2
Notes here about the product |
16.01 |
Demo Drug nelDemo |
Notes about medicines |
16.01 |
Demo Drug nelDemo |
Restricted to In Area 3 |
06.06.02 |
Denosumab Xgeva® |
For specialist use only in line with NICE TA265
|
06.06.02 |
Denosumab Prolia® |
Dudley
Sandwell
ESCA-Denosumab-Sandwell only
Walsall
Wolverhampton
with RiCaD
Wolverhampton only |
13.08.02 |
Dermablend® |
- Specialist recommendation
|
13.10.05 |
Dermabond ProPen® |
Hospital only |
13.08.02 |
Dermacolor® |
- First line
- Specialist recommendation
- 100 shades available
- FP10 prescriptions should be endorsed "ACBS"
|
13.02.01 |
Dermatonics Once Heel Balm |
Specialist recommendation for epidermolysis bullosa only |
A5.13 |
Dermatonics Once Heel Balm |
Preferred local option Podiatry recommendation only Cream containing 25% urea Type of wound product is suitable for To moisturise dry skin on the soles of feet For use on adults and children over 12 years of age Frequency of use Reapply daily Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Allergy or hypersensitivity to any of the ingredients, contains beeswax and lanolin Not to be used on children under 12 Rationale for inclusion in formulary Treatment of dry skin conditions of the foot. Dermatology approved |
15.02 |
Dermogesic spray |
Hospital only |
A5.13 |
Dermol 500 lotion |
Emollient lotion containing an antimicrobial Type of wound product is suitable for For dry and pruritic skin conditions including eczema and dermatitis. Can be applied to skin as an emollient or used as a soap substitute Frequency of use Reapply daily Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Allergy or hypersensitivity to any of the ingredients, contains benzalkonium chloride, 0.1%, chlorhexidine hydrochloride 0.1%, liquid paraffin, isopropyl myristate. Should not be used unless infection is present or is a frequent complication Rationale for inclusion in formulary Treatment of dry skin requiring antimicrobial properties Dermatology approved |
13.02.01.01 |
Dermol 600® Emollient Bath Additive |
Over the counter preparation suitable for self-care/purchase if appropriate |
13.02.01 |
Dermol® 500 |
For short term use only
Over the counter preparation suitable for self-care/purchase if appropriate |
09.01.03 |
Desferrioxamine Mesilate |
NHSE commissioned |
15.01.02 |
Desflurane Suprane® |
HOSPITAL ONLY |
06.05 |
Desmopressin Desmotabs® |
Primary Nocturnal enureis -Paediatrics |
06.05 |
Desmopressin |
Paediatric Nocturnal enuresis
Diabetes Insipidus |
06.05 |
Desmopressin |
Diabetes Insipidus |
06.05 |
Desmopressin |
|
07.03.02.01 |
Desogestrel 75mcg |
Prescribe generically |
09.04.01 |
Desserts |
Low-protein foods
These products are not available to purchase in supermarkets
They are important to provide essential energy and variety to aid the palatability of low protein diets. They are important for good metabolic control of the patient. Poor access to these products could lead to poor dietary adherence. This will cause poor metabolic control which may lead to irreversible brain damage
The NSPKU guidelines for prescription of low protein foods can be used for other amino acid disorderssuch as MSUD, homocystinuria, tyrosinaemia and pyridoxine response epilepsy
Protein free - necessary for children and adults with inborn errors of protein metabolism who do not tolerate very little natural protein
The specialist dietician will make individual reccomendations based on diagnosis,protein recommendations, weight etc.
- Important protein-free foods to provide important energy, assist dietary adherence and provide variety when natural protein tolerance is very limited. Necessary for children and adults with inborn errors of protein metabolism who tolerate very little natural protein
|
04.06 |
Dexamethasone |
For use in palliative care only |
04.06 |
Dexamethasone |
For resistant nausea and vomiting only
£££££ |
06.03.02 |
Dexamethasone |
|
11.04.01 |
Dexamethasone Maxidex® |
For use on the advice of a specialist |
11.04.01 |
Dexamethasone 700mcg Ozurdex® |
For macular oedema secondary to retinal vein occlusion - use in line with NICE TA229
For diabetic macular oedema - use in line with NICE TA349 |
11.04.01 |
Dexamethasone eye drops |
Branded preservative free drops i.e. single use drops should be prescribed where available as manufactured 'specials' cost significantly more and don't have a product license
Restricted to patients needing preservative free For use on the advice of a specialist For post corneal transplants or OSD
Use the agent with the lowest acquisition cost |
06.03.02 |
DEXAMETHASONE PHOSPHATE INJECTION |
|
12.01.01 |
Dexamethasone with Antibacterial Sofradex® |
|
12.01.01 |
Dexamethasone with neomycin and glacial acetic acid Otomize® |
|
11.04.01 |
Dexamethasone with Neomycin and Polymyxin B sulphate Maxitrol® |
Steroid- antibiotic combination eye drops are only recommended for use under close specialist supervision and after ocular surgery. On specialist ophthalmologist recommendation |
11.04.01 |
Dexamethasone with tobramycin Tobradex® |
|
04.04 |
Dexamfetamine |
Please note that commissioning discussion is underway. However the present status is as follows:-
Age 6 and over - Solihull practices. Supported with ESCA
Age 16 and over - Birmingham practices. Supported with ESCA
Age under 16 - Birmingham practices
Supported with an ESCA - Sandwell & West Birmingham CCG for patients seen by the Black Country ADHD Services |
08.01 |
Dexrazoxane Savene® |
|
09.04 |
Dialamine® |
- Protein and carbohydrate
- This is a source of essential amino acids for use in low protein diets with urea cycle disorders. The dose and type of product should always be advised by the specialist dietitian according to the needs of the patient
- Hypoproteinaemia, chronic renal failure, wound fistula leakage with excessive protein loss, conditions requiring a controlled nitrogen intake, and haemodialysis
- Not suitable for child under 6 months
|
04.07.02 |
Diamorphine salts |
|
04.01.02 |
Diazepam |
|
04.01.02 |
Diazepam |
|
04.01.02 |
Diazepam |
Inpatient use and prison settings only |
04.08.02 |
Diazepam Rectal tubes |
|
04.10 |
Diazepam |
|
04.10.01 |
Diazepam |
|
10.02.02 |
Diazepam |
|
15.01.04.01 |
Diazepam |
Hospital only |
04.01.01 |
Diazepam liquid |
Inpatient use and prison settings only |
10.01.01 |
Diclofenac |
Enteric coated tablets (most cost effective choice) Not first line NSAID treatment choice
Renal colic and other acute severe painful conditions Assess CVD risk
For short term use only - no information on their use for longer than 3 months. Dispersible tablets reserved for paediatric use and those patients with swallowing difficulties or specific clinical need |
10.01.01 |
Diclofenac |
£££££
Short term use only
Assess CVD risk
Not first line NSAID
For patients with swallowing difficulties
Renal colic and severe acute painful conditions |
11.08.02 |
Diclofenac Voltarol® Ophtha SDU |
For use on advice of specialist |
15.01.04.02 |
Diclofenac |
Post operative use only then switch to oral ibuprofen or naproxen. |
13.08.01 |
Diclofenac 3% gel Solaraze® |
Apply thinly twice a day. Max 8g daily Treat for 60-90 days ( effect may not be seen until 30 days after stopping use). For specialist initiation |
11.08.02 |
Diclofenac Sodium Voltarol® Ophtha multidose |
For use on advice of specialist Restricted to patients who need preservative free |
05.05 |
Diethylcarbamazine |
|
08.03.01 |
Diethylstilbestrol |
For oncological treatment by an experienced specialist |
13.04 |
Diflucortolone valerate 0.3% oily cream |
Potency - Very potent |
02.01 |
Digoxin |
Use only if still symptomatic despite optimal treatment of HF with atrial fibrillation Take special care in elderly who may be more susceptible to digitalis toxicity |
02.01 |
Digoxin |
|
02.01 |
Digoxin |
Use only if still symptomatic despite optimal treatment of HF with atrial fibrillation Take special care in elderly who may be more susceptible to digitalis toxicity |
02.01.01 |
Digoxin specific antibody fragments |
|
04.07.02 |
Dihydrocodeine |
Tablets
Oral solution for patients with swallowing difficulties |
05.04 |
Diloxanide |
|
02.06.02 |
Diltiazem |
|
01.07.04 |
Diltiazem Cream 2% Anoheal |
£££££
Unlicensed - for use only in patients intolerant of or unresponsive to GTN ointment
Store in the fridge
One tube will last a month if used as 2cm apllication TWICE DAILY
Topical diltiazem 2% may be used twice daily [unlicensed indication] in patients with chronic anal fissures unresponsive or intolerant to topical nitrates and before considering surgery |
08.02.04 |
Dimethyl fumarate Tecfidera® |
For use in relapsing - remitting Multiple Sclerosis
In line with NICE |
13.05.03 |
Dimethyl fumarate Skilarence® |
For use in moderate to severe plaque psoriasis- CCG commissioned
In line with NICE |
07.04.04 |
DIMETHYL SULPHOXIDE Bladder Instillation 50% |
Hospital only |
13.10.04 |
Dimeticone Hedrin® |
Over the counter preparation suitable for self-care/purchase if appropriate |
02.14 |
Dinoprostone Prostin E2® |
|
07.01.01 |
Dinoprostone Prostin E2® Propess ® |
For Specialist/ Hospital Use Only |
07.01.01.01 |
Dinoprostone |
|
08.02.03 |
Dinutuximab Qarziba® |
In line with NICE |
13.14.07 |
Diphenylcyclopropenone in acetone 0.00001-6.0% w/v |
|
02.09 |
Dipyridamole |
With specialist initiation |
02.09 |
Dipyridamole MR Persantin Retard® |
With specialist initiation |
21 |
Disodium pamidronate |
- For Acute Trusts and Hospices.
- Specialist recommendation.
|
01.01 |
Disodium pamidronate |
|
06.06 |
Disodium Pamidronate |
|
04.10.01 |
Disulfiram Antabuse® |
|
13.05.02 |
Dithranol Dithrocream® |
All strengths-specialist recommendation only. 0.1% - 0.5% cream suitable for overnight treatment, 1% - 2% cream for maximum 1 hour Stains everything including skin, linen, bathroom furniture and may cause skin irritation. |
13.14.05 |
Dithranol in Lassar’s paste 0.1% w/w |
|
13.14.05 |
Dithranol in Lassar’s paste 0.5% w/w |
|
13.14.05 |
Dithranol in Lassar’s paste 1% w/w |
|
13.14.05 |
Dithranol in Lassar’s paste 10% w/w |
|
13.14.05 |
Dithranol in Lassar’s paste 15% w/w |
|
13.14.05 |
Dithranol in Lassar’s paste 2% w/w |
|
13.14.05 |
Dithranol in Lassar’s paste 4% w/w |
|
13.14.05 |
Dithranol in Lassar’s paste 8% w/w |
|
13.14.05 |
Dithranol pomade 0.4% w/w |
Dithranol 0.4% w/w, salicylic acid 2% w/w, emulsifying wax BP 25% & liquid paraffin to 100% |
02.07 |
Dobutamine |
|
08.01.05 |
Docetaxel Taxotere® |
In line with NICE
Hospital only |
09.04 |
DocOmega® |
- DHA supplement for low chain fatty acid and low protein diets
- The only ACBS prescribed DHA supplement for low protein diets. The dose and frequency of administration will be determined by the specialist dietitian
- Nutritional supplement for the dietary management of inborn errors of metabolism for adults and children from birth
|
01.06.02 |
Docusate Sodium |
Capsules 100mg, Liquid 50mg/5ml
Solution is utterly unpalatable- only fit for use down tubes
Probably acts as a softening laxative as well as a stimulant
Time to effect is approximately 24 to 48 hours |
05.03.01 |
Dolutegravir Tivicay ® |
|
05.03.01 |
Dolutegravir with rilpivirine Juluca® |
|
01.02 |
Domperidone |
The MHRA has issued new advice for domperidone which states that it is no longer licensed for the relief of nausea and vomiting in children under the age of 12 years or those weighing less than 35kg (16th December 2019).
See MHRA Dug Safety Update
Domperidone is no longer recommended for managing heartburn,bloating and stomach discomfort
It should only be used for relief of nausea and vomiting at low doses for short periods (generally upto 1 week)
MHRA advice on domperidone |
04.06 |
Domperidone |
Tablets - short term use only
Suppositories
SF suspension £££££ - for patients with swallowing difficulties only |
04.11 |
Donepezil |
- Tablets
- Orodispersible 10mg tablets sugar free (pack of 28)
|
02.07 |
Dopamine |
|
05.03.01 |
Doravirine Pifeltro® |
|
03.07 |
Dornase Alfa Pulmozyme® |
Commissioned by NHSE for Cystic Fibrosis only |
11.06 |
Dorzolamide 2% |
On Specilaist Ophthalmologist Recommendation |
11.06 |
Dorzolamide 2% with Timolol 0.5% SDU Eye Drops Cosopt® |
On Specilaist Ophthalmologist Recommendation |
11.06 |
Dorzolomide 2% Trusopt® |
On Specialist Ophthalmologist Recommendation |
11.06 |
Dorzolomide 2% with Timolol 0.5% |
On Specialist Ophthalmologist Recommendation |
08.01.05 |
Dostarlimab Jemperli® |
In line with NICE |
13.02.01 |
Doublebase |
Over the counter preparation suitable for self-care/purchase if appropriate |
03.05.01 |
Doxapram Dopram® |
|
03.05.01 |
Doxapram |
|
15.01.07 |
Doxapram Dopram® |
Hospital only |
02.05.04 |
Doxazosin |
|
07.04.01 |
Doxazosin |
Reduce BP - care with other antihypertensives Caution in elderly Care with hepatic and severe renal impairment Contraindicated in postural hypotension or micturition syncope
MODIFIED RELEASE TABLETS ARE NON-FORMULARY |
13.03 |
Doxepin hydrochloride Xepin® |
Supported by a RICaD |
08.01.02 |
Doxorubicin Hydrochloride |
Commissioned by NHSE Hospital only |
08.01.02 |
Doxorubicin Hydrochloride Myocet® |
Commissioned by NHSE Hospital only |
05.01.03 |
Doxycycline |
|
05.04 |
Doxycycline |
|
05.04 |
Doxycycline Vibramycin-D® |
|
13.06.02 |
Doxycycline |
•Topical treatments should be used first line. •Oral antibiotics should be reserved for acne, if topical treatment is not adequately effective or if it is inappropriate Take with or after food and avoid sunlight Please refer to Primary Care Antimicrobial Guidelines
|
02.03.02 |
Dronedarone |
In line with NICE TAG TA197
Use current status at Place/Trust
Sandwell
Wolverhampton
ESCA Dronedarone-Wolverhampton only
Walsall
Dudley
ESCA Dronedarone-Dudley only
|
03.01.05 |
Drug Delivery Device |
- Aerochamber Plus
- Aerochamber Plus Flow-vu Anti-static
- Aerochamber Plus Flow-vu Anti-static With Adult Large Mask
- Aerochamber Plus Flow-vu Anti-static With Adult Small Mask
- Aerochamber Plus Flow-vu Anti-static With Medium Mask Child 1-5 Years
- Aerochamber Plus Flow-vu Anti-static With Small Mask Infant 0-18 Months
- Aerochamber Plus Flow-vu Anti-static Youth 5
- Aerochamber Plus With Adult Mask
- Aerochamber Plus With Child Mask
- Aerochamber Plus With Infant Mask
- Volumatic
- Volumatic With Paediatric Mask
- Zerostat Vt Spacer
|
14.04 |
DTaP/IPV/Hib/HepB Infanrix-hexa®, Vaxelis® |
|
06.01.02.03 |
Dulaglutide Trulicity® |
PLEASE PRESCRIBE BY BRAND - NICE Guidance on prescribing
|
04.03.04 |
Duloxetine Cymbalta® |
|
04.07.03 |
Duloxetine Cymbalta® |
Third line after gabapentin
On advice of specilaist - initiate at 30 mg OD for 1 month, then 60 mg OD
More cost effective options available
NICE suggests 1st line for Diabetic neuropathy
Low abuse potential , high cost £££££
Not licensed for use in children |
06.01.02.03 |
Duloxetine |
Prescribe generically as 30mg & 60mg.
90 and 120mg not cost-effective |
07.04.02 |
Duloxetine |
|
09.04 |
Duocal® Super Soluble |
- Fat and Carbohydrate
- For renal children with fluid restriction
- Disease-related malnutrition, malabsorption states, or other conditions requiring fortification with a high fat (or fat and carbohydrate) supplement
|
19.12 |
DuoDERM® Extra Thin |
Light Exudate Only Indications: necrotic, sloughy, granulating and epithelialising wounds. Primary dressing which provides moist environment for autolysis. Waterproof and requires 1.5-2cm margin around wound to ensure adhesion and to reduce leakage. Warm with hands to make more pliable and adhesive. To remove press down on skin and carefully lift corners stretching the edges until free. Not suitable for infected wounds as they are occlusive (unless aerobic infection isolated). Not suitable for heavily exuding wounds as they have limited absorption capacity. Contains porcine extract Without porcine extract: Hydrocolloid dressings are available without porcine extract. Please contact Tissue Viability Service for advice if required.
|
19.12 |
DuoDERM® Signal |
Light to moderate exudate Indications: necrotic, sloughy, granulating and epithelialising wounds. Primary dressing which provides moist environment for autolysis. Waterproof and requires 1.5-2cm margin around wound to ensure adhesion and to reduce leakage. Warm with hands to make more pliable and adhesive. To remove press down on skin and carefully lift corners stretching the edges until free. Not suitable for infected wounds as they are occlusive (unless aerobic infection isolated). Not suitable for heavily exuding wounds as they have limited absorption capacity. Contains porcine extract Without porcine extract: Hydrocolloid dressings are available without porcine extract. Please contact Tissue Viability Service for advice if required.
|
A5.02.04 |
DuoDERM® |
Preferred local option The adhesive layer forms a cohesive gel when in contact with wound exudate Available as Extra thin or Signal (Bordered) Type of wound product is suitable for Dry to lightly exuding wounds Non infected Acute or Chronic wounds Duration dressing remains on wound before changing Up to 7 days maximum Frequency of dressing change 3-7 days Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Not suitable for infected wounds, full thickness burns or wounds with exposed bone, muscle or tendon or wounds that are likely to macerate, particularly on plantar surface of foot Not for diabetic foot ulcers Not for ischaemic wounds Known product or component sensitivity Rationale for inclusion in formulary Conformable, waterproof, aids autolysis. Protect surrounding skin , reduced risk of blistering. Cost effective |
03.04.03 |
Dupilumab Dupixent® |
|
08.01.05 |
Dupilumab Dupixent® |
|
08.01.05 |
Durvalumab Imfinzi® |
In line with NICE |
06.04.02 |
Dutasteride Avodart® |
|
09.04 |
EAA Supplement |
- Consists of essential amino acids for the treatment of urea cycle disorders
- Essential amino acid supplement for use in urea cycle disorders and the cerebral creatine deficiency syndrome: guanidinoacetate methyltransferase (GAMT) deficiency. The only pre-measured sachet of essential amino acids with added vitamins and minerals for the treatment of urea cycle disorders. This is particularly important as most of our families with UCD do not speak English as their first language so require pre-measured products. Unmeasured use of essential amino acid supplements in UCD could lead to hyperammonaemia, acute brain encephalopathy and ITU admission. The dose and frequency of administration will be determined by the specialist dietitian
- Nutritional supplement for the dietary management of disorders of protein metabolism including urea cycle disorders in children over 3 years
|
A5.11 |
Easy-Slide |
Preferred local option Application aid for open toe compression garments |
A5.01.02 |
Eclypse® |
Approved June 2018 to replace Flivasorb® |
07.02.02 |
Econazole Gyno-Pevaryl® |
|
11.03.02 |
Econazole 1% eye drops |
|
02.08 |
Edoxaban |
|
15.01.06 |
Edrophonium |
Hospital only |
10.02.01 |
Edrophonium Chloride |
Hospital use only |
05.03.01 |
Efavirenz with emtricitabine and tenofovir disoproxil |
|
05.03.01 |
Elbasvir with grazoprevir Zepatier® |
|
09.04.02 |
Elemental 028® Extra |
- Less than 1 kcal/mL and less than 5g protein/100 mL
- Amino acid formula (essential and non-essential amino acids)
- Pts with IBD, multiple allergy
- Short bowel syndrome, intractable malabsorption, proven inflammatory bowel disease, bowel fistula
|
09.04.02 |
Elemental 028® Extra |
- Less than 1 kcal/mL and less than 5 g protein/100 mL
- Amino acid formula (essential and non-essential amino acids)
- Pts with IBD, multiple allergies. For tube feed and oral feeding. Alter concentration of feed to support individual patient’s nutritional needs.
- Short bowel syndrome, intractable malabsorption, proven inflammatory bowel disease, bowel fistula
|
09.08.01 |
Eliglustat Cerdelga® |
In line with NICE Highly Specialised Technology guidance- NHSE commissioned |
06.04.01.01 |
Elleste Solo |
|
06.04.01.01 |
Elleste-Duet Conti® |
|
09.01.04 |
Eltrombopag Revolade® |
In line with NICE TA293. |
05.03.01 |
Elvitegravir with cobicistat, emtricitabine and tenofovir alafenamide Genvoya® |
|
06.01.02.03 |
Empagliflozin |
For treating type 2 diabetes Do not use SGLT2-inhibitors in patients with T1DM, regardless of CKD and/or heart failure status due to risk of DKA (diabetic ketoacidosis)
treatment of all grades of symptomatic heart failure
SGLT2 inhibitors: updated advice on the risk of diabetic ketoacidosis
MHRA: SGLT2 inhibitors: updated advice on increased risk of lower-limb amputation (mainly toes) |
06.01.02.03 |
Empagliflozin / Metformin Synjardy ® |
|
06.01.02.03 |
Empagliflozin/Linagliptin |
|
05.03.01 |
Emtricitabine Emtriva® |
|
05.03.01 |
Emtricitabine 200mg, Rilpivirine 25mg and Tenofovir 245mg Eviplera® |
Blueteq /prior approval form |
05.03.01 |
Emtricitabine with rilpivirine and tenofovir alafenamide Odefsey® |
|
05.03.01 |
Emtricitabine with tenofovir alafenamide Descovy® |
|
05.03.01 |
Emtricitabine with tenofovir disoproxil |
|
A5.14 |
Emulsifying ointment |
Preferred local option Emollient ointment containing emulsifying wax, white soft paraffin and liquid paraffin Type of wound product is suitable for For treatment of dry skin conditions Frequency of use Daily Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Allergy or hypersensitivity to any of the ingredients Rationale for inclusion in formulary Treatment of dry skin Dermatology approved |
13.02.01 |
Emulsifying Ointment BP |
Most greasy option
Over the counter preparation suitable for self-care/purchase if appropriate Use frequently and liberally. prescribe in adequate quantities In generalised eczema, an adult will require 500g per week and a child will require 250g a week |
08.01.05 |
Encorafenib plus cetuximab Braftovi® + Erbitux® |
In line with NICE |
08.01.05 |
Encorafenib with binimetinib Braftovi® + Mektovi ® |
In line with NICE
Providers are NHS hospital trusts
|
09.04 |
Energivit® |
- Fat and Carbohydrate
- Infant feed - Metabolic disorder pts
- Also protein-free (containing fat, carbohydrate, vitamins and minerals) powder necessary for infants with inborn errors of protein metabolism. It is the only protein-free infant feed for patients with urea cycle disorders and organic acidaemias. It is commonly used in combination with a measured amount of natural protein e.g. expressed breast milk. It will help meet essential energy and nutrient requirements. The dose and type of product should always be advised by the specialist dietitian according to the needs of the patient
- For children requiring additional energy, vitamins, minerals, and trace elements following a protein-restricted diet
|
05.03.01 |
Enfuvirtide Fuzeon® |
|
02.08.01 |
Enoxaparin |
Use current Place/Trust Status and local guidelines
Sandwell
Single use in suspected DVT
Pregnant women - see URGENT PRESCRIBING OF ENOXAPARIN IN PROPHYLYAXIS OF VENOUS THROMBOEMBOLISM (VTE) IN PREGNANCY
For all other indications
The APC's view is that on clinical grounds, the status for certain indications approved by APC should be Amber Shared Care, supported by an ESCA. These indications are:
- Deep vein thrombosis (including paediatrics)
- Pulmonary embolism (including paediatrics)
- Intolerance/unsuitable for oral anticoagulants
- Certain cancer patients
- Injectable drug users
HOWEVER, until the commissioning arrangements have been agreed to allow safe transfer of patient care, the status will remain RED (ESCAs to be developed). This should not prevent individuals in primary care providing initial prescriptions in urgent situations e.g. pregnancy where there is a high thrombotic risk (see guidance linked below).
Wolverhampton
Walsall
Preferred brand-Inhixa and Clexane
Dudley
|
02.01.02 |
Enoximone |
|
09.04 |
Enshake® |
- Protein, fat, and carbohydrate
- First choice for patients with very high energy requirement eg. cystic fibrosis
- In adults with cystic fibrosis, nutritional advice and interventions should be aimed at maintaining a BMI of 22kg/m2 in women and 23kg/m2 in men, as these are associated with better lung function (Nutritional management of CF – Consensus document – 2016)
- Disease-related malnutrition, malabsorption states, or other conditions requiring fortification with a high fat or carbohydrate (with protein) supplement. Not suitable for child under 1 year; use with caution in child 1–6 years
|
09.04.02 |
Ensure® Twocal |
- More than 1.5 kcal/mL and 5g (or more) protein/100 mL
- High calorie vegetarian fish oil free
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula ; also haemodialysis and CAPD
|
04.09.01 |
Entacapone |
|
05.03.03 |
Entecavir Baraclude® |
|
05.03.03 |
Entecavir |
|
15.01.02 |
Entonox® |
HOSPITAL ONLY |
08.01.05 |
Entrectinib Rozlytrek® |
In line with NICE |
08.03.04.02 |
Enzalutamide Xtandi® |
Commissioned by NHS England
Hospital only
In line with NICE and available from day 91 following publication of TA |
13.14.07 |
Eosin solution 2% w/v |
|
13.02.01 |
Epaderm |
Over the counter preparation suitable for self-care/purchase if appropriate |
A5.14 |
Epaderm ointment |
Emollient ointment containing liquid paraffin, yellow soft paraffin and emulsifying wax Type of wound product is suitable for For use on all dry skin conditions and with dry or wet wrapping techniques Frequency of use Daily or more frequently if required Caution/contraindications Non listed Rationale for inclusion in formulary Treatment of dry skin conditions. Dermatology approved |
02.07 |
Ephedrine |
|
12.02.02 |
Ephedrine 0.5% |
Short Term Use Only
Do not exceed 7 days use. Rebound congestion may occur on withdrawal Maximum of 5 days in children aged 6-12 years. Do not use in children under 6 years. |
03.01.01.02 |
Ephedrine Hydrochloride |
|
13.02.01 |
Epimax |
|
08.01.02 |
Epirubicin hydrochloride |
Commissioned by NHSE Hospital only |
02.02.03 |
Eplerenone |
|
09.01.03 |
Epoetin beta NeoRecormon® |
•NHSE commissioned for use in renal dialysis
•Primary Care commissioned for use in cancer- in line with NICE TA323
|
02.08 |
Epoprostenol Flolan® |
|
02.06 |
Eptifibatide |
|
04.07.04.02 |
Erenumab Aimovig® |
In line with NICE |
09.06.04 |
Ergocalciferol |
20,000 units solution capsules (Osto D2) injection-hospital only |
07.01.01 |
Ergometrine Maleate |
For Specialist/ Hospital Use Only |
07.01.01 |
Ergometrine Maleate and Oxytocin Syntometrine® |
For Specialist/ Hospital Use Only |
08.01.05 |
Eribulin Halaven® |
In line with NICE
Hopsital ONLY - NHSE Commissioned |
08.01.05 |
Erlotinib Tarceva® |
In line with NICE and available from day 91 following pubication of TA |
05.01.02.02 |
Ertapenem |
Amber Rec under OPAT Scheme in Primary care
Hospital use under microbiological advice |
06.01.02.03 |
Ertugliflozin |
In line with NICE
Do not use SGLT2-inhibitors in patients with T1DM, regardless of CKD and/or heart failure status due to risk of DKA (diabetic ketoacidosis)
|
05.01.05 |
Erythromycin |
|
05.01.05 |
Erythromycin ethyl succinate |
|
05.01.05 |
Erythromycin lactobionate |
|
04.08.01 |
Eslicarbazepine |
Should only be considered following referral to a tertiary care specialists and after oxcarbazepine has been tried
Supported by an ESCA |
02.04 |
Esmolol |
Hospital use only |
01.03.05 |
Esomeprazole |
|
01.03.05 |
Esomeprazole injection |
|
06.04.01.01 |
Estraderm MX® |
|
06.04 |
Estradiol 10mg Vagifem®, Vagirux® |
Pessary
|
06.04 |
Estradiol 1mg /2mg |
|
06.04 |
Estradiol hemihydrate lenzetto 153 mg/spray ® |
|
07.03.01 |
Estradiol/dienogest Qlaira® |
•Phasic (28-day ‘Every day’ preparation) •Only for Synphase® failure |
06.04 |
Estradiol/dydrogesterone |
|
06.04 |
Estradiol/Medroxyprogesterone |
|
06.04 |
Estradiol/Norethisterone |
2nd line to patches
https://pcwhf.co.uk/wp-content/uploads/2021/02/Prescribing-HRT-3.pdf |
06.04.01.01 |
Estradot® |
|
08.01.01 |
Estramustine phosphate Estracyt® |
Commissioned by NHSE |
06.04 |
ESTRIOL 0.01% Cream |
|
06.04.01.01 |
Estriol® 0.01% |
|
02.11 |
Etamsylate Dicynene® |
|
10.01.03 |
Etanercept Enbrel® |
Hospital use only
Use in children is commissioned by NHSE specialised commissioning not SWB CCG |
13.05.03 |
Etanercept |
In line with NICE |
09.05.01.02 |
Etelcalcetide Parsabiv® |
Commissioned by NHS England
In line with NICE |
05.01.09 |
Ethambutol |
Hospital use only under microbiological and Tuberculosis specialist advice
Ethambutol liquid 400mg in 5ml (unlicensed) |
06.04.01.01 |
Ethinylestradiol |
|
07.03.01 |
Ethinylestradiol / levonorgestrel phased pill TriRegol® |
Phasic Standard Strength (21 Day preparation) Phased peparations are generally reserved for women who either do no have withdrawal bleeding or who have breakthrough bleeding with monophasic products. Note BNF contraindications and cautions in migraine. Advise all women to report increase in headache frequency and stop if focal symptoms not typical of aura > 1 hour. Carry small increased risk of venous thromboembolism, higher with desogestrel and gestodene than other progestogens. Use low strength if risk factors for circulatory disease and COC is otherwise suitable. |
07.03.01 |
Ethinylestradiol 20 mcg / norethisterone 1mg Loestrin 20® |
Monophasic LOW strength (21 Day preparation)
For pubertal induction in adolescent patients or premature ovarian failure ONLY. |
07.03.01 |
Ethinylestradiol 20mcg / desogestrel 150mcg Gedarel®20/150, Lestramyl®20/150 |
Lestramyl is the preferred brand however if there are supply issues use Gedarel. Monophasic LOW strength (21 Day preparation) Use low strength if risk factors for circulatory disease and COC is otherwise suitable. Note BNF contraindications and cautions in migraine. Advise all women to report increase in headache frequency and stop if focal symptoms not typical of aura > 1 hour. Carry small increased risk of venous thromboembolism, higher with desogestrel and gestodene than other progestogens. |
07.03.01 |
Ethinylestradiol 20mcg / gestodene 75 mcg Millinette®20/75 |
Monophasic LOW strength (21 Day preparation) |
07.03.01 |
Ethinylestradiol 30 mcg / drospirenone 3 mg |
•Monophasic standard strength (21-day preparation) APC approved brands: Yacella® Acondro® Dretine® |
07.03.01 |
Ethinylestradiol 30mcg / desogestrel 150mcg Gedarel®30/150, Lestramyl®30/150 |
Lestramyl preferred brand however if supply issues use Gedarel. Monophasic standard strength (21 Day preparation) Use standard monophasic for most women. Use phased preparations for those who do not have withdrawal bleeding or experience breakthrough bleeding with monophasic. Note BNF contraindications and cautions in migraine. Advise all women to report increase in headache frequency and stop if focal symptoms not typical of aura > 1 hour. Carry small increased risk of venous thromboembolism, higher with desogestrel and gestodene than other progestogens. Use low strength if risk factors for circulatory disease and COC is otherwise suitable. |
07.03.01 |
Ethinylestradiol 30mcg / gestodene 75 mcg Millinette®30/75 |
Monophasic standard strength (21 Day preparation)
|
07.03.01 |
Ethinylestradiol 30mcg / levonorgestrel 150mcg Microgynon 30 ED® |
Monophasic standard strengh (28-day "Everyday" preparation) |
07.03.01 |
Ethinylestradiol 30mcg / levonorgestrel 150mcg Rigevidon®, Levest® |
Monophasic standard strength (21 Day preparation)
Rigevidon®
Levest® Use standard monophasic for most women. Use phased preparations for those who do not have withdrawal bleeding or experience breakthrough bleeding with monophasic. Note BNF contraindications and cautions in migraine. Advise all women to report increase in headache frequency and stop if focal symptoms not typical of aura > 1 hour. Carry small increased risk of venous thromboembolism, higher with desogestrel and gestodene than other progestogens. Use low strength if risk factors for circulatory disease and COC is otherwise suitable. |
07.03.01 |
Ethinylestradiol 35 mcg / noresthisterone 500mcg Brevinor® |
Monophasic Standard Strength (21 Day preparation) Use standard monophasic for most women. Use phased preparations for those who do not have withdrawal bleeding or experience breakthrough bleeding with monophasic. Note BNF contraindications and cautions in migraine. Advise all women to report increase in headache frequency and stop if focal symptoms not typical of aura > 1 hour. Carry small increased risk of venous thromboembolism, higher with desogestrel and gestodene than other progestogens. Use low strength if risk factors for circulatory disease and COC is otherwise suitable. |
07.03.01 |
Ethinylestradiol 35 mcg / norgestimate 250 mcg Lizinna® |
Monophasic Standard Strength (21 Day preparation) Use standard monophasic for most women. Use phased preparations for those who do not have withdrawal bleeding or experience breakthrough bleeding with monophasic. Note BNF contraindications and cautions in migraine. Advise all women to report increase in headache frequency and stop if focal symptoms not typical of aura > 1 hour. Carry small increased risk of venous thromboembolism, higher with desogestrel and gestodene than other progestogens. Use low strength if risk factors for circulatory disease and COC is otherwise suitable. |
07.03.01 |
Ethinylestradiol/cyproterone acetate Dianette® |
|
07.03.01 |
Ethinylestradiol/norelgestromin Evra® |
For patients with poor compliance or absorption problems
Restricted to women likely to comply poorly with combined oral contraceptives and those with metabolic problems. The risk of venous thromboembolism with transdermal patches may be slightly increased compared with combined oral contraceptives that contain levonorgestrel. Note BNF contraindications and cautions in migraine. Advise all women to report increase in headache frequency and stop if focal symptoms not typical of aura > 1 hour. |
07.03.01 |
Ethinylestradiol/norethisterone Synphase® |
•Phasic 21-day preparation •Added to formulary May 2017 as alternative to Trinovum which was discontinued in 2016 |
04.08.01 |
Ethosuximide |
On specialist advice
MHRA Advice When prescribing for epilepsy, the potential for clinically relevant differences to exist between different manufacturers' product is considered to be extremely low. However, consider otherpatient / carer related factors, such as negative perceptions about alternative products and/or other issues related to the patient such co-morbid autism, mental health issues, or learning disability |
15.02 |
Ethyl Chloride Cryogesic® Spray |
Hospital only |
06.06.02 |
Etidronate disodium |
In line with NICE |
15.01.01 |
Etomidate Etomidate-Lipuro® |
HOSPITAL ONLY |
15.01.01 |
Etomidate Hypnomidate® |
HOSPITAL ONLY |
07.03.02.02 |
Etonogestrel Nexplanon® |
|
08.01.04 |
Etoposide |
Commissioned by NHSE
Hospital only |
15.01.04.02 |
Etoralac |
Hospital only |
05.03.01 |
Etravirine Intelence® |
|
13.02.01 |
Eucerin® 10% urea Intensive |
Over the counter preparation suitable for self-care/purchase if appropriate |
08.01.05 |
Everolimus Votubia® |
|
08.01.05 |
Everolimus Afinitor® |
In line with NICE
Hospital only |
08.02.02 |
Everolimus Certican® |
In line with NICE |
02.12 |
Evolocumab Repatha® |
In line with NICE. |
06.04.01.01 |
Evorel Conti® |
|
06.04 |
EVOREL SEQUI PATCH |
|
06.04.01.01 |
Evorel® |
|
08.03.04.01 |
Exemestane |
|
06.01.02.03 |
Exenatide |
- prolonged-release suspension for injection
|
02.12 |
Ezetimibe Ezetrol® |
In line with NICE. |
02.11 |
Factor VIIa (Recombinant) Eptacog alfa (activated) |
|
05.03.02.01 |
Famciclovir |
Second line for Shingles |
10.01.04 |
Febuxostat Adenuric® |
Second line choice as per APC minutes (June 2019)
For use in line with NICE guidance for patients intolerant of allopurinol (due to adverse effects sufficient to warrant discontinuation, or to prevent full dose escalation for optimal effectiveness) or for whom allopurinol is contraindicated. |
08.01.05 |
Fedratinib Inrebic® |
In line with NICE |
02.06.02 |
Felodipine |
|
06.04 |
Femoston Conti ® |
|
06.04 |
Femoston Sequential ® |
|
06.04.01.01 |
Femseven ® |
|
06.04.01.01 |
Femseven Conti® |
|
06.04.01.01 |
Femseven Sequi® |
2nd line to Evorel Sequi® |
02.12 |
Fenofibrate |
|
04.07.02 |
Fentanyl |
Palliative care use only |
04.07.02 |
Fentanyl |
|
04.07.02 |
Fentanyl |
Palliative care use only |
04.07.02 |
Fentanyl |
For patients with swallowing difficulties on stable doses of opiates or on pain team specialist advice when morphine is not suitable. Prescribe by brand. Follow Optimise Rx advice for most cost effective brand |
15.01.04.03 |
Fentanyl |
Hospital only |
21 |
Fentanyl |
|
09.01.01.02 |
Ferric Carboxymaltose Ferinject® |
Hospital only |
09.01.01.01 |
Ferric maltol Feraccru® |
- Approved on formulary December 2017
- For the treatment of iron deficiency anaemia (IDA) in patients with inflammatory bowel disease (IBD), unable to tolerate other oral iron formulations
- Supported by a RICaD
|
09.01.01.01 |
Ferrous Fumarate |
|
09.01.01.01 |
Ferrous Fumarate Fersamal® |
|
09.01.01.01 |
Ferrous Gluconate |
For patients intolerant to ferrous sulphate. |
09.01.01.01 |
Ferrous Sulphate |
|
03.04.01 |
Fexofenadine |
|
03.04.01 |
Fexofenadine Telfast® |
|
05.01.07 |
Fidaxomicin |
On Microbiological advice only |
10.01.03 |
Filgotinib Jyseleca® |
In line with NICE |
09.01.06 |
Filgrastim |
Hospital only |
06.04.02 |
Finasteride |
|
13.09 |
Finasteride 1mg Propecia ® |
For hyperandrogenism in women (unlicensed)
Black listed in NHS primary care
Link to Section 13.9 |
08.02.04 |
Fingolimod |
In line with NICE |
A5.03.04 |
Flaminal® Forte Gel |
Alginate gel. Moderate to heavily exuding wounds. Contains antimicrobial enzymes. Type of wound product is suitable for Colonised wound bed. More suited to sloughy wounds. Can be used on all wound types Useful for cavity wounds and sinus’s Requires a secondary dressing Duration dressing remains on wound before changing 1-7 days Frequency of dressing change 1-7 days dependent on exudate levels Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Sensitivity to alginate dressings or polyethylene glycol Full thickness burns Rationale for inclusion in formulary 1st line antimicrobial in paediatrics Consider as first line product if signs of colonisation or clinical infection Does not cause cellular damage |
A5.03.04 |
Flaminal® Hydro Gel |
Alginate gel. Low to moderate exuding wounds. Contains antimicrobial enzymes Type of wound product is suitable for Colonised wound bed. More suited to sloughy wounds. Can be used on all wound types Useful for cavity wounds and sinus’s Requires a secondary dressing Duration dressing remains on wound before changing 1-7 days Frequency of dressing change 1-7 days dependent on exudate levels Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Sensitivity to alginate dressings or polyethylene glycol Full thickness burns Rationale for inclusion in formulary 1st line antimicrobial in paediatrics Consider as first line product if signs of colonisation or clinical infection Does not cause cellular damage |
07.03.04 |
Flat spring diaphragm |
Sizes 55-95mm (rising in 5mm) |
09.04 |
FlavourPac |
Flavouring preparations
- For flavouring unpalatable flavouring amino acid supplements or feeds in inborn errors of metabolism
- Essential for flavouring different unflavoured amino acid supplements in inborn errors of metabolism particularly for non PKU conditions. They offer common children’s favourite flavours: e.g. orange or raspberry. Flavourings are important, as amino acid formulations are unpalatable and unacceptable particularly for patients with late diagnosed conditions.
- They cannot be purchased from a supermarket
- For use with Vitaflo's range of unflavoured protein substitutes for metabolic diseases; not suitable for child under 3 years
|
02.03.02 |
Flecainide |
|
02.03.02 |
Flecainide |
Use current status at Place/Trust
Sandwell
Initiation under specialist supervision Contraindicated in heart failure or abnormal left ventricular function Rhythm control should be used when: symptomatic; under 65's; first time -lone AF; secondary to treated or corrected precipitant with congestive heart failure. Beta-blockers are first line, flecainide is a second line option when there is no structural heart disease:
Wolverhampton
Walsall
Dudley
|
01.06.05 |
Fleet Phospho-soda® |
For use in hospital prior to bowel procedures |
19.06 |
Flivasorb |
Superabsorbent dressing Alternative to KerraMax Care® if patient discharged from hospital with. Type of wound product is suitable for For heavily exuding wounds Can be used under compression bandages Secondary Dressing Only Duration dressing remains on wound before changing Up to 7 days Frequency of dressing change When exudate levels determine Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Known sensitivity to any components of the dressing Lightly exuding wounds Must not be cut or torn Rationale for inclusion in formulary Management of heavily exuding wounds. Cost effective. Must be applied white side to the wound bed. |
09.04.01 |
Flour mixes and egg substitutes |
Low-protein foods
These products are not available to purchase in supermarkets
They are important to provide essential energy and variety to aid the palatability of low protein diets. They are important for good metabolic control of the patient. Poor access to these products could lead to poor dietary adherence. This will cause poor metabolic control which may lead to irreversible brain damage
The NSPKU guidelines for prescription of low protein foods can be used for other amino acid disorderssuch as MSUD, homocystinuria, tyrosinaemia and pyridoxine response epilepsy
Protein free - necessary for children and adults with inborn errors of protein metabolism who do not tolerate very little natural protein
The specialist dietician will make individual reccomendations based on diagnosis,protein recommendations, weight etc.
- Essential protein-free basic products. Necessary for children and adults with inborn errors of protein metabolism who tolerate very little natural protein. 1 ordinary egg = 6g protein. 100g flour = 10g protein
|
13.04 |
Flucinolone Acetonide 0.0025% Synalar 1 in 10 Dilution® |
Potency: mild Paediatric use only |
13.04 |
Flucinolone Acetonide 0.025% Synalar® Gel |
Potency - potent Gel only |
05.01.01.02 |
Flucloxacillin |
|
05.01.01.02 |
Flucloxacillin |
|
05.02.01 |
Fluconazole |
|
05.02.01 |
Fluconazole |
Capsules
Suspension - Only for patients with swallowing difficulties |
07.02.02 |
Fluconazole |
For other oral treatments please see primary care antimicrobial guidelines in chapter 5 |
05.02 |
Flucytosine |
|
05.02.05 |
Flucytosine Ancotil® |
|
08.01.03 |
Fludarabine Phosphate |
Commissioned by NHSE Injection-hospital only |
06.03.01 |
Fludrocortisone Acetate |
|
13.04 |
Fludroxycortide tape Previously known as Haelan® |
Potency - moderate |
A5.16 |
Fludroxycortide tape |
Specialist recommendation only Adhesive, waterproof, occlusive tape impregnated with 4mg/cm2 fludroxycortide (topical steroid) Type of wound product is suitable for Chronic over granulation, non acute or weeping. Duration dressing remains on wound before changing Cut the tape to size. Apply for 12 hours at a time, remove and discard. Apply to clean, dry skin that is shorn of any hair. Frequency of dressing change Apply daily for 12 hours at a time. Maximum treatment time 7 days. Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Chicken pox Tuberculosis of the skin Hypersensitivity to any components in the tape (steroid fludroxycortide) Facial rosacea Acne vulgaris Perioral dermatitis Perianal and genital pruritis Dermatoses in infants Dermatitis napkin eruption Bacterial, viral and fungal infections Keep away from the eyes Avoid prolonged use on the face Not for untreated bacterial, fungal or viral skin lesions Rationale for inclusion in formulary Treatment of over granulation |
15.01.07 |
Flumazenil Anexate® |
Hospital only |
12.01.01 |
Flumetasone with Clioquinol Locorten-Vioform® |
|
04.07.04.02 |
Flunarizine |
Unlicensed medicine
Specialist use only
|
13.04 |
fluocinolone acetonide 0.025% with clioquinol 3% Synalar C® |
Potency - Potent
REPLACES BETNOVATE C Cream Ointment Restricted to use in inflammatory conditions associated with an infection with confirmed susceptibility to the antimicrobial component. Use for short periods - typically no more than one week |
11.04.01 |
Fluocinolone intravitreal implant Iluvien® |
For specialist use only in line with NICE |
11.04.01 |
Fluorometholone FML® |
Recommended second line for patients who have experienced a rise in intraocular pressure with other corticosteroids
On specialist ophthalmologist recommendation |
08.01.03 |
Fluorouracil |
Commissioned by NHSE
Hospital only |
11.99.99.99 |
Fluorouracil |
Hospital only |
13.08.01 |
Fluorouracil Efudix® |
|
13.08.01 |
Fluorouracil 0.5% & salicylic acid 10% Actikerall® |
For hyperkaratotic lesions |
04.03.03 |
Fluoxetine |
|
04.03.03 |
Fluoxetine |
|
04.02.01 |
Flupentixol |
Supported by ESCA |
04.02.02 |
Flupentixol Decanoate |
The APC's view is that, on clinical grounds, the status of antipsychotic depot injections should be amber with a framework in place in Primary Care before transfer
HOWEVER, until the commissioning arrangements have been agreed to allow safe transfer of patient care, the status will remain RED |
04.02.02 |
Fluphenazine Decanoate Modecate® |
The APC's view is that, on clinical grounds, the status of antipsychotic depot injections should be amber with a framework in place in Primary Care before transfer
HOWEVER, until the commissioning arrangements have been agreed to allow safe transfer of patient care, the status will remain RED
Discontinued by UK manufacturer by the end of 2018 |
08.03.04.02 |
Flutamide |
|
03.02 |
Fluticasone |
- Flixonase Nasal Drops
- Flixotide Nebuliser Liquid
|
03.02 |
Fluticasone and salmeterol Seretide® |
For paediatric use ONLY (i.e. up to 18 years of age)
- Seretide Evohaler- 50mg and 125mg only .
- Should be prescribed by the intended brand to ensure patients are maintained on the formulation they are used to.
How to use an Accuhaler Inhaler How to use a Metered Dose Inhaler How to use a Metered Dose Inhaler with a Large Volume Spacer Device How to use a Metered Dose Inhaler with a Small Volume Spacer Device
|
12.02.01 |
Fluticasone furoate Avamys® |
Approved for use in children and adults
Previous APC decision reviewed in December 2015 |
12.02.01 |
Fluticasone furoate |
Hospital only |
03.02 |
Fluticasone furoate & vilanterol Relvar Ellipta® |
How to use an Ellipta Inhaler
|
03.02 |
Fluticasone Nasal Spray |
BRANDS
|
03.02 |
Fluticasone Nasal Spray Avamys® |
|
03.02 |
Fluticasone propionate Flixotide® |
How to use an Accuhaler Inhaler How to use a Metered Dose Inhaler How to use a Metered Dose Inhaler with a Large Volume Spacer Device How to use a Metered Dose Inhaler with a Small Volume Spacer Device |
12.02.01 |
Fluticasone Propionate Flixonase Nasule® |
Specialist recommendation only for nasal polyps |
03.02.03 |
Fluticasone/vilanterol/Umeclidinium Trelegy Ellipta® |
|
09.01.02 |
Folic Acid |
Tablets
Sugar Free Solution Lexpec®
|
02.08 |
Fondaparinux Arixtra® |
Hospital Only |
09.04 |
Food First |
Where clinically appropriate encourage a nutrient dense food and fluid intake for patients at risk of malnutrition |
09.04.02 |
Food First |
Where clinically appropriate encourage a nutrient dense food and fluid intake for patients at risk of malnutrition. |
09.04 |
Foodlink® Complete |
First line product
- More than 1.5 kcal/mL and 5g (or more) protein/100 mL
- Not suitable for CKD 4-5, renal pts.
- Not suitable for lactose intolerance
- Not suitable for bile acid malabsorption or fat maldigestion associated with biliary diseases/conditions
- To be made up with whole milk
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula
|
09.04 |
Foodlink® Complete with Fibre |
First line with added fibre
- More than 1.5 kcal/mL and 5g (or more) protein/100 mL
- Not suitable for CKD 4-5, renal pts.
- Not suitable for lactose intolerance
- Not suitable for bile acid malabsorption or fat maldigestion associated with biliary conditions
- To be made up with whole milk
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula
|
03.01.01.01 |
Formoterol Fumarate Oxis Turbohaler® |
|
09.04.02 |
Fortini® |
- More than 1 kcal/ml and less than 4g protein/100ml
- Sip feed for children over 8kg with faltering growth
- Disease-related malnutrition and growth failure in child 1–6 years, body-weight 8–20 kg
|
09.04.02 |
Fortini® Compact Multi Fibre |
- Child: More than 1 kcal/mL and less than 4 g protein/100 mL
- Low volume supplement
- Supporting an unmet paediatric nutritional need
- No other product is current available to meet this need
|
09.04.02 |
Fortini® Creamy Fruit |
- Child: More than 1 kcal/mL and less than 4 g protein/100 mL
- High energy fruit pudding for children with faltering growth
|
09.04.02 |
Fortini® Multi Fibre |
- Child: More than 1 kcal/mL and less than 4 g protein/100 mL
- Sip feed for children over 8kg with faltering growth, with added fibre
- Disease-related malnutrition and growth failure in child 1–6 years, body-weight 8–20 kg
|
09.04.02 |
Fortini® Smoothie Multi Fibre |
- Child: More than 1 kcal/mL and less than 4 g protein/100 mL
- Sip feed for children over 8kg with faltering growth
|
09.04.02 |
Fortini®1.0 Multi Fibre |
Child under 12 years
- 1 kcal/mL and less than 4g protein/100 mL
- Standard 1 kcal/mL with fibre
|
09.04 |
Fortisip® |
- Restricted for use where fluid volume is a benefit
- Restricted for patients who are lactose intolerant
- Maybe used as an alternative as a bolus feeds
- Low fibre
- Low osmolality
- More than 1.5 kcal/mL and 5g (or more) protein/100 mL
- Low volume supplement and for bolus feeding
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula
- Not suitable for child under 3 years; use with caution in child 3–5 years
- Second line choice for 200ml ready-made. If powder is not tolerated or contraindicated
|
09.04 |
Fortisip® 2kcal |
- More than 1.5 kcal/mL and 5g (or more) protein/100 mL
- For bolus tube feeding only
- Only on dietetic advice sip feed in small volum.
- Nutritionally complete in 2 bottles
|
09.04 |
Fortisip® Bottle |
- 1.5 kcal/mL and 5g (or more) protein/100 mL
- Restricted for use where fluid volume is a benefit
- Restricted for patients who are lactose intolerant
- Maybe used as an alternative as a bolus feeds
- Low fibre
- Low osmolality.
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula
- Not suitable for child under 3 years; use with caution in child 3–5 years
|
09.04 |
Fortisip® Compact |
Second line supplements choice
- More than 1.5 kcal/mL and 5g (or more) protein/100 mL
- Low volume supplement and for bolus feeding
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula
- Not suitable for child under 3 years; use with caution in child 3–5 years
|
09.04 |
Fortisip® Compact Fibre |
Second line supplements choice for use when fibre in indicated as advised by dietitan only
- More than 1.5 kcal/mL and 5g (or more) protein/100 mL
- Low volume supplement and for bolus feeding
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula
- Not suitable for child under 3 years; use with caution in child 3–5 years
|
09.04 |
Fortisip® Compact Protein |
- More than 1.5 kcal/mL and 5 g (or more) protein/100 mL
- Not to be used without dietetic advice that higher protein is clinically appropriate
- With added protein
- Low volume supplement and for bolus feeding advised by dietitian only
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula.
- Not suitable for child under 3 years; use with caution in child 3–5 years.
|
09.04 |
Fortisip® Yogurt Style |
- 1.5 kcal/mL and 5g (or more) protein/100 mL
- For dysgeusia and flavour fatigue only
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula
- Not suitable for child under 3 years
|
09.04 |
Fortisip® Yogurt Style |
- 1.5 kcal/mL and 5g (or more) protein/100 mL
- For dysgeusia and flavour fatigue only
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula. Not suitable for child under 3 years
|
05.03.01 |
Fosamprenavir Telzir® |
|
05.03.02.02 |
Foscarnet Sodium |
|
05.03.02.02 |
Foscarnet Sodium Foscavir® |
|
05.01.13 |
Fosfomycin |
Second line treatment for sensitivities |
05.01.13 |
Fosfomycin Injection |
Hospital use only under microbiological advice |
04.07.04.02 |
Fremanezumab Ajovy® |
In line with NICE |
02.11 |
Fresh Frozen Plasma |
|
09.04 |
Fresubin 2 kcal Fibre Drink |
- More than 1.5 kcal/mL and 5g (or more) protein/100 mL
- Used where 2kcal/ml sip feed in small volume with fibre is required
- High Cal low Vol with added fibre
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula ; also CAPD, haemodialysis.
- Not suitable for use in child under 1 year; use with caution in child 1–5 years
|
09.04 |
Fresubin® 2 kcal Drink |
First line choice for 2kcal/ml sip feed
- More than 1.5 kcal/mL and 5g (or more) protein/100 mlL
- Small volume required and based on taste preference
- Nutritionally complete in 2 bottles
- High Cal low Vol
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula; also CAPD, haemodialysis.
- Not suitable for use in child under 1 year; use with caution in child 1–5 years
|
09.04.02 |
Fresubin® HP Energy |
- 1.5 kcal/mL and 5g (or more) protein/100 mL
- Only available product with high protein and high MCT (burns pts, tumour pts, and liver pts.)
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula ; also CAPD and haemodialysis
|
09.04.02 |
Fresubin® HP Energy Fibre |
- 1.5 kcal/mL and 5g (or more) protein/100 mL
- Only available product with high protein and high MCT with fibre (burns pts, tumour pts, liver pts)
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula
|
09.04 |
Fresubin® Jucy Drink |
- More than 1 kcal/mL and less than 5 g protein/100 mL
- Juice style fat free, low K+
- Patients who dislike milky tasting drinks
- Caution advised – not milk free and high sugar content
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula ; also CAPD, haemodialysis
|
09.04 |
Fresubin® Thickened |
- 1.5 kcal/mL and 5g (or more) protein/100 mL
- Used for dysphagia pts only
- Dysphagia or disease-related malnutrition. Not suitable for child under 3 years; use with caution in child 3–4 years.
|
09.04 |
Fresubin® YOcreme |
- For dysgeusia and flavour fatigue only
- Not recommended by SALTs for use as a dysphagia product
- Low energy per serving as a semi-solid supplement where low volume is required only
|
09.04 |
Fructose |
- Special additives for conditions of intolerance
- Used as a partial CHO source in modular feeds for infants and children with malabsorption secondary to short bowel syndrome or other malabsorption states
- (Laevulose) For proven glucose/galactose intolerance
|
09.06.07 |
FruitVits® |
- For patients with inborn errors of metabolism and for enteral feed patients
- For use in children 3 years and over with inborn errors of metabolism. This is a small volume, flavoured, carbohydrate free vitamin/mineral supplement used in conditions like citrin deficiency. There are no other carbohydrate free preparations available. It cannot be purchased from a supermarket. The dose and type of product should always be advised by the specialist dietitian according to the needs of the patient
- Vitamin, mineral, and trace element supplement in children 3–10 years with restrictive therapeutic diets
|
08.03.04.01 |
Fulvestrant Faslodex® |
|
02.02.02 |
Furosemide |
|
21 |
Furosemide |
- Syringe driver use for symptom management in heart failure at EOL
|
05.01.07 |
Fusidic acid |
|
11.03.01 |
Fusidic acid |
NICU Use as per guideline - 1st line
Bacterial conjunctivitis infection 2nd line per Antimicrobial Guidelines
|
13.10.01.02 |
Fusidic Acid 2% |
|
09.04 |
GA Amino 5 |
- Amino acid supplement without lysine – low in tryptophan for infants with GA1 - used for tube feeding in emergencies
- The only pre-measured amino acid supplement without lysine, low in tryptophan for children with GA1 that can be administered via a tube in emergency feeds. It is essential it is easy to use in an emergency and pre-measured is safer, particularly for non-English speaking families. It can also be used in pyridoxine responsive epilepsy
|
09.04 |
GA Anamin Junior |
- An unthickened amino acid supplement without lysine, low in tryptophan for children with GA1 that can be given as a drink. It can also be used in pyridoxine responsive epilepsy
|
09.04 |
GA Express 15 (not ACBS approved) |
- Amino acid supplement without lysine and low in tryptophan for children and adults with GA1
- The only low volume, vitamin and mineral amino acid supplement without lysine, low in tryptophan for use in patients > the age of 6 years’ children and adults with GA1 and pyridoxine responsive epilepsy
|
09.04 |
GA Gel® |
- Amino acid supplement without lysine – low in tryptophan for infants with GA1
- The only weaning (thickened) amino acid supplement without lysine, low in tryptophan for children with GA1. It can also be used in pyridoxine responsive epilepsy
- Nutritional supplement for dietary management of type 1 glutaric aciduria in children 6 months–10 years
|
09.04 |
GA1 Anamix® Infant |
- Amino acid supplement without lysine – low in tryptophan for infants with GA1
- The only amino acid supplement without lysine, low in tryptophan for infants with GA1 and pyridoxine responsive epilepsy
- Nutritional supplement for the dietary management of proven glutaric aciduria (type 1) in children from birth to 3 years
|
04.07.03 |
Gabapentin |
2nd line
Be aware of abuse and addiction potential associated with this class of agent Due to the risk of adverse effects associated with Gabapentin,start with the lowest effective dose and titrate up to the minimum effective dose. Educate patient on titration At follow up, check patient's tolerance of treatment and understanding of dose titration See Gabapentin leave sheet for dose titration information Reduce dose in renal impairment |
04.08.01 |
Gabapentin |
On advice of specialist
Tablets £££££, capsules are more cost effective
MHRA Advice For patients being treated for epilepsy , it is usually unnecessary to ensure that patiemts are maintained on a specific manufacturer's product unless there are specific reasons such as patient anxiety and risk of confusion or dosing errors |
04.08.01 |
Gabapentin |
On advice of specialist
MHRA Advice It is usually unnecessary to ensure that patients are maintained on a specific maufacturer's product unless there are specific reasons such as patient anxiety and risk of confusion or dosing errors |
09.04 |
Galactomin 17® |
- Specialised formulas: Infant and child: Residual lactose formula
- Lactose free feed for use in adults metabolic disease only
- Used as a milk alternative in adults, lactose free with galactosaemia. This is not used for infants by Birmingham Children’s Hospital. The dose and type of product should always be advised by the specialist dietitian according to the needs of the patient
- Proven lactose intolerance in pre-school children, galactosaemia, and galactokinase deficiency
|
09.04 |
Galactomin 19® |
- Specialised formulas: Infant and child: Fructose-based formula
- Disease specific fructose containing formula for infants and children with glucose galactose malabsorption.
- Conditions of glucose plus galactose intolerance
|
04.11 |
Galantamine |
- Tablets
- M/R capsules
- Oral solution
|
04.07.04.02 |
Galcanezumab Emgality® |
In line with NICE |
A5.05.01 |
Gamgee UHB burns unit ONLY |
Sterile or non sterile highly absorbent cotton wool enclosed in an absorbent cotton cover Type of wound product is suitable for Full thickness burns Can be cut to required size Secondary dressing Duration dressing remains on wound before changing Dependent on exudate levels Frequency of dressing change Dependent on exudate levels Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Not to be used as a primary dressing Only to be used in UHB burns unit Rationale for inclusion in formulary UHB burns unit only |
05.03.02.02 |
Ganciclovir |
|
05.03.02.02 |
Ganciclovir Cymevene® |
|
11.03.03 |
Ganciclovir Virgan® |
Use on specialist ophthalmologist recommendation |
01.01.02 |
Gaviscon Infant |
Oral powder |
08.01.05 |
Gefitinib Iressa® |
Commissioned by NHSE |
09.02.02.02 |
Gelatin Gelofusine® |
For use by endoscopy speciality at Sandwell and West Birmingham NHS Trust |
12.03.01 |
Gelclair® |
Oncology & haematology use only |
20 |
Gelofusion and indigocarmine for submucosal injection for endoscopic mucosal resection |
For use by endoscopy speciality at Sandwell and West Birmingham NHS Trust |
08.01.03 |
Gemcitabine Gemzar® |
Commissioned by NHSE Hospital only |
07.01.01 |
Gemeprost |
For Specialist/ Hospital Use Only |
08.02.03 |
Gemtuzumab ozogamicin Mylotarg® |
Hospital use only
In line with NICE |
03.13 |
Gentamicin |
|
03.13 |
Gentamicin |
Hospital only |
05.01.04 |
Gentamicin |
For hospital use only |
11.03.01 |
Gentamicin |
Possible second line after chloramphenicol on specialist ophthalmologist recommendation |
11.03.01 |
Gentamicin |
For the treatment of corneal abscess only on specialist ophthalmologist advice. |
12.01.01 |
Gentamicin 0.3% Genticin® |
Only with positive culture/sensitivity data |
08.01.05 |
Gilteritinib Xospata® |
In line with NICE |
08.02.04 |
Glatiramer Acetate Copaxone® |
Hospital use only |
05.03.03.02 |
Glecaprevir-pibrentasvir Maviret® |
In line with NICE |
06.01.02.01 |
Gliclazide |
- Tablets
- Modified Release Tablets
Check OptimiseRx for most cost effective brand |
06.01.02.01 |
Glimepiride |
|
06.01.04 |
Glucagon GlucaGen® HypoKit |
|
06.01.04 |
GlucoGel® |
|
06.01.04 |
Glucose |
|
06.01.04 |
Glucose |
|
06.01.04 |
Glucose |
|
09.04 |
Glucose |
- Special additives for conditions of intolerance
- Used as a partial CHO source in modular feeds for infants and children with malabsorption secondary to short bowel syndrome or other malabsorption states
- (Dextrose monohydrate) For use as an energy supplement in sucrose-isomaltase deficiency
|
21 |
Glucose 4% and Sodium Chloride 0.18% |
|
06.01.06 |
Glucose interstitial fluid detection sensors FreeStyle Libre 2 Sensor ® |
in Type I Diabetes
in Type II Diabetes in line with RMOC criteria |
09.02.02.01 |
Glucose Intravenous |
Hospital use only |
09.08.01 |
Glutamine |
|
13.07 |
Glutaraldehyde 10% |
Over the counter preparation suitable for self-care/purchase if appropriate |
09.04.01 |
Gluten Free Foods |
Department of Health and Social Care (DHSC) guidance –
- GF, GF & Wheat Free (WF) bread (includes rolls, part baked bread, and pizza bases)
- GF, GF&WF mixes
Follow Coeliac UK prescribing guidance for monthly quantities (based on age) |
01.06.02 |
Glycerol (Glycerin) Suppositories |
|
01.07.04 |
Glyceryl Trinitrate 0.4% Ointment Rectogesic® |
|
02.06.01 |
Glyceryl Trinitrate 400mcg/ dose Spray |
|
02.06.01 |
Glyceryl trinitrate buccal |
|
02.06.01 |
Glyceryl Trinitrate Injection |
Secondary Care use only |
02.06.01 |
Glyceryl Trinitrate Sublingual tablets |
|
02.06.01 |
Glyceryl Trinitrate Transdermal Patches |
|
07.04.04 |
Glycine |
For Specialist / Hospital Use Only |
13.14.07 |
Glycopyrrolate 0.05% w/v in water |
|
13.14.07 |
Glycopyrrolate 2% w/w in cetomacrogol cream |
|
13.12 |
Glycopyrronium |
Unlicensed
Specialist initiation for hyperhidrosis |
15.01.03 |
Glycopyrronium |
HOSPITAL ONLY |
21 |
Glycopyrronium |
|
04.12 |
Glycopyrronium bromide Sialanar® |
£££££
Specilaist initiation and stabilisation
Approved on formualry December 2017
|
03.01.04 |
Glycopyrronium/formoterol Bevespi Aerosphere® |
|
09.04 |
Glycosade® |
- Slow release CHO to prevent hypoglycaemia in GSD
- The only specially formulated slow release carbohydrate to prevent hypoglycaemia in severe forms of GSD e.g. Type I and III which allows extended fasting time. The dosage is dependent on age, weight and clinical symptoms of hypoglycaemia. Doses may be given at regular intervals during the day and night or at bedtime only. The dose and frequency of dose should always be advised by the specialist dietitian according to the needs of the patient. Glycosade is in a pre-measured sachet. The dose and type of product should always be advised by the specialist dietitian according to the needs of the patient
- A nutritional supplement for use in the dietary management of glycogen storage disease and other metabolic conditions where a constant supply of glucose is essential. Not suitable for use in children under 2 years
|
09.04 |
Glytactin Bettermilk 15 |
- A low phenylalanine supplement derived from whey protein for children and adults with phenylketonuria. It is more palatable than amino acid supplements and associated with better utilisation of protein. Very useful for adult patients trying to return to diet or children / adults struggling to take their amino acid product because of its taste. Suitable from aged 4 years
|
09.04 |
Glytactin Bettermilk RTD 15 (original and chocolate) |
- A low phenylalanine supplement derived from whey protein for children and adults with phenylketonuria. It is more palatable than amino acid supplements and associated with better utilisation of protein. Very useful for adult patients trying to return to diet or children / adults struggling to take their amino acid product because of its taste. Suitable from aged 4 years
|
01.05 |
Golimumab Simponi® |
Specialist use only in line with NICE TA |
10.01.03 |
Golimumab Simponi® |
Hospital only
Available via Home Care
|
06.05 |
GONADORELIN |
HRF - Red
Powder For - Red |
06.07.02 |
Goserelin |
BRANDS
|
08.03.04.02 |
Goserelin Zoladex® |
Advanced prostate cancer |
08.03.04.02 |
Goserelin Zoladex® LA |
Advanced prostate cancer |
A5.09.01 |
Graduated compression hosiery |
Based on assessment |
04.06 |
Granisetron Sancuso® |
Hospital use only for oncology patients |
04.06 |
Granisetron |
Hospital only |
A5.02.04 |
Granuflex® |
Specialist recommendation only Type of wound product is suitable for Hyperkeratosis, granulating wounds, forms cohesive gel on contact with exudate Duration dressing remains on wound before changing Up to 7 days Frequency of dressing change 3-7 days Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Known sensitivity to ingredients - contains pectin and gelatine Not for diabetic foot ulcers or ischaemic wounds Not for infected wounds Rationale for inclusion in formulary Comformable waterproof dressing, aids rehydration. Reduces and softens hyperkeratosis |
03.04.02 |
Grass and Tree Pollen Extract Pollinex® |
For hospital use only |
03.04 |
Grass pollen extract Pollinex ® |
|
03.04 |
Grass pollen extract Grazax® |
|
05.02.05 |
Griseofulvin |
|
09.04 |
GTO oil |
- A cooking oil for dietary treatment of adrenoleukodystrophy. The dose and type of product should always be advised by the specialist dietitian according to the needs of the patient
|
04.04 |
Guanfacine Intuniv® |
For the treatment of ADHD in children and adolescents 6-17 years old for whom stimulants are not suitable, not tolerated or have been shown to be ineffective |
13.05.03 |
Guselkumab Tremfya® |
In line with NICE |
14.04 |
Haemophilus Type B Menigococcal Group C Conjugate Vaccine Menitorix® |
|
01.07.01 |
Haemorrhoid relief ointment |
|
01.07.01 |
Haemorrhoid relief suppositories |
|
04.02.01 |
Haloperidol |
For rapid tranquilisation
Not to be used for psychiatric / anxiolytic purposes in Primary Care |
04.02.01 |
Haloperidol |
tablets capsules SF liquid Supported by an ESCA |
04.02.02 |
Haloperidol Haldol Decanoate® |
The APC's view is that, on clinical grounds, the status of antipsychotic depot injections should be amber with a framework in place in Primary Care before transfer
HOWEVER, until the commissioning arrangements have been agreed to allow safe transfer of patient care, the status will remain RED |
04.09.03 |
Haloperidol |
|
09.04 |
HCU Anamix® Infant |
- Amino acid supplement without methionine for infants with homocystinuria
- The only amino acid supplement without methionine for infants with homocystinuria. It is given to screened infants for HCU. The dose and type of product should always be advised by the specialist dietitian according to the needs of the patient
- Nutritional supplement for the dietary management of proven vitamin B6 non-responsive homocystinuria or hypermethioninaemia in children from birth to 3 years
|
09.04 |
HCU cooler® 10 |
- Amino acid supplement without methionine for children and adults with homocystinuria
- The only liquid amino acid supplement without methionine for children with homocystinuria aged 3 to 6 years. Larger pouches are unacceptable for this age group of children and provide in excess of protein requirements
|
09.04 |
HCU cooler® 15 |
- Amino acid supplement without methionine for teenagers and adults with homocystinuria
- The only liquid amino acid supplements without methionine for children with homocystinuria aged 7 to 12 years. Larger pouches are unacceptable for this age group of children and provide in excess of protein requirements
|
09.04 |
HCU cooler® 20 |
- Amino acid supplement without methionine for teenagers and adults with homocystinuria
- One of two liquid amino acid supplements without methionine for children with homocystinuria aged >12 years. They need the larger sachets (20g protein equivalent) meet their non-methionine protein requirements
|
09.04 |
HCU Express® 15 |
- Amino acid supplement without methionine for teenagers and adults with homocystinuria
- The only powdered amino acid supplement without methionine that provides 15g protein equivalent per sachet for children with homocystinuria aged 7 to 12 years. Larger sachets are unacceptable for this age group of children and provide in excess of protein requirements
- A methionine-free protein substitute for use as a nutritional supplement in children over 8 years with homocystinuria
|
09.04 |
HCU Express® 20 |
- Amino acid supplement without methionine for teenagers and adults with homocystinuria
- One of 2 powdered amino acid supplements without methionine that provides 20g protein equivalent per sachet for teenagers with homocystinuria aged >12 years. They need the larger pouches to meet their non-methionine protein requirements. It is important we have a choice of more than 1 product for this age group as adherence is poor
- A methionine-free protein substitute for use as a nutritional supplement in children over 8 years with homocystinuria
|
09.04 |
HCU gel® |
- Amino acid supplement without methionine for children with homocystinuria
- The only weaning (thickened) amino acid supplement without methionine for children with homocystinuria
- A methionine-free protein substitute for use as a nutritional supplement for the dietary management of children 1–10 years with homocystinuria
|
09.04 |
HCU Lophlex® LQ 20 |
- Amino acid supplement without methionine for teenagers and adults with homocystinuria
- One of 2 powdered amino acid supplements without methionine that provides 20g protein equivalent per sachet for teenagers with homocystinuria aged >12 years. They need the larger pouches to meet their non-methionine protein requirements. It is important we have a choice of more than 1 product for this age group as adherence is poor
- Nutritional supplement for the dietary management of homocystinuria in children over 3 years
|
09.06.07 |
Healthy Start Vitamins |
Available free of charge from designated centres. |
01.03 |
Helicobacter Stool Antigen Test |
In line with NICE / PHE guidance
Check availability of test in local laboratory |
01.03 |
Helicobacter Urea Breath Test |
In line with NICE / PHE guidance |
02.08.01 |
Heparin Sodium |
|
13.13 |
Heparinoid 0.3% Hirudoid® |
|
14.04 |
Hepatitis A and Typhoid ViATIM® |
|
14.04 |
Hepatitis A vaccine Paediatric Single Component HAvrix ® Junior Monodose, VAQTA ® Paediatric |
|
14.04 |
Hepatitis A vaccine Single Component Havrix ® Monodose, AVAXIM ®, VAQTA ® Adult |
|
14.04 |
Hepatitis A vaccine with Hepatitis B vaccine Twinrix® Adult, Twinrix® Paediatric, Ambirix® |
|
14.05.02 |
Hepatitis B immunoglobulin |
|
14.04 |
Hepatitis B vaccine Single Component Engerix B® Fendrix® HBvaxPRO® |
|
13.11.02 |
Hibitane Obstetric® |
|
13.10.05 |
Histoacryl® |
Hospital only
For use by endoscopy speciality at Sandwell and West Birmingham NHS Trust |
20 |
Histoacyl and lipiodol for gastric varices |
For use by endoscopy speciality at Sandwell and West Birmingham NHS Trust |
09.04 |
Homemade milkshake |
Where clinically appropriate encourage a standardised home-made nutritious drink at least equivalent to a standard 1.5KCal/ml prescribed bottle supplement in terms of calories and protein |
09.04.02 |
Homemade milkshake |
Where clinically appropriate encourage a standardised home-made nutritious drink equivalent to a standard 1.5 KCal/mL prescribed bottle supplement in terms of calories and protein. |
03.04 |
House dust mite extract Mitizax® |
|
03.04 |
House dust mite extract Acarizax® |
|
06.05 |
Human Chorionic Gonadotrophin |
HUMAN MENOPAUSAL GONADOTROPHINS - Red
HUMAN MENOPAUSAL GONADOTROPHINS / Menogon - Red |
02.11 |
Human fibrinogen / Human thrombin Evicel® |
|
09.08.02 |
Human hemin Normasang® |
NHSE commissioned |
12.04 |
Human papilloma virus vaccine Gardasil® |
For use by ENT Specialists in recurrent respiratory papillomatosis (RRP) |
14.04 |
Human papilloma virus vaccine Gardasil®, Gardasil®9 |
|
14.04 |
Human Papilloma virus vaccine Cervarix ® |
Use Gardasil first line |
14.04 |
Human papolloma virus vaccine |
For use by ENT Specialist only in recurrent respiratory papillomatosis (RRP) |
11.99.99.99 |
Hyaluronidase Hyalase® |
Hospital only |
02.05.01 |
Hydralazine |
|
01.05.02 |
Hydrocortisone |
|
06.03.02 |
Hydrocortisone |
- SODIUM SUCCINATE
- SODIUM PHOSPHATE
|
06.03.02 |
Hydrocortisone |
|
13.04 |
Hydrocortisone 0.25% Crotamiton 10% Eurax-Hydrocortisone® |
Potency-mild
Post scabies once infection cleared but itch still present. |
13.04 |
Hydrocortisone 0.5% |
Potency-mild Cream Ointment |
13.04 |
Hydrocortisone 0.5% ,chlorhexidine HCl 1% & nystatin Nystaform-HC® |
Potency - mild Paediatric use only Replacement for discontinued Vioform HC |
13.04 |
Hydrocortisone 1% |
Potency-mild Cream Ointment |
13.04 |
Hydrocortisone 1% and oxytetracycline 3% Terra-Cortril® ointment |
Potency-mild |
13.04 |
Hydrocortisone 1% with Clotrimazole 1% Canesten HC® |
Potency-mild |
13.04 |
Hydrocortisone 1% with Miconazole Nitrate 2% Daktacort® cream |
Potency-mild |
12.03.01 |
Hydrocortisone 2.5mg |
Specialist recommendation only |
10.01.02.02 |
Hydrocortisone acetate Hydrocortistab® |
For hospital use |
13.04 |
Hydrocortisone Acetate 1% with Fusidic Acid 2% Fucidin H® cream |
Potency-mild
|
12.01.01 |
Hydrocortisone Acetate 1% with Gentamicin 0.3% Gentisone® HC |
Only with positive culture/sensitivity data |
13.04 |
Hydrocortisone Butyrate 0.1% Locoid® |
Potency - potent Cream Lipocream Ointment Scalp lotion |
01.05.02 |
Hydrocortisone foam enema Colifoam ® |
For specialist initiation
Foam enema 125mg /metered application
|
01.07 |
Hydrocortisone with lidocaine |
|
A5.02.02 |
Hydrofilm® |
Preferred local option Vapour-permeable adhesive film Type of wound product is suitable for Dry non infected wounds, retention of lines, fixation of secondary dressings, protection of intact skin, protection of skin against friction, protection of newly epithelialized wounds Duration dressing remains on wound before changing Up to 7 days Frequency of dressing change Up to 7 days Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Clinically infected wounds, bleeding or exuding wounds Rationale for inclusion in formulary Retention of lines, protection of intact skin, fixation of other dressings. Cost effective Waterproof |
12.03.04 |
Hydrogen peroxide mouthwash BP |
|
13.11.06 |
Hydrogen peroxide Crystacide® |
|
13.11.06 |
Hydrogen Peroxide Solution |
3% (10 vols) 6% (20 vols) |
09.04 |
Hydrolysed whey protein maltodextrin powder |
- High-energy supplements: protein
- Hydrolysed protein powder to be used in a modular feed
|
13.02.01 |
Hydromol® |
Over the counter preparation suitable for self-care/purchase if appropriate |
13.02.01 |
Hydromol® |
Over the counter preparation suitable for self-care/purchase if appropriate |
13.02.01.01 |
Hydromol® Bath and Shower Emollient |
Over the counter preparation suitable for self-care/purchase if appropriate |
13.14.07 |
Hydroquinone 5% w/w, hydrocortisone 1% w/w & tretinoin 0.1% w/w in a non-aqueous gel 0.3% w/v |
|
13.02.01 |
Hydrous ointment BP |
Over the counter preparation suitable for self-care/purchase if appropriate |
09.01.02 |
Hydroxocobalamin |
|
08.01.05 |
Hydroxycarbamide |
For myeloproliferative disorders
Supported by an ESCA (in developement)
Fopr use in sickle cell - see Chapter 9
|
09.01.03 |
Hydroxycarbamide |
For use in sickle cell. |
13.05.03 |
Hydroxycarbamide |
|
10.01.03 |
Hydroxychloroquine |
Please note: ESCA is not required - Common practice |
10.01.03 |
Hydroxychloroquine |
|
13.05.03 |
Hydroxychloroquine |
|
03.04.01 |
Hydroxyzine |
|
11.08.01 |
HYLO NIGHT® Formally known as VitA POS® |
Name change from VitA POS to HLYO NIGHT (April 2020) |
04.02.03 |
Hyoscine |
For hypersalivation caused by antipsychotics in line with Green status for hypersalivation use in Parkinson's Disease |
01.02 |
Hyoscine Butylbromide |
10mg Tablet
20mg/ml Injection |
04.06 |
Hyoscine Hydrobromide |
|
15.01.03 |
Hyoscine Hydrobromide |
|
15.01.03 |
Hyoscine hydrobromide |
|
15.01.03 |
Hyoscine hydrobromide |
For hyoscine patch, see Chapter 4.6 |
21 |
Hyoscine Hydrobromide |
- Not used as frequently in palliative care due to side-effects and cost.
|
21 |
Hyoscine Hydrobromide |
- Indictaion " drooling in chronic neurological disease".
|
04.06 |
Hyosine Scopaderm |
£££££
1.5mg patch releases 1mg of hyoscine over 72 hours
Tablets more cost effective |
03.07 |
Hypertonic sodium chloride |
VIALS
AMPOULES
- Bronchlear 3%
- Mucoclear 3%
- Nebusal 7%
- Pulmoclear 3%
- Pulmoclear 7%
- Resp-ease 3%
- Resp-ease 7%
- Respi-clear 7%
- Salineb 7%
|
11.08.01 |
Hypromellose 0.5% |
All other strengths are non-formulary |
06.06 |
Ibandronic acid |
Dudley
Sandwell
ESCA Sandwell only
Walsall
Wolverhampton
|
06.06 |
Ibandronic acid |
|
06.06 |
Ibandronic acid |
|
08.01.05 |
Ibrutinib Imbruvica® |
In line with NICE
Hospital ONLY - NHSE commisssioned |
02.14 |
Ibuprofen Pedea® |
|
10.01.01 |
Ibuprofen |
This remains the first-line NSAID. If a patient has tried ibuprofen, check that they have taken an anti-inflammatory dose at least 400mg TDS regularly. Also indicated for use in dysmenorrhoea. Suspension is reserved for paediatric use, patients with swallowing difficulties or specific clinical need. The lowest effective dose should be used for the shortest duration necessary to control symptoms. A patient’s need for symptomatic relief and response to treatment should be re-evaluated periodically. |
10.01.01 |
Ibuprofen |
For patients with swallowing difficulties
Paediatric use |
10.03.02 |
Ibuprofen 5 % gel |
Prescribe generically. Follow Optimise Rx advice for any preferred brand |
03.04.03 |
Icatibant Firazyr® |
Hospital only- NHSE Commissioned |
13.14.04 |
Ichthammol 1% w/w & zinc oxide 15% w/w in YSP |
|
A5.08.09 |
Ichthopaste |
Preferred local option Specialist recommendation only Zinc and Ichthammol bandage. Type of wound product is suitable for Venous leg ulcers Chronic eczema Dermatitis Duration dressing remains on wound before changing Up to 7 days Frequency of dressing change Daily up to weekly dependant on skin and wound management. Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Do not use in any cases of sensitivity or allergy to ingredients Rationale for inclusion in formulary For treatment of dermatitis and chronic eczema when venous insufficiency is present. |
02.12 |
Icosapent ethyl |
|
19.49 |
Icthopaste® |
Zinc Paste Bandage has been used with compression bandaging for the treatment of venous leg ulcers. However, paste bandages are associated with hypersensitivity reactions and should be used with caution.
|
08.01.02 |
Idarubicin Hydrochloride |
Commissioned by NHSE Injection-hospital only |
02.08 |
Idarucizumab |
|
08.01.05 |
Idelalisib Zydelig® |
NHSE is responsible commissioner for its use in chronic lymphocytic leukaemia (as per NICE TA359)
|
09.08.01 |
Idursulfase Elaprase® |
NHSE commissioned |
08.01.01 |
Ifosfamide |
Commissioned by NHSE Hospital only |
02.05.01 |
Iloprost |
|
02.05.01 |
Iloprost nebules Vantavis® |
NHS England commissioned |
08.01.05 |
Imatinib Glivec® |
Commissioned by NHSE
In line with NICE |
05.01.02.02 |
Imipenem with Cilastatin Primaxin® |
For hospital use only |
05.01.02.02 |
Imipenem with Cilastatin |
For hospital use only |
05.01.02.02 |
Imipenem with cilastatin and relebactam Recarbrio® |
|
04.03.01 |
Imipramine |
|
13.07 |
Imiquimod Aldara® |
|
13.08.01 |
Imiquimod 3.75% Zyclara® |
For field changes >25cm2 |
13.08.01 |
Imiquimod 5% Aldara® |
|
14.04 |
Inactivated Influenza Vaccine |
|
19.21 |
Inadine® Povidine-Iodine Dressing. |
Indications: sloughy, exuding wounds. Bactericidal and are very effective against MRSA. Need secondary dressings. CAUTION: hyperthyroidism, concurrent lithium therapy, severe renal impairment – discuss with GP first before prescribing. Contra-indications: known or suspected iodine sensitivity, not recommended for use in children or in pregnancy or lactation.Iodine may be absorbed particularly if large wounds treated. NB: Destroyed by sloughy exudate. Max 4 dressings at same time. Orange goes to white antimicrobial activity is reduced after 2 days. Superficial/low to moderate exuding infected wounds
|
A5.03.02 |
Inadine® |
Preferred local option Non-adherent dressing impregnated with povidone iodine (10%) Type of wound product is suitable for Mild local infection where there is low exudate levels, ischaemic wounds, dry, gangrenous digits with the aim to desiccate and auto-amputate. Dry-manage fixator sites Minor burns or skin trauma with local infection Duration dressing remains on wound before changing 1-3 days depending on uptake of iodine from dressing Frequency of dressing change 1-3 days depending on uptake of iodine from dressing Look at colour change of dressing (orange initially to white when all used) Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Iodine allergy or sensitivity Thyroid disorders Renal impairment Not suitable for children, pregnant or lactating women Rationale for inclusion in formulary Topical antimicrobial Non-adherent/pain free use No damage to granular or epithelial cells Easy application and removal Drying properties Efficacy against bacteria, fungi and viruses Cost effective. |
02.12 |
Inclisiran Leqvio® |
Inclisiran is covered by NICE TA 733. |
02.02.01 |
Indapamide |
Use 2.5mg standard release tablets only. |
02.02.01 |
Indapamide MR |
|
13.10.05 |
Indermil® |
Hospital only |
20 |
Indigo carmine |
For use by endoscopy only |
06.04.01.01 |
Indivina® |
|
02.14 |
Indometacin Indocid PDA® |
|
10.01.01 |
Indometacin |
For use in gout and resistant cases |
10.01.01 |
Indomethacin |
£££££
Special product (100ml)
For use in gout and special cases |
20 |
Infacol and N acetyl cysteine for mucosal cleansing |
For use by endoscopy speciality at Sandwell and West Birmingham NHS Trust |
14.04 |
Infanrix-IPV® |
|
09.04 |
Infatrini® |
- Child: 1 kcal/ml and less than 4g protein/100ml
- 1 kcal infant feed for faltering growth
- Varying volume size available to support nutritional requirements of the patients
- Single use only in acute setting – risk of increased waste. Once open must be used within 24 hours
- Failure to thrive, disease-related malnutrition and malabsorption, in child from birth up to body-weight 8 kg. Up to 18 months
|
09.04 |
Infatrini® Peptisorb |
- Infant and child: Hydrolysate formula
- Whey hydrolysate. Use in infants (birth – 18 mths) who are unable to tolerate Infatrini (eg gut intolerance) and also require a higher calorie feed for faltering growth
- Use as tube or oral feed
- Disease-related malnutrition, intractable malabsorption, proven inflammatory bowel disease, short bowel syndrome, bowel fistula, and intolerance to whole protein feeds
|
01.05.03 |
Infliximab Remicade® |
For specialist use only in line with NICE guidance Commissioned in paediatrics by NHSE
£££££ |
10.01.03 |
Infliximab |
Hospital use only
Biosimilar brands of Remicade available:
- Flixabi®
- Inflectra®
- Remsima®
- Zessly®
Paediatric use is commissioned by NHSE |
14.04 |
Influenza vaccine Fluenz Tetra® |
|
06.01.01.03 |
Injection Devices |
- AllStar Pro hypodermic insulin injection pen reusable for 3ml cartridge 1 unit dial up / range 1-80 units
- Autopen
- Autopen 24 hypodermic insulin injection pen reusable for 3ml cartridge 1 unit dial up / range 1-21 units
- Autopen 24 hypodermic insulin injection pen reusable for 3ml cartridge 2 unit dial up / range 2-42 units
- Autopen Classic hypodermic insulin injection pen reusable for 3ml cartridge 1 unit dial up / range 1-21 units
- Autopen Classic hypodermic insulin injection pen reusable for 3ml cartridge 2 unit dial up / range 2-42 units
- HumaPen Ergo
- HumaPen Luxura
- HumaPen Luxura HD hypodermic insulin injection pen reusable for 3ml cartridge 0.5 unit dial up / range 1-30 units
- HumaPen Savvio hypodermic insulin injection pen reusable for 3ml cartridge 1 unit dial up / range 1-60 units
- JuniorSTAR hypodermic insulin injection pen reusable for 3ml cartridge 0.5 unit dial up / range 1-30 units
- NovoPen
- NovoPen 5 hypodermic insulin injection pen reusable for 3ml cartridge 1 unit dial up / range 1-60 units
- NovoPen Echo hypodermic insulin injection pen reusable for 3ml cartridge 0.5 unit dial up / range 0.5-30 units
- OptiPen Pro 1
- mhi-500
|
05.03.02.01 |
Inosine Pranobex Imunovir® |
|
08.02.03 |
Inotuzumab ozogamicin Besponsa® |
Hospital use only
In line with NICE |
06.01.01.01 |
Insulin |
- Actrapid
- Humulin S
- Insuman Rapid
|
06.01.01.01 |
Insulin Humulin R 500 units in 1mL® |
|
06.01.01.01 |
Insulin Aspart |
- Fiasp
- Fiasp FlexTouch
- Fiasp Penfill
- NovoRapid
- NovoRapid FlexPen
- NovoRapid FlexTouch
- NovoRapid Penfill
- Trurapi
|
06.01.01.02 |
Insulin Degludec Tresiba® |
- Tresiba FlexTouch 100units/ml
- Tresiba Penfill 100units/ml
|
06.01.01.02 |
Insulin Degludec Tresiba Flextouch ® |
- Tresiba FlexTouch 200units/ml
Type I Diabetes
Type II Diabetes |
06.01.01.02 |
Insulin degludec/liraglutide |
|
06.01.01.02 |
Insulin Detemir |
- Levemir FlexPen
- Levemir InnoLet
- Levemir Penfill
|
06.01.01.02 |
INSULIN GLARGINE |
- Abasaglar KwikPen
- Lantus
- Toujeo
- Toujeo DoubleStar
|
06.01.01.02 |
Insulin glargine Semglee® |
First line insulin for new patients initiated on insulin glargine 100units/ml and existing patients on Lantus |
06.01.01.01 |
Insulin Glulisine |
BRANDS
|
06.01.01.01 |
Insulin lispro |
BRANDS
|
06.01.01.02 |
Insulin Lispro |
- Admelog
- Humalog 100units/ml
- Humalog KwikPen
- Lyumjev
- Lyumjev KwikPen
- Lyumjev Junior KwikPen
|
06.01.01.03 |
Insulin Pen Needles Insupen 4mm/32g pen needles |
|
06.01.01.03 |
Insulin Pen Needles Insupen 5mm/31g pen needles |
|
06.01.01.03 |
Insulin Pen Needles BD Viva 4mm/32g pen needles |
|
06.01.01.03 |
Insulin Pen Needles GlucoRx Carepoint 5mm/31g pen needles |
|
06.01.01.03 |
Insulin Pen Needles BD Viva 5mm/31g pen needles |
|
06.01.01.03 |
Insulin Pen Needles Microdot MAX safety pen needles 5mm/30g ® |
There are used primarily to protect any individuals administering insulin as a third party
|
08.02.04 |
Interferon Alfa |
Hospital only
In line with NICE |
08.02.04 |
Interferon alfa-2a Roferon-A ® |
Commissioned by NHSE for the treatment of Hepatitis B and C
Hospital only |
08.02.04 |
Interferon alfa-2b IntronA ® |
Commissioned by NHSE for the treatment of Hepatitis B and C
Hospital only |
08.02.04 |
Interferon Beta Avonex® |
|
08.02.04 |
Interferon Beta Betaferon® |
|
08.02.04 |
Interferon Beta Proleukin® |
|
08.02.04 |
Interferon Beta Rebif® |
|
08.02.04 |
Interferon beta Extavia® |
|
08.02.04 |
Interferon gamma-1b Immukin ® |
Hospital only |
14.05 |
INTERFERON GAMMA-1b |
|
28.01 |
Intrathecal Fluorescein Sodium |
For diagnosis of CSF leak |
07.03.04 |
Intra-uterine Contraceptive Devices T-Safe® CU 380 A QuickLoad |
|
07.03.04 |
Intra-uterine Contraceptive Devices Mini TT® 380 Slimline |
|
07.03.04 |
Intra-uterine Contraceptive Devices Nova-T® 380 |
|
07.03.02.03 |
Intra-uterine Progestogen Only System Mirena® |
- GP will not prescribe for supply. Only prescribe if fitting
- Effective for 5 years
|
07.03.02.03 |
Intra-uterine Progestogen Only System Kyleena® |
- Prescribe by brand name to reduce risk of confusion between products
- Low-dose levonorgestrel releasing IUS effective for 5 years
|
07.03.02.03 |
Intra-uterine Progestogen Only System Jaydess® |
•GP will not prescribe for supply. Only prescribe if fitting •Effective for 3 years |
06.02.02 |
Iodine and Iodide |
|
A5.03.02 |
Iodoflex |
Cadexomer dressing containing iodine Preferred local option Type of wound product is suitable for Iodine paste in mesh form for chronic infected, sloughy wounds with moderate exudate eg pressure ulcers, leg ulcers, diabetic foot ulcers Can be used under compression bandaging Duration dressing remains on wound before changing Up to 3 days Frequency of dressing change Daily for acute infection Up to 3 days for chronic wounds and infection, depending on exudate levels Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Allergy or sensitivity to iodine Precaution with large wounds due to absorption. Do not use more than 50g in a single application and no more than 150g in 7 days Dry necrotic wounds Thyroid disorders Renal impairment Not suitable for children, pregnant or lactating mothers Concurrent Lithium therapy Rationale for inclusion in formulary Anti microbial, broad spectrum, long acting/high absorption capacity Removes slough and debris to clean the wound bed Can be moulded to shape of the wound Alternative to honey products if allergy to bees |
19.21 |
Iodoflex® |
Indications: sloughy, exuding wounds. Bactericidal and are very effective against MRSA. Need secondary dressings. Moderate to highly exuding infected wounds. CAUTION: hyperthyroidism, concurrent lithium therapy, severe renal impairment – discuss with GP first before prescribing. Contra-indications: known or suspected iodine sensitivity, not recommended for use in children or in pregnancy or lactation. Iodine may be absorbed, particularly from large wounds or during prolonged use. Single Use = 50g Weekly = 150g 3 months MAX |
A5.03.02 |
Iodosorb |
Preferred local option Cadexomer powder or ointment with iodine Type of wound product is suitable for Chronic exuding sloughy wounds eg leg ulcers, pressure ulcers, diabetic foot ulcers. Can be used under compression bandaging Duration dressing remains on wound before changing Up to 3 days Frequency of dressing change Daily for acute infection Up to 3 days for chronic infection Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Allergy to iodine products Dry necrotic tissue Not suitable for Children, pregnant or lactating mothers Thyroid disorders Renal impairment Needs at least twice weekly dressings for iodine to be effective Rationale for inclusion in formulary Antimicrobial, broad spectrum, long acting De-slough and cleans wound debris Non-adherant. Reduces trauma to wound and pain on dressing changes Easy application. Can fill cavities or awkward shaped wounds Alternative to honey based products if allergy to bees |
08.01.05 |
Ipilimumab Yervoy® |
Commissioned by NHSE Hospital only |
03.01.02 |
Ipratropium bromide |
|
02.05.05.02 |
Irbesartan |
|
06.01.02.03 |
Irbesartan |
|
09.01.01.01 |
Iron and Folic Acid Pregaday® |
|
09.01.01.02 |
Iron isomaltoside Monofer® |
Hospital only |
09.01.01.02 |
Iron Sucrose Venofer® |
Hospital use only |
A5.12 |
Irripod |
Preferred local option Sterile sodium chloride solution Type of wound product is suitable for Wound cleansing, for topical irrigation of the eye Duration dressing remains on wound before changing As required Frequency of dressing change As required Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Single use External use only Rationale for inclusion in formulary Cost effective Cleansing of wounds |
08.01.05 |
Isatuximab |
In line with NICE |
05.02.01 |
Isavuconazole |
|
15.01.02 |
Isoflurane |
HOSPITAL ONLY |
15.01.02 |
Isoflurane AErrane® |
HOSPITAL ONLY |
09.04 |
Isoleucine 1000® |
- Used as an inpatient only
- Used at the time of diagnosis when on haemofiltration and an isoleucine supplement is necessary
|
09.04 |
Isoleucine50® |
- To correct isoleucine deficiency in MSUD
- The only pre-measured sachet of isoleucine that provides 50 mg/dose to correct isoleucine deficiency in MSUD. A pre-measured sachet is particularly important as most of our families with MSUD do not speak English as their first language so require pre-measured products. The dose and frequency of administration will be determined by the specialist dietitian
- Nutritional supplement for use in the dietary management of inborn errors of amino acid metabolism in adults and children from birth
|
05.01.09 |
Isoniazid |
Hospital use only under microbiological and Tuberculosis specialist advice |
05.01.09 |
Isoniazid |
Unlicensed special. |
06.01.01.02 |
Isophane Insulin |
- Humulin I
- Humulin I KwikPen
- Insulatard
- Insulatard InnoLet
- Insulatard Penfill
- Insuman Basal
- Insuman Basal SoloStar
|
02.07 |
Isoprenaline |
|
02.06.01 |
Isosorbide Dinitrate |
|
02.06.01 |
Isosorbide Mononitrate |
Brand prescribe modified release preparations
Follow Optimise Rx advice for new initiations
|
02.06.01 |
Isosorbide Mononitrate |
|
09.04 |
Isosource Junior® |
-
Isosource® Junior Mix is a nutritionally complete 1.2kcal/ml standard enteral tube feed, containing some blended food ingredien (rehydrated Chicken meat & vegetables, peach puree, orange juice from concentrate).
- Indicated for: Short bowel syndrome; intractable malabsorption; preoperative preparation of undernourished patients; inflammatory bowel disease; total gastrectomy; dysphagia; bowel fistulae; feeding intolerances, developmental disabilities, disease related malnutrition for children greater than 1 year of age
|
13.06.02 |
Isotretinoin |
Oral retinoid should only be prescribed under the supervision of a consultant dermatologist.
Contraindicated in pregnancy. |
01.06.01 |
Ispaghula Husk |
Follow Optimise Rx recommendation on which brand to choose
Adequate fluid intake is important to prevent obstruction (6-8 cups per day) and should not be taken immediatley before bed
Unsuitable for frail patients who are likely to drink less than daily required volume of fluid
Fluid thickens on standing so should be taken as soon as possible after mixing
Time to effect is approximately 48-72 hours |
05.02.01 |
Itraconazole oral presentations |
Capsules more cost effective
SF Liquid £££££ |
05.02.01 |
Itraconazole |
|
A5.02.02 |
IV3000 |
Specialist recommendation only Fixation dressing Type of wound product is suitable for For fixation of intravenous and subcutaneous catheter sites Duration dressing remains on wound before changing Up to 7 days Frequency of dressing change Up to 7 days or when wet/soiled Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Sensitivity to any of the product components Not for use on pressure ulcers, burns or donor sites Strips and documentation label are not to be used as suture replacements or primary wound closure methods Rationale for inclusion in formulary Fixation of intravenous and subcutaneous devices |
09.04 |
IVA Anamix® Infant |
- Amino acid supplement without leucine for infants with isovaleric acidaemia
- The only infant amino acid supplement without leucine, for infants with isovaleric acidaemia. The dose and type of product should always be advised by the specialist dietitian according to the needs of the patient
- Nutritional supplement for the dietary management of proven isovaleric acidaemia or other proven disorders of leucine metabolism in children from birth to 3 years
|
02.06.03 |
Ivabradine |
For use on the advice of a specialist in line with NICE TA267
|
03.07 |
Ivacaftor Kalydeco® |
In line with NICE |
05.05 |
Ivermectin |
Unlicensed, for crusted scabies, on specialist advice |
13.06.03 |
Ivermectin Soolantra® |
For topical treatment of inflammatory lesions of rosacea (papulopustular) in adults. Alternative treatment option to metronidazole 0.75% cream/gel or azelaic acid 15% gel |
05.05 |
Ivermectin > Soolantra |
|
08.01.05 |
Ixazomib |
In line with NICE
Hospital only - NHSE commissioned |
08.01.05 |
Ixazomib Ninlaro® |
|
13.05.03 |
Ixekizumab Taltz® |
In line with NICE |
A5.17 |
Jelonet® |
Hospital use only Paraffin gauze dressing Type of wound product is suitable for As a primary layer for use with Flamazine® or Flammercerium® Duration dressing remains on wound before changing 24 hours Frequency of dressing change Daily- occasionally alternate day Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Allergy to any ingredients. Rationale for inclusion in formulary Cost effective primary layer |
09.04.02 |
Jevity® |
- 1 kcal/ml and less than 5g protein/100ml
- Pt requires 1 kcal/ml vegetarian feed fish oil free (contains fibre)
- Standard ACBS indications: Disease -related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula except bowel fistula. Not suitable for child under 2 years
|
09.04.02 |
Jevity® 1.5kcal |
- 1.5 kcal/mL and 5g (or more) protein/100 mL
- High energy vegetarian feed, fish oil free with fibre
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula. Not suitable for children under 2 years; not recommended for child 2 - 10 years
|
09.04.02 |
Jevity® Plus |
- Less than 1.5 kcal/mL and 5g (or more) protein/100 mL
- Pt requires 1.2kcal/mL, fibre, vegetarian feed fish oil free
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula. Not suitable for child under 2 years; not recommended for child 2 - 10 years
|
09.04.02 |
Jevity® Plus HP |
- Less than 1.5 kcal/mL and 5g (or more) protein/100 mL
- Pt requires 1.3kcal/mL, high protein, fibre, vegetarian feed fish oil free
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula; also CAPD, heamodialysis. Not suitable for child under 2 years; not recommended for child 2 - 10 years
|
09.04.02 |
Jevity® Promote |
- Less than 1.5 kcal/mL and 5g (or more) protein/100 mL
- Pt requires 1 kcal/mL, fibre, vegetarian feed fish oil free
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula. Not suitable for child under 2 years; not recommended for child 2 - 10 years
|
09.05.02.01 |
Joules phosphate solution |
Paediatrics only |
19.37 |
K-BAND® |
Lightweight conforming bandages are used for dressing retention, with the aim of keeping the dressing close to the wound without inhibiting movement or restricting blood flow. |
A5.03.04 |
Kendall® AMD |
Specialist use only for pin sites Absorbent, non adherent foam disc impregnated with PHMB. Double sided with a centre hole and radial slit Type of wound product is suitable for For use on pin sites, drains and tubes. Duration dressing remains on wound before changing 1-7 days Frequency of dressing change 1-7 days dependent on exudate levels Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Not intended as a primary treatment for infection Do not use as a primary treatment for full thickness burns Not for patients sensitive to PHMB Rationale for inclusion in formulary Provides local exudate management and antimicrobial properties Absorbent Non adherent and semi occlusive |
A5.17 |
Kerlix |
Specialist recommendation only Gauze roll containing 0.2% Polyhexamethylene Biguanide (PHMB) Type of wound product is suitable for Colonised or infected wounds, with moderate to heavy exudate Duration dressing remains on wound before changing 3 days Frequency of dressing change 3 days Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Allergy to PHMB Do not use with Sodium hypochlorite ( Eusol) solutions, as this will deactivate PHM Do not apply gauze circumferentially as it has no stretch, and can become tight restricting circulation Rationale for inclusion in formulary Broad-spectrum antimicrobial agent that reduces bacterial colonization within the dressing and bacterial penetration through the dressing. Can be used in conjunction with Renasys Negative Pressure Therapy |
13.08.02 |
Keromask® |
- Specialist recommendation
- FP10 prescriptions should be endorsed "ACBS"
|
19.06 |
KerraMax Care® |
HOSPITAL USE ONLY Superabsorbent dressing Type of wound product is suitable for Highly exuding wounds as a primary or secondary dressing. Can be used under compression therapy Stackable as no backing present to hold exudate Duration dressing remains on wound before changing 1-7 days. Frequency of dressing change Dependent on level of exudate, usually daily or more frequently Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Do not cut or tear Rationale for inclusion in formulary Required for heavily exuding wounds. |
A5.01.02 |
KerraMax Care® |
HOSPITAL USE ONLY Superabsorbent dressing Type of wound product is suitable for Highly exuding wounds as a primary or secondary dressing. Can be used under compression therapy Stackable as no backing present to hold exudate Duration dressing remains on wound before changing 1-7 days. Frequency of dressing change Dependent on level of exudate, usually daily or more frequently Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Do not cut or tear Rationale for inclusion in formulary Required for heavily exuding wounds. |
A5.16 |
Kerraped |
First consider clients own footwear options Preferred local option A shoe to accommodate bandages and offload pressure from the front of the foot Type of wound product is suitable for Neuropathic foot ulcers or patients with bulky bandages who cannot wear their own footwear Duration product remains on wound before changing As required Frequency of use As required Caution/contraindications (when not to use the dressing, patient groups to avoid etc. Ensure correct size is selected Rationale for inclusion in formulary Only footwear available for patients with neuropathic ulcers or bulky bandages |
A5.16 |
KerraPro® |
Preferred local option Silicone pads designed to redistribute pressure from bony prominences. Type of wound product is suitable for Prevention and treatment of category (Stage/Grade) 1 pressure ulcers Duration dressing remains on wound before changing As required. Check skin daily. Frequency of dressing change As required, check skin daily. Pads will last up to 3 months Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Must only be used as part of a pressure ulcer prevention programme Not to be used on a grade 2, 3 4, unstageable or deep tissue injury pressure ulcer unless directed by a clinical specialist Known sensitivity to silicone Do not use as a wound dressing Do not apply directly onto broken skin If skin macerates beneath, ensure the area is being checked and washed daily and consider utilising a cotton stockinette to reduce humidity Rationale for inclusion in formulary Cost effective Available in a large range of shapes and sizes Accessible pressure ulcer prevention medical device Reusable on the same patient for up to 3 months by washing with soap and water and thoroughly drying |
15.01.01 |
Ketamine (preservative free) |
HOSPITAL ONLY |
15.01.01 |
Ketamine injection Ketalar® |
HOSPITAL ONLY |
09.04 |
Ketocal® 2.5:1 LQ |
- The only complete tube feed which meets requirements for the older age group beyond 8 years of age
- Nutritionally complete
|
09.04 |
KetoCal® 3:1 |
- Specialised formulas for specific clinical conditions
- High fat, low carbohydrate, nutritionally complete formula for infants and children from birth to 6 yrs, or as a supplementary feed for children over 6 years and adults on a ketogenic diet. May also be used in cooking
- Enteral feed or nutritional supplement as part of ketogenic diet in management of drug resistant epilepsy or other conditions for which a ketogenic diet is indicated in children from birth to 6 years; as a nutritional supplement in children over 6 years
|
09.04 |
KetoCal® 4:1 |
- Specialised formulas for specific clinical conditions
- High fat, low carbohydrate powdered formula for children on a ketogenic diet as oral or tube feed, or used in cooking or as a supplementary feed for adults on a ketogenic diet
- Enteral feed or nutritional supplement as part of ketogenic diet in management of epilepsy resistant to drug therapy, in children over 1 year, only on the advice of secondary care physician with experience of ketogenic diet
|
09.04 |
KetoCal® 4:1 LQ |
- Specialised formulas for specific clinical conditions
- High fat, low carbohydrate nutritionally complete liquid for children over 1 year of age and adults on a ketogenic diet, suitable for oral or tube feeding
- Enteral feed or nutritional supplement as part of ketogenic diet in management of drug resistant epilepsy or other conditions for which a ketogenic diet is indicated in children 1–10 years; as a nutritional supplement in children over 10 years
|
05.02.02 |
Ketoconazole |
Specialist use only |
06.07 |
Ketoconazole |
|
13.10.02 |
Ketoconazole 2% cream |
|
13.09 |
Ketoconazole 2% shampoo |
Over the counter preparation suitable for self-care/purchase if appropriate |
06.01.06 |
Ketones Test Strips FreeStyle Optium beta-ketone testing strips® |
- FreeStyle Optium beta-ketone testing strips
|
06.01.06 |
Ketones Test Strips KetoSens testing strips ® |
|
06.01.06 |
Ketones Test Strips Glucofix Tech beta-ketone Sensor testing strips ® |
|
11.08.02 |
Ketorolac Acular® |
For use on advice of specialist |
21 |
Ketorolac |
|
15.01.04.02 |
Ketorolac trometamol Toradol® |
Hospital only |
09.04 |
KeyOmega® |
- Long chain fatty acid supplementation in very low fat diets
- Nutritional supplement for the dietary management of inborn errors of metabolism
|
19.47 |
K-FOUR ® Compression Bandaging Kit |
Indications: venous leg ulceration. Doppler assessment (ABPI) and/or specialist assessment are required before use. Only to be applied by trained individuals – refer to manufacturer’s application guidelines for details.
Prescribe as individual items and quantities NOT as a ‘kit’. System used is dependent upon ankle circumference which should be re-measured at each dressing change to ensure that the system used is still safe and effective.
The ‘gold standard’ for immobile/poor mobility patients to achieve healing by graduated compression. |
19.11 |
Kliniderm® |
•November 2016: approved for use, replacing Mepilex® Polyurethane foam with adhesive silicone wound contact layer Type of wound product is suitable for Suitable for acute and chronic wounds including leg ulcers, pressure ulcers, superficial and partial thickness burns, donor sites, post operative wounds and skin abrasions. Suitable for low to moderately exuding wounds for patients with fragile skin Available in border and non border Duration dressing remains on wound before changing Up to 7 days Frequency of dressing change 1-7 days – dependant on exudate level Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Known product or component sensitivity eg Silicone Rationale for inclusion in formulary Wound contact surface is coated with a layer of soft silicone which reduces trauma to delicate tissue. Range of shapes and sizes available. |
A5.02.03 |
Kliniderm® |
November 2016: approved for use, replacing Mepilex® Polyurethane foam with adhesive silicone wound contact layer Type of wound product is suitable for Suitable for acute and chronic wounds including leg ulcers, pressure ulcers, superficial and partial thickness burns, donor sites, post operative wounds and skin abrasions. Suitable for low to moderately exuding wounds for patients with fragile skin Available in border and non border Duration dressing remains on wound before changing Up to 7 days Frequency of dressing change 1-7 days – dependant on exudate level Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Known product or component sensitivity eg Silicone Rationale for inclusion in formulary Wound contact surface is coated with a layer of soft silicone which reduces trauma to delicate tissue. Range of shapes and sizes available. |
06.04.01.01 |
Kliofem® |
|
06.04.01.01 |
Kliovance® |
|
A5.08.04 |
K-Lite |
Preferred local option Lightweight knitted bandage Type of wound product is suitable for Designed for use on sprains/strains Can be used to prevent oedema, would require a wadding bandage to be applied beneath It is the second layer of a four layer compression bandage kit Where there is open skin, a primary dressing must be used Duration dressing remains on wound before changing Change in line with primary dressing Frequency of dressing change 1-7 days Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Known allergy to any components Not suitable for application of pressure on its own and therefore should be used with other bandage components for the treatment of venous ulcers Caution over bony prominences where the bandage can cause pressure Rationale for inclusion in formulary Cost effective Essential for providing support to a limb and as part of a bandage compression therapy kit |
19.41 |
K-LITE® |
Indications: venous leg ulceration. Doppler assessment (ABPI) and/or specialist assessment are required before use. Only to be applied by trained individuals – refer to manufacturer’s application guidelines for details.
Prescribe as individual items and quantities NOT as a ‘kit’. System used is dependent upon ankle circumference which should be re-measured at each dressing change to ensure that the system used is still safe and effective.
The ‘gold standard’ for immobile/poor mobility patients to achieve healing by graduated compression. |
A5.08.02 |
Knit-Band |
Preferred local option Cellulose contour bandage used for retention of non adhesive dressing products Type of wound product is suitable for Retention bandage Duration dressing remains on wound before changing Change in line with dressing change Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Take care to apply joint below to joint above. Always use a primary dressing Rationale for inclusion in formulary Most cost effective choice |
19.47 |
KO-FLEX® Compression Bandage Class 3b Cohesive |
Indications: venous leg ulceration. Doppler assessment (ABPI) and/or specialist assessment are required before use. Only to be applied by trained individuals – refer to manufacturer’s application guidelines for details.
Prescribe as individual items and quantities NOT as a ‘kit’. System used is dependent upon ankle circumference which should be re-measured at each dressing change to ensure that the system used is still safe and effective.
The ‘gold standard’ for immobile/poor mobility patients to achieve healing by graduated compression. |
A5.08.06 |
Ko-Flex® |
Preferred local option A water resistant vapour permeable cohesive bandage Type of wound product is suitable for Venous ulceration, oedema, Managing sprains and strains and following orthopaedic surgery Forms part of the K four bandage system Duration dressing remains on wound before changing 1 to 7 days Frequency of dressing change Dependant on exudate levels if wound present or oedema management . Caution/contraindications (when not to use the dressing, patient groups to avoid etc. Not recommended on those patients with an ABPI lower than 0.8. Contains latex Rationale for inclusion in formulary Cohesive bandage that can be used alongside other formulary products Forms the 4th layer of a four layer compression bandage system |
19.41 |
K-PLUS® |
Indications: venous leg ulceration. Doppler assessment (ABPI) and/or specialist assessment are required before use. Only to be applied by trained individuals – refer to manufacturer’s application guidelines for details.
Prescribe as individual items and quantities NOT as a ‘kit’. System used is dependent upon ankle circumference which should be re-measured at each dressing change to ensure that the system used is still safe and effective.
The ‘gold standard’ for immobile/poor mobility patients to achieve healing by graduated compression. |
A5.08.07 |
K-Soft |
Preferred local option An absorbent non –woven, sub bandage wadding. Type of wound product is suitable for Provides padding , shaping and protection of the limb prior to the application of compression bandage therapy. Duration dressing remains on wound before changing Up to 7 days Frequency of dressing change Daily up to weekly dependant on exudate and oedema management. Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Advised not to apply directly to skin as can cause irritation. Rationale for inclusion in formulary Essential for protecting a limb, padding and shaping Forms part of the compression bandage regime. Suitable for use with other formulary products. |
19.46 |
K-SOFT® Absorbent Wadding |
|
19.47 |
K-THREE ® |
Indications: venous leg ulceration. Doppler assessment (ABPI) and/or specialist assessment are required before use. Only to be applied by trained individuals – refer to manufacturer’s application guidelines for details.
Prescribe as individual items and quantities NOT as a ‘kit’. System used is dependent upon ankle circumference which should be re-measured at each dressing change to ensure that the system used is still safe and effective.
The ‘gold standard’ for immobile/poor mobility patients to achieve healing by graduated compression. |
A5.03.04 |
KytoCel |
Preferred local option Absorbent gelling fibre wound dressing
Type of wound product is suitable for Moderate to heavily exuding chronic and acute wounds that are sloughy and clinically infected. Haemostatic properties for minor bleeds in superficial wounds Autolytic debridement properties Duration dressing remains on wound before changing 1-3 days Frequency of dressing change 1-3 days, dependent on exudate levels Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Allergy to Shellfish (Chitin) Full thickness burns Heavily bleeding wounds Dry wounds Rationale for inclusion in formulary Cost effective Alternative to available antimicrobials Can be used on heavily exuding wounds |
02.04 |
Labetalol |
|
02.04 |
Labetolol |
|
04.08.01 |
Lacosamide |
Tablets
Syrup
Supported by an ESCA |
01.06 |
Lactulose |
|
05.03.01 |
Lamivudine Epivir®, Zeffix® |
|
05.03.01 |
Lamivudine |
|
05.03.01 |
Lamivudine with dolutegravir Dovato® |
|
05.03.01 |
Lamivudine with tenofovir disoproxil and doravirine Delstrigo® |
|
04.02.03 |
Lamotrigine |
On specialist advice. |
04.08.01 |
Lamotrigine |
Tablets
Dispersible tablets
On specialist advice
MHRA Advice Care should be taken when switching between oral formulations. The need for continued supply of a particular manufacturer's product should be based on clinical judgement and consultation with patient and/or carer, taking into account factors such as seizure frequency and treatment history |
03.04.03 |
Lanadelumab Takhzyro® |
In line with NICE
Highly specialist allergy centre- NHSE commissioned |
08.03.04.03 |
Lanreotide Somatuline® LA |
NHSE: Commissioned in cancer; product with lowest procurement cost to be used Palliative Care use only For Oncology
For Acromegaly |
08.03.04.03 |
Lanreotide Somatuline Autogel® |
NHSE: Commissioned in cancer; product with lowest procurement cost to be used
Palliative Care Use Only For Oncology
For Acromegaly |
01.03.05 |
Lansoprazole |
Capsules are more cost effective than tablets
Can be opened and beads swallowed without crushing or can be mixed with food or drink |
01.03.05 |
Lansoprazole |
Capsules are more cost effective than tablets
Can be opened and beads swallowed without crushing or can be mixed with food or drink
dfsdfsdfsdfdsdf |
01.03.05 |
Lansoprazole dispersible |
Orodispersible tablets 15mg, 30mg Orodispersible tablets cost twice as much as capsules
For use in patients with swallowing difficulties or who are on enteral tube feeding
|
09.05.02.02 |
Lanthanum |
- Specialist recommendation
- No ESCA
- Common Practice
NHSE commissioned when used for renal dialysis in most circumstances |
08.01.05 |
Lapatinib Tyverb® |
Not routinely commissioned by NHSE |
09.08.01 |
L-arginine |
tablets
oral solution
infusion 100ml
capsules
|
08.01.05 |
Larotrectinib Vitrakvi® |
In line with NICE |
A5.10 |
LarvE |
Specialist recommendation only Free range: Biomonde Larvae 100/200 or BioBag Biosurgical treatment for the debridement and cleansing of wounds consisting of aseptically produced living larvae. The BioBag is presented in the five (5) configurations listed below. The larvae are Lucilia sericata contained in a sterile polyester net bag with a sterile PVA spacer cube, presented in a sterile transport container. BioBag 50 at least 50 larvae 25 x 40mm 1 8x8x10 BioBag 100 at least 100 larvae 50 x 40mm 1 12x12x10 BioBag 200 at least 200 larvae 60 x 50mm 1 25x10x10 BioBag 300 at least 300 larvae 120 x 60mm 2 25x10x10 BioBag 400 at least 400 larvae 100 x 100mm 2 25x10x10 Free range larvae, larvae and 30 x 30 flat retention net plus kit pack, larvae and 40 x 60cm boot retention net plus kit pack. Additional 100 or 200 larvae available. Type of wound product is suitable for The BioMonde Larval Debridement Therapy Products are indicated for debridement of non-healing necrotic skin and soft tissue wounds, including pressure ulcers, venous stasis ulcers, neuropathic foot ulcers, and non-healing traumatic or post-surgical wounds. Duration dressing remains on wound before changing and frequency of dressing change An application of BioBag can be left in place for up to 4 days, dependent on the condition of the wound. If the wound is not sufficiently debrided after 4 days, the treatment can be repeated with a fresh application of BioBag. The treatment should be stopped as soon as the wound is sufficiently debrided or if no improvement is observed after 3 or more applications. The total number of treatment cycles will depend on the characteristics of the wound, the response of the patient to LDT and the aim of the therapy. Most ulcers are completely debrided within 1 to 6 treatment cycles. If exudate production is excessive, the secondary dressing may be changed as required while leaving the BioBag undisturbed. Frequent removal of the outer dressing will also help to control the odour associated with the liquefied necrotic tissue Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Larvae should not be used in patients with known hypersensitivities to fly larvae, polyester, PVA (polyvinyl alcohol) or the components of the media on which the larvae are raised (including soya protein, yeast protein, potato starch and bovine protein) as this may result in dermatitis or more severe immunological reactions in susceptible individuals. If treatment is undertaken then these patients should be under strict medical supervision for the duration of the treatment with immediate access to care. Patients with life or limb-threatening, rapidly advancing infections should not be treated with as LDT may interfere with the close and frequent observation that these patients require. Should not be used as first line therapy of infected tendon and bone. These wounds should be treated surgically and/or with antibiotics before using LDT. Should not be used to treat wounds which are not directly exposed to the outside. Wounds should never be allowed to close over the larvae either intentionally or unintentionally. Should not be used on wounds with an inadequate blood supply as this ultimately reduces the ability of the wound to heal. LDT will enlarge the wound as necrotic tissue is debrided but the resulting clean wound is at risk from re-infection. Although some mild bleeding is common during LDT, larvae should not be used on wounds that have a tendency to bleed or wounds close to an exposed major blood vessel, especially if considered to be necrotic as this can lead to rupture of the blood vessels which could be life-threatening. If LDT is attempted, the patient must remain under strict medical supervision for the duration of the treatment. Should not be used on patients with an inborn or medication-induced coagulopathy or in patients being treated with anticoagulants. If these patients are treated with LDT, they should remain under strict medical supervision for the duration of the treatment. Should never be used in sterile body cavities. Should be used with caution on wounds over adjacent exposed organs or leading to a body cavity, and only under close medical supervision for the duration of the treatment. Data are not available concerning the antibiotic / antiseptic activity of maggots and therefore any infected wound should receive standard antibiotic care. Rationale for inclusion in formulary Only available larval therapy on prescription. Rapid debridement of chronic wounds Can be utilised in the community |
11.06 |
Latanoprost |
Ist line
On Specialist Ophthalmologist Recommendation |
11.06 |
Latanoprost Monopost ® |
1st Line PF option
On Specialist Ophthalmologist Recommendation |
11.06 |
Latanoprost 0.005% with Timolol 0.5% |
On Specialist Ophthalmologist Recommendation |
11.06 |
Latanoprost with Timolol preservative free Fixapost® |
Specialist Ophthalmologist Recommendation |
09.08.01 |
L-carnitine |
NHSE commissioned
liquid-specialist advice only
injection |
09.08.01 |
L-citrulline |
|
05.03.03.02 |
Ledipasvir/sofosbuvir Harvoni® |
In line with NICE |
10.01.03 |
Leflunomide |
Supported by an ESCA |
08.02.04 |
Lenalidomide |
In line wth NICE |
09.01.06 |
Lenograstim |
Hospital only |
08.01.05 |
Lenvatinib Kisplyx® |
In line with NICE |
02.08 |
Lepirudin |
|
02.06.02 |
Lercanidipine |
|
05.03.02.02 |
Letermovir Prevymis® |
In line with NICE |
08.03.04.01 |
Letrozole |
|
06.07.02 |
Leuprorelin Prostap 3 DCS® |
|
06.07.02 |
Leuprorelin Prostap SR DCS® |
|
06.07 |
LEUPRORELIN ACETATE |
Amber Initiation - Prostap 3 DCS
Amber Initiation - Prostap SR DCS |
08.03.04.02 |
Leuprorelin Acetate Prostap® SR |
Advanced prostate cancer |
08.03.04.02 |
Leuprorelin Acetate Prostap® 3 |
Advanced prostate cancer |
05.05 |
Levamisole |
Unlicensed |
05.05 |
Levamisole > Ergamisol |
|
04.08.01 |
Levetiracetam Desitrend® |
Paediatrician initiation
For patients up to and including 16 years of age who are unable to swallow tablets and in whom the liquid formulation is not appropriate or tolerated
MHRA Advice It is usually unnecessary to ensure that patients are maintained on a specific maufacturer's product unless there are specific reasons such as patient anxiety and risk of confusion or dosing errors
|
04.08.01 |
Levetiracetam |
Tablets
SF oral solution
Coated granules in sachets (see Desitrend®)
On specialist advice
MHRA Advice It is usually unnecessary to ensure that patients are maintained on a specific manufacturer's product unless there are specific reasons such as patient anxiety and riak of confusion or dosing errors |
15.02 |
Levobupivacaine Chirocaine® |
Hospital only |
15.02 |
Levobupivacaine 0.1% with Fentanyl 2mcg/ml |
Hospital only |
15.02 |
Levobupivacaine 0.1% with Fentanyl 4mcg/ml |
Hospital only |
05.01.12 |
Levofloxacin |
- For multi resistant organisms, based on Microbiological sensitivity
|
05.01.12 |
Levofloxacin |
|
11.03.01 |
Levofloxacin Oftaquix® |
2nd line
Use SDU if using 1 or 2 hourly or if significant OSD/toxicity
For use by consultant ophthalmologists in patients undergoing surgical procedures who are allergic to chloramphenicol or in patients undergoing intravitreal injections who are allergic to chloramphenicol and allergic to/intolerant of preservatives More cost effective option available |
04.02.01 |
Levomepromazine |
Supported by ESCA |
04.02.01 |
Levomepromazine |
Not to be used for psychiatric / anxiolytic purposes in Primary Care |
04.06 |
Levomepromazine |
For palliative care only |
07.03.05 |
Levonorgestrel Levonelle® 1500 |
Less effective than insertion of IUD. Effective up to 72 hours post-coitus Effectiveness of EHC reduced in women taking enzyme inducing drugs, IUD preferred option, see MHRA link below regarding dose adjustment. Use barrier contraception until next period. Available free of charge via some community pharmacies |
07.03.02.01 |
Levonorgestrel 30mcg Norgeston® |
|
06.02.01 |
Levothyroxine |
|
15.01 |
Lidocaine Versatis® |
For use in neuropathic pain on advice of pain clinic only
RICaD required for prescribing in primary care. |
15.02 |
Lidocaine |
|
12.03.01 |
Lidocaine 10% |
Hospital only |
15.02 |
Lidocaine 10% |
Hospital only |
15.02 |
Lidocaine 2% adrenaline 1:200,000 |
|
15.02 |
Lidocaine 2% adrenaline 1:80,000 |
|
15.02 |
Lidocaine 2% with Chlorhexidine 0.25% Instillagel® |
|
15.02 |
Lidocaine 2.5% with Prilocaine 2.5% EMLA® |
|
15.02 |
Lidocaine 4% laryngojet® |
Hospital only
Dental use under review |
15.02 |
Lidocaine 4% LMX® |
For paediatric use only |
15.02 |
Lidocaine 5% |
|
15.02 |
Lidocaine 5% and Phenylephrine 0.5% |
Hospital only |
04.07.03 |
Lidocaine 5% patch Versatis® |
Approved only in patients who have been treated in line with NICE CG173: Neuropathic pain in adults: pharmacological management in non-specialist settings but are still experiencing neuropathic pain associated with previous hepes zoster infection (post-herpetic neuralgia)
Following the policy - Items which should not routinely be prescribed in Primary Care. There is an exception for lidocaine for treatment of neuropathic pain in adults.
|
02.03.02 |
Lidocaine hydrochloride |
|
15.02 |
Lidocaine with Adrenaline Lignospan® |
|
15.02 |
Lidocaine with Adrenaline Xylocaine® |
|
15.02 |
Lidocaine with tetracaine Pliaglis® |
Hospital only |
15.02 |
Lidocaine, adrenaline & tetracaine LAT® |
Hospital only |
15.02 |
Lignocaine |
Hospital only |
A5.11 |
LimbO Waterproof Protector |
Waterproof protector, non slip latex free with a flexible seal at the opening Type of wound product is suitable for Used to keep arm, PICC, leg and foot dressings dry, can be fully submerged in water Rationale for inclusion in formulary Multiple sizing for legs and arms |
01.06.07 |
Linaclotide Constella® |
For moderate to severe IBS-Constipation
For patients who have not responded adequately to or cannot tolerate all other suitable treatment options BUT BEFORE other agents with higher costs
Supported by a RICaD (in development)
|
06.01.02.03 |
Linagliptin |
In line with NICE Linagliptin has no significant clinical benefit or renoprotective effect in patients with CKD.
Sitagliptin should be used first line at the appropriate renal dose where a DPP4 inhibitor is indicated
No significant clinical benefit when used in combination with Insulin – avoid using together
|
06.01.02.03 |
Linagliptin/ Metformin Jentadueto ® |
A variety of combinations tablets (dual therapies) of oral diabetes medication can be prescribed and are available in the Drug Tariff.
Overall, they may improve compliance in patients, however some combinations would then not allow the flexibility in dosing that is required for diabetes management and in some cases increase the tablet burden. There are specific sick-day rules related to stopping certain medication which would be further complicated where they are not prescribed in their separate formulations.
Furthermore, for the overall health economy not all combination therapies are cost-effective and this will be increasingly so as the patents expire over the near future. There are some combination therapies that are not recommended in the oral guidance and clinicians are guided to review and discuss these with patients as part of shared -care decision making.
There are complexities also around the lack of licensing of dual therapies in specific cohorts of patients, related to prescribing for the indication of heart failure or renal disease, making this a complex area for prescribing in primary care
|
05.01.07 |
Linezolid |
For hospital use only |
05.01.07 |
Linezolid |
For hospital use only |
06.02.01 |
Liothyronine |
|
06.02.01 |
Liothyronine |
|
20 |
Lipiodol |
For andoscopy use only |
09.04 |
Lipistart® (Vitaflo) |
- Specialised formulas: Infant and child: MCT-enhanced formula
- Essential for infants/children with long chain fatty acid oxidation disorders who need a high intake of MCT but require normal proportions of carbohydrate e.g. CPT1 and CPT2 deficiency. High carbohydrate formulas are unnecessary
- Also essential for infants/children with long chain fatty acid oxidation disorders who need a high intake of MCT but require normal proportions of carbohydrate e.g. CPT1 deficiency (i.e. high carbohydrate formulas may be unnecessary). There should always be 2 powdered high MCT formulae in the formulary in case of supply issues. The dose and type of product should always be advised by the specialist dietitian according to the needs of the patient
- Dietary management of fat malabsorption, long-chain fatty acid oxidation disorders, and other disorders requiring a high MCT, low LCT formula
|
13.02.01 |
Liquid and White Soft Paraffin Ointment (50:50) |
Most greasy option
Over the counter preparation suitable for self-care/purchase if appropriate |
A5.13 |
Liquid paraffin/white soft paraffin 50:50 |
Preferred local option Emollient ointment containing liquid paraffin and white soft paraffin To assist the skin in retaining moisture Type of wound product is suitable for For use on all dry skin conditions including eczema and psoriasis Frequency of use Daily or more frequently if required Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Allergy or hypersensitivity to any of the ingredients Rationale for inclusion in formulary Treatment of dry skin conditions. Dermatology approved |
09.04 |
Liquigen® |
- High-energy supplements: fat
- Used as a source of MCT when required for children and adults with LCT intolerance and on a low LCT diet and for adults and children on a ketogenic diet - ££
- Also this is used as a milk replacement and as part of module tube feeds for patients with long chain fatty acid disorders such as LCHADD and VLCADD who require ≥10% fat calories from long chain fat and a diet supplemented with MCT. It is essential to provide essential energy on fat restricted diets if MCT is tolerated by the patient. The dose and type of product should always be advised by the specialist dietitian according to the needs of the patient
- Steatorrhoea associated with cystic fibrosis of the pancreas, intestinal lymphangiectasia, intestinal surgery, chronic liver disease, liver cirrhosis, other proven malabsorption syndromes, ketogenic diet in epilepsy, and in type 1 lipoproteinaemia
- Not suitable for child under 1 year
|
06.01.02.03 |
Liraglutide Saxenda® |
PLEASE PRESCRIBE BY BRAND - NICE Guidance on prescribing
• Injection • For weight loss/ obesity • Use according to NICE guidance
The use of Liraglutide for this indication is restricted to prescribing in secondary care by a specialist multidisciplinary Tier 3 weight management service with a commercial agreement in place.
Prescribe by brand (Saxenda ®) to avoid patients inadvertently receiving a different product licensed for type 2 diabetes
|
06.01.02.03 |
Liraglutide Victoza® |
PLEASE PRESCRIBE BY BRAND - NICE Guidance on prescribing
Use according to NICE guidance
For the treatment of type 2 diabetes ONLY
THIS IS FOR DIABETES ONLY. Prescribe by brand (Victoza®) to avoid patients inadvertently receiving a different product licensed for obesity. |
04.04 |
Lisdexamphetamine Elvanse® |
Please note that commissioning discussion is underway. However the present status is as follows:-
Age 6 and over - Solihull practices. Supported with ESCA
Age 16 and over - Birmingham practices. Supported with ESCA
Age under 16 - Birmingham practices
Age 6 and over - Sandwell and West Birmingham CCG. Supported with ESCA
|
02.05.05.01 |
Lisinopril |
|
06.01.05 |
Lisinopril |
|
04.02.03 |
Lithium Carbonate |
- Supported by ESCA-requires regular review in secondary care. Full discharge at 12 months
- APC preferred brand is Priadel, however there are other brands available and you should continue to prescribe the brand that the patient is stable on
- Below is an ESCA link for patients seen by the Black Country Mental Health Services
|
04.02.03 |
Lithium Citrate |
- Supported by an ESCA-requires regular review in secondary care. Full discharge at 12 months
- APC preferred brand is Priadel, however there are other brands available and you should continue to prescribe the brand that the patient is stable on
- Below is an ESCA link for patients seen by the Black Country Mental Health Services
|
06.01.02.03 |
Lixisenatide |
|
A5.03.01 |
L-Mesitran® |
UHB specialists only A hydro active gel dressing containing medical grade honey available without or with an adhesive film border. L- Mesitran has anti bacterial properties and can debride and reduce malodour. Type of wound product is suitable for Burns, chronic wounds, necrotic/sloughy wounds, surgical wounds, diabetic ulcers with caution, donor sites, fungating wounds. Max Duration dressing remains on wound before changing 3-7 days Frequency of dressing change 3- 7 days, dependent on exudate level Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Known sensitivity to dressing and any of its components use with caution in patients with bee venom allergy Not suitable for full thickness burns/deep narrow cavities Caution must be exercised when applying to diabetic patients. Blood glucose levels must be monitored. Rationale for inclusion in formulary Desloughing, Antimicrobial, Deodorising |
09.04 |
Locasol® |
- Specialised formulas: Infant and child: Low calcium formula
- Use in children with high blood calcium levels eg. Noonan’s syndrome
- Conditions of calcium intolerance requiring restriction of calcium and vitamin D intake
|
04.03.01 |
Lofepramine |
|
04.10.03 |
Lofexidine BritLofex® |
|
08.01.01 |
Lomustine |
Commissioned by NHSE |
01.04.02 |
Loperamide |
Capsules are more cost effective than tablets
Loperamide melts (orodispersible) tablets are reserved for high risk stoma output patients and patients with swallowing difficulty only
Not to be used if C.diff is suspected
Caution in patients with a history of recent or repeated antibiotic use as increased risk of C.diff infection in this group |
01.04.02 |
Loperamide with simeticone |
|
09.04 |
Lophlex® |
- A supplement without phenylalanine for teenagers and adults with phenylketonuria
- One of 2 powdered amino acid supplement without phenylalanine for teenagers and adults with phenylketonuria that will meet their higher amino acid requirements. This age group need the larger sachets (20g protein equivalent) to meet their non-phenylalanine protein requirements. It is important we have a choice of more than 1 product for this age group as compliance is reported to be poor and the potential outcome of poor compliance is poor executive functioning. The 2 different products have a different degree of sweetness and range of flavours
- Nutritional supplement for the dietary management of proven phenylketonuria in children over 8 years and adults including pregnant women
|
05.03.01 |
Lopinavir and Ritonavir Kaletra® |
|
05.03.01 |
Lopinavir with Ritonavir |
|
09.04 |
Loprofin SnoPro® |
- Specialised formulas for specific clinical conditions
- Low protein, low potassium, low Phosphate milk substitute , used as a milk replacement in children with renal disease and IMD
- Nutritional supplement for the dietary management of phenylketonuria, chronic renal failure and other inborn errors of amino acid metabolism
|
09.04 |
Loprofin® PKU Drink |
- Low protein milk for children and adults with phenylketonuria and other disorders of protein metabolism
- Low energy protein milk for children and adults with phenylketonuria and other disorders of protein metabolism who are overweight
- Nutritional supplement for the dietary management of phenylketonuria in children over 1 year and adults
|
09.04 |
Loprofin® Sno-Pro |
- Low protein milk for children and adults with phenylketonuria and other disorders of protein metabolism
- High energy low protein milk for children and adults with phenylketonuria and other disorders of protein metabolism who are underweight. Unsuitable for MSUD
- Nutritional supplement for the dietary management of phenylketonuria, chronic renal failure and other inborn errors of amino acid metabolism
|
03.04.01 |
Loratadine |
OTC preparation suitable for self-care/purchase if appropriate |
04.01.02 |
Lorazepam |
|
04.01.02 |
Lorazepam |
|
15.01.04.01 |
Lorazepam |
Hospital only |
21 |
Lorazepam |
- For breathlessness where anxiety is predominant feature
- Genus brand for sublingual use (blue tablets)
|
09.04 |
Lorenzo’s oil |
- For dietary treatment of adrenoleukodystrophy. The dose and type of product should always be advised by the specialist dietitian according to the needs of the patient
|
08.01.05 |
Lorlatinib Lorviqua® |
In line with NICE |
09.08.01 |
L-ornithine L-aspartate |
|
02.05.05.02 |
Losartan |
|
06.01.02.03 |
Losartan Potassium |
|
11.04.01 |
Loteprednol Lotemax® |
|
09.04 |
Low fat +1 module |
- Specialised formulas: Infant and child: MCT-enhanced formula
- Children and adults with a fatty acid disorder
- Also fat free preparation. Used by patients with long chain fatty acid oxidation disorders who cannot tolerate MCT and require a very low-fat diet. Suitable for children and adults with a fatty acid disorder. The dose and type of product should always be advised by the specialist dietitian according to the needs of the patient
|
03.01.05 |
Low range peak flow meter |
BRANDS
- Rossmax Peak Flow Meter
- Easy Peak Flow Meter Low Range
|
06.04.01.01 |
Lubion® |
Fertility use only |
20 |
Lugol’s iodine for assessment of squamous dysplasis/cancer |
For use by endoscopy speciality at Sandwell and West Birmingham NHS Trust |
03.07 |
Lumacaftor with ivacaftor Orkambi® |
In line with NICE |
03.13 |
Lumacaftor with ivacaftor Orkambi® |
|
03.14 |
Lumacaftor with Ivacaftor Orkambi® |
|
09.01.04 |
Lusutrombopag Mulpleo® |
Use in line with NICE |
08.03.04.03 |
Lutetium (177Lu) oxodotreotide Lutathera® |
Hospital use only
In line with NICE |
05.01.03 |
Lymecycline oral presentations |
|
13.06.02 |
Lymecycline |
- Topical treatments should be used first line.
- Oral antibiotics should be reserved for acne, if topical treatment is not adequately effective or if it is inappropriate.
|
A5.09.02 |
Lymphoedema garments |
Based on assessment |
02.05 |
Macitentan Opsumit® |
NHS England commissioned |
01.06 |
Macrogol 3350 with anhydrous sodium sulfate, ascorbic acid, potassium chloride, sodium ascorbate and sodium chloride |
|
01.06 |
Macrogol 3350 with anhydrous sodium sulfate, potassium chloride, sodium bicarbonate and sodium chloride |
|
01.06 |
Macrogol 3350 with potassium chloride, sodium bicarbonate and sodium chloride |
|
01.06.04 |
Macrogols Laxido® |
Follow Optimise Rx recommendation on the most cost effective brand to prescribe
Prescribe as Laxido |
01.06.05 |
Macrogols Klean-Prep® |
|
01.06.05 |
Macrogols Moviprep® |
|
11.08.01 |
Macrogols Systane® |
Non-formulary For existing patients only |
09.05.01.03 |
Magnaspartate® |
|
09.05.01.03 |
Magnesium citrate |
|
01.06 |
Magnesium citrate with sodium picosulfate |
|
09.05.01.03 |
Magnesium glycerophosphate |
|
09.05.01.03 |
Magnesium Sulphate Injection |
For use in hospital only |
13.10.05 |
Magnesium Sulphate Paste |
Over the counter preparation suitable for self-care/purchase if appropriate |
01.01.01 |
Magnesium Trisilicate Mixture BP |
Suspension
High sodium content
Use with caution in patients with renal impairment |
03.13 |
Magnessium sulfate |
Severe acute asthma,Continuing respiratory deterioration in anaphylaxis |
A5.11 |
Magnide |
Preferred local option Application of closed toe compression garments |
13.10.04 |
Malathion |
Over the counter preparation suitable for self-care/purchase if appropriate |
02.02.05 |
Mannitol |
Hospital use only |
03.07 |
Mannitol Bronchitol® |
Hospital only Commissioned by NHSE |
03.07 |
Mannitol inhalation Bronchitol ® |
|
05.03.01 |
Maraviroc |
|
05.03.01 |
Maraviroc Celsentri® |
|
09.04 |
Maxijul® Super Soluble |
- High-energy supplements: carbohydrate
- High calorie modular powder, to be added to other food, drink and feeds e.g. faltering growth, to increase carbohydrate content
- Also used as an additional energy supplement when IMD patients require a modified, low protein or low-fat feed or are on a glucose polymer based energy supplement and require other Nutricia products such as Monogen or Nutrini fibre, so it can be delivered using the same home delivery service so less burdensome for families. It is also used as a core ingredient for glucose based emergency feeds. The dose and type of product should always be advised by the specialist dietitian according to the needs of the patient
- Disease-related malnutrition, malabsorption states, or other conditions requiring fortification with a high or readily available carbohydrate supplement
|
09.04 |
MCT Pepdite® +1 |
- Not used, other preparation more nutritionally complete
|
09.04 |
MCT Procal® |
- Protein, fat, and carbohydrate
- Used in children and adults on a ketogenic diet as an energy source for use with long chain fatty acid disorders and in metabolic disorders
- Used in liver/hepatobiliary disease/conditions
- Essential for use with log chain fatty acid disorders such as LCHADD, VLCADD, CACT. It provides a pre-measured source of MCT energy at breakfast, midday and evening to ensure patients do not become energy depleted when performing usual daytime activities. The dose and type of product should always be advised by the specialist dietitian according to the needs of the patient
- Dietary management of disorders of long-chain fatty acid oxidation, fat malabsorption, and other disorders requiring a low LCT, high MCT supplement
- Not suitable for child under 1 year
|
14.04 |
Measles, Mumps and Rubella Vaccine, Live (MMR) Priorix ® MMRVaxPRO® |
|
05.05 |
Mebendazole |
Also available to buy OTC |
05.05 |
Mebendazole > Vermox |
|
01.02 |
Mebeverine Hydrochloride |
|
19.20 |
MEDIHONEY ® Antibacterial Honey Apinate Non adherent calcium alginate dressing impregnated with medical grade honey |
Indications: sloughy, necrotic or granulating wounds. Honey has an osmotic effect that helps deslough wounds and maintain a moist environment. Antibacterial activity against common wound pathogens, including MRSA.
Can be left on for up to 7 days dependent upon exudate. Deodorises the wound as bacteria adhere to sugar present. Exudate levels may increase and pain may be experienced owing to the osmotic action. Use a barrier cream to protect wound edges. Wound may appear larger and deeper initially as dead tissue is removed but an improvement in appearance should follow.
SAFE to use on diabetic patients just monitor blood sugars. Do NOT use if sensitive to honey or bees. |
19.20 |
MEDIHONEY ® Antibacterial Medical Honey 20g and 50g tube Apply 3mm deep only |
Indications: sloughy, necrotic or granulating wounds. Honey has an osmotic effect that helps deslough wounds and maintain a moist environment. Antibacterial activity against common wound pathogens, including MRSA.
Can be left on for up to 7 days dependent upon exudate. Deodorises the wound as bacteria adhere to sugar present. Exudate levels may increase and pain may be experienced owing to the osmotic action. Use a barrier cream to protect wound edges. Wound may appear larger and deeper initially as dead tissue is removed but an improvement in appearance should follow.
SAFE to use on diabetic patients just monitor blood sugars. Do NOT use if sensitive to honey or bees.
Medical grade honey is applied directly to the wound and covered with primary low adherence wound dressing; as additional secondary dressing may be required for exuding wounds |
19.20 |
MEDIHONEY ® Antibacterial Wound Gel 80% antibacterial medical honey + natural waxes / oils to form gel |
Indications: sloughy, necrotic or granulating wounds. Honey has an osmotic effect that helps deslough wounds and maintain a moist environment. Antibacterial activity against common wound pathogens, including MRSA.
Can be left on for up to 7 days dependent upon exudate. Deodorises the wound as bacteria adhere to sugar present. Exudate levels may increase and pain may be experienced owing to the osmotic action. Use a barrier cream to protect wound edges. Wound may appear larger and deeper initially as dead tissue is removed but an improvement in appearance should follow.
SAFE to use on diabetic patients just monitor blood sugars. Do NOT use if sensitive to honey or bees. Not recommended for deep wounds or cavities where removal of waxes may be difficult |
19.20 |
MEDIHONEY ® Gel Sheet Sodium Alginate dressing impregnanted with medihoney |
Indications: sloughy, necrotic or granulating wounds. Honey has an osmotic effect that helps deslough wounds and maintain a moist environment. Antibacterial activity against common wound pathogens, including MRSA.
Can be left on for up to 7 days dependent upon exudate. Deodorises the wound as bacteria adhere to sugar present. Exudate levels may increase and pain may be experienced owing to the osmotic action. Use a barrier cream to protect wound edges. Wound may appear larger and deeper initially as dead tissue is removed but an improvement in appearance should follow.
SAFE to use on diabetic patients just monitor blood sugars. Do NOT use if sensitive to honey or bees. |
A5.15 |
Medihoney barrier cream |
Specialist recommendation only Barrier cream containing active Medihoney. Helps to reduce inflammation. Type of wound product is suitable for Treatment of incontinence related lesions Blistered skin Prevention and treatment of maceration and excoriation Treats candidiasis and intertrigo Duration dressing remains on wound before changing At each episode of hygiene Frequency of dressing change At each episode of hygiene Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Patch test before use
Suitable for neonates and children Treats fungal infections as well as incontinence associated lesions Reduces inflammation Can be applied to broken skin |
09.04 |
Medium-chain Triglyceride (MCT) Oil |
- High-energy supplements: fat
- Used as a source of energy for children and adults requiring a low LCT/ High MCT diet
- Also this is used as a MCT cooking oil to improve diet palatability in patients with long chain fatty acid disorders such as LCHADD and VLCADD who require ≥10% fat calories from long chain fat. It is used to make MCT margarine, add to toast or to cook potatoes and other vegetables. It is essential to provide essential energy on fat restricted diets if MCT is tolerated by the patient. The dose and type of product should always be advised by the specialist dietitian according to the needs of the patient
- Nutritional supplement for steatorrhoea associated with cystic fibrosis of the pancreas, intestinal lymphangiectasia, intestinal surgery, chronic liver disease and liver cirrhosis, other proven malabsorption syndromes, ketogenic diet in management of epilepsy, type 1 hyperlipoproteinaemia
|
06.04.01.02 |
Medroxyprogesterone Acetate Depo -Provera® |
|
06.04.01.02 |
Medroxyprogesterone Acetate Climanor® |
|
06.04.01.02 |
Medroxyprogesterone Acetate Provera® |
|
06.04.01.02 |
Medroxyprogesterone Acetate Sayana press® |
Suitable for self injection in patients who have had appropriate tranining |
07.03.02.02 |
Medroxyprogesterone acetate Sanyana Press® |
Suitable for self-injection in patients who have had appropriate training |
07.03.02.02 |
Medroxyprogesterone Acetate Depo-Provera® |
Short or long term – lasts 12 weeks In adolescents, medroxyprogesterone acetate should be used only when other methods of contraception are inappropriate; In all women, the benefits of using medroxyprogesterone acetate beyond 2 years should be evaluated against the risks; In women with risk factors for osteoporosis, a method of contraception other than medroxyprogesterone acetate should be considered. |
08.03.02 |
Medroxyprogesterone Acetate |
|
10.01.01 |
Mefenamic Acid |
For dysmenorrhoea - NSAIDs significantly reduce menstrual blood loss compared with placebo. There is no significant difference between mefenamic acid and naproxen, or between NSAIDs and oral progesterone given in the luteal phase
Ibuprofen or naproxen can also be prescribed for the treatment of dysmenorrhoea |
19.32 |
MEFIX ® Only to be used for securing dresings |
|
A5.07.03 |
Mefix® |
Preferred local option Permeable, aperture non woven, synthetic adhesive tape For securing dressings. Frequency of dressing change Determined by wound type and dressing change Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) None listed Rationale for inclusion in formulary Available on drug tariff. Different availability of sizes in comparison to Clinipore® for difficult to dress areas. Some stretch and flexibility to improve conformity and adhesion. Can be used to secure dressings rather than bandages. |
05.04 |
Mefloquine |
|
05.04 |
Mefloquine Lariam® |
Private prescription in Primary Care |
08.03.02 |
Megestrol Acetate |
|
04.01.01 |
Melatonin |
|
04.01.01 |
Melatonin 3mg tablets |
REM sleep behaviour disorder and circadian rhythm sleep-wake disorder in adults in line with ESCA
For all other indications |
04.01.01 |
Melatonin MR Circadin ® |
Sandwell & West Birmingham CCG for patients seen by the Black Country ADHD Services.
REM sleep behaviour disorder and circadian rhythm sleep-wake disorder in adults in line with ESCA
For all other indications |
08.01.01 |
Melphalan |
Commissioned by NHSE Injection-hospital only |
04.11 |
Memantine |
|
09.06.06 |
Menadiol Sodium Phosphate |
|
14.04 |
Meningococcal A, C, W135, and Y conjugate vaccine Menveo® Nimenrix® |
|
14.04 |
Meningococcal group B Vaccine Bexsero® |
|
14.04 |
Meningococcal group C conjugate vaccine Menjugate Kit® Neis Vac-C® |
|
13.03 |
Menthol in Aqueous cream |
Over the counter preparation suitable for self-care/purchase if appropriate |
05.04 |
Mepacrine |
|
13.15 |
Mepacrine Hydrochloride |
For Discoid lupus erythematosus (DLE)
See Chapter 5, section 05.04.04
|
A5.04.02 |
Mepiform® |
Specialist recommendation only Silicone sheet for scar treatment Type of wound product is suitable for Not for use on open wounds- to be applied on healed scar only. This is not a dressing but a scar treatment Duration dressing remains on wound before changing 23 hours Frequency of dressing change Daily Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Do not use on open or infected wounds. Do not use on skin affected by acne. Discontinue use if a rash or itching occur. Rationale for inclusion in formulary Scar therapy Silicone sheets have been shown to soften, flatten scarring aiding movement, nerve sensations and function. Cost effective. |
A5.02.03 |
Mepitel® |
Specialist recommendation only Soft polymer non-adherent dressing without pad Type of wound product is suitable for Primary wound contact layer, non adherent, traumatic and chronic wounds Requires secondary dressing Duration dressing remains on wound before changing Up to 7 days Frequency of dressing change Up to 7 days Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Heavily bleeding wounds Any sensitivity to silicone Rationale for inclusion in formulary Non-adherent primary wound contact layer to protect skin tears, fragile skin, primary contact layer for use under topical negative pressure |
15.02 |
Mepivacaine Scandonest Plain® |
Hospital only |
03.14 |
Mepolizumab Nucala® |
In line with NICE |
19.03 |
Mepore® |
Type of wound product is suitable for
Post operative closed surgical wounds or simple wounds with up to light amounts of exudate.
Can be used as a protective dressing for sutured post operative wounds. Can be used as a protective dressing for newly epithelialized wounds. Can be used for small traumatic wounds.
Duration dressing remains on wound before changing
Up to 7 days
Frequency of dressing change
1-7 days. If daily change is required - review product choice
Caution/contraindications (when not to use the dressing, patient groups to avoid etc.)
Known product or component sensitivity
Rationale for inclusion in formulary
Sutured surgical wounds for protection. Can be used as a protective dressing for newly epithelialized wounds. Can be used for small traumatic wounds. |
A5.01.02 |
Mepore® |
Type of wound product is suitable for Post operative closed surgical wounds or simple wounds with up to light amounts of exudate. Can be used as a protective dressing for sutured post operative wounds. Can be used as a protective dressing for newly epithelialized wounds. Can be used for small traumatic wounds. Duration dressing remains on wound before changing Up to 7 days Frequency of dressing change 1-7 days. If daily change is required - review product choice Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Known product or component sensitivity Rationale for inclusion in formulary Sutured surgical wounds for protection. Can be used as a protective dressing for newly epithelialized wounds. Can be used for small traumatic wounds. |
04.07.02 |
Meptazinol Meptid® |
|
09.08.01 |
Mercaptamine Cystagon® |
NHSE commissioned
Hospital use only |
01.05.03 |
Mercaptopurine |
Maintenance of remission of acute ulcerative colitis and Crohn’s disease in adults – unlicensed but in line with national guidelines
For use in Inflammatory Bowel Disease (IBD)
Walsall
Amber Initiation- Walsall only
Wolverhampton
Amber Shared Care- Wolverhampton only
ESCA Mercaptopurine-Wolverhampton only
Sandwell
Amber Shared Care- Sandwell only
ESCA Mecaptopurine (Sandwell only)
Dudley
Amber Shared Care Dudley only
ESCA Mecaptopurine (Dudley only) |
08.01.03 |
Mercaptopurine |
Red for cancer indications |
09.04 |
Meritene Shake |
- Prescribed for liver patients, at request of UHB liver/dietetic team only
- For patients with high protein needs and low phosphate requirements
- Use for renal patients
- Use in Liver/hepatobiliary and pancreatic conditions
- Supported by an ESCA
|
03.13 |
Meropenem |
|
05.01.02.02 |
Meropenem |
Primary care-Amber Rec under agreed OPAT Pathway
Secondary care-Microbiological advice |
05.01.02.02 |
Meropenem with vaborbactam Vaborem® |
|
01.05 |
Mesalazine |
Mesalazines should be prescribed by brand.
Please refer to Optimise Rx messages for the preferred brand to be prescribed. Brands include – Pentasa®, Asacol®, Asacol MR®, Salofalk® (granules/enema), Mezavant XL®, Octasa® |
08.01 |
Mesna |
|
07.03.01 |
Mestranol/norethisterone Norinyl-1® |
Monophasic Standard Strength (21 Day preparation)
For patients who need high oestrogen
For patients on anticonvulsant treatment |
A5.15 |
Metanium ointment |
Preferred local option Specialist recommendation only Barrier preparation Type of wound product is suitable for For relief of the symptoms of nappy rash Frequency of use Spread the ointment thinly so the skin texture can be clearly seen through it. Repeat at each nappy change. Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Not to be used on adults in conjunction with containment products for incontinence due to the inclusion of light liquid and white paraffin in the ingredients, which will repel urine/faeces back onto the skin. Any allergy to the listed ingredients Overdose is unlikely when Metanium Nappy Rash Ointment is used as instructed for treating nappy rash. However, as this product contains titanium salicylate, accidental ingestion or excessive topical application could lead to symptoms of salicylate poisoning. Rationale for inclusion in formulary Dermatology approved |
13.02.02 |
Metanium® |
On specialist recommendation only
Over the counter preparation suitable for self-care/purchase if appropriate |
02.07 |
Metaraminol |
|
06.01.02.02 |
Metformin |
Check Optimise Rx for most cost effective brand |
06.01.02.02 |
Metformin |
|
06.01.02.02 |
Metformin |
For patients with swallowing difficulties only.
Tablets more cost effective. |
06.01.02.02 |
Metformin |
Patients with swallowing difficulties |
04.07.02 |
Methadone |
For use in opiod dependence, see section 4.10.3
|
04.10.03 |
Methadone |
|
04.10.03 |
Methadone |
|
04.10.03 |
Methadone |
For use under specialist addiction services |
21 |
Methadone |
|
03.09 |
Methadone Hydrochloride |
For use in palliative care only |
03.09 |
Methadone Hydrochloride Physeptone ® |
For Palliative care use only |
03.09 |
Methadone Hydrochloride oral solution Metharose ® |
For Palliative care use only |
03.09 |
Methadone Hydrochloride oral solution Methadose ® |
For Palliative care use only |
03.09 |
Methadone Hydrochloride oral solution Physeptone ® |
For Palliative care use only |
03.09 |
Methadone Linctus |
For Palliative care use only |
05.01.13 |
Methenamine hippurate |
- On Microbiology/Urology advice
- Prescribing to be retained by Secondary care
|
01.05.03 |
Methotrexate |
Tablets 2.5mg (2.5mg tablets preferred as per NPSA alert)
Cytotoxic - do not crush and disperse in water
For use in active Crohn's disease
For specialist initiation only
Wolverhampton Amber Shared Care Wolverhampton only
ESCA :Methotrexate (Wolverhampton only):
Walsall
Amber Initiation Walsall only
Sandwell
Amber Shared Care Sandwell only
ESCA:Methotrexate in active Crohn's disease (Sandwell only)
Dudley
Amber Shared Care Dudley only
ESCA:Methotrexate (Dudley only) |
03.12 |
Methotrexate |
Sandwell
Amber SC Supported by ESCA
ESCA for Sandwelll
Walsall
Not on Formulary
Dudley
Not on Formulary
Wolverhampton
Amber SC Supported by ESCA
ESCA for Wolverhampton only |
04.13 |
Methotrexate |
Specialist use only for neurological conditions |
08.01.03 |
Methotrexate |
Commissioned by NHSE for treatment of cancer Injection-hospital only |
10.01.03 |
Methotrexate Metoject® |
Metoject is APC preferred brand in view of additional patient safety characteristics
For use under the supervision of a specialist
Supported by an ESCA
Check cytotoxic disposal arrangements locally |
10.01.03 |
Methotrexate |
Only 2.5mg tablets to be prescribed (Local agrement following National Patient Safety Agency (NPSA) alert)
Supported by an ESCA
To be prescribed once weekly as a single dose on the same day each week Folic acid 5mg should normally be taken on the non methotrexate day Cytotoxic, do not crush or disperse the tablets in water |
13.05.03 |
Methotrexate |
Initiated by hospital only ONCE WEEKLY DOSING |
09.01.03 |
Methoxy polyethylene glycol-epoetin beta Mircera® |
•NHSE commissioned for use in renal dialysis
•Primary Care commissioned for use in cancer- in line with NICE TA323
|
13.05.02 |
Methoxypsoralen |
|
13.08.01 |
Methyl aminolevulinate Metvix® |
|
02.05.02 |
Methyldopa |
|
04.04 |
Methylphenidate |
Please note that commissioning discussion is underway. However the present status is as follows:-
Age 6 and over - Solihull practices. Supported with ESCA
Age 16 and over - Birmingham practices. Supported with ESCA
Age under 16 - Birmingham practices
Age 6 and over - Sandwell and West Birmingham CCG. Supported with ESCA
Supported with an ESCA -Sandwell & West Birmingham CCG for patients seen by the Black Country ADHD Services
The immediate release preparation may be prescribed generically |
04.04 |
Methylphenidate |
Please note that commissioning discussion is underway. However the present status is as follows:-
Age 6 and over - Solihull practices. Supported with ESCA
Age 16 and over - Birmingham practices. Supported with ESCA
Age under 16 - Birmingham practices
Age 6 and over - Sandwell and West Birmingham CCG. Supported with ESCA
Supported with an ESCA - Sandwell & West Birmingham CCG for patients seen by the Black Country ADHD Services
|
02.05 |
Metirosine |
|
01.02 |
Metoclopramide |
Nausea and vomiting
Not recommended for patients under 20 years of age due to risk of dystonic reactions
For restrictions for use in younger patients see MHRA guidance below
|
04.06 |
Metoclopramide |
Palliative care
All other indications |
04.06 |
Metoclopramide |
Tablets
SF solution £££££ - for patients with swallowing difficulties only
Nausea and vomiting
Not recommended for patients under 20 years of age due to risk of dystonic reactions
For restrictions for use in younger patients see MHRA guidance below |
02.02.01 |
Metolazone |
Specialist recommendation
|
02.04 |
Metoprolol tartrate |
|
02.04 |
Metoprolol tartrate |
|
06.02.01 |
Metoprolol Tartrate |
|
05.01.11 |
Metronidazole |
|
05.01.11 |
Metronidazole |
|
05.01.11 |
Metronidazole |
Tablets
Suspension £££££ |
05.04 |
Metronidazole Rozex ® |
For acne rosacea only NOT infected wounds. |
05.04 |
Metronidazole Zidoval® |
|
05.04 |
Metronidazole Anabact® |
For wounds, malodorous tumours and skin ulcers. |
05.04 |
Metronidazole Metrogel® |
|
05.04 |
Metronidazole |
|
05.04 |
Metronidazole Acea ® |
For acne rosacea only NOT infected wounds. |
05.04 |
Metronidazole Rosiced® |
|
05.04 |
Metronidazole |
|
A5.16 |
Metronidazole Anabact® |
Specialist recommendation only Type of wound product is suitable for Malodourous fungating wounds Requires a secondary dressing Duration dressing remains on wound before changing Apply 1-2 times daily following cleansing Frequency of dressing change 1-2 times daily for a maximum of 8 weeks Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Avoid exposure to strong sunlight or UV light Not to be used on a patient with known sensitivity to any components avoid contact with eyes Not for use on any other aetiology of wound as odour control Rationale for inclusion in formulary Odour control for fungating tumours |
06.07 |
Metyrapone Metopirone® |
|
10.02.02 |
Mexiletine 167mg hard capsules Namuscla® |
In line with NICE
For use in Ventricular Arrythmia use this link to Chapter 2
|
02.03.02 |
Mexiletine hydrochloride |
|
02.03.02 |
Mexiletine unlicensed special |
|
05.02.04 |
Micafungin |
|
07.02.02 |
Miconazole Gyno-Daktarin® |
- 2% intravaginal cream
- 1.2g ovule (vaginal capsule) - discontinued by manufacturer 2018
|
12.03.02 |
Miconazole |
|
11.03.02 |
Miconazole 1% eye drops |
|
13.10.02 |
Miconazole 2% |
Cream Dusting powder |
04.08.02 |
Midazolam Buccolam® |
On specialist advice |
15.01.04.01 |
Midazolam |
Palliative care
All other indications-hospital only |
02.07 |
Midodrine |
Use current status at Place/Trust
Sandwell
ESCA Midodrine- Sandwell only
Wolverhampton
Walsall
Dudley
Unclassified
|
08.01.05 |
Midostaurin Rydapt® |
In line with NICE |
08.02.04 |
Mifamurtide |
In line with NICE |
07.01.02 |
Mifepristone Mifegyne® |
For Specialist/ Hospital Use Only |
04.07.04 |
Migraleve ® pink |
|
02.05 |
Milrinone Primacor® |
|
02.05.01 |
Minoxidil Loniten® |
Use on specialist advice only |
07.04.02 |
Mirabegron Betmiga® |
Specialist Initiated
In line with NICE
For patients not tolerating / with contra-indications to antimuscarinics Only to be used instead of anticholinergics if: Anticholinergics contraindicated Severe side effects with anticholinergics At least two anticholinergics not effective Prescribing mirabegron in combination with anticholinergics is not supported by trial data and therefore non-formulary |
04.03.04 |
Mirtazapine |
- Tablets
- Orodispersible tablets ££
|
21 |
Mirtazapine |
- Pain under Specialist Initiation.
- Limited RCT evidence, for 3rd or 4th line pain where patient has low mood.
|
01.03 |
Misoprostol |
|
01.03.04 |
Misoprostol Cytotec® |
For specialist initiation only |
08.01.02 |
Mitomycin |
Commissioned by NHSE Hospital only |
11.99.99.99 |
Mitomycin C |
Hospital only |
08.01.05 |
Mitotane Lysodren® |
Commissioned by NHSE |
08.01.02 |
Mitoxantrone |
Commissioned by NHSE Hospital only |
15.01.05 |
Mivacurium Chloride Mivacron® |
Hospital only |
09.04 |
MMA/PA A,omp 5 |
- Methionine, threonine and valine free, and low isoleucine aa supplement
- The only pre-measured sachet of methionine, threonine, valine free and low isoleucine amino acid supplement for patients with propionic acidaemia and methyl malonic acidaemia reliant on tube feeding. A pre-measured sachet is particularly important as most of our families with MSUD do not speak English as their first language so require pre-measured products
|
09.04 |
MMA/PA Anamix® Infant |
- Amino acid supplement without methionine, threonine, valine and isoleucine for infants with propionic acidaemia and methyl malonic acidaemia
- The only infant amino acid supplement without methionine, threonine, valine and isoleucine for patients with propionic acidaemia and methyl malonic acidaemia
- Nutritional supplement for the dietary management of proven methylmalonic acidaemia or propionic acidaemia in children from birth to 3 years
|
04.03.02 |
Moclobemide |
|
04.04 |
Modafinil |
- Specialist initiation only for use in narcolepsy
|
09.04 |
Modjul® Flavour System |
Flavouring preparations
- For flavouring unpalatable flavouring amino acid supplements or feeds in inborn errors of metabolism
- Essential for flavouring different unflavoured amino acid supplements in inborn errors of metabolism- particularly for non PKU conditions. They offer alternative flavours to Vitaflo pacs. This is important as amino acid formulations are unpalatable and unacceptable particularly for patients with late diagnosed conditions
- They cannot be purchased from a supermarket
- For use with unflavoured SHS products based on peptides or amino acids; not suitable for child under 6 months
|
09.04 |
Modulen IBD® |
- Specialised formulas for specific clinical conditions
- For treatment of Crohn’s Disease
- Crohn's disease active phase, and in remission if malnourished
|
08.01.05 |
Mogamulizumab Poteligeo® |
In line with NICE |
03.02 |
Mometasone |
|
12.02.01 |
Mometasone Furoate |
|
13.04 |
Mometasone Furoate 0.1% |
Potency - potent Cream Ointment Scalp lotion £££ Avoid prolonged use in children Prescribe as acute prescription for 7 - 14 days only |
09.04 |
Monogen® |
- Specialised formulas: Infant and child: MCT-enhanced formula
- Used in infants who require high MCT feed eg following chylothorax and in inborn errors of metabolism where MCT is required
- Also essential for infants/children with long chain fatty acid oxidation disorders who need a high intake of MCT and high intake of carbohydrate e.g. LCHADD and trifunctional protein deficiency (i.e. lower carbohydrate formulas are inappropriate). There should always be 2 powdered high MCT formulae in the formulary in case of supply issues. The dose and type of product should always be advised by the specialist dietitian according to the needs of the patient
- Long-chain acyl-CoA dehydrogenase deficiency (LCAD), carnitine palmitoyl transferase deficiency (CPTD), primary and secondary lipoprotein lipase deficiency, chylothorax, and lymphangiectasia
|
03.03.02 |
Montelukast |
Use in line with recommendations in BTS-SIGN asthma guideline |
04.07.02 |
Morphine |
Tablets
M/R tablets
M/R capsules
Oral solution
Injection
Suppositories
100mg/100ml PCA
5mg/5ml intrathecal injection
pre-filled syringe
Specialist initiation- pain clinic Modified release(MR) preparation should be used for regular dosing. Immediate release preparations may be associated with tolerance and problem drug use. Follow Optimise Rx advice for most cost effective brand / formulation Injectable formulations for palliative care only |
15.01.04.03 |
Morphine |
Hospital only in context of chapter 15. See chapter 4 for other indications. |
21 |
Morphine |
- Topical use for painful wounds where systemic opioids are effective but dose limited due to side-effects
|
03.09 |
Morphine modified release capsule Zomorph® |
For Palliative care use only |
03.09 |
Morphine modified release tablet MST Continus ® |
For Palliative care use only |
03.09 |
Morphine oral solution |
For Palliative care use only |
03.09 |
Morphine oral solution |
For Palliative care use only |
03.09 |
Morphine solution for infusion |
For Palliative care use only |
03.09 |
Morphine solution for injection |
For Palliative care use only |
03.09 |
Morphine tablet Sevredol® |
For Palliative care use only |
05.01.12 |
Moxifloxacin |
Hospital use only under microbiological advice |
02.05.02 |
Moxonidine |
|
09.04 |
MSUD Amino 5 |
- Amino acid supplement without leucine, valine and isoleucine for infants/children with MSUD
- The only pre-measured amino acid supplement, without leucine, valine, isoleucine for infants/children with maple syrup urine disease used for emergency regimens and tube feeds. This is particularly important as most of our families with MSUD do not speak English as their first language
|
09.04 |
MSUD Anamix® Infant |
- Amino acid supplement without leucine, valine and isoleucine for infants with MSUD
- The only infant amino acid supplement without leucine, valine, isoleucine for maple syrup urine disease
- Nutritional supplement for the dietary management of proven maple syrup urine disease in children from birth to 3 years
|
09.04 |
MSUD Anamix® Junior |
- Amino acid supplement without leucine, valine and isoleucine for children with MSUD
- The only infant amino acid supplement without leucine, valine, isoleucine for maple syrup urine disease
- Nutritional supplement for the dietary management of maple syrup urine disease in children 1–10 years
|
09.04 |
MSUD Anamix® Junior LQ |
- Amino acid supplement without leucine, valine and isoleucine for children with MSUD
- Can be used in adults
- An unthickened powdered amino acid supplement without leucine, valine, isoleucine for children aged 1 to 10y with maple syrup urine disease which can be given as a drink
- Nutritional supplement for the dietary management of maple syrup urine disease in children 1–10 years
|
09.04 |
MSUD cooler® 10 |
- Amino acid supplement without leucine, valine and isoleucine for children and adults with MSUD
- An oral liquid amino acid supplement without leucine, valine, isoleucine formulated for children aged 3 to 6 years with maple syrup urine disease. Larger pouches are unacceptable for this age group of children and provide in excess of protein requirements
|
09.04 |
MSUD cooler® 15 |
- Amino acid supplement without leucine, valine and isoleucine for teenagers with MSUD
- An oral liquid amino acid supplement without leucine, valine, isoleucine for children aged 7 to 12 years with maple syrup urine disease. Larger pouches are unacceptable for this age group of children and provide in excess of protein requirements
|
09.04 |
MSUD cooler® 20 |
- Amino acid supplement without leucine, valine and isoleucine for teenagers and adults with MSUD
- One of 2 oral flavoured liquid amino acid supplements without leucine, valine, isoleucine for teenagers over 12 years of age and adults. This age group need the larger pouches to meet their non-leucine protein requirements. It is important we have a choice of more than 1 product as compliance is poor. It is essential that patients are offered choice of more than 1 protein substitute
|
09.04 |
MSUD express® 15 |
- Amino acid supplement without leucine, valine and isoleucine for teenagers and adults with MSUD
- The only powdered amino acid supplement without leucine, valine, isoleucine for 7 to 12-year olds with maple syrup urine disease. Larger sachets are unacceptable for this age group of children and provide in excess of protein requirements
- Nutritional supplement for the dietary management of maple syrup urine disease in children over 8 years and adults
|
09.04 |
MSUD express® 20 |
- Amino acid supplement without leucine, valine and isoleucine for teenagers and adults with MSUD
- The only powdered amino acid supplement without leucine, valine, isoleucine for teenagers and adults with maple syrup urine disease that will met their higher BCAA-free amino acid requirements. This age group need the larger sachets (20g protein equivalent) to meet their non-methionine protein requirements
- Nutritional supplement for the dietary management of maple syrup urine disease in children over 8 years and adults
|
09.04 |
MSUD Gel® |
- Amino acid supplement without leucine, valine and isoleucine for children with MSUD
- The only weaning (thickened) amino acid supplement without leucine, valine, isoleucine for infants/young children with maple syrup urine disease
- Nutritional supplement for the dietary management of maple syrup urine disease in children 1–10 years
|
09.04 |
MSUD Lophlex® LQ 20 |
- Amino acid supplement without leucine, valine and isoleucine for teenagers and adults with MSUD
- One of 2 oral flavoured amino acid supplement without leucine, valine, isoleucine for teenagers over 12 years of age and adults with maple syrup urine disease. They need the larger pouches to meet their BCAA-free amino acid requirements. It is important we have a choice of more than 1 product for this age group as compliance is poor. It is essential that patients are offered choice of more than 1 protein substitute
- Nutritional supplement for the dietary management of maple syrup urine disease in children over 3 years
|
09.06.07 |
Multivitamin preparations Dalivit® |
Patients should be referred to healthy start vitamins scheme where eligible. Limit prescribing to patients with clinical deficiency. Dalivit and alternatives are available for purchase for general needs. |
09.06.07 |
Multivitamin preparations Abidec® |
Contains arachis ( peanut) oil Patients should be referred to healthy start vitamins scheme where eligible. Limit prescribing to patients with clinical deficiency. Abidec and alternatives are available for purchase for general needs. |
09.06.07 |
Multivitamin Supplement Paravit-CF® |
Specialist initiation or recommendation for GP initiation by specialist in Cystic Fibrosis |
09.06.07 |
Multivitamins |
|
09.06.07 |
Multivitamins (vitamin capsules) |
Contains vitamin A, vitamin D, Vitamin C, and B bitamins (riboflavin, nicotinamide and thiamine) Eligible patients should be referred to health start vitamins scheme. Prescribing of vitamins should be limited to patients with clinical deficiencies or malabsorption syndromes. |
12.02.03 |
Mupirocin 2% Bactroban Nasal® |
|
13.10.01.01 |
Mupirocin 2% Bactroban® |
Please refer to Primary Care Antimicrobial Guidelines
|
04.13 |
Mycophenolate |
Specialist use only for neurological conditions |
13.05.03 |
Mycophenolate |
In line with ESCA (to be developed) |
08.02.01 |
Mycophenolate Mofetil |
Prescribing to remain with the specialist for this patient group
Renal Post transplant- new patients Renal Post transplant-patients initiated pre April 2013
For use in connective tissue diseases (Rheumatology), click here
|
10.02.01 |
Mycophenolate mofetil |
For use in connective tissue diseases
For specialist initiation and dose stabilisation
Supported by an ESCA |
20 |
N acetyl cysteine |
For use in endoscopy |
19.01 |
N-A® Ultra |
Type of wound product is suitable for
For flat granulating and epithelising wound for non to heavy exudate levels where adherence may occur. To be used as a primary dressing with a secondary for absorption.
Duration dressing remains on wound before changing
7 days maximum
Frequency of dressing change
1-7 days, depending on levels of exudate
Caution/contraindications (when not to use the dressing, patient groups to avoid etc.)
Known product or component sensitivity eg silicone. Use with care if wound is bleeding heavily.
Rationale for inclusion in formulary
To be used to reduce adherence to wound bed. |
A5.01.01 |
N-A® Ultra |
Preferred local option Type of wound product is suitable for For flat granulating and epithelising wound for non to heavy exudate levels where adherence may occur. To be used as a primary dressing with a secondary for absorption. Duration dressing remains on wound before changing 7 days maximum Frequency of dressing change 1-7 days, depending on levels of exudate Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Known product or component sensitivity eg silicone. Use with care if wound is bleeding heavily. Rationale for inclusion in formulary To be used to reduce adherence to wound bed. |
03.07 |
N-Acetylcysteine nebulised |
Hospital only |
02.06.04 |
Naftidrofuryl Oxalate |
|
01.06.06 |
Naldemedine Rizmoic® |
For treating opioid-induced constipation in line with NICE |
04.10.01 |
Nalmefene |
Restricted to Specialist Substance Misuse Services only (as per the local authority public health approved pathways) Reach Out Recovery (CRI) in Birmingham. Single point of contact 24/7 Tel: 0121 227 5890 Link Reach Out Recovery website
Swanswell in Sandwell Tel: 0121 553 1333 Link to Swanswell website
SIAS in Solihull Tel:0121 301 3600 Link to SIAS website
The Nalmefen for reducung alcohol consumption technology appraisal (TA325) recommends this drug as a possible treatment for people with alcohol dependence who:
- are still drinking more than 7.5 units per day (men) and more than 5 units per day (women) 2 weeks after an initial assessement and
- do not have physical withdrawal symptoms and
- do not need to either stop drinking straight away or stop drinkling completely
The guidance also recommends that nalmefene should only be prescribed in conjunction with continuous psychosocial support focused on treatment adherence and reducing alcohol consumption |
01.06.06 |
Naloxegol Moventig® |
£££££
For treating opioid-induced constipation in line with NICE
|
04.10 |
Naloxone |
|
04.10.03 |
Naloxone |
Used to reverse opioid overdose |
15.01.07 |
Naloxone |
Hospital only |
04.10.01 |
Naltrexone |
Useful as an adjunct in the treatment of alcohol dependence after a successful withdrawal |
04.10.03 |
Naltrexone Nalorex® |
On recommendation from specialist service |
10.01.01 |
Naproxen |
Naproxen EC tablets - Non-formulary This has a half-life of 14 hours, so is useful if a sustained effect is required Also indicated for use in dysmenorrhoea Recommended for use in gout |
08.02.04 |
Natalizumab Tysabri® |
Commissioned by NHSE Hospital only |
02.04 |
Nebivolol |
Follow Optimise Rx advice for new initiations |
06.01.01.03 |
Needle free administration device |
BRANDS
- Injex 10ml vial adaptor pack
- Injex 4 monthly refill pack
- Injex ampoule pack
- Injex starter set
- InsuJet 10ml vial adaptor pack 5 pieces
- InsuJet 3ml cartridge adaptor pack 5 pieces
- InsuJet nozzle pack 5 pieces
- InsuJet starter set
|
08.01.03 |
Nelarabine Atriance® |
Funding may be available from cancer drug fund
Hospital only |
09.04 |
Neocate Syneo® |
Infant formula powder and is amino acid-based. |
09.04 |
Neocate® Junior |
- Infant and child: Amino acid-based formula
- Replacement for Neocate Active and Neocate Advance on the formulary
- Use in children over 12 mths who require amino acid based feed / have multiple food allergies
- Used as tube or oral feed, provides complete nutritional support
- For the dietary management of proven whole protein allergy, short bowel syndrome, intractable malabsorption and other gastrointestinal disorders where an amino acid diet is recommended, for children from 1 year onwards
- ACBS Indications: Proven whole protein intolerance, short bowel syndrome, intractable malabsorption, or other gastro-intestinal disorders where an elemental diet is indicated
|
09.04 |
Neocate® LCP |
- Infant and child: Amino acid-based formula
- Use in infants ( birth – 12 months) who have multiple food allergies / faltering growth / require amino acid based feed as unable to tolerate standard or peptide feed. Used as tube and oral feed
- Cows' milk allergy, multiple food protein intolerance, and conditions requiring an elemental diet
- ACBS Indications: Proven whole protein intolerance, short bowel syndrome, intractable malabsorption, or other gastro-intestinal disorders where an elemental diet is indicated
|
11.04.02 |
Neodocromil Rapitil® |
|
10.02.01 |
Neostigmine |
|
10.02.01 |
Neostigmine |
Hospital use only |
15.01.06 |
Neostigmine metilsulfate |
Hospital only |
09.04 |
Nepro® |
- Specialised formulas for specific clinical conditions
- Used for renal in and outpatients – adults only
- Useful on occasion due to reduced Vitamin A content – adults only
- Enteral feed or nutritional supplement in patients with chronic renal failure who are on haemodialysis or CAPD, or with cirrhosis, or other conditions requiring a high energy, low fluid, low electrolyte diet
- Not suitable for child under 1 year; use with caution in child 1–5 years
|
08.01.05 |
Neratinib Nerlynx® |
In line with NICE |
05.03.01 |
Nevirapine |
|
05.03.01 |
Nevirapine Viramune® |
|
02.06.02 |
Nicardipine Cardene® |
|
05.05 |
Niclosamide |
|
02.06 |
Nicorandil Ikorel® |
Specialist initiation |
09.06.02 |
Nicotinamide |
|
13.06.01 |
Nicotinamide 4% |
3rd line |
04.10.02 |
Nicotine replacement therapy |
|
02.06.02 |
Nifedipine |
|
07.01.03 |
Nifedipine |
|
21 |
Nifedipine |
- Hiccup, Tenesmus - Off-label use according to WMPCP Palliative Care Physicians Guidelines.
|
08.01.05 |
Nilotinib Tasigna® |
Commissioned by NHSE
In line with NICE |
02.06.02 |
Nimodipine Nimotop® |
|
03.11 |
Nintedanib Vargatef® |
Hospital ONLY
NHSE comissioned
In line with NICE and available from day 91 following publication of TA |
03.11 |
Nintedanib Ofev® |
Hospital only- NHSE commissioned
In line with NICE and available from day 91 following publication of TA |
08.01.05 |
Niraparib Zejula® |
Hospital Only
In line with NICE |
05.03.01 |
Nirmatrelvir With Ritonavir |
|
05.01.07 |
Nitazoxanide Alinia® |
For Hospital Use Only |
05.04.04 |
Nitazoxanide |
Not in BNF (Phase 2 trials) |
09.08.01 |
Nitisinone Orfadin® |
NHSE commissioned |
05.01.13 |
Nitrofurantoin |
Modified release capsules preferred formulation-First line
Oral Suspension £££££ |
15.01.02 |
Nitrous oxide |
HOSPITAL ONLY |
08.02.03 |
Nivolumab Opdivo® |
Hospital Only
In line with NICE |
01.03.01 |
Nizatidine |
|
19.31 |
NON-WOVEN FABRIC SWAB Drug Tariff Specification 28 |
Alternative to gauze Lint/cotton, swabs/cotton wool should NOT be used - fibres can remain in the wound bed. Gauze should NOT be used as a primary dressing |
02.07 |
Noradrenaline / Norepinephrine |
|
06.04 |
NORETHISTERONE |
|
07.03.02.01 |
Norethisterone Noriday® |
Alternative to discontinued Micronor® |
08.03.02 |
Norethisterone |
|
05.01.12 |
Norfloxacin |
Hospital use only under microbiological advice |
14.05 |
Normal immunoglobulin |
Normal immunoglobulin (IV or SC) is commissioned by NHS England not CCG
For subcutaneous use: Gammanorm Hizentra Subcuvia Subgam
For intravenous use: Flebogamma Gammaplex Octagam Vigam
For intramuscular use
List of brands available for use:
- Intratect (5%)
- Gammaplex
- Subgam
- Hizentra
- Privigen
- Gamunex (10%)
- Iqymune
- Gammanorm
- Octagam 10%
- Panzyga
- Cuvitru
- Subcuvia
|
14.05.01 |
Normal immunoglobulin |
Normal immunoglobulin for intramuscular use Normal immunoglobulin for subcutaneous use:
|
06.04.01.01 |
Novofem® |
|
10.02 |
Nusinersen Spinraza® |
In line with NICE |
09.09 |
Nutilis® Clear |
- Recommended by SALTs for patients with dysphagia requiring thickened fluids
- For thickening of liquids or foods in dysphagia. Not suitable for children under 3 years
- Gum based products are generally preferred as they thicken to a more stable end point (unlike starch based products, they do not continue thickening over time) and provide a smoother texture, which improves acceptability and palatability for patients
|
09.04 |
Nutilis® Complete Stage 1 |
- More than 1.5 kcal/mL and 5g (or more) protein/100 mL
- Used for dysphagia pts only
- Where first line pre-thickened product – Slo Milkshake – is not suitable
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula
- Not suitable for child under 3 years; use with caution in child 3–5 years
|
09.04 |
Nutramigen® 1 with LGG (previous name Nutramigen® Lipil 1) |
- Specialised formulas: Infant and child: Hydrolysate formula
- Casein hydrolysate. Use in infants (from birth – 6 mths) who have cow’s milk protein intolerance / allergy
- Tube or oral feed
- Nutramigen has all the fat as LCT and CHO as glucose polymer and is more suitable for CMPI
- If patient has a cow’s milk protein intolerance / allergy GP may initiate Nutramigen® Lipil 1 and refer to dietetics – in line NICE CG 116
- Disaccharide and/or whole protein intolerance where additional medium chain triglycerides are not included
|
09.04 |
Nutramigen® 2 with LGG (previous name Nutramigen® Lipil 2) |
- Specialised formulas: Infant and child: Hydrolysate formula
- Casein hydrolysate. Use in infants from 6 mths who have cow’s milk protein intolerance/ allergy and soya intolerance/allergy
- Tube or oral feed
- If patient has a cow’s milk protein intolerance / allergy GP may initiate Nutramigen® Lipil 2 and refer to dietetics – in line NICE CG 116
- Established disaccharide and/or whole protein intolerance (where additional chain triglycerides are not indicated)
- Not suitable for child under 6 months
|
09.04 |
Nutramigen® Puramino |
- Infant and child: Amino acid-based formula
- Use in infants (birth – 12 months) who have multiple food allergies / faltering growth / require amino acid based feed. Unlike other products contains 33% MCT fat so useful in children requiring amino acid feed who also have fat malabsorption
- Used as tube and oral feed
- For use in the management of severe protein intolerance, multiple food intolerance and other gastro-intestinal disorders where an amino acid based diet is specifically indicated for infants and young children
- ACBS Indications: Proven whole protein intolerance, short bowel syndrome, intractable malabsorption, or other gastro-intestinal disorders where an elemental diet is indicated
|
09.04 |
Nutricrem® |
- More than 1.5 kcal/mL and 5g (or more) protein/100 mL
- Lactose free diet
- Low energy per serving as a semi-solid supplement where low volume is required only
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula
- Not suitable for child under 3 years; use with caution in child 3–6 years.
|
09.04.02 |
Nutrini® |
- Child: 1 kcal/ml and less than 4g protein/100ml
- 1 kcal feed without fibre, used in children 8-20kg. Up to 6 years.
- Also essential low protein tube feed for children with inborn errors of protein metabolism (e.g. organic acidaemias, urea cycle disorders) aged 2 to 10y due to its low protein and amino profile as a source of natural protein. It is used when IMD children cannot tolerate fibre. To change to an alternative enteral feed with children with metabolic disorders would potentially require hospital admission to ensure stabilisation with a new enteral feed. The dose and type of product should always be advised by the specialist dietitian according to the needs of the patient
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula and growth failure in child 1–6 years, body-weight 8–20 kg
|
09.04.02 |
Nutrini® Low Enery Multi Fibre |
Child under 12 years
- Low energy with fibre. 8-20kg
- Less than 1 kcal/mL and less than 4g protein/100 mL
- Paediatric ACBS indications: Disease-related malnutrition, intractable malabsorption, growth failure, pre-operative preparation of malnourished patients, dysphagia, short-bowel syndrome, bowel fistula except bowel fistula, in child 1–6 years, body-weight 8–20 kg
|
09.04.02 |
Nutrini® Energy |
- Child: 1.5 kcal/mL and more than 4g protein/100 mL
- 1.5kcal/ml tube feed for children over 8kg
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula and growth failure in child 1–6 years, body-weight 8–20 kg
|
09.04.02 |
Nutrini® Energy Multi Fibre |
- Child: 1.5 kcal/mL and more than 4g protein/100 mL
- 1.5kcal/ml tube feed for children over 8kg with added fibre
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula and growth failure in child 1–6 years, body-weight 8–20 kg
|
09.04.02 |
Nutrini® Multi fibre |
- Child: 1 kcal/ml and less than 4g protein/100ml
- 1 kcal feed with fibre, used in children 8-20kg. Up to 6 years
- Also, used in low protein tube feeds for children with inborn errors of protein metabolism (e.g. organic acidaemias, urea cycle disorders) aged 2 to 10y due to its protein and amino acid profile. It provides a source of natural protein. It is used in IMD children who can tolerate fibre. To change to an alternative enteral feed with children with metabolic disorders would potentially require hospital admission to ensure stabilisation with a new enteral feed. The dose and type of product should always be advised by the specialist dietitian according to the needs of the patient.
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula and growth failure in child 1–6 years, body-weight 8–20 kg
|
09.04.02 |
Nutrini® Peptisorb |
- Hydrolysate formula
- 1.0kcal/ml polymeric feed used 8 -20kg where hydrolysed protein is required
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula and growth failure in child 1–6 years, body-weight 8–20 kg Follow trust guidance on use of acidic tube feeds.
|
09.04.02 |
Nutrini® Peptisorb Energy |
- Child: 1.5 kcal/mL and more than 4g protein/100 mL
- 1.5kcal/ml hydrolysed protein feed used in children over 8kg where whole protein is not tolerated. Additional information re pH of the product?
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula and growth failure in child 1–6 years, body-weight 8–20 kg
|
09.04.02 |
Nutriprem® 1 |
For premature infant up to 2kg
- Less than 1 kcal/mL and less than 4g protein/100 mL
- Low birth - weight formula
|
09.04.02 |
Nutriprem® 2 |
Child under 12 years
- Less than 1 kcal/mL and less than 4g protein/100 mL
- Post discharge formula for pre-term infants
- Catch-up growth in pre-term infants (less than 35 weeks at birth) and small for gestational-age infants up to 6 months corrected age
|
09.04.02 |
Nutriprem® 2 |
Child under 12 years
- Less than 1 kcal/mL and less than 4g protein/100 mL
- Post discharge formula for pre-term infants <34 weeks to aid growth, for immunocompromised infants
- Catch-up growth in pre-term infants (less than 35 weeks at birth) and small for gestational-age infants up to 6 months corrected age
|
09.04.02 |
Nutrison Peptisorb Plus HEHP Liquid tube feed |
- For large volumes use Nutrison Peptisorb Plus HEHP. For small er volumes 200ml use Vital®1.5 kcal.
- Nutrison Peptisorb Plus HEHP is a Food for Special Medical Purposes for use under medical supervision.
- Nutrison Peptisorb Plus HEHP is a peptide based, nutritionally complete*, ready to use, high energy (1.5kcal/ml), high protein (7.5g/100ml, 20% of energy from protein) tube feed, for the dietary management of disease related malnutrition in patients with malabsorption and/or maldigestion.
- Suitable as a sole source of nutrition.
- ACBS approved: for adults with disease related malnutrition, short bowel syndrome, intractable malabsorption, bowel fistulae, inflammatory bowel disease, total gastrectomy and for the pre-operative preparation of patients who are malnourished.
|
09.04.02 |
Nutrison Peptisorb® |
- 1 kcal/mL and less than 5g protein/100 mL
- Peptide-based formula
- Pts with malabsorption
- Short bowel syndrome, intractable malabsoprtion, proven inflammatory bowel disease, bowel fistula.
- Follow Trust guidance on use of acidic tube feeds
|
09.04.02 |
Nutrison® |
First line
- 1 kcal/mL and less than 5 g protein/100 mL
- Standard 1 kcal/mL. No fibre
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula
|
09.04.02 |
Nutrison® 1000 Complete Multi Fibre |
- Less than 1.5 kcal/mL and 5g (or more) protein/100 mL
- 1000 kcal/L, nutritionally complete in 1 litre, low volume
- Disease related malnutrition in patients with low energy and/or low fluid requirements
|
09.04.02 |
Nutrison® 1200 Complete Multi Fibre |
- Less than 1.5 kcal/mL and 5g (or more) protein/100 mL
- 1200 kcal/L, nutritionally complete in 1 litre, low volume
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula
|
09.04.02 |
Nutrison® 800 Complete Multi Fibre |
- Less than 1.5 kcal/mL and 5g (or more) protein/100 mL
- 800 kcal/L, nutritionally complete in 1 litre, low volume
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula. Not suitable for child under 6 years, not recommended for child 6 - 12 years
|
09.04.02 |
Nutrison® Concentrated |
- More than 1.5 kcal/mL and 5g (or more) protein/100 mL
- High calorie (2000 kcal/L), low volume, low potassium
- First line in CF and renal patients
|
09.04.02 |
Nutrison® Energy |
- 1.5 kcal/mL and 5g (or more) protein/100 mL
- High energy feed
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula
|
09.04.02 |
Nutrison® Energy Multi Fibre |
- 1.5 kcal/mL and 5g (or more) protein/100 mL
- High energy feed with fibre
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula
|
09.04.02 |
Nutrison® MCT |
- Less than 1.5 kcal/mL and 5g (or more) protein/100 mL
- Pts with chyle leaks following upper GI surgery
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula
|
09.04.02 |
Nutrison® Multi Fibre |
First line
- 1 kcal/mL and less than 5 g protein/100 mL
- Standard 1 kcal/mL, With fibre
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula
|
09.04.02 |
Nutrison® Protein Plus |
- Less than 1.5 kcal/mL and 5g (or more) protein/100 mL
- Lower calorie, high protein feed. Fibre free
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula
|
09.04.02 |
Nutrison® Protein Plus Multi Fibre |
- Less than 1.5 kcal/mL and 5g (or more) protein/100 mL
- Lower calorie, high protein feed. Added fibre
|
09.04.02 |
Nutrison® Soya |
- 1 kcal/mL and less than 5g protein/100 mL
- Soya protein formula
- Dietary restriction or intolerance to standard feeds
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula; also cows'milk protein and lactose intolerance
|
09.04.02 |
Nutrison® Soya Multi Fibre |
- 1 kcal/mL and less than 5g protein/100 mL
- Soya protein formula
- Dietary restriction or intolerance to standard feeds requiring fibre
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula
|
05.02 |
Nystatin |
Not sugar Free |
12.03.02 |
Nystatin 100,000units/ml |
Do not prescribe as Sugar free (SF) |
A5.05.02 |
Oakmed Option Wound Manager |
Specialist recommendation only Wound drainage system consisting of a hydrocolloid adhesive wafer and a drainable drainage bag Type of wound product is suitable for Complex abdominal wounds, moderate to large fistula’s, orthopaedic wounds or fungating wounds with high levels of exudate, that are unmanaged with conventional dressings. Max duration dressing remains on wound before changing Empty drainage bag as required. If no port for drainage, change as required. Frequency of dressing change As long as adhesive remains intact whilst being mindful of skin integrity Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Known product component sensitivity to hydrocolloid (Gelatine and Pectin) Low to moderate exuding wounds Do not use if a conventional dressing can manage the exudate levels Rationale for inclusion in formulary Various size selection with drainage ports and windows For highly exuding wounds that conventional dressings cannot manage the exudate levels |
01.09 |
Obeticholic acid Ocaliva® |
NHSE commissioned
In line with NICE |
08.02.03 |
Obinutuzumab Gazyvaro® |
In line with NICE
Hospital only |
08.02.03 |
Ocrelizumab Ocrevus® |
Hospital Only
In line with NICE |
11.08.02 |
Ocriplasmin Jetrea® |
|
12.02.03 |
Octenidine hydrochloride Octenisan® ms Nasal gel |
- Classed as a medical device
- Listed in drug tariff - 6ml tube
- Added to the formulary as alternative to Bacroban® nasal ointmnet in view of supply issues
|
13.11.02 |
Octenisan antimicrobial wash lotion |
For MRSA skin decolonisation if chlorhexidine sensitivity is a problem. |
13.01 |
Octenisan® |
For MRSA skin decolonisation , if chlorhexidine sensitivity is a problem |
01.09 |
Octreotide |
For specialist gastroenterologist initiation for intestinal secretions |
01.09 |
Octreotide |
|
06.05 |
OCTREOTIDE |
Olatuton - Red
Sandostatin - Red
Sandostatin LAR - Red |
08.03.04.03 |
Octreotide Sandostatin Lar® |
NHSE commissioned in cancer: Use the product with the lowest acquisition cost. Palliative Care Use Only For Oncology
For Acromegaly |
08.03.04.03 |
Octreotide Sandostatin® |
NHSE commissioned in cancer: Use the product with the lowest acquisition cost. Palliative Care Use Only For Oncology
For Acromegaly |
21 |
Octreotide |
- For high volume vomiting, increased gastric secretion.
|
06.04 |
Oestrogel® |
|
07.02.01 |
Oestrogens, Topical Estring® |
|
07.02.01 |
Oestrogens, Topical Gynest® |
CAUTION CONTAINS ARACHIS (PEANUT) OIL Topical oestrogens should be used in the smallest effective amount to minimise systemic effects. The risk of endometrial hyperplasia and carcinoma is increased when systemic oestrogens are administered alone for prolonged periods. The endometrial safety of long-term or repeated use of topical vaginal oestrogens is uncertain; treatment should be reviewed at least annually, with special consideration given to any symptoms of endometrial hyperplasia or carcinoma. |
07.02.01 |
Oestrogens, Topical Ovestin® |
Topical oestrogens should be used in the smallest effective amount to minimise systemic effects. The risk of endometrial hyperplasia and carcinoma is increased when systemic oestrogens are administered alone for prolonged periods. The endometrial safety of long-term or repeated use of topical vaginal oestrogens is uncertain; treatment should be reviewed at least annually, with special consideration given to any symptoms of endometrial hyperplasia or carcinoma. |
07.02.01 |
Oestrogens, Topical Ortho-Gynest® |
Topical oestrogens should be used in the smallest effective amount to minimise systemic effects. The risk of endometrial hyperplasia and carcinoma is increased when systemic oestrogens are administered alone for prolonged periods. The endometrial safety of long-term or repeated use of topical vaginal oestrogens is uncertain; treatment should be reviewed at least annually, with special consideration given to any symptoms of endometrial hyperplasia or carcinoma. |
08.02.03 |
Ofatumumab Arzerra® |
NHSE is responsible commissioner for its use in untreated chronic lymphocytic leukaemia (as per NICE TA344)
Hospital only
Use in line with NICE |
05.01.12 |
Ofloxacin |
Hospital use only under microbiological advice /GUM |
11.03.01 |
Ofloxacin |
For use on advice of specialist. Not be used for the treatment of bacterial conjunctivitis |
04.02.01 |
Olanzapine |
Supported by ESCA |
04.02.02 |
Olanzapine Embonate ZypAdhera® |
The APC's view is that, on clinical grounds, the status of antipsychotic depot injections should be amber with a framework in place in Primary Care before transfer
HOWEVER, until the commissioning arrangements have been agreed to allow safe transfer of patient care, the status will remain RED |
08.01.05 |
Olaparib Lynparza® |
Hospital ONLY
NHSE commissioned
In line with NICE and available from day 91 following publication of TA |
08.01.05 |
Olaratumab Lartruvo® |
In line with NICE |
12.01.03 |
Olive Oil Ear Drops |
|
11.04.02 |
Olopatadine Opatanol® |
Sodium cromoglicate more cost effective |
03.04.02 |
Omalizumab Xolair® |
For specialist use only in line with NICE TAs Commissioned by NHSE |
03.14 |
Omalizumab Xolair® |
For specialist use only in line with NICE guidance below
NHS England is the responsible commissioner for use in Asthma
|
13.05.03 |
Omalizumab |
In line with NICE |
01.03.05 |
Omeprazole |
Capsules are more cost effective than tablets
Most brands of capsules can be opened and beads swallowed without crushing or can be mixed with food or drink
|
01.03.05 |
Omeprazole Dispersible tablets |
££ - Orodispersible tablets are significantly more expensive than capsules
For use in swallowing difficulties or via nasogastric tubes when beads in the capsules are too large and lansoprazole orodispersible are not acceptable (e.g. children with fine NG tubes) |
01.03.05 |
Omeprazole IV |
Hospital use only |
06.01.01.03 |
Omnican fine |
|
A5.07.05 |
Omnistrip® |
Adhesive wound closure strip Type of wound product is suitable for For atraumatic closure of minor wounds or surgical incisions Require a secondary dressing Duration dressing remains on wound before changing As necessary, up to 14 days Frequency of dressing change As necessary Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) None Rationale for inclusion in formulary Cost effective Essential for closure of minor injuries |
04.06 |
Ondansetron |
Preparations available:
- Tablets
- Melt tablets
- Suppositories
- Injection
- SF syrup- for patients with swallowing difficulties only
Chemotherapy patients only Hyperemesis in pregnancy (off label) Palliative care (off label)
|
04.09.01 |
Opicapone Ongentys® |
Second-line therapy to entacapone, in patients who fail to respond to, or are intolerant of, entacapone, in situations where apomorphine therapy has been considered
Supported by an ESCA |
12.03.01 |
Orabase® |
|
12.03.01 |
Orahesive® |
|
01.04 |
Oral Rehydration Salts |
Follow OptimiseRx advice for most cost-effective prescribing option |
01.04 |
Oral Rehydration Salts |
Follow scriptswitch advice for cost-effective brand prescribing |
09.02.01.02 |
Oral rehydration salts |
|
04.05.01 |
Orlistat |
Can prescribe in accordance with NICE guidance
Orlistat 60mg capsules - Over the counter preparation suitable for self-care/purchase if appropriate |
05.03.04 |
Oseltamivir |
-For Primary Care- Green only during Flu season and on authorisation by NHS England/Department of Health & Social Care or via commissioned service for out of season supply |
05.03.04 |
Oseltamivir Tamiflu® |
-For Primary Care- Green only during Flu season and on authorisation by NHS England/Department of Health & Social Care or via commissioned service for out of season supply |
08.01.05 |
Osimertinib |
In line with NICE |
09.04.02 |
Osmolite 1.5kcal |
- 1.5 kcal/mL and 5g (or more) protein/100 mL
- High energy vegetarian fish oil free (Nil fibre)
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula
|
09.04.02 |
Osmolite® |
- 1 kcal/mL and less than 5 g protein/100 mL
- Pt requires 1 kcal/mL, vegetarian feed fish oil free (Nil fibre)
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula
|
09.04.02 |
Osmolite® Plus |
- Less than 1.5 kcal/mL and 5g (or more) protein/100 mL
- Alternative standard feed, vegetarian fish oil free (1200 kcal/L) (Nil fibre)
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula. Not suitable for child under 10 years.
|
09.05.02.02 |
Osvaren® |
Specialist recommendation |
06.04.01.01 |
Ovestin ® |
|
04.01.02 |
Oxazepam |
|
04.08.01 |
Oxcarbazepine |
Tablets
Oral suspension
On specialist advice
MHRA Advice Care should be taken when switching between oral formulations. The need for continued supply of a particluar manufacturer's product should be based on clinical judgement and consultation with patient and/or carer, taking into account factors such as seizure frequency and treatment history |
07.04.02 |
Oxybutynin |
Normal release tablets more cost effective. Do not offer to frail older women. |
07.04.02 |
Oxybutynin |
2.5mg and 5mg tablets ONLY
3mg tablets are non-formulary |
13.12 |
Oxybutynin |
For hyperhidrosis (off label use)after trial of aluminium salts |
07.04.02 |
Oxybutynin Hydrochloride Kentera® |
Only to be used if patients benefit from oral oxybutynin but cannot tolerate the side effects or oral agents |
04.07.02 |
Oxycodone |
|
04.07.02 |
Oxycodone |
Capsules
M/R tablets
SF solution
For patients who do not tolerate morphine
Specialist initiation Pain clinic and palliative care use only
|
21 |
Oxycodone |
- With specialist advice, may be used for symptom control only where Morphine is not tolerated.
|
03.06 |
Oxygen |
|
03.06 |
Oxygen |
|
05.01.03 |
Oxytetracycline oral |
Recommended by Dermatologist |
13.06.02 |
Oxytetracycline |
•Topical treatments should be used first line. •Oral antibiotics should be reserved for acne, if topical treatment is not adequately effective or if it is inappropriate. Oxytetracycline - take 1 hour before food or on a empty stomach. Avoid calcium, iron and indigestion remedies at the same time.
Please refer to Primary Care Antimicrobial Guidelines
|
07.01.01 |
Oxytocin Syntocinon® |
For Specialist/ Hospital Use Only |
09.06.02 |
Pabrinex |
Hospital only |
08.01.05 |
Paclitaxel |
Funding may be available from the Cancer Drug Fund
In line with NICE |
08.01.05 |
Paclitaxel albumin-bound Abraxane® |
NHSE commissioned
In line with NICE |
09.04.02 |
Paediasure® |
- Child: 1 kcal/ml and less than 4g protein/100ml
- 1 kcal per ml low carbohydrate sip feed for children
- Paediatric ACBS indications: Disease-related malnutrition, intractable malabsorption, growth failure, pre-operative preparation of malnourished patients, dysphagia, short-bowel syndrome, bowel fistula in child 1–10 years, body-weight 8–30 kg
|
09.04.02 |
Paediasure® Peptide |
- Child: 1 kcal/ml and less than 4g protein/100ml
- Peptide based sip feed used in pts with gut failure
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula and growth failure in child 1–10 years, body-weight 8–30 kg
|
09.04.02 |
Paediasure® Plus |
- Child: 1.5 kcal/mL and more than 4g protein/100 mL
- Lower Carbohydrate, 1.5kcal/ml sip feed, used in children with CHO intolerance
- Paediatric ACBS indications: Disease-related malnutrition, intractable malabsorption, growth failure, pre-operative preparation of malnourished patients, dysphagia, short-bowel syndrome, bowel fistula in child 1–10 years, body-weight 8–30 kg
|
09.04.02 |
Paediasure® Plus |
- Child: 1.5 kcal/mL and more than 4g protein/100 mL
- Lower Carbohydrate, 1.5kcal/ml sip feed, used in children with CHO intolerance
- Paediatric ACBS indications: Disease-related malnutrition, intractable malabsorption, growth failure, pre-operative preparation of malnourished patients, dysphagia, short-bowel syndrome, bowel fistula in child 1–10 years, body-weight 8–30 kg
|
09.04.02 |
Paediasure® Plus Fibre |
- Child: 1.5 kcal/mL and more than 4g protein/100 mL
- Lower Carbohydrate, 1.5kcal/ml sip feed, used in children with CHO intolerance with added fibre
- Paediatric ACBS indications: Disease-related malnutrition, intractable malabsorption, growth failure, pre-operative preparation of malnourished patients, dysphagia, short-bowel syndrome, bowel fistula in child 1–10 years, body-weight 8–30 kg. Not suitable for use in child under 1 year
|
09.06.07 |
Paediatric Seravit® |
- Used in children and low weight adults on very restricted diets who are not meeting vitamin and mineral requirements and in enteral feed patients
- For use in infants - unflavoured vitamin and mineral supplement given to infants and young children on low protein or low-fat diets who require vitamin and mineral supplementation. There are no other powdered preparations available that meet the requirements of infants on very limited diets with inherited metabolic disorders of metabolism. It cannot be purchased from a supermarket. The dose and type of product should always be advised by the specialist dietitian according to the needs of the patient
- Vitamin, mineral, and trace element supplement in infants and children with restrictive therapeutic diets
|
08.01.05 |
Palbociclib Ibrance® |
In line with NICE
Hospital only-NHSE commissioned |
04.02.02 |
Paliperidone Trevicta® |
The APC's view is that, on clinical grounds, the status of antipsychotic depot injections should be amber with a framework in place in Primary Care before transfer
HOWEVER, until the commissioning arrangements have been agreed to allow safe transfer of patient care, the status will remain RED |
04.02.02 |
Paliperidone Xeplion® |
The APC’s view is that, on clinical grounds, the status of antipsychotic depot injections should be amber with a framework in place in Primary Care before transfer
HOWEVER, until the commissioning arrangements have been agreed to allow safe transfer of patient care, the status will remain RED |
05.03.05 |
Palivizumab Synagis® |
|
04.06 |
Palonosetron Aloxi® |
|
06.06 |
PAMIDRONATE DISODIUM |
|
01.09.04 |
Pancreatin Pancrex V® |
For Specialist initiation
Counsel patient on need for adequate hydration
Prescribe by Brand only
Use brand and strength recommended by specialist |
01.09.04 |
Pancreatin Creon 10,000 ®, Creon 25,000 ® |
For specialist initiation
Counsel patient on need for adequate hydration
Prescribe by Brand only
Use brand and strength recommended by specialist
|
15.01.05 |
Pancuronium Bromide |
Hospital only |
08.01.05 |
Panitumumab Vectibix® |
|
08.01.05 |
Panobinostat Farydak® |
Hospital only- NHSE commissioned
In line with NICE and available from day 91 following publication of TA |
04.07.01 |
Paracetamol Perfal® |
|
04.07.01 |
Paracetamol |
Tablets
SF suspension
500mg soluble tablets - high sodium content. Only for patients with swallowing difficulties |
04.07.01 |
Paracetamol |
|
04.07.01 |
Paracetamol and codeine Co-codamol ®15/500 |
£££££
Limited evidence
Only for patients with swallowing difficulties
For elderly community who would not tolerate separate ingredients and to support a step down review
High sodium content
Tablets and capsules more cost effective
|
04.07.01 |
Paracetamol and codeine Co-codamol 30/500 |
Use with caution in patients over 65s
Contraindicated in children below the age of 12
Use in chronic pain only |
04.07.01 |
Paracetamol and codeine Co-codamol 30/500 |
£££££
High sodium content
Only for use in patients with swallowing difficulties
Tablets and capsules more cost effective
For use in chronic pain |
04.07.01 |
Paracetamol and codeine Co-codamol 15/500 |
£££££
Limited evidence
For elderly community who would not tolerate separate ingredients and to support a step down review |
04.08.02 |
Paraldehyde |
|
15.01.04.02 |
Parecoxib Dynastat® |
Hospital only |
09.03 |
Parenteral Nutrition (TPN or PN) |
For hospital use only
|
09.06.04 |
Paricalcitol |
Hospital only |
05.04 |
Paromomycin |
Unlicensed |
04.03.03 |
Paroxetine |
|
09.04.01 |
Pasta |
Low-protein foods
These products are not available to purchase in supermarkets
They are important to provide essential energy and variety to aid the palatability of low protein diets. They are important for good metabolic control of the patient. Poor access to these products could lead to poor dietary adherence. This will cause poor metabolic control which may lead to irreversible brain damage
The NSPKU guidelines for prescription of low protein foods can be used for other amino acid disorderssuch as MSUD, homocystinuria, tyrosinaemia and pyridoxine response epilepsy
Protein free - necessary for children and adults with inborn errors of protein metabolism who do not tolerate very little natural protein
The specialist dietician will make individual reccomendations based on diagnosis,protein recommendations, weight etc.
- Essential protein-free basic products. Necessary for children and adults with inborn errors of protein metabolism who tolerate very little natural protein. 100g pasta = 10g protein
|
09.02.01.01 |
Patiromer Veltassa® |
In line with NICE
In emergency care for acute life-threatening hyperkalaemia alongside standard care
for people with persistent hyperkalaemia and chronic kidney disease stage 3b to 5 or heart failure, with RICaD
|
08.01.05 |
Pazopanib Votrient® |
|
14.04 |
Pediacel® |
|
09.04.02 |
PEG feeding products |
Usually via Homecare |
08.01.05 |
Pegaspargase Oncaspar® |
Hospital ONLY
NHSE commissioned
In line with NICE and available from day 91 following publication of TA |
08.01.05 |
Pegcetacoplan Aspaveli® |
In line with NICE |
09.01.06 |
Pegfilgrastim |
Hospital only |
05.03 |
Peginterferon Alfa |
Hospital only
In line with NICE |
05.03 |
Peginterferon Alfa Pegasys® |
Hospital only
In line with NICE |
08.02.04 |
Peginterferon Alfa |
Hospital only
In line with NICE |
08.02.04 |
Peginterferon alfa-2a Pegasys ® |
Commissioned by NHSE for the treatment of Hepatitis B and C
|
08.02.04 |
Peginterferon alfa-2b ViraferonPeg |
Commissioned by NHSE for the treatment of Hepatitis B and C |
08.02.04 |
Peginterferon beta-1a Plegridy® |
In line with NICE |
08.01.05 |
Pembrolizumab Keytruda® |
Hospital Only
NHS England is responsible commisioner in line with NICE (see links below)
|
08.01.03 |
Pemetrexed Alimta® |
Funding may be available from cancer drug fund Hospital only |
08.01.05 |
Pemigatinib Pemazyre® |
Use in line with NICE |
06.01.01.03 |
Penfine classic |
|
04.02.01 |
Penfluridol |
|
09.08.01 |
Penicillamine |
Specialist recommendation with ESCA |
10.01.03 |
Penicillamine |
Supported by an ESCA |
11.03.01 |
Penicillin |
Hospital use only on advice of specialist ophthalmologists |
05.04 |
Pentamidine |
|
05.04 |
Pentamidine > Pentacarina |
|
05.04.08 |
Pentamidine Isetionate Pantacarinat® |
|
07.04.03 |
Pentosan polysulfate sodium Elmiron® |
In line with NICE |
01.02 |
Peppermint Oil |
Prescribe as capsules E/C 0.2ml |
01.02 |
Peppermint water |
Peppermint water is an unlicensed special and should only be prescribed (initiation and maintenance) by specialists, where no suitable alternative exists
For specialist use only |
01.01.02 |
Peptac |
|
09.04.02 |
Peptamen® |
- 1 kcal/mL and less than 5g protein/100 mL
- Peptide-based formula
- Where hydrolysate is required
- Short bowel syndrome, intractable malabsorption, proven inflammatory bowel disease, bowel fistula
|
09.04.02 |
Peptamen® AF |
Hospital use only
- Less than 1.5 kcal/mL and 5g (or more) protein/100 mL
- Used in critical care settings
|
09.04.02 |
Peptamen® HN |
- Less than 1.5 kcal/mL and 5g (or more) protein/100 mL
- Step down from Peptamen® AF
- Intolerance to other feed
- Hydrolysate 1300 kcal/L nutritionally complete in 1 litre
- For patients with malabsorption where requirements (high protein/low volume) cannot be met with a standard 1Kcal/ml MCT peptide feed. Used in liver/hepatobiliary disease/conditions
- Short bowel syndrome, intractable malabsorption, proven inflammatory bowel disease, bowel fistula. Not suitable for child under 3 years
|
09.04.02 |
Peptamen® Junior |
- Hydrolysate Formula
- Powdered preparation only
- Used in children requiring hydrolsate, ability to concentrate or dilute to meed specific calorie density requirements
- Short bowel syndrome, intractable malabsorption, proven inflammatory bowel disease, bowel fistula, in child 1–10 years
|
09.04.02 |
Peptamen® Junior |
- Hydrolysate Formula
- Ready to use, neutral pH, 1kcal/ml
- Short bowel syndrome, intractable malabsorption, proven inflammatory bowel disease, bowel fistula, in child 1–10 years
|
09.04.02 |
Peptamen® Junior Advance |
- Child: 1.5 kcal/mL and more than 4g protein/100 mL
- 1.5kcal/ml hydrolysed protein feed used in children over 8kg where whole protein is not tolerated. Increased MCT for use in liver failure.
- Intractable malabsorption, short-bowel syndrome, bowel fistula, and proven inflammatory bowel disease in child 1–10 years
|
04.08.01 |
Perampanel Fycompa® |
On specialist advice with an ESCA
MHRA Advice When prescribing for epilepsy the patient should be assessed to make a clinical judgement if the same manufacturer's product/brand is necessary taking into account factors such as seizure frequency and treatment history. Also take into account patient/carer related factors such as their negative perceptions about alternative products and/or other issues related to the patient such as co-morbid autism, mental health issues or learning disability
|
04.02.01 |
Pericyazine |
Supported by ESCA
£££££ |
02.05.05.01 |
Perindopril erbumine |
DO NOT PRESCRIBE as perindopril arginine salt-Perindopril arginine is Black on the formulary |
13.10.04 |
Permethrin 5% Lyclear® Dermal Cream |
Over the counter preparation suitable for self-care/purchase if appropriate |
04.02.01 |
Perphenazine |
Supported by ESCA |
14.04 |
Pertussis (acelluar) low dose with low dose diptheria, tetanus and inactivated poliomyelitis vaccine (dTap/IPV) Boostrix®-IPV, Repevax® |
|
08.01.05 |
Pertuzumab Perjeta® |
In line with NICE
Hospital only |
04.07.02 |
Pethidine |
|
15.01.04.03 |
Pethidine |
Hospital only |
02.08 |
Phenindione |
Use on the advice of a specialist only |
04.08.01 |
Phenobarbital |
Tablets
Elixir
On specialist advice
MHRA Advice Patients being treated for epilepsy should be maintained on a specific manufacturer's product
Safety Information
Prescriptions for Phenobarbital for children should be prescribed as "unlicensed phenobarbital oral solution 50mg in 5ml (alcohol free)" APC descision September 2021
|
01.07.03 |
Phenol |
|
13.14.07 |
Phenol 2% w/w in compound zinc paste BP |
|
02.05.04 |
Phenoxybenzamine |
|
05.01.01.01 |
Phenoxymethylpenicillin |
|
02.07 |
Phenylephrine |
|
11.05 |
Phenylephrine Hydrochloride Minims® Phenylephrine Hydrochloride |
Mydriatic. For use prior to eye procedure
Only for use in patients with known hypersensitivity to preservatives |
04.08.01 |
Phenytoin |
Capsules
Suspension
On specialist advice
MHRA Advice Patients being treated for epilepsy should be maintained on a specific manufacturer's product |
09.04 |
Phlexy-10® Exchange System |
- Tablets maybe used in pregnancy, when suffering from morning sickness
- Nutritional supplement for the dietary management of phenylketonuria
|
09.04 |
Phlexy-Vits® |
- Vitamin and mineral supplement for teenagers and adults with phenylketonuria and other inborn errors of protein metabolism
- The only suitable low volume (powder and tablets) comprehensive vitamin and mineral supplement for teenagers and adults that has been formulated for patients with phenylketonuria and other inborn errors of protein metabolism requiring very restrictive diets. The dose and type of product should always be advised by the specialist dietitian according to the needs of the patient
- For use as a vitamin and mineral component of restricted therapeutic diets in children over 11 years and adults with phenylketonuria and similar amino acid abnormalities
|
03.09 |
Pholcodine Linctus, BP |
OTC preparation suitable for self-care/purchase if appropriate |
03.09 |
Pholcodine Linctus, Strong, BP |
OTC preparation suitable for self-care/purchase if appropriate |
09.05.02.01 |
Phosphate |
Hospital only |
01.06.04 |
Phosphate enema |
Fletchers phosphate enema®
Fleet ready to use enema®
|
09.05.02.01 |
Phosphate supplements Phosphate-Sandoz® |
|
01.06 |
Phosphates (rectal) |
|
09.06.06 |
Phytomenadione |
Konakion® MM and Konakion® MM Paediatric
1mg capsules |
A5.06.01 |
PICO products |
Specialist recommendation only Consider standard interactive dressings first
Disposable and portable system designed to kick start wound healing. Required components: One PICO device, 2 dressings per kit. Type of wound product is suitable for Acute, chronic, dehisced, partial thickness burns, flaps, grafts and traumatic wounds. Duration dressing remains on wound before changing Twice a week dressing change, PICO device weekly change Frequency of dressing change Determined by exudate levels. Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) It should not be used on: Confirmed and untreated osteomyelitis Malignancy in wound bed or wound margins Exposed blood vessels Organs Unexplored fistulae Necrotic wounds Anastomotic sites Emergency airway aspiration Pleural, mediastinal or chest tube drainage and surgical suction Rationale for inclusion in formulary These devices promote patient mobility at a cost effective price and is available on drug tariff which other comparable models are not. |
01.06.05 |
Picolax® |
|
11.06 |
Pilocarpine |
Used as add-on therapy. A darkly pigmented iris will tend to require higher strength products. On Specialist Ophthalmologist Recommendation |
21 |
Pilocarpine |
- Oral use for dry mouth where routine oral mouth care and saliva substitutes have failed.
|
12.03.05 |
Pilocarpine Hydrochloride Salagen® |
- Licensed for the treatment of xerostomia (dry mouth) following irradiation for head and neck cancer; dry mouth and dry eyes in Sjögren's syndrome
- Effective only in patients who have residual salivary gland function
|
11.06 |
Pilocarpine Preservative Free |
Hospital only |
13.05.03 |
Pimecrolimus Elidel® |
In line with NICE |
06.01.02.03 |
Pioglitazone |
|
05.01.01.04 |
Piperacillin and Tazobactam |
For hospital use only |
04.09.03 |
Piracetam |
Tablets
Oral solution |
20 |
PIRENZEPINE 50mg tabs |
Hospital only |
04.02.03 |
Pirenzipine (unlicensed) |
Hospital use only |
03.11 |
Pirfenidone Esbriet® |
Hospital only - NHSE commissioned |
05.01.01.05 |
Pivmecillinam Hydrochloride |
|
08.01.05 |
Pixantrone |
|
04.07.04.02 |
Pizotifen |
|
09.04.01 |
Pizza bases |
Low-protein foods
These products are not available to purchase in supermarkets
They are important to provide essential energy and variety to aid the palatability of low protein diets. They are important for good metabolic control of the patient. Poor access to these products could lead to poor dietary adherence. This will cause poor metabolic control which may lead to irreversible brain damage
The NSPKU guidelines for prescription of low protein foods can be used for other amino acid disorderssuch as MSUD, homocystinuria, tyrosinaemia and pyridoxine response epilepsy
Protein free - necessary for children and adults with inborn errors of protein metabolism who do not tolerate very little natural protein
The specialist dietician will make individual reccomendations based on diagnosis,protein recommendations, weight etc.
- Important protein-free foods to provide important energy, assist dietary adherence and provide variety when natural protein tolerance is very limited. Necessary for children and adults with inborn errors of protein metabolism who do not tolerate very little natural protein. One regular pizza likely to provide 20g + protein
|
09.04 |
PKU Air 15 |
- A liquid amino acid which is lower in calories for children and adults with phenylketonuria
|
09.04 |
PKU Air 20 |
- A supplement which is lower in calories for children and adults with phenylketonuria
|
09.04 |
PKU Anamix first spoon |
- A supplement without phenylalanine for children with phenylketonuria
- One of 2 powdered weaning (thickened) amino acid supplement without phenylalanine for infants/young children with phenylketonuria. The consistency can be adjusted to suit the developmental age of the older baby/toddler. This is our preferable product because it has added long chain fatty acids
- Nutritional supplement for the dietary management of proven phenylketonuria in children from 6 months to 5 years
|
09.04 |
PKU Anamix® Infant |
- A supplement without phenylalanine for infants with phenylketonuria
- The only infant amino acid supplement without phenylalanine for infants with phenylketonuria
- Nutritional supplement for the dietary management of proven phenylketonuria in children from birth to 3 years
|
09.04 |
PKU cooler 10® |
- A supplement without phenylalanine for children and adults with phenylketonuria
- An oral liquid amino acid supplement without phenylalanine formulated for children aged 3 to 6 years with phenylketonuria. Larger pouches are unacceptable for this age group of children and provide in excess of protein requirements. The 3 different products have a different degree of sweetness and range of flavours
- Nutritional supplement for the dietary management of phenylketonuria in children over 3 years
|
09.04 |
PKU cooler 15® |
- A supplement without phenylalanine for children and adults with phenylketonuria
- One of three oral liquid amino acid supplements without phenylalanine for children aged 7 to 12 years with phenylketonuria. Larger pouches are unacceptable for this age group of children and provide in excess of protein requirements
|
09.04 |
PKU cooler 20® |
- A supplement without phenylalanine for teenagers and adults with phenylketonuria
- One of 3 liquid amino acid supplement without phenylalanine for teenagers and adults (>12 years of age) with phenylketonuria that will meet their higher amino acid requirements. This age group need the larger sachets (20g protein equivalent) to meet their non-phenylalanine protein requirements. It is important there is a choice of more than 1 product for this age group as compliance is poor and the potential outcome of poor compliance. The 3 different products have a different degree of sweetness and range of flavours
- Nutritional supplement for the dietary management of phenylketonuria in children over 3 years
|
09.04 |
PKU Explore 10® |
- Contains 10g of protein equivalent
- Contains all the vitamins, minerals adn consists of low fat and low carbohydrate
|
09.04 |
PKU Explore 5® |
- Contains 5g of protein equivalent
- Contains all the vitamins, minerals adn consists of low fat and low carbohydrates
|
09.04 |
PKU express15® |
- A supplement without phenylalanine for teenagers and adults with phenylketonuria
- The only powdered amino acid supplement without phenylalanine for 7 to 12-year olds with phenylketonuria. Larger sachets are unacceptable for this age group of children and provide in excess of protein requirements
- Nutritional supplement for the dietary management of phenylketonuria. Not recommended for children under 3 years
|
09.04 |
PKU express20® |
- A supplement without phenylalanine for teenagers and adults with phenylketonuria
- One of 2 powdered amino acid supplement without phenylalanine for teenagers and adults with phenylketonuria that will meet their higher amino acid requirements. This age group need the larger sachets (20g protein equivalent) to meet their non-phenylalanine protein requirements. It is important there is a choice of more than 1 product for this age group as compliance is poor. The 2 different products have a different degree of sweetness and range of flavours
- Nutritional supplement for the dietary management of phenylketonuria. Not recommended for children under 3 years
|
09.04 |
PKU Lophlex® LQ 10 |
- A supplement without phenylalanine for children and adults with phenylketonuria
- One of three liquid amino acid supplement without phenylalanine formulated for children aged 3 to 6 years with phenylketonuria. Larger pouches are unacceptable for this age group of children and provide in excess of protein requirements. The 3 different products have a different degree of sweetness and range of flavours
- Nutritional supplement for the dietary management of phenylketonuria in children over 4 years and adults including pregnant women
|
09.04 |
PKU Lophlex® LQ 20 |
- A supplement without phenylalanine for teenagers and adults with phenylketonuria
- One of 3 liquid amino acid supplements without phenylalanine for teenagers and adults (>12 years of age) with phenylketonuria that will met their higher amino acid requirements. This age group need the larger sachets (20g protein equivalent) to meet their non-phenylalanine protein requirements. It is important there is a choice of more than 1 product for this age group as compliance is poor. The 3 different products have a different degree of sweetness and range of flavours
- Nutritional supplement for the dietary management of phenylketonuria in children over 4 years and adults including pregnant women
|
09.04 |
PKU sphere 15 |
- A low phenylalanine supplement derived from whey protein for children and adults with phenylketonuria. It is more palatable than amino acid supplements and associated with better utilisation of protein. Very useful for adult patients trying to return to diet or children / adults struggling to take their amino acid product because of its taste. Suitable from aged 4 years
|
09.04 |
PKU Sphere 20 |
- A low phenylalanine supplement derived from whey protein for children and adults with phenylketonuria. It is more palatable than amino acid supplements and associated with better utilisation of protein. Very useful for adult patients trying to return to diet or children / adult struggling to take their amino acid product because of its taste. Suitable from aged 4 years
|
09.04 |
PKU Start® |
- For use in the dietary management of phenylketonuria
- Amino acid supplement. Without phenylalanine for infants with phenylketonuria
|
09.01.07 |
Plerixafor |
Hospital only, NHSE commissioned. |
14.04 |
Pneumococcal polysaccharide conjugate vaccine (adsorbed) Synflorix® |
|
14.04 |
Pneumococcal polysaccharide conjugate vaccine (adsorbed) Prevenar 13® |
Protects against 13 strands of pneumococcus For use in: the childhood immunisation programme individuals with an underlying medical condition which puts them at increased risk from pneumococcal disease. |
14.04 |
Pneumococcal polysaccharide vaccine Pneumovax® |
23-valent pneumococcal polysaccharide vaccine (PPV) containing 23-serotypes |
13.07 |
Podophyllotoxin Condyline® |
|
13.07 |
Podophyllotoxin Warticon® |
|
13.07 |
Podophyllum |
|
08.01.05 |
Polatuzumab Polivy® |
Hospital use only
Use in line with NICE |
14.04 |
Poliomyelitis Vaccine inactivated (Salk) |
The polio vaccine is only given as part of combined products:
- diphtheria/tetanus/acelluar pertussis/inactivated polio vaccine/Haemophilus influenzae type b (dTaP/IPV/Hib)
- diphtheria/tetanus/acelluar pertussis/inactivated polio vaccine (DTaP/IPV or dTaP/IPV)
- tetanus/diphtheria/inactivated polio vaccine (Td/IPV)
|
09.04 |
Polycal® |
- High-energy supplements: carbohydrate
- Ready to use. Requires no specific instruction to prepare e.g. energy supplement/ used as pre and post bolus with patients with glycogen storage disease to prevent hypoglycaemia, also used in fatty acid oxidation disorders
- There is no other liquid glucose supplement on ACBS prescription.
- Also energy supplements/ used as pre-and post-bolus tube feeds with patients with glycogen storage disease to prevent hypoglycaemia. Also use as a quick access, liquid energy supplement in patients with fatty acid oxidation disorders. There is no other liquid glucose supplement on ACBS prescription. The dose and type of product should always be advised by the specialist dietitian according to the needs of the patient
- Disease-related malnutrition, malabsorption states, or other conditions requiring fortification with a high or readily available carbohydrate supplement
|
A5.17 |
Polyfax® |
Hospital use only Type of wound product is suitable for Partial thickness facial burns and healing graft sites, infected/colonised wounds
2 days or 2-3 times a day depending on injury site and type (as directed by Burns team) Frequency of dressing change 2 days or 2-3 times a day Caution/contraindications (when not to use the dressing, patient groups to avoid etc) Allergy to Polymixin B sulphate or Bacitracin zinc No more than 200g of Polyfax ointment per day Rationale for inclusion in formulary Prevent and treat bacterial infections in burns |
A5.07.01 |
Polyfield Nitrile Patient Pack |
Sterile dressing pack Type of wound product is suitable for To be used on all wounds requiring aseptic dressing procedures Duration dressing remains on wound before changing Single use Frequency of dressing change Determined by wound type Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) None listed Rationale for inclusion in formulary Available on drug tariff, cost effective and incorporates a measure guide which would be an additional cost with other packs |
A5.02.05 |
PolyMem® |
Specialist recommendation only Foam dressing that contains a cleansing agent and glycerol Type of wound product is suitable for Low to moderately exuding wound including skin tears, and other traumatic wounds, superficial and partial thickness wounds, burns, donor and graft sites and radiotherapy induces reactions Duration dressing remains on wound before changing 2-7 days Frequency of dressing change Up to 7 days dependent on exudate levels Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Sensitivity to ingredients contained within the dressing Not for full thickness burns Not for ischaemic wounds Not for diabetic foot wounds Not in conjunction with solutions containing hypochlorite Rationale for inclusion in formulary Suitable for fragile and sensitive skin, Soft and comformable, Easy to redress awkward areas Wide range of sizes including digit shaped dressings |
14.04 |
Polysaccharide Typhoid Vaccine Typherix® |
|
14.04 |
Polysaccharide Typhoid vaccine for injection Typhim Vi® |
|
14.04 |
Polysaccharide vaccine with hepatitis A vaccine |
|
09.02.01.01 |
Polystyrene Sulphonate Resins |
|
13.09 |
Polytar ® |
Contains peanut oil
Over the counter preparation suitable for self-care/purchase if appropriate |
13.09 |
Polytar Plus® |
Over the counter preparation suitable for self-care/purchase if appropriate |
08.02.04 |
Pomalidomide Imnovid® |
In line with NICE |
08.01.05 |
Ponatinib Iclusig® |
In line with NICE |
08.02.04 |
Ponesimod Ponvory® |
In line with NICE |
03.05.02 |
Poractant Alfa Curosurf® |
For Hospital use only
Commissioned by NHSE |
05.02.01 |
Posaconazole |
|
09.05.02.01 |
Potassium acid phosphate |
|
09.02.01.01 |
Potassium chloride |
Potassium Chloride efferevescent tablets (Sando-K®) Potassium Chloride MR tablets (Slow-K®)
SF syrup (Kay-Cee-L®) specialist recommendation only
|
09.02.02.01 |
Potassium Chloride and Glucose Intravenous Infusion |
Hospital use only |
09.02.02.01 |
Potassium Chloride and Sodium Chloride Intravenous Infusion |
Hospital use only |
09.02.02.01 |
Potassium Chloride Concentrate (Sterile) |
Hospital use only |
09.02.02.01 |
Potassium Chloride, Sodium Chloride and Glucose Intravenous Infusion |
Hospital use only |
07.04.03 |
Potassium citrate |
|
06.02.02 |
Potassium iodate |
|
06.02.02 |
Potassium iodide |
|
13.11.06 |
Potassium Permanganate |
SAFETY: Risk of death or serious harm if swallowed National Patient Safety Alert on the inadvertent oral administration of potassium permanganate April 2022.
If using or prescribing potassium permanganate ensure actions in alert are taken, including:
- If to be used in a patient’s home, a risk assessment must be undertaken before prescribing
- All patients must be supplied with a patient information leaflet
- Include clear instructions on prescription to dilute before use
- Do not issue on repeat prescription.
|
13.11.04 |
Povidone-iodine preparations |
10% antiseptic 10% ointment 7.5% surgical scrub |
04.09.01 |
Pramipexole |
Please note that MODIFIED RELEASE preparation's are non-formulary and for existing patients only |
07.02.01 |
Prasterone Intrarosa® |
Approved by APC in July 2021
Place in thetrapy relevant to available treatments: 2nd
GP to seek specialist guidance prior to consideration
Prasterone is biochemically and biologically identical to endogenous dehydroepiandrosterone (DHEA), and is converted to oestrogens and androgens |
02.09 |
Prasugrel Efient® |
In line with NICE |
02.12 |
Pravastatin |
|
05.05 |
Praziquantel |
Unlicensed
On Specialist advice only |
05.05 |
Praziquantel > Cysticide |
|
03.02 |
Prednisolone |
|
03.12 |
Prednisolone |
•Plain tablets (not enteric coated) •In conjunction with azathioprine for ILD |
06.03 |
Prednisolone |
|
10.01.02.01 |
Prednisolone |
Do not prescribe EC tablets
Second line choice for the treatment of gout
|
10.01.02.01 |
Prednisolone |
Only for use in paediatric patients or patients with swallowing difficulties. Prednisolone 5mg in 5ml oral solution is a cost effective alternative to soluble tablets. |
10.01.02.01 |
Prednisolone |
Cost effective alternative to soluble tablets for paediatric patients and those with swallowing difficulties. |
10.01.04 |
Prednisolone |
Second line for gout
Do not prescribe EC tablets
Prednisolone 5mg in 5ml oral solution is a cost effective alternative to soluble tablets for paediatric patients and those with swallowing difficulties. |
11.04.01 |
Prednisolone |
For use on the advice of a specialist ophthalmologist |
11.04.01 |
Prednisolone Pred Forte® |
On specialist ophthalmologist recommendation
For the treatment of anterior uveitis in A&E-prednisolone acetate 1% as the drug of choice unless the patient has a preference for dexamethasone 0.1% |
01.05.02 |
Prednisolone (oral) |
Tablets 5mg, EC2.5mg, 5mg, Soluble 25mg
Plain tablets are first line option
EC tablets are more expensive than plain tablets without any substantial evidence that they confer any GI benefits
25mg tablets are more expensive per mg than 5mg tablets
Soluble tablets are significantly more expensive than normal tablets which can be crushed and dispersed (unlicensed)
For short term use in acute exacerbation or "flare-ups" of relevant conditions
|
11.04.01 |
Prednisolone preservative free Minims SDU® |
Restricted to those needing preservative free
On specialist ophthalmologist recommendation
To be used in patients with severe Chronic Allergic Eye Disease who present to A&E with a flare up |
04.03.04 |
Pregabalin |
£££££
For generalised anxiety disorder
Please follow Optimise Rx for most cost effective brand |
04.07.03 |
Pregabalin |
4th line after duloxetine
On the advice of a specialist where duloxetine is unsuitable
Please be aware of abuse potential associated with this class of agent
From 17th July 2017, clinicians can now return to normal practice when prescribing pregabalin and no longer need to specify a brand name when prescribing for neuropathic pain |
04.08.01 |
Pregabalin |
On advice of specialist
Please follow Optimise Rx for most cost effective brand |
21 |
Pregabalin |
- For pain.
- Second line to Gabapentin if intolerant.
- Useful if anxiety also present.
|
06.04.01.01 |
Premarin® |
|
06.04.01.01 |
Premique® low dose |
|
06.04.01.01 |
Premique® modified release |
|
15.02 |
Prilocaine Hydrochloride 1% Citanest® |
Hospital only |
15.02 |
Prilocaine Hydrochloride with Felypressin Citanest with Octapressin® |
Hospital only |
05.04.01 |
Primaquine |
|
04.08.01 |
Primidone |
On specialist advice
MHRA Advice Patients being treated for epilepsy should be maintained on a specific manufacturer's product |
04.09.03 |
Primidone |
|
10.01.04 |
Probenecid |
|
15.02 |
Procaine Hydrochloride |
Hospital only |
05.01.01.01 |
Procaine Penicillin G |
for hospital use only as advised by GUM |
09.04 |
Pro-Cal® Shot |
- Protein, fat, and carbohydrate
- Used where energy and protein is required in small volume – only on recommendation of dietitian
- Disease-related malnutrition, malabsorption states, or other conditions requiring fortification with a high fat or carbohydrate (with protein) supplement
- Not suitable for child under 3 years
|
09.04 |
Pro-Cal® Singles |
- Protein, fat, and carbohydrate
- Used where energy and protein is required in small volume, where measured doses are required – only on recommendation of dietitian
- Disease-related malnutrition, malabsorption states, or other conditions requiring fortification with a high fat or carbohydrate (with protein) supplement
- Not suitable for child under 3 years
|
08.01.05 |
Procarbazine |
Commissioned by NHSE |
04.06 |
Prochlorperazine |
Inappropriate for elderly patients
Tablets
Buccal tablets
Syrup
Injection |
04.02.03 |
Procyclidine |
|
04.09.02 |
Procyclidine |
Tablets
SF syrup |
04.09.02 |
Procyclidine |
Injection |
13.10.05 |
Proflavine cream BPC |
Hospital only |
06.04.01.02 |
Progesterone |
BRANDS
- Cyclogest pessary
- Lutigest pessary
|
06.04.01.02 |
Progesterone (micronised) Utrogestan ® |
|
05.04 |
Proguanil |
Private Prescription in Praimary care |
05.04 |
Proguanil > Paludrine |
Private prescription in Praimary care |
05.04.01 |
Proguanil Hydrochloride |
Private prescription in Primary Care |
05.04 |
Proguanil Hydrochloride with Atovaquone |
Private prescription in Primary Care |
06.04 |
Progynova TS patch |
|
06.04.01.01 |
Progynova® |
Progynova® 1mg and 2mg tablets |
03.04.01 |
Promethazine |
OTC preparation suitable for self-care/purchase if appropriate |
04.01.01 |
Promethazine Hydrochloride |
|
04.06 |
Promethazine hydrochloride |
|
A5.12 |
Prontosan Wound Irrigation solution |
See under antimicrobials
|
A5.03.04 |
Prontosan® Wound Gel |
Specialist recommendation only A gel containing betaine, a surfactant to remove biofilm and debris and PHMB to help control bacterial bioburden. Type of wound product is suitable for Cleansing, decontamination and moisturising of acute and chronic wounds including 1st and 2nd degree burns. Duration dressing remains on wound before changing Apply at each dressing change Frequency of dressing change As determined by the wound and exudate levels Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) None Rationale for inclusion in formulary Gel to cleanse and decontaminate wounds Antimicrobial Breaks down biofilms in chronic wounds |
A5.03.04 |
Prontosan® Wound Irrigation Solution |
Wound irrigation solution containing betaine a surfactant to remove biofilm and debris and PHMB to help control bacterial bioburden. Type of wound product is suitable for Cleansing, decontamination and moisturising of acute and chronic wounds including 1st and 2nd degree burns. Duration dressing remains on wound before changing Apply at each dressing change Frequency of dressing change As determined by the wound and exudate levels Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) None Rationale for inclusion in formulary Solution to cleanse and decontaminate wounds Antimicrobial Breaks down biofilms in chronic wounds Can be used as an irrigation fluid with V.A.C. VERAFLO® |
02.03.02 |
Propafenone |
|
13.12 |
Propantheline |
•For hyperhidrosis (licensed indication) •Specialist recommendation |
15.01.01 |
Propofol |
HOSPITAL ONLY |
15.01.01 |
Propofol Diprivan® |
HOSPITAL ONLY |
02.04 |
Propranolol |
|
04.07.04.02 |
Propranolol |
|
04.09.03 |
Propranolol |
|
06.02 |
Propranolol |
|
06.02 |
Propranolol |
For Paediatric use |
02.04 |
Propranolol Hydrochloride Half-Inderal® LA |
|
02.04 |
Propranolol Hydrochloride Inderal® LA |
|
13.14.01 |
Propylene glycol 20% w/w in aqueous cream |
|
13.14.02 |
Propylene glycol 40% w/w in Dermovate® cream |
|
06.02.02 |
Propylthiouracil |
|
A5.15 |
ProShield |
Skin cleanser for use in patients with chronic diarrhoea or incontinence of urine. Type of wound product is suitable for To cleanse intact or injured skin from contamination of urine or faeces Frequency of use Apply at each episode of hygiene Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) External use only Avoid contact with eyes Known allergic sensitivity to any of the components Keep out of reach of children Rationale for inclusion in formulary For skin cleansing related to incontinence. Only skin cleanser available on drug tarrif |
A5.15 |
ProShield Plus |
Skin protectant Type of wound product is suitable for To treat injured skin associated with incontinence where a dressing seal cannot be achieved Frequency of use Apply at each episode of hygiene Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) External use only Avoid contact with eyes Known allergic sensitivity to any of the components Keep out of reach of children Do not apply to pressure ulcers or leg ulcers Not to be used as a first line barrier cream Not to be used to protect peri wound Not to be used as an emollient Rationale for inclusion in formulary For treatment of incontinence lesions where a standard dressing seal cannot be achieved |
09.04 |
ProSource® Jelly |
- High-energy supplements: protein
- Liver/hepatobiliary disease/conditions
- Other patients groups, based on clinical assessment
- Pts requiring increased protein in a low volume
- Hypoproteinaemia
- Not recommended for child under 3 years
|
09.04 |
ProSource® Liquid |
- Protein and carbohydrate
- Pts requiring low volume, low cal, low CHO protein supplement (10g/30ml) for oral and tube feeders. Useful in allergy to milk and soya proteins. For high protein requirements
- Liver/hepatobiliary disease/conditions
- Biochemically proven hypoproteinaemia
- Not recommended for child under 3 years
|
09.04 |
ProSource® Plus |
- Protein and carbohydrate
- Pts requiring low volume, low cal, low CHO protein supplement (15g/30ml) for oral and tube feeders
- Useful in allergy to milk and soya proteins
- Liver/hepatobiliary disease/conditions
- Hypoproteinaemia
- Not recommended for child under 3 years
|
09.04 |
ProSource® TF |
- Protein and carbohydrate
- Pts requiring low volume, low cal, low CHO protein supplement (11g/30ml) specifically formulated for tube feeders
- Useful in allergy to milk and soya proteins
- Low osmolality
- Liver/hepatobiliary disease/conditions
|
02.08 |
Protamine |
|
05.01.09 |
Prothionamide |
Hospital use only under microbiological and Tuberculosis specialist advice |
02.11 |
Prothrombin complex injection |
|
09.04 |
Protifar® |
- High-energy supplements: protein
- High protein modular powder, to be added to other food, drink and feeds in a range of conditions
- Nutritional supplement for use in biochemically proven hypoproteinaemia
|
09.04 |
ProZero® |
- Low protein milk replacer in children and adults with inborn errors of protein metabolism on low protein diets
- A protein-free milk in children and adults with inborn errors of protein metabolism on low protein diets. It contains equal calories per 100 ml to cow’s milk. It is particularly suitable for MSUD patients. Available in 1 litre /250 ml cartons. The dose and frequency of administration will be determined by the specialist dietitian
- A protein-free nutritional supplement for the dietary management of inborn errors of metabolism in children over 6 months and adults
|
01.06.07 |
Prucalopride Resolor ® |
For use in men and women for chronic constipation
Supported by a RICaD (in development) |
03.10 |
Pseudoephedrine Hydrochloride |
OTC suitbale for self-care/purchase if appropraie |
05.01.09 |
Pyrazinamide |
Pyrazinamide liquid 500mg in 5ml (unlicensed)
Hospital use only under microbiological and Tuberculosis specialist advice |
10.02.01 |
Pyridostigmine Bromide Mestinon® |
|
09.06.02 |
Pyridoxine Hydrochloride |
|
05.04 |
Pyrimethamine Daraprim® |
|
05.04 |
Pyrimethamine |
|
05.04 |
Pyrimethamine with Sulfadoxine Fansidar® |
|
04.02.01 |
Quetiapine |
- Supported by ESCA
- Rationale for prescribing rather than first line antipsychotics to be provided with ESCA
APC preferred brands, choose most cost effective option:
- Biquelle XL
- Sondate XL
- Zaluron XL
- Choose most cost-effective option
|
04.02.01 |
Quetiapine |
- Prescribe standard release tablets
- Supported by ESCA
|
06.07 |
Quinagolide Norprolac® |
|
05.04 |
Quinine |
|
05.04 |
Quinine Bisulphate |
|
05.04 |
Quinine Dihydrochloride |
|
05.04.01 |
Quinine Sulphate |
|
10.02.02 |
Quinine Sulphate |
Short term use only - MHRA guidance
Not to be routinely prescribed for nocturnal leg cramps |
14.05 |
Rabies immunoglobulin |
Use in line with protocol |
16.01 |
Radium-223 Xofigosup>® |
- Hospital only- NHSE commissioned
- In line with NICE and available from day 91 following publication of TA.
|
16.01 |
Radium-223 Xofigo® |
- Hospital only- NHSE commissioned
- In line with NICE and available from day 91 following publication of TA.
|
16.06 |
Radium-223 Xofigo® |
- Hospital only- NHSE commissioned
- In line with NICE and available from day 91 following publication of TA.
|
06.04.01.01 |
Raloxifene |
|
05.03.01 |
Raltegravir Isentress ® |
|
08.01.03 |
Raltitrexed Tomudex® |
Commissioned by NHSE - only for use in the context of appropriately designed clinical trials. Hospital only |
02.05.05.01 |
Ramipril |
Prescribe as capsules |
11.08.02 |
Ranibizumab Lucentis® |
Use in line with NICE |
01.03.01 |
Ranitdine IV |
For specialist use only |
01.03.01 |
Ranitidine |
For use in patients with swallowing difficulties or via nasogastric tubes only |
01.03.01 |
Ranitidine |
|
01.03.01 |
Ranitidine |
The European Medicines Agency (EMA) Human Medicines Committee (CHMP) has recommended the suspension of all ranitidine medicines due to the presence of low levels of the impurity N-nitrosodimethylamine (NDMA). (30 April 2020)
|
02.06 |
Ranolazine Ranexa® |
Use current status at Place/Trust
Sandwell
Supported by RICaD
RICaD Ranolazine-Sandwell only
Wolverhampton
Walsall
Dudley
|
04.09.01 |
Rasagiline Azilect® |
|
10.01.04 |
Rasburicase Fastertec® |
Hospital only |
09.01.03 |
Ravulizumab Ultomiris® |
Use in line with NICE |
13.14.07 |
Reflectant (Dundee) sunscreens coffee, coral pink, beige |
coffee
coral pink
beige |
08.01.05 |
Regorafenib Stivarga® |
In line with NICE |
06.07 |
RELUGOLIX/ ESTRADIOL/ NORETHISTERONE ACETATE |
|
05.03 |
Remdesivir Veklury® |
|
15.01.04.03 |
Remifentanil Ultiva® |
Hospital only |
09.04 |
Renapro® |
- Specialised formulas for specific clinical conditions
- For patients with high protein needs, low volume, low phosphate requirements.
- Used in renal patients
- Used in liver/hepatobiliary diseases/conditions
|
09.04 |
Renapro® shot |
Renapro Shot is described as "low fat, high protein and low carbohydrate"
- For patients with high protein needs, low phosphate requirements
- Used for renal patients
- Used in liver/hepatobiliary diseases/conditions
- Specialist dietician recommendation
|
09.04 |
Renastart® |
- Specialised formulas for specific clinical conditions
- Used in infants and children with renal disease when low Potassium and Low phosphate feed is required
- Can be given orally or as a tube feed
- Dietary management of renal failure in child from birth to 10 years
|
09.04 |
Renastep® |
- ACBS criteria: For the dietary management of renal failure from 3 years of age
- Ready to use high energy formula
- Low in potassium, phosphate and vitamin A content
- Patients with renal failure from 3 years of age
- Use under medical supervision.
- Not suitable for use as a sole source of nutrition.
- Suitable from 3 years of age onwards.
- Regular monitoring of nutritional status and electrolyte levels is required.
- For enteral use only
|
A5.06.01 |
Renasys products |
Specialist recommendation only The use of sub atmospheric pressure to promote or assist wound healing or to remove fluids from a site. Required components: Pump, Dressings foam or gauze, tubing and canister. Type of wound product is suitable for Acute, chronic and traumatic wounds. Can be used as a adjunct to surgery and for salvage procedures such as wound dehiscence. Benefits are that it removes excess fluid that may contain bacterial pathogens, reduces soft tissue oedema, promotes granulation and provides a moist wound healing environment. Consider standard interactive dressings first. Duration dressing remains on wound before changing Every three days Frequency of dressing change Determined by exudate levels. Different canister sizes available Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) It should not be used on: Grossly infected or bleeding wounds Malignancy Exposed blood vessels Organs Unexplored fistulae Extensive necrotic wounds Caution with foam, document the number inserted, ensure all pieces are retrieved. Rationale for inclusion in formulary It removes excess fluid that may contain bacterial pathogens, reduces soft tissue oedema, promotes granulation and provides a moist wound healing environment. Both companies products are included due to different contracting arrangements. Can be used on large open wounds to increase speed of wound healing |
09.06.07 |
Renavit® |
In line with ACBS criteria: Dietary management of water-soluble vitamin deficiency in adults with renal failure on dialysis
- For renal patients as per APC formulary
- Dietary management of water-soluble vitamin deficiency in adults with renal failure on dialysis
- Dietary management of water-soluble vitamine deficiency in adults with renal failure on dialysis
|
09.04 |
Renilon® 7.5 |
- More than 1.5 kcal/mL and 5g (or more) protein/100 mL
- Low potassium, low phosphate sip feed
- Dietetic advice
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula
- Not suitable for child under 3 years; use with caution in child 3–5 years
|
06.01.02.03 |
Repaglinide |
|
14.04 |
Repevax®, Boostrix-IPV® |
|
03.14 |
Reslizumab Cinqaero® |
For specialist use only in line with NICE
NHS England is the responsible commissioner for use in Asthma |
09.04.02 |
Resource® Energy |
- 1.5 kcal/mL and 5g (or more) protein/100 mL
- Paediatrics and specialists adults use only
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula. Not suitable for use in child under 3 years
|
09.04.02 |
Resource® Junior |
First Choice
- Child: More than 1 kcal/mL and less than 4 g protein/100 mL
- Alternative to Fortini, for patients who have taste fatigue - long term use
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula. Not suitable for use in child under 3 years
|
09.04 |
Resource® Optifibre |
- High-fibre supplements
- A fibre source added to oral and tube feeds
- This is added to low protein tube feeds for patients with propionic acidaemia, methyl malonic acidaemia to provide a source of fibre. Children with these conditions become easily constipated leading to metabolic instability and hospital admissions so an additional source extra to fibre content of existing enteral feeds is essential. this product cannot be purchased from the supermarket and is essential. The dose and type of product should always be advised by the specialist dietitian according to the needs of the patient
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula except dysphagia
- Not suitable for child under 5 years
|
09.09 |
Resource® ThickenUp Clear |
- Recommended by SALTs for patients with dysphagia requiring thickened fluids
- Gum based products are generally preferred as they thicken to a more stable end point (unlike starch based products, they do not continue thickening over time) and provide a smoother texture, which improves acceptability and palatability for patients
|
02.10 |
Reteplase |
Hospital only |
14.04 |
Revaxis® |
|
05.03.05 |
Ribavirin |
|
08.01.05 |
Ribociclib Kisqali® |
In line with NICE
Hospital only-NHSE commissioned |
09.06.02 |
Riboflavin |
Specialist recommendation only for inherited metabolic diseases |
05.01.09 |
Rifabutin |
Hospital use only under microbiological and Tuberculosis specialist advice |
05.01.09 |
Rifampicin |
Hospital use only under microbiological and Tuberculosis specialist advice |
05.01.09 |
Rifampicin |
|
13.06.02 |
Rifampicin |
Specialist initiation |
05.01.09 |
Rifampicin and Isoniazid Rifinah® 300 |
Hospital use only under microbiological and Tuberculosis specialist advice |
05.01.09 |
Rifampicin and Isoniazid Rifinah® 150 |
Hospital use only under microbiological and Tuberculosis specialist advice |
05.01.09 |
Rifampicin and Isoniazid and Pyrazinamide Rifater® |
Hospital use only under microbiological and Tuberculosis specialist advice |
05.01.09 |
Rifampicin, isoniazid, pyrazinamide and ethambutol Voractiv® |
Hospital use only under microbiological and Tuberculosis specialist advice |
01.09 |
Rifaximin |
In line with NICE, supported by RICaD (In development)
|
05.01.07 |
Rifaximin oral presentations |
|
05.03.01 |
Rilpivirine hydrochloride Edurant® |
|
05.03.01 |
Rilpivirine hydrochloride Rekambys® |
|
04.09.03 |
Riluzole Rilutek® |
Supported by an ESCA |
09.02.02.01 |
Ringer's Solution for Injection |
Hospital use only |
13.05.02 |
Risankizumab Skyrizi |
In line with NICE |
10.02 |
Risdiplam Evrysdi® |
In line with NICE |
06.06 |
RISEDRONATE SODIUM 30mg |
|
04.02.01 |
Risperidone |
Supported by ESCA |
04.02.02 |
Risperidone Risperdal Consta® |
The APC's view is that, on clinical grounds, the status of antipsychotic depot injections should be amber with a framework in place in Primary Care before transfer
HOWEVER, until the commissioning arrangements have been agreed to allow safe transfer of patient care, the status will remain RED |
05.03.01 |
Ritonavir |
|
08.02.03 |
Rituximab MabThera® |
NHSE is the responsible commissioner
In line with NICE |
10.01.03 |
Rituximab (rheumatology) MabThera® |
Hospital use only
Commissioned by NHSE for paediatrics (where adult TA available; anca-positive vasculitis; SLE; neuromyelitis optica |
02.08 |
Rivaroxaban |
|
04.11 |
Rivastigmine |
- Capsules
- Patches - preferred brand is Alzest®
|
04.07.04.01 |
Rizatriptan |
Tablets Orodispersible tablets SF-reserved for patients who are vomiting due to migraine
Wafer/oral lyophilisates SF £££££
|
15.01.05 |
Rocuronium Bromide Esmeron® |
Hospital only |
03.03.03 |
Roflumilast Daxas® |
In line with NICE |
09.01.04 |
Romiplostim Nplate® |
Hospital use only in line with NICE TA221. |
06.06 |
ROMOSOZUMAB |
Evenity - Red |
04.09.01 |
Ropinirole |
Brand preference SWB CCG Ippinia XL® (September 2020) |
04.09.01 |
Ropinirole |
For use in Restless Legs, supported by an ESCA, see link below |
04.09.04 |
Ropinirole |
For use in Restless Legs, supported by an ESCA, see link below |
15.02 |
Ropivacaine Hydrochloride 75mg/10ml Naropin® |
Hospital only |
02.12 |
Rosuvastatin |
Restricted to patients unable to tolerate other low cost generic statins. |
14.04 |
Rotavirus vaccine Rotarix® |
|
04.09.01 |
Rotigotine |
|
08.01.05 |
Rucaparib Rubraca® |
In line with NICE |
04.08.01 |
Rufinamide |
For Lennox-Gastaut syndrome only
Supported by an ESCA
MHRA Advice MHRA advises that when prescribing for epilepsy the patient should be assessed to make a clinical judgement if the same manufacturer's product/brand is necessary taking into account factors such as seizure frequency and treatment history. Also take into account patient/carer related factors such as their negative perceptions about alternative products and/or other issues related to the patient such as co-morbid autism, mental health issues or learning disability |
08.01.05 |
Ruloxitinib Jakavi® |
Hospital ONLY
NHS Engalnd is responsible commissioner
In line with NICE and available from day 91 following publication of TA |
28.01 |
Ruxolitinib (INC424) Incyte® |
Approved for 2nd line compassionate treatment in patients with high risk myelofibrosis (Cons. Haematologist) |
09.04 |
S.O.S® |
- High-energy supplements: carbohydrate
- Individual dose sachets, to be made as needed –pre measured dose to be made up by parents
- Essential for use in an emergency regimen in inborn errors of metabolism / module in tube feed for low amino acid or fat diets / energy supplement
- Also essential core ingredient in emergency feeds for inborn errors of metabolism / or used as an Individual carbohydrate module in tube feeds for low amino acid or fat diets / or as an energy supplement. Particularly important to use with non-English speaking families and vulnerable families as it is supplied in pre-measured sachets. Research as shown that it is safer to use than conventional glucose polymer powders. The dose and type of product should always be advised by the specialist dietitian according to the needs of the patient
- For use as an emergency regimen in the dietary management of inborn errors of metabolism in adults and children from birth
|
02.05.05 |
Sacubitril valsartan Entresto® |
Use current status at Place/Trust
Sandwell
Supported by RICaD
Sacubatril valsartan(Entresto) RICaD -Sandwell only
Wolverhampton
Walsall
Dudley
Entresto-Implementation of Entresto (Sacubitril/Valsartan) in Dudley Health Economy |
03.01.01.01 |
Salbutamol |
- Salbutamol IV
- Ventolin Solution for Infusion
- Ventolin Solution for Injection
|
03.01.01.01 |
Salbutamol |
BRANDS/FORMULATION
- Easyhaler
- Ventolin Accuhaler
- Salamol
- Salamol Easi-Breathe
How to use a Metered Dose Inhaler How to use a Metered Dose Inhaler with a Large Volume Spacer Device How to use a Metered Dose Inhaler with a Small Volume Spacer Device How to use an Accuhaler inhaler How to use an Easyhaler Inhaler How to use an Easi-Breathe Inhaler |
03.01.01.01 |
Salbutamol Nebuliser Liquid ® |
Green-Nebuliser Liquid
Amber Recommended- Nebuliser Liquid in Paediatrics |
07.01.03 |
Salbutamol |
|
13.14.06 |
Salicylic acid 10% w/w in emulsifying ointment |
|
13.07 |
Salicylic Acid 16.7% with Lactic Acid 16.7% paint Salactol® |
Over the counter preparation suitable for self-care/purchase if appropriate |
13.14.06 |
Salicylic acid 2% w/w & sulphur 2% w/w in aqueous cream |
|
13.14.06 |
Salicylic acid 2% w/w in emulsifying ointment |
|
13.14.06 |
Salicylic acid 20% w/w in emulsifying ointment |
|
13.14.02 |
Salicylic acid 5% w/w & propylene glycol 47.5% w/w in Dermovate® cream |
|
13.14.06 |
Salicylic acid 5% w/w in emulsifying ointment |
|
13.07 |
Salicylic Acid gel Salatac® |
Over the counter preparation suitable for self-care/purchase if appropriate |
13.07 |
Salicylic Acid Ointment Verrugon® |
Over the counter preparation suitable for self-care/purchase if appropriate |
12.03.05 |
Saliveze® |
Approved for ACBS conditions i.e. patients suffering from xerostomia (dry mouth) as a result of having or having undergone radiotherapy or sicca syndrome Palliative care Dental Practitioners |
12.03.05 |
Salivix® |
Approved for ACBS conditions i.e. patients suffering from xerostomia (dry mouth) as a result of having or having undergone radiotherapy or sicca syndrome. Palliative care Dental practitioners Only useful in patients who have residual salivary gland function |
09.05.01.01 |
Sandocal-1000® |
|
06.04 |
Sandrena gel |
|
09.04.01 |
Sapropterin Dihydrochloride Kuvan® |
Use in line with NICE |
08.02.04 |
Sarilumab Kevzara® |
In line with NICE |
28.01 |
Sativex “Cannabis Extract” |
For muscle spasticity, to be funded by Neurosciences directorate |
09.04.01 |
Savory meals and mixes |
Low-protein foods
These products are not available to purchase in supermarkets
They are important to provide essential energy and variety to aid the palatability of low protein diets. They are important for good metabolic control of the patient. Poor access to these products could lead to poor dietary adherence. This will cause poor metabolic control which may lead to irreversible brain damage
The NSPKU guidelines for prescription of low protein foods can be used for other amino acid disorderssuch as MSUD, homocystinuria, tyrosinaemia and pyridoxine response epilepsy
Protein free - necessary for children and adults with inborn errors of protein metabolism who do not tolerate very little natural protein
The specialist dietician will make individual reccomendations based on diagnosis,protein recommendations, weight etc
- Important protein-free foods to provide important energy, assist dietary adherence and provide variety when natural protein tolerance is very limited. Necessary for children and adults with inborn errors of protein metabolism who tolerate very little natural protein-. 1 ordinary meal is likely to provide ≥25g protein
|
09.04 |
Scandishake® Mix |
- Protein, fat, and carbohydrate
- Second choice for patients with very high energy requirement eg. cystic fibrosis
- In adults with cystic fibrosis, nutritional advice and interventions should be aimed at maintaining a BMI of 22kg/m2 in women and 23kg/m2 in men, as these are associated with better lung function (Nutritional management of CF – Consensus document – 2016)
- Disease-related malnutrition, malabsorption states, or other conditions requiring fortification with a high fat or carbohydrate (with protein) supplement
- Not suitable for child under 3 years
|
01.07.02 |
Scheriproct® |
|
13.05.02 |
Sebco® |
|
13.05.03 |
Secukinumab Cosentyx® |
Specialist use only in line with NICE. |
08.04 |
Selective internal radiation therapies |
In line with NICE |
04.09.01 |
Selegiline Hydrochloride |
Tablets
Oral lyophilisate are reserved for patients with swallowing difficulties in advanced Parkinson's disease
|
09.05.05 |
Selenium Selenase® |
Specialist recommendation |
09.05.05 |
Selenium |
Hospital only |
13.09 |
Selenium Sulphide Selsun® |
Over the counter preparation suitable for self-care/purchase if appropriate |
08.01.05 |
Selpercatinib Retsevmo® |
In line with NICE |
06.01.02.03 |
Semaglutide Rybelsus®▼ |
PLEASE PRESCRIBE BY BRAND - NICE Guidance on prescribing
Rybelsus is a tablet for once-daily oral use but has special administration directions:
- It must be taken on an empty stomach at any time of the day.
- Patients are required to wait at least 30 minutes before eating/drinking or taking other oral medicinal products. Waiting less than 30 minutes decreases absorption.
- It should be swallowed whole with a sip of water (up to half a glass of water equivalent to 120 ml).
|
06.01.02.03 |
Semaglutide Wegovy ® |
PLEASE PRESCRIBE BY BRAND - NICE Guidance on prescribing
Semaglutide is a biological medicine. Biological medicines must be prescribed and dispensed by brand name, see Biological medicines and Biosimilar medicines, under Guidance on Prescribing; manufacturer advises to record the brand name and batch number after each administration.
The use of semaglutide for this indication is restricted to prescribing by commissioned clinics in secondary care by a consultant led specialist multidisciplinary Tier 3 weight management service with a commercial agreement in place.
Prescribe by brand (Wegovy®) to avoid patients inadvertently receiving a different product licensed for type 2 diabetes.
|
01.06.02 |
Senna |
Tablets 7.5mg, Syrup 7.5mg/5ml
Syrup is currently more cost effective than tablets
Time to effect approximately 8 to 12 hours |
05.01.04 |
Septopal |
|
04.03.03 |
Sertraline |
|
09.05.02.02 |
Sevelamer |
Specialist Recommendation • No ESCA • Common Practice |
15.01.02 |
Sevoflurane |
HOSPITAL ONLY |
02.05.01 |
Sildenafil |
|
10.04 |
Sildenafil tablets GENERIC |
- Use in digital ulceration is commissioned by NHS England
- All prescribing retained in Secondary Care
- Off label use
|
A5.16 |
Silver nitrate |
NOT 1ST LINE TREATMENT ONLY TO BE USED IN A CLINIC SETTING OR BY A CLINICAL SPECIALIST Type of wound product is suitable for For treatment of chronic overgranulation, non acute or weeping. Duration product remains on wound before changing Apply moistened caustic pencil tip for 1-2 mins, whilst protecting the surrounding skin with soft paraffin. Frequency of use Maximum treatment: 3 applications Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Keep away from the eyes Not suitable for use on the face, ano-genital region or large areas Not for untreated bacterial, fungal or viral skin lesions Can cause chemical burns Rationale for inclusion in formulary Treatment of overgranulation |
13.07 |
Silver nitrate 95% caustic applicator |
|
13.07 |
Silver Nitrate 95% with Potassium Nitrate 5% Caustic pencil AVOCA® |
Over the counter preparation suitable for self-care/purchase if appropriate |
13.07 |
Silver nitrate applicators |
40% 75% 95%
Over the counter preparation suitable for self-care/purchase if appropriate |
13.10.01.01 |
Silver Sulfadiazine Flamazine® |
For infected burns under specialist supervision |
A5.17 |
Silver sulfadiazine 1% Flamazine® |
Burns specialist recommendation only Type of wound product is suitable for Partial thickness & full thickness burn injuries. Sloughy burn wounds or areas of graft loss Duration preparation remains on wound before changing 24-48 hours Frequency of use Daily- occasionally alternate day Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Allergy to any ingredients. Not to use in pregnancy or breast feeding Take care if: suffer kidney or liver problems, deficiency of the enzyme known as glucose 6- phosphate dehydrogenase. Taking tablets prescribed for epilepsy Rationale for inclusion in formulary Prevent and treat bacterial infections in burns, skin graft donor sites. |
A5.17 |
Silver sulfadiazine 1.0g & Cerium nitrate 2.2g Flammercerium® |
Hospital use only Type of wound product is suitable for Partial thickness & full thickness burn injuries. Duration preparation remains on wound before changing 24-48 hours Frequency of use Daily- occasionally alternate day Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Allergy to any ingredients. Not to use in pregnancy or breast feeding, infants or babies under the age of 2 years. Take care if: suffer kidney or liver problems, deficiency of the enzyme known as glucose 6- phosphate dehydrogenase. Taking tablets prescribed for epilepsy Rationale for inclusion in formulary Prevent and treat bacterial infections in burns |
01.01.01 |
Simeticone |
Drops
For use in infantile colic |
03.09.02 |
Simple Linctus, BP |
OTC preparation suitable for self-care/purchase if appropriate |
03.09.02 |
Simple Linctus, Paediatric BP |
OTC preparation suitable for self-care/purchase if appropriate |
02.12 |
Simvastatin |
|
08.02.04 |
Siponimod Mayzent® |
In line with NICE |
08.02.02 |
Sirolimus Rapamune® |
Commissioned by NHSE for post transplant patients. Prescribing to remain with the specialist for this patient group
Post transplant- if prescribing is NOT established with GP before 1st April 2013
Post transplant- if prescribing IS established with GP before 1st April 2013
|
06.01.02.03 |
Sitagliptin |
To be used in line with NICE
First line treatment option where a DPP-4 inhibitor is indicated.
No significant clinical benefit when used in combination with Insulin – avoid using together
|
06.01.02.03 |
Sitagliptin and Metformin |
A variety of combinations tablets (dual therapies) of oral diabetes medication can be prescribed and are available in the Drug Tariff.
Overall, they may improve compliance in patients, however some combinations would then not allow the flexibility in dosing that is required for diabetes management and in some cases increase the tablet burden. There are specific sick-day rules related to stopping certain medication which would be further complicated where they are not prescribed in their separate formulations.
Furthermore, for the overall health economy not all combination therapies are cost-effective and this will be increasingly so as the patents expire over the near future. There are some combination therapies that are not recommended in the oral guidance and clinicians are guided to review and discuss these with patients as part of shared -care decision making.
There are complexities also around the lack of licensing of dual therapies in specific cohorts of patients, related to prescribing for the indication of heart failure or renal disease, making this a complex area for prescribing in primary care
|
A5.16 |
Skin tissue adhesive LiquiBand® Optima |
Preferred local option Tissue Adhesive Type of wound product is suitable for Closure of minor skin wounds from surgical incisions and simple traumatic lacerations Duration dressing remains on wound before changing Single application should be sufficient to close the wound. If this does not maintain the wound edges, refer to a medic for consideration of other wound closure Frequency of dressing change As necessary Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) May cause skin sensitivities Do not use on any wound with evidence of active infection, gangrene or wounds of pressure aetiology Do not use on mucosal surfaces or on skin that may be regularly exposed to bodily fluids or with dense natural hair Do not use on patients with a known sensitivity to formaldehyde or cyanoacrylate Rationale for inclusion in formulary Necessary for closure of minor wounds |
09.04 |
Slo drinks milkshakes |
First Line
- For dysphagia pts only
- Not suitable for CKD 4-5, renal pts
- Not suitable for lactose intolerance
- Not suitable for bile acid malabsorption or fat maldigestion associated with biliary diseases/conditions
- To be made up with whole milk
- Contains 24g protein per serving as served
|
09.09 |
SLO Drinks® |
- Used in a complex specific patient group advised by a SALT specialist
- Nutritional supplement for patient hydration in the dietary management of dysphagia
- Not suitable for children under 3 years
|
09.04 |
SMA Althera® |
|
09.04 |
SMA LF® Lactose Free Formula (previous name SMA® LF) |
- Specialised formulas: Infant and child: Residual lactose formula
- Can be purchased over the counter
- Only prescribable for patients who currently do not pay for formula feeds (eg healthy start scheme)
- For infants with lactose intolerance
- Proven lactose intolerance
|
09.04.02 |
SMA PRO High Energy (previous name SMA® High Energy |
Child under 12 years
- Less than 1 kcal/mL and less than 4g protein/100 mL
- High energy feed for faltering growth
- Single use only in acute setting – risk of increased waste
- Once open must be used within 24 hours
- Disease-related malnutrition, malabsorption, and growth failure in infancy
|
09.04.02 |
SMA® PRO Gold Prem 2 (previous name SMA® gold Prem 2 |
Child under 12 years
- Less than 1 kcal/mL and less than 4g protein/100 mL
- Post discharge formula for pre term infants
- Powder feed
- Partially hydrolysed
- For catch-up growth in preterm infants and small for gestational age babies on discharge from hospital until 6 months corrected age. It may be used as the sole source of nutrition until complementary feeding commences
|
01.06 |
Sodium acid phosphate with sodium phosphate |
|
01.03 |
Sodium alginate with calcium carbonate and sodium bicarbonate |
|
01.03 |
Sodium alginate with potassium bicarbonate |
|
10.01.03 |
Sodium aurothiomalate Myocrisin® |
Supported by an ESCA |
07.04.03 |
Sodium bicarbonate |
|
09.02.01.03 |
Sodium bicarbonate |
Specialist recommendation |
12.01.03 |
Sodium Bicarbonate 5% |
|
09.02.02.01 |
Sodium bicarbonate infusion |
Hospital use only |
03.01.05 |
Sodium Chloride |
|
09.02.01.02 |
Sodium chloride |
Sodium chloride M/R Tablets
Sodium chloride 5mmol solution
Sodium chloride 1mmol/mL oral solution - Specialist recommendation
|
11.08.01 |
Sodium Chloride Minims® Saline |
Hospital only
Diluent for impregnated dye strips |
12.02.02 |
Sodium Chloride |
|
03.07 |
Sodium chloride 0.9% |
|
03.07 |
Sodium chloride 0.9% |
|
07.04.04 |
Sodium Chloride 0.9% |
For Specialist / Hospital Use Only |
13.11.01 |
Sodium Chloride 0.9% |
|
21 |
Sodium chloride 0.9% |
|
11.08.01 |
Sodium Chloride 0.9% Solutions |
Hospital only - Theatre use |
11.08.01 |
Sodium chloride 5% |
On Specialist Ophthalmologist Recommendation |
11.08.01 |
Sodium Chloride 5% PF drops (Moorfields) |
On Specialist Ophthalmologist Recommendation |
03.07 |
Sodium Chloride 7% |
|
09.02.02.01 |
Sodium Chloride and Glucose Intravenous Infusion |
Hospital use only |
09.02.02.01 |
Sodium Chloride Intravenous infusion |
Hospital use only |
07.04.04 |
Sodium Citrate |
Hospital Only |
06.06 |
Sodium Clodronate Calsteon®, Loron 520® |
Dudley
Sandwell
ESCA- Sandwell
Walsall
Wolverhampton
|
11.04.02 |
Sodium Cromoglicate |
|
11.04.02 |
Sodium cromoglicate Catacrom® |
On specialist ophthalmologist recommendation as Catacrom |
09.01.01.01 |
Sodium Feredetate SF Elixir Sytron® |
|
09.05.03 |
Sodium Flouride Toothpaste 0.619% (2800ppm) DPF |
Dental prescribing ONLY |
09.05.03 |
Sodium Flouride Toothpaste 1.1% (5000ppm) DPF |
Dental prescribing ONLY |
09.05.03 |
Sodium Fluoride Mouthwash BP |
Dental prescribing ONLY |
05.01.07 |
Sodium fusidate |
|
05.01.07 |
Sodium fusidate |
|
11.08.01 |
Sodium Hyaluronate 0.15% Multi Hyabak® |
On Specialist Ophthalmologist Recommendation |
11.08.01 |
Sodium Hyaluronate 0.2% PF Multi Hylo-Forte® |
On Specialist Ophthalmologist Recommendation |
11.08.01 |
Sodium Hyaluronate 0.2% Preservative Free Evolve HA® |
Approved onto the formulary January 2019
Specialist Ophthalmologist Recommendation |
11.08.01 |
Sodium Hyaluronate 0.4% SDU Clinitas ® |
On Specialist Ophthalmologist Recommendation
Single use restricted to patients needing preservative free
Each unit is re-sealable and may be used for up to 12 hours |
02.05.01 |
Sodium nitroprusside |
Injection (Secondary Care only) |
01.06 |
Sodium Picosulfate |
|
21 |
Sodium Picosulfate |
|
05.05 |
Sodium Stibogluconate Pentostam® |
|
02.13 |
Sodium Tetradecyl Sulphate Fibro-Vein® |
|
04.08.01 |
Sodium Valproate |
E/C tablets
M/R tablets
Crushable tablets
SF liquid
M/R granules see Episenta®
On specialist advice
Use in men and women of non-child bearing potential
Use in women and girls of childbearing potential (all indications).
Contraindicated in women of childbearing potential unless part of the Pregnancy Prevention Programme. See MHRA guidance
MHRA Advice Care should be taken when switching between oral formulations. The need for continued supply of a particular manufacturer’s product should be based on clinical judgement and consultation with patient and/or carer, taking into account factors such as seizure frequency and treatment history |
04.08.01 |
Sodium valproate prolonged release Episenta® |
Paediatrician initiation for patients with epilepsy aged up to and including 16 years of age unable to swallow tablets and who require a modified release formulation in whom other formulations are more expensive or not appropriate
Contraindicated in women of childbearing potential unless part of the Pregnancy Prevention Programme. See MHRA guidance
MHRA Advice Care should be taken when switching between oral formulations. The need for continued supply of a particular manufacturer’s product should be based on clinical judgement and consultation with patient and/or carer, taking into account factors such as seizure frequency and treatment history |
09.02.01.01 |
Sodium zirconium cyclosilicate Lokelma® |
In line with NICE
In emergency care for acute life-threatening hyperkalaemia alongside standard care
For people with persistent hyperkalaemia and chronic kidney disease stage 3b to 5 or heart failure, pending publication of RICaD |
05.03.03.02 |
Sofosbuvir Sovaldi® |
|
05.03.03.02 |
Sofosbuvir/velpatasvir Epclusa® |
In line with NICE |
05.03.03.02 |
Sofosbuvir/Velpatasvir/Voxilaprevir Vosevi® |
In line with NICE |
19.03 |
Softpore® self adhesive |
Type of wound product is suitable for Low to moderately exuding wounds, superficial wounds (closed), light amounts of exudate. Use alone without other products, also can be used as a protective dressing for sutured post operative wounds. Can be used as a protective dressing for newly epithelialised wounds. Can be used for minor traumatic wounds Duration dressing remains on wound before changing Maximum 7 days, dependent on exudate levels Frequency of dressing change If daily change is required; review dressing type Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Known product or component sensitivity Rationale for inclusion in formulary Sutured/Post-surgical wound for protection . Most cost effective option. Can be used as a protective dressing for newly epithelialized wounds. Can be used for minor traumatic wounds |
A5.01.02 |
Softpore® self adhesive |
Preferred local option Type of wound product is suitable for Low to moderately exuding wounds, superficial wounds (closed), light amounts of exudate. Use alone without other products, also can be used as a protective dressing for sutured post operative wounds. Can be used as a protective dressing for newly epithelialised wounds. Can be used for minor traumatic wounds Duration dressing remains on wound before changing Maximum 7 days, dependent on exudate levels Frequency of dressing change If daily change is required; review dressing type Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Known product or component sensitivity Rationale for inclusion in formulary Sutured/Post-surgical wound for protection . Most cost effective option. Can be used as a protective dressing for newly epithelialized wounds. Can be used for minor traumatic wounds |
07.04.02 |
Solifenacin |
|
04.04 |
Solriamfetol Sunosi® |
In line with NICE |
06.05.01 |
Somatropin |
Genotropin GoQuick powder/solvent for |
Genotropin MiniQuick powder/solvent for injection |
Genotropin powder/solvent for injection |
Humatrope powder/solvent for injection |
Norditropin FlexPro |
Norditropin NordiFlex |
Norditropin SimpleXx |
NutropinAq |
Omnitrope |
Omnitrope SurePal |
Saizen |
Saizen powder/solvent for injection |
Zomacton powder/solvent for injection |
|
08.01.05 |
Sorafenib Nexavar® |
Funding may be available from cancer drugs fund |
19.17 |
Sorbsan ® Packing |
Moderate to heavilty exuding cavity wounds. Pack only 80% of the cavity to allow for dressing to swell and leave 2.5cm tail of dressing exposed to facilitate removal. |
19.17 |
Sorbsan ® Plus Border |
Shower proof with adhesive border.
Indications: sloughy, granulating wounds, moderate to heavy exudate. Forms a gel which provides a “moist wound environment”, encouraging autolytic debridement and facilitating wound healing. All dressing residue must be irrigated away to avoid an inflammatory response. Do NOT use on dry, lightly exuding or dry necrotic wounds. Have limited lateral absorbency, hence do not need to be cut to shape.
|
19.17 |
Sorbsan ® Ribbon |
Moderate to heavily exuding cavity wounds. Pack only 80% of the cavity to allow for dressing to swell and leave 2.5cm tailof dressing exposed to facilitate removal. |
19.17 |
Sorbsan® Flat |
Can be multilayered if needed.
Indications: sloughy, granulating wounds, moderate to heavy exudate. Forms a gel which provides a “moist wound environment”, encouraging autolytic debridement and facilitating wound healing. All dressing residue must be irrigated away to avoid an inflammatory response. Do NOT use on dry, lightly exuding or dry necrotic wounds. Have limited lateral absorbency, hence do not need to be cut to shape. |
19.17 |
Sorbsan®Plus |
Highly absorbent.
Indications: sloughy, granulating wounds, moderate to heavy exudate. Forms a gel which provides a “moist wound environment”, encouraging autolytic debridement and facilitating wound healing. All dressing residue must be irrigated away to avoid an inflammatory response. Do NOT use on dry, lightly exuding or dry necrotic wounds. Have limited lateral absorbency, hence do not need to be cut to shape.
|
A5.02.06 |
Sorbsan® range |
Preferred local option Calcium alginate dressing Type of wound product is suitable for Use in moderate to highly exuding wounds with a sloughy or granulating wound bed. Also helps with haemostasis in wounds with minor bleeding or where blood is present in the exudate. Available in flat and rope dressing Primary dressing only. Secondary dressing will be required. Duration dressing remains on wound before changing Can be left in place for approximately 4 days Frequency of dressing change 1-4 days dependent on exudate levels Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Do not use in individuals with a known sensitivity to any of the components of the dressing Do no use on dry or lightly exuding wounds as adherence is an issue Extreme caution if used for tumours with friable tissue Rationale for inclusion in formulary</> Sorbsan® can facilitate debridement, absorb exudate and is a haemostat Cost effective Biodegradable |
02.04 |
Sotalol |
Anti-arrhythmic
|
08.01.05 |
Sotorasib Lumykras® |
In line with NICE |
05.02.05 |
Sotrovimab |
|
07.03.03 |
Spermicidal Contraceptives Gygel®2% Gel |
|
05.05 |
Spiramycin |
Unlicensed |
13.11.01 |
Spiriclens |
Hospital only |
02.02.03 |
Spironolactone |
|
09.04.01 |
Spreads |
Low-protein foods
These products are not available to purchase in supermarkets
They are important to provide essential energy and variety to aid the palatability of low protein diets. They are important for good metabolic control of the patient. Poor access to these products could lead to poor dietary adherence. This will cause poor metabolic control which may lead to irreversible brain damage
The NSPKU guidelines for prescription of low protein foods can be used for other amino acid disorderssuch as MSUD, homocystinuria, tyrosinaemia and pyridoxine response epilepsy
Protein free - necessary for children and adults with inborn errors of protein metabolism who do not tolerate very little natural protein
The specialist dietician will make individual reccomendations based on diagnosis,protein recommendations, weight etc.
- Important protein-free foods to provide important energy, assist dietary adherence and provide variety when natural protein tolerance is very limited. Necessary for children and adults with inborn errors of protein metabolism who tolerate very little natural protein. 1 portion ordinary spread likely to provide 2-5g protein
|
01.04 |
St Mark’s powder & solution (unlicensed) |
UNLICENSED
Specialist use only |
01.04 |
St Mark's recipe |
For fluid and electrolye replacement following diarrhoea
Click here for St Mark's recipe |
03.01.05 |
Standard range peak flow meter |
BRANDS
- Easy Peak Flow Meter
- Rossmax Peak Flow Meter
|
04.08.01 |
Stiripentol Diacomit® |
Severe myoclonic epilepsy of infancy (Dravet syndrome) APC supports use in Adults: for continuation of therapy started in childhood. (Note Off Label use in adults) |
02.10 |
Streptokinase |
Hospial only |
05.01.09 |
Streptomycin Sulphate |
|
06.06.02 |
Strontium ranelate |
|
01.03.03 |
Sucralfate Tablet 1g. Suspension 500mg/5ml |
For specialist initiation only |
09.05.02.02 |
Sucroferric oxyhydroxide Velphoro® |
2nd or 3rd line for those intolerant to Sevelamer
Specialist use only |
A5.15 |
Sudocrem |
Barrier cream Type of wound product is suitable for Intact skin, not to be applied to a wound. To protect the skin from moisture, irritation and chafing. To protect the peri wound when utilising free range larvae Frequency of use Application at every episode of hygiene. Apply a thin layer sparingly. Remove with olive oil. Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Not to be used in conjunction with containment products for incontinence due to the inclusion of lanolin in the ingredients, which will repel urine/faeces back onto the skin. Any allergy to the listed ingredients Rationale for inclusion in formulary Dermatology approved |
13.02.02 |
Sudocrem® |
Use for areas around stoma, bedsores and pressure areas where the skin is intact
Avoid use with continence pads
Over the counter preparation suitable for self-care/purchase if appropriate |
15.01.06 |
Sugammadex Bridion® |
Hospital only |
05.04.07 |
Sulfadiazine |
|
05.05 |
Sulfadiazine |
|
01.05.01 |
Sulfasalazine |
Plain tablets are more cost effective than enteric coated tablets
Walsall
Green -Walsall only
Sandwell
Amber Recommended -Sandwell only
Wolverhampton
Amber SC-Wolverhampton only
ESCA Sulfasalazine-Wolverhampton only
Dudley
Amber SC-Dudley only
ESCA Sulfasalazine (Dudley only) |
10.01.03 |
Sulfasalazine EC |
Supported by an ESCA |
10.01.01 |
Sulindac |
For hospital use only in Polyhydramnios (women only) |
04.02.01 |
Sulpiride |
Supported by ESCA |
04.07.04.01 |
Sumatriptan |
Tablets (prescribe as generic)
Nasal spray £££££
Injection £££££
|
08.01.05 |
Sunitinib Sutent® |
Commissioned by NHS England in line with NICE |
13.08.01 |
Sunsense® Ultra lotion (SPF 50) |
Non-formulary if not for ACBS approved indication |
09.03 |
Supplementary Preparations Addiphos® |
For hospital use only |
09.03 |
Supplementary Preparations Additrace® |
For hospital use only |
09.03 |
Supplementary Preparations Peditrace® |
For hospital use only |
09.03 |
Supplementary Preparations Solivito N® |
For hospital use only |
09.03 |
Supplementary Preparations Vitlipid N® |
For hospital use only |
A5.03.04 |
Suprasorb® X+PHMB |
Hospital use only
Biocellulose gel sheet dressing with PHMB antimicrobial properties Type of wound product is suitable for Light to moderately, critically colonised or infected exuding wounds Can be used on all wound types at all stages of wound healing Can be cut or folded to wound shape size Duration dressing remains on wound before changing 1-3 days Frequency of dressing change 1-3 days, dependent on exudate levels Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Known sensitivity to PHMB or any components of the dressing Heavily exuding wounds Rationale for inclusion in formulary Light to moderate exudate in clinically infected wounds. Suitable for all wounds at all stages of wound healing Doesn’t affect healthy cells, suitable for long term use when necessary
|
A5.02.03 |
Surprasorb X |
Specialist recommendation only Bio-cellulose gel sheet dressing Type of wound product is suitable for Light to moderately, non infected exuding wounds Duration dressing remains on wound before changing 1-7 days Frequency of dressing change 1-7 days, dependent on exudate levels Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Known sensitivity to any components of the dressing Rationale for inclusion in formulary Light to moderate exudate. |
15.01.05 |
Suxamethonium Chloride Anectine® |
Hospital only |
04.13 |
Tacrolimus |
Specialist use only for neurological conditions |
08.02.02 |
Tacrolimus AdoPORT® |
|
08.02.02 |
Tacrolimus Prograf® |
Prescribe by brand name only to minimise the risk of inadvertent switching between products, which has been associated with reports of toxicity and graft rejection (June 2012)
Commissioned by NHSE for post transplant patients
Prescribing to remain with the specialist for this patient group
Prograf ®: immediate release/standard release capsule, twice daily dosage
Post transplant- if prescribing is NOT established with GP before 1st April 2013
Post transplant - if prescribing IS established with GP before 1st April 2013
|
08.02.02 |
Tacrolimus Modigraf® |
Prescribe by brand only to minimise the risk of inadvertent switching between products, which has been associated with reports of toxicity and graft rejection (June 2012)
Commissioned by NHSE for post transplant patients
Prescribing to remain with the specialist for this patient group
Modigraf®: immediate release formulation, twice daily dosage
Post transplant- if prescribing is NOT established with GP before 1st April 2013
Post transplant - if prescribing IS established with GP before 1st April 2013
|
08.02.02 |
Tacrolimus Advagraf ® |
Prescribe by brand name only to minimise the risk of inadvertent switching between products, which has been associated with reports of toxicity and graft rejection (June 2012)
Commissioned by NHSE for post transplant patients
Prescribing to remain with the specialist for this patient group
Advagraf ®: prolonged release capsule, once daily dosage
Post transplant- if prescribing is NOT established with GP before 1st April 2013
Post transplant - if prescribing IS established with GP before 1st April 2013
|
13.05.03 |
Tacrolimus Protopic® |
Initiated by hospital only In line with NICE 0.03% 0.1% |
13.14.07 |
Tacrolimus 0.1% w/w in Orabase® |
|
13.14.07 |
Tacrolimus 0.3% w/w in Orabase® |
|
07.04.05 |
Tadalafil |
More cost effective options available
Erectile Dysfunction Only
On demand preparation only
SLS criteria still apply
Quanties in line with HSC Guidance
Maxiumum 4 tablets per month (NOT DAILY)
for Lower Urinary tract symptoms in Benign Prostatic Hyperplasia |
11.06 |
Tafluprost |
2nd line PF option
On Specialist Ophthalmologist Recommendation |
08.01.05 |
Talimogene Iaherparepvec Imlygic® |
Hospital ONLY - NHS England commissioned
In line with NICE and available from day 91 following publication of TA
|
06.07 |
TAMOXIFEN |
|
08.03.04.01 |
Tamoxifen |
|
07.04.01 |
Tamsulosin |
Reduce BP - care with other antihypertensives Caution in elderly Care with hepatic and severe renal impairment Contraindicated in postural hypotension or micturition syncope |
04.07.02 |
Tapentadol Palexia® |
|
13.05.02 |
Tars - bath preparations Psoriderm® emulsion |
|
02.08 |
TauroLock TauroLock HEP 500® |
|
05.01 |
Tedizolid Oral and IV |
|
A5.02.05 |
Tegaderm Foam Adhesive |
Type of wound product is suitable for Wound management by secondary intention on acute, chronic, full thickness or partial thickness or shallow granulating wounds including pressure ulcers, leg ulcers, diabetic foot ulcers, malignant wounds, surgical wounds, donor sites and fungating ulcers Can be used as a primary or secondary dressing Film border increases adherence Duration dressing remains on wound before changing Can stay in place up to 3-7 days Frequency of dressing change Dependent on exudate levels Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Care with fragile skin Rationale for inclusion in formulary Can be used for low to moderate exudate levels Different sizes and shapes available Conformability around difficult areas such as heels and elbows Can be used on sacral and buttock wounds where incontinence is an issue due to film backing and border. |
19.10 |
Tegaderm® Film |
Indications: shallow, lightly exuding wounds, adhesive primary or secondary dressing. Properties include: provide protection from exposure to friction, maintain moisture to prevent scab formation, vapour permeable to water and oxygen but impermeable to micro-organisms, for use when occlusion is required. Allow 4cm skin overlap when applying dressing, stretch film parallel to skin to release adhesives and prevent trauma to skin on removal. NOT suitable for infected wounds Caution: exudate may accumulate under the dressing which can lead to tissue maceration,
|
19.16 |
Tegadern Foam Adhesive |
Indications: granulating, epithelialising or wounds with minimal slough and moderate exudate (of limited value in dry/necrotic wounds). Primary or secondary dressing which should overlap wound edge by 2-3cm. ‘Erythematous reaction’ (redness in the shape of the dressing) may be observed when dressing is removed due to increased blood flow following thermal insulation, or lateral wicking of exudate to peri-wound skin. |
05.01.07 |
Teicoplanin |
For hospital use only |
05.01 |
Telavancin |
|
19.03 |
Telfa® |
PODIATRY USE ONLY Thin absorbent cotton pad with non adherent film Type of wound product is suitable for Dry or lightly exuding wounds Duration dressing remains on wound before changing 1-7 days Frequency of dressing change As exudate levels determine Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) None Rationale for inclusion in formulary Cost effective. Non adherent dressing for dry or lightly exuding wounds |
A5.01.02 |
Telfa® |
PODIATRY USE ONLY Thin absorbent cotton pad with non adherent film Type of wound product is suitable for Dry or lightly exuding wounds Duration dressing remains on wound before changing 1-7 days Frequency of dressing change As exudate levels determine Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) None Rationale for inclusion in formulary Cost effective. Non adherent dressing for dry or lightly exuding wounds |
04.01.01 |
Temazepam |
From Monday 1st June 2015, prescriptions for temazepam will be required to meet full prescription requirements for Schedule 3 controlled drugs (CDs)
Legislative changes to prescription writing requirements for temazepam
|
04.01.01 |
Temazepam |
£££££
From Monday 1st June 2015, prescriptions for temazepam will be required to meet full prescription requirements for Schedule 3 controlled drugs (CDs)
Legislative changes to prescription writing requirements for temazepam
|
15.01.04.01 |
Temazepam |
Hospital only |
05.01.01.02 |
Temocillin Negaban® |
|
05.01.01.02 |
Temocillin |
|
08.01.05 |
Temozolomide Temodal® |
|
08.01.05 |
Temsirolimus Torisel® |
Hospital only |
02.11 |
Tenecteplase |
Hospital only |
05.03.03.01 |
Tenofovir alafenamide Vemlidy® |
|
05.03.03.01 |
Tenofovir Disproxil |
|
05.03.01 |
Tenofovir, cobicistat, elvitegravir & emtricitabine Stribild® |
|
15.01.04.02 |
Tenoxicam |
Hospital only |
09.04.02 |
Tentrini® |
- Child: 1 kcal/ml and less than 4g protein/100ml
- Polymeric feed, used in children 20-45kg as tube feed, no added fibre
- Also essential low protein tube feeds for teenagers with inborn errors of protein metabolism (e.g. organic acidaemias, urea cycle disorders) due to its protein profile. It provides a natural protein source. It is used when IMD teenagers cannot tolerate fibre. To change to an alternative enteral feed with teenagers with metabolic disorders would potentially require hospital admission to ensure stabilisation with a new enteral feed. The dose and type of product should always be advised by the specialist dietitian according to the needs of the patient.
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula and growth failure in child 7–12 years, body-weight 21–45 kg
|
09.04.02 |
Tentrini® Energy |
- Child: 1.5 kcal/mL and more than 4g protein/100 mL
- 1.5kcal/ml tube feed for children 20-45kg
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula and growth failure, in child 7–12 years, body-weight 21–45 kg
|
09.04.02 |
Tentrini® Energy Multi Fibre |
- Child: 1.5 kcal/mL and more than 4g protein/100 mL
- 1.5kcal/ml tube feed for children 20-45kg with added fibre
- Paediatric ACBS indications: Disease-related malnutrition, intractable malabsorption, growth failure, pre-operative preparation of malnourished patients, dysphagia, short-bowel syndrome, bowel fistula and proven inflammatory bowel disease, in child 7–12 years, body-weight 21–45 kg
|
09.04.02 |
Tentrini® Multi Fibre |
- Child: 1 kcal/ml and less than 4g protein/100ml
- Polymeric feed, used in children 20-45kg as tube feed, added fibre
- Also essential in low protein tube feeds for teenagers with inborn errors of protein metabolism (e.g. organic acidaemias, urea cycle disorders) due to its protein profile. It provides a natural protein source. It is used when IMD teenagers cannot tolerate fibre. To change to an alternative enteral feed with teenagers with metabolic disorders would potentially require hospital admission to ensure stabilisation with new enteral feed. The dose and type of product should always be advised by the specialist dietitian according to the needs of the patient
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula except bowel fistula, and growth failure in child 7–12 years body-weight 21–45 kg
|
08.01.05 |
Tepotinib Tepmetko® |
In line with NICE |
05.02 |
Terbinafine |
|
13.10.02 |
Terbinafine 1% cream |
First line for dermatophyte skin infection. |
03.01.01.01 |
Terbutaline Bricanyl® |
How to use a Turbohaler Inhaler |
03.01.01.01 |
Terbutaline |
How to use a Turbohaler Inhaler |
07.01.03 |
Terbutaline |
For Specialist/ Hospital Use Only |
08.02.04 |
Teriflunomide Aubagio® |
In line with NICE
Commissioned by NHSE for multiple sclerosis |
06.06 |
Teriparatide |
Red - Forsteo
Red - Movymia
Red - Terrosa |
01.09 |
Terlipressin Glypressin® |
|
06.05 |
TERLIPRESSIN |
Glypressin - Red |
06.01.06 |
Test strips |
BRANDS
- Aviva testing strips
- FreeStyle Optium testing strips
- On Call Extra testing strips
|
06.01.06 |
Test strips |
BRANDS-Use in line with local guidance
- CareSens PRO testing strips
- Contour Next testing strips
- Contour Plus testing strips
- Instant testing strips
- TEE2 testing strips
- WaveSense JAZZ Duo testing strips
- WaveSense JAZZ testing strips
|
06.04.02 |
Testosterone Sustanon 250® |
|
06.04.02 |
Testosterone gel |
|
06.04.02 |
Testosterone Propionate |
|
06.04.02 |
Testosterone undecanoate Nebido® |
|
14.05.02 |
Tetanus immunoglobulin |
|
04.09.03 |
Tetrabenazine |
Tablets |
15.02 |
Tetracaine (Amethocaine) 4% Ametop® |
First line at Birmingham Children's Hospital |
06.05 |
TETRACOSACTIDE |
BRANDS
- Synacthen
- Synacthen Depot
|
05.01.03 |
Tetracycline |
Specialist Advice for H. pylori relapse only |
05.01.10 |
Thalidomide oral presentations |
|
08.02.04 |
Thalidomide |
In line with NICE
Commissioned by NHSE |
13.05.03 |
Thalidomide |
NHSE commissioned |
03.01.03 |
Theophylline Uniphyllin Continus |
|
09.06.02 |
Thiamine |
|
15.01.01 |
Thiopental |
HOSPITAL ONLY |
08.01.01 |
Thiotepa |
Commissioned by NHSE Hospital only |
09.09 |
Thixo-D® |
- Intolerance to locust bean gum in children under 1
- For thickening of foods in dysphagia
- Not suitable for children under 1 year except in cases of failure to thrive
|
06.05 |
THYROTROPIN ALFA Thyrogen® |
|
05.05 |
Tiabendazole 500mg tabs |
|
06.04 |
Tibolone Livial® |
|
02.09 |
Ticagrelor Brilique® |
|
05.01.03 |
Tigecycline |
|
13.05.03 |
Tildrakizumab Ilumya® |
In line with NICE |
13.04 |
Timodine® |
Potency-mild
Use for short periods - typically no more than one week |
11.06 |
Timolol |
On Specialist Ophthalmologist Recommendation |
11.06 |
Timolol LA |
On Specialist Ophthalmologist Recommendation
Once daily preparation |
11.06 |
Timolol Unit Dose Tiopex ® |
On Specialist Ophthalmologist Recommendation
Once daily preparation |
05.05 |
Tinidazole |
|
02.08.01 |
Tinzaparin |
Use current Place/Trust status and local guidelines
Sandwell
Single use in suspected DVT
For all other indications
The APC's view is that on clinical grounds, the status for certain indications approved by APC should be Amber Shared Care, supported by an ESCA. These indications are:
- Deep vein thrombosis (including paediatrics)
- Pulmonary embolism (including paediatrics)
- Intolerance/unsuitable for oral anticoagulants
- Certain cancer patients
- Injectable drug users
- Pregnant women
HOWEVER, until the commissioning arrangements have been agreed to allow safe transfer of patient care, the status will remain RED (ESCAs to be developed). This should not prevent individuals in primary care providing initial prescriptions in urgent situations e.g. pregnancy where there is a high thrombotic risk.
Wolverhampton
Walsall
Dudley
|
08.01.03 |
Tioguanine |
Commissioned by NHSE |
03.01.02 |
Tiotropium Spiriva Respimat® |
How to use a Respimat Inhaler |
03.01.04 |
Tiotropium & Olodaterol Spiolto® Respimat® |
How to use a Respimat Inhaler
|
02.06 |
Tirofiban Aggrastat® |
|
02.09 |
Tirofiban Aggrastat® |
|
08.01.05 |
Tisagenlecleucel Kymriah® |
In line with NICE
Providers - NHS hospital trusts |
02.11 |
Tisseel® |
|
08.01.05 |
Tivozanib Fotivda® |
In line with NICE |
10.02.02 |
Tizanidine |
|
03.13 |
Tobramycin |
|
05.01.04 |
Tobramycin Munuza ®
| |
05.01.04 |
Tobramycin Bramitob® |
|
05.01.04 |
Tobramycin Tymbrineb ® |
|
05.01.04 |
Tobramycin Vantobra ® |
|
05.01.04 |
Tobramycin TOBI Podhaler® |
For specialist prescribing only
|
05.01.04 |
Tobramycin |
|
10.01.03 |
Tocilizumab RoActemra® |
Hospital use only
In line with NICE
Paediatric use is commissioned by NHSE |
01.05.03 |
Tofacitinib Xeljanz® |
In line with NICE
Tofacitinib for moderately to severe active ulcerative colitis - providers are NHS hospital trusts |
06.01.02.01 |
Tolbutamide |
|
07.04.02 |
Tolterodine |
|
07.04.02 |
Tolterodine |
Normal release tablets more cost effective. |
06.05.02 |
Tolvaptan Samsca® |
|
06.05.02 |
Tolvaptan Jinarc® |
|
A5.06.01 |
Topical Negative Pressure Therapy |
Specialist recommendation only The use of sub atmospheric pressure to promote or assist wound healing or to remove fluids from a site. Required components: Pump, dressings foam or gauze, tubing and canister. Type of wound product is suitable for Acute, chronic and traumatic wounds. Can be used as a adjunct to surgery and for salvage procedures such as wound dehiscence. Benefits are that it removes excess fluid that may contain bacterial pathogens, reduces soft tissue oedema, promotes granulation and provides a moist wound healing environment. Consider standard interactive dressings first. Duration dressing remains on wound before changing Every three days Frequency of dressing change Determined by exudate levels. Different canister sizes available Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) It should not be used on: Grossly infected or bleeding wounds Malignancy Exposed blood vessels Organs Unexplored fistulae Extensive necrotic wounds Caution with foam, document the number inserted, ensure all pieces are retrieved. Rationale for inclusion in formulary It removes excess fluid that may contain bacterial pathogens, reduces soft tissue oedema, promotes granulation and provides a moist wound healing environment. Both companies products are included due to different contracting arrangements. Can be used on large open wounds to increase speed of wound healing |
04.07.04.02 |
Topiramate |
For migraine prophylaxis as per guidance
On specialist recommendation |
04.08.01 |
Topiramate |
On specialist advice
MHRA Advice MHRA advises that when prescribing for epilepsy the patient should be assessed to make a clinical judgement if the same manufacturer's product/brand is necessary taking into account factors such as seizure frequency and treatment history. Also take into account patient/carer related factors such as their negative perceptions about alternative products and/or other issues related to the patient such as co-morbid autism, mental health issues or learning disability |
08.01.05 |
Topotecan Hyxamtin® |
In line with NICE
Commissioned by NHSE
Hospital only |
04.07.02 |
Tramadol |
Third line after morphine and codeine
Please note modified release preparations are non-formulary |
04.07.02 |
Tramadol |
Third line after morphine and codeine
Only for patients with swallowing difficulties
Capsules more cost effective
|
15.01.04.03 |
Tramadol |
Hospital only |
02.11 |
Tranexamic Acid |
|
02.11 |
Tranexamic Acid |
Palliative use only |
21 |
Tranexamic acid |
- The risk of bleeding can be affected by other factors such as the presence of fungating or infected wounds. Smaller bleeds can be palliated using topical tranexamic acid.
|
02.11 |
Tranexamic acid 5% mouthwash |
|
02.11 |
Tranexamic Acid Injection |
Injection (Secondary Care only) |
12.03.04 |
Tranexamic Acid Mouthwash |
Hospital use only |
08.01.05 |
Trastuzumab Herceptin® |
Funding may be available from cancer drug fund
Hospital only
In line with NICE |
08.01.05 |
Trastuzumab Enhertu® |
Hospital Trust use only
Use in line with NICE |
08.01.05 |
Trastuzumab emtansine Kadcyla® |
In line with NICE |
04.03.01 |
Trazodone |
Tablets
Capsules
SF Liquid |
03.04 |
Tree pollen extract Pollinex Trees ® |
|
03.04 |
Tree pollen extract Pollinex trees ® |
|
08.01.01 |
Treosulfan |
In line with NICE
Commissioned by NHSE Injection-hospital only |
10.01.02.02 |
Triamcinolone Acetonide |
|
13.14.07 |
Triamcinolone acetonide 0.1% w/w in Orabase® |
|
13.14.07 |
Trichloroacetic acid 90% w/v |
|
06.04.01.01 |
Tridestra® |
|
09.08.01 |
Trientine Dihydrochloride |
For specialist initiation only. For use in Wilson's disease in patients intolerant of penicillamine. |
04.02.01 |
Trifluoperazine |
tablets SF solution Supported by ESCA |
11.03.03 |
Trifluorothymidine |
|
08.01.03 |
Trifluridine-tipiracil Lonsurf® |
£££££
In line with NICE
Hospital only
NHSE commissioned |
04.02.03 |
Trihexyphenidyl |
|
04.09.02 |
Trihexyphenidyl |
Tablets |
05.01.08 |
Trimethoprim |
|
05.01.08 |
Trimethoprim |
|
05.01.13 |
Trimethoprim |
Second choice in UTI |
13.06.02 |
Trimethoprim |
Off label use-specialist initiation. |
13.04 |
Trimovate® |
Potency: moderate
Restricted to use in inflammatory conditions associated with an infection with confirmed susceptibility to the antimicrobial component
Use for short periods - typically no more than one week |
06.07 |
TRIPTORELIN |
|
06.07 |
TRIPTORELIN |
|
06.07.02 |
Triptorelin Decapeptyl SR® |
|
06.07.02 |
Triptorelin Salvacyl® |
|
08.03.04.02 |
Triptorelin Decapeptyl® SR |
Accepted on formulary January 2017 following new drug application
Cost-effective alternative to current formulary options and a longer administration interval |
06.04 |
Trisequens ® |
|
09.08.02 |
Trometamol 7% |
NHSE commissioned |
11.05 |
Tropicamide Mydriacyl® |
Hospital only |
11.05 |
Tropicamide Single Use Minims® Tropicamide |
Hospital only |
07.04.02 |
Trospium Regurin® XL |
For patients over 65 years of age |
07.04.02 |
Trospium |
For patients over 65 years old |
04.03.04 |
Tryptophan |
Hospital use only |
A5.08.03 |
Tubegauz® |
PODIATRY USE ONLY-NOT PRESCRIBABLE ON NHS Surgical stockinette 100% cotton Type of wound product is suitable for PODIATRY ONLY for digital dressings Duration dressing remains on wound before changing As required Frequency of dressing change As required Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) None listed Rationale for inclusion in formulary Only product that has finger and toe sizes in 100% cotton |
14.04 |
Tuberculin PPD injection |
|
08.01.05 |
Tucatinib Tukysa® |
In line with NICE |
14.04 |
Typhoid and Hepatitis A ViATIM® |
|
14.04 |
Typhoid Live Oral vaccine Vivotif® |
|
09.04 |
TYR Anamix® Infant |
- A supplement without tyrosine and phenylalanine for infants with tyrosinaemia
- The only infant amino acid supplement without tyrosine and phenylalanine for infants with tyrosinaemia
- Nutritional supplement for the dietary management of proven tyrosinaemia where plasma-methionine concentrations are normal in children from birth to 3 years
|
09.04 |
TYR Anamix® Junior |
- A supplement without tyrosine and phenylalanine for children with tyrosinaemia
- An unthickened powdered amino acid supplement without tyrosine and phenylalanine for children aged 1 to 10y with tyrosinaemia
- Nutritional supplement for the dietary management of proven tyrosinaemia in children 1–10 years
|
09.04 |
TYR Anamix® Junior LQ |
- A supplement without tyrosine and phenylalanine for children with tyrosinaemia
- A liquid amino acid supplement without tyrosine and phenylalanine for children aged 1 to 10y with tyrosinaemia. Ready to use. Can be delivered via a tube
- Nutritional supplement for the dietary management of tyrosinaemia type 1 (when nitisinone (NTBC) is used, see "nitisinone"), type II, and type III, in children over 1 year
|
09.04 |
TYR cooler® 10 |
- A supplement without tyrosine and phenylalanine for children and adults with tyrosinaemia
- An oral liquid amino acid supplement without tyrosine and phenylalanine formulated for children aged 3 to 6 years with tyrosinaemia. Larger pouches are unacceptable for this age group of children and provide in excess of protein requirements. The 2 different products have a different degree of sweetness and range of flavours
- Nutritional supplement for the dietary management of tyrosinaemia in children over 3 years and adults
|
09.04 |
TYR cooler® 15 |
- A supplement without tyrosine and phenylalanine for teenagers and adults with tyrosinaemia
- One of two oral liquid amino acid supplements without tyrosine and phenylalanine for children aged 7 to 12 years with tyrosinaemia. Larger pouches are unacceptable for this age group of children and provide in excess of protein requirements
- Nutritional supplement for the dietary management of tyrosinaemia in children over 3 years and adults
|
09.04 |
TYR cooler® 20 |
- A supplement without tyrosine and phenylalanine for teenagers and adults with tyrosinaemia
- One of 2 liquid amino acid supplements without tyrosine and phenylalanine for teenagers and adults (>12 years of age) with tyrosinaemia that will meet their higher amino acid requirements. This age group needs the larger sachets (20g protein equivalent) to meet their non-tyrosine/phenylalanine protein requirements. It is important we have a choice of more than 1 product for this age group as compliance is poor. The 2 different products have a different degree of sweetness and range of flavours
|
09.04 |
TYR express15® |
- A supplement without tyrosine and phenylalanine for teenagers and adults with tyrosinaemia
- The only powdered amino acid supplement without tyrosine and phenylalanine for 7 to 12-year olds with tyrosinaemia. Larger sachets are unacceptable for this age group of children and provide in excess of protein requirements
- Nutritional supplement for the dietary management of tyrosinaemia in children over 8 years and adults
|
09.04 |
TYR express20® |
- A supplement without tyrosine and phenylalanine for teenagers and adults with tyrosinaemia
- One of 2 powdered amino acid supplements without tyrosine phenylalanine for teenagers and adults with phenylketonuria that will meet their higher amino acid requirements. This age group need the larger sachets (20g protein equivalent) to meet their non-tyrosine/phenylalanine protein requirements. It is important we have a choice of more than 1 product for this age group as compliance is poor. The 2 different products have a different degree of sweetness and range of flavours
- Nutritional supplement for the dietary management of tyrosinaemia in children over 8 years
|
09.04 |
TYR Gel® |
- A supplement without tyrosine and phenylalanine for teenagers with tyrosinaemia
- The only weaning (thickened) amino acid supplement without tyrosine and phenylalanine for infants/young children with tyrosinaemia
- Nutritional supplement for the dietary management of tyrosinaemia in children 1–10 years
|
09.04 |
TYR Lophlex® LQ 20 |
- A supplement without tyrosine and phenylalanine for teenagers with tyrosinaemia
- One of 2 liquid amino acid supplements without tyrosine and phenylalanine for teenagers and adults (>12 years of age) with tyrosinaemia that will meet their higher amino acid requirements. This age group need the larger sachets (20g protein equivalent) to meet their non-tyrosine/phenylalanine protein requirements. It is important we have a choice of more than 1 product for this age group as compliance is reported to be poor. different products have a different degree of sweetness and range of flavours
- Nutritional supplement for the dietary management of tyrosinaemia in children over 3 years and adults
|
09.04 |
UCD Amino5 |
- Essential amino acid supplement for use in urea cycle disorders
- Essential amino acid supplement for use in urea cycle disorders and the cerebral creatine deficiency syndrome: guanidinoacetate methyltransferase (GAMT) deficiency. The only pre-measured sachet of essential amino acids without vitamins and minerals (designed for tube feeding) for the treatment of urea cycle disorders. This is particularly important as most of our families with urea cycle disorders do not speak English as their first language so require pre-measured products. Unmeasured use of essential amino acid supplements in UCD could lead to hyperammonaemia, acute brain encephalopathy and ITU admission. The dose and frequency of administration will be determined by the specialist dietitian
|
A5.05.03 |
UCS® Debridement |
Single use pre- moistened cloth for wound debridement. Can be used to remove hyperkeratosis.
Type of wound product is suitable for
All acute and chronic wounds including pressure ulcers, leg ulcers, diabetic foot ulcers.
Hyperkeratosis
Duration dressing remains on wound before changing Not applicable
Frequency of dressing change At each dressing change or as required
Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Heavy slough and necrotic tissue may require autolytic debridement to soften prior to use Thick hyperkeratosis may take more than one treatment
Rationale for inclusion in formulary Lifts wound debris, superficial slough and exudate, without inhibiting granulation tissue formation Compatible with subsequent use of any type of dressing. Lifts hyperkeratosis and dry flaking skin to peri-wound Convenient, pre- moistened, easy to use, disposable single use cloth
|
07.03.05 |
Ulipristal EllaOne® |
Can be used up to 5 days post-coitus For use where copper IUD not preferred/tolerated |
03.01.02 |
Umeclidinium Incruse® Ellipta® |
How to use an Ellipta Inhaler
|
03.01.04 |
Umeclidinium & vilanterol Anoro Ellipta® |
How to use an Ellipta Inhaler
|
01.07.02 |
Uniroid HC® |
Contains the same ingredients as Proctosedyl® but is much more cost effective |
10.01.03 |
Upadacitinib Rinvoq® |
In line with NICE
Providers are NHS Hospital Trusts
|
01.03 |
Urea |
|
A5.08.08 |
Urgo K4 range® |
Preferred local option Multi layer compression system Type of wound product is suitable for Venous and mixed aetiology leg ulcers and associated conditions Duration dressing remains on wound before changing 1 to 7 days Frequency of dressing change Daily up to weekly dependant on exudate and oedema management. Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Not recommended for patients with a ABPI of less than 0.8 Contains latex Kit size determined by measuring the ankle after padding with the tape measure pulled taught Rationale for inclusion in formulary Compression system consisting of K-Soft , K-Lite, K-Plus or K-ThreeC (dependent on ankle size) and Ko-Flex Component bandages available in longer lengths for larger limbs |
A5.02.04 |
UrgoClean® Dressings |
Type of wound product is suitable for
All non-infected sloughy wounds including diabetic foot ulcers, burns, leg and pressure ulcers
Duration dressing remains on wound before changing
UrgoClean Pad should be changed every 1 to 2 days during the wound desloughing phase, then as often as required (up to 7 days) depending on the level of exudate and the clinical condition of the wound
Frequency of dressing change
Can be left in place for up to 7 days
Caution/Contraindiciations (when not to use the dressing, patient groups to avoid etc.)
Do not use if there is a known sensitivity to UrgoClean
Do not use Urgoclean as a surgical sponge for heavily bleeding wounds
Rational for inclusion to formulary
No other comparable dressing available
|
A5.08.08 |
UrgoKTwo® |
Two layer bandage system consisting of elastic and inelastic components that provide a sustained graduated compression,. Also available in UrgoKTwo reduced compression. Type of wound product is suitable for Treatment of venous leg ulcers, venous oedema and lymphoedema Duration dressing remains on wound before changing 1 to 7 days Frequency of dressing change Daily up to weekly dependant on exudate and oedema management. Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Arterial disease Diabetic Microangiplathy Ischaemic Phlebitis Septic thrombosis Allergy to any components in particular latex (available in latex free ) Rationale for inclusion in formulary Two layer compression kit. Essential for treating venous leg ulceration 2 layer less bulky for community use and enabling patients to wear foot wear Available in latex free option and reduced compression option |
A5.03.03 |
UrgoSorb Silver range |
Specialist recommendation only Alginate and hydrocolloid dressings containing silver Type of wound product is suitable for Management of moderate to heavily exuding wounds that are clinically infected. Absorbs and gels on contact with wound exudate which facilitates debridement of devitalised tissue. Dressing has haemostatic properties Duration dressing remains on wound before changing 1-3 days dependent on exudate levels Frequency of dressing change 1-3 days dependent on exudate levels Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Known sensitivity to any of the dressing components Contraindicated in 3rd degree burns, dry necrotic eschar Low exudate or dry wounds Removal on those undergoing MRI scans Avoid contact with electrodes or conductive gels during electronic measurement procedures Rationale for inclusion in formulary Can be used for moderate to heavily exuding clinically infected wounds Can be used for debriding sloughy and wet necrotic wounds Haemostatic |
A5.02.06 |
UrgoSorb® range |
Specialist recommendation only Type of wound product is suitable for Management of moderate to heavily exuding wounds. Absorbs and gels on contact with wound exudate which facilitates debridement of devitalised tissue. Dressing has haemostatic properties Duration dressing remains on wound before changing 1-7 days dependent on exudate levels Frequency of dressing change 1-7 days dependent on exudate levels Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Known sensitivity to any of the dressing components Contraindicated in 3rd degree burns, dry necrotic eschar Low exudate or dry wounds Rationale for inclusion in formulary Can be used for moderate to heavily exuding wounds Can be used for debriding sloughy and wet necrotic wounds Haemostatic |
A5.04.01 |
UrgoSTART ® Plus Border/UrgoSTART® Plus Pad range |
A polyabsorbent fibre pad containing a protease inhibitor (TLC-NOSF Healing Matrix), polyabsorbent fibres, a superabsorbent layer and a silicone border with waterproof backing.
Type of wound product is suitable for
All stages (from desloughing to complete healing) of exuding wounds including leg ulcers, diabetic foot ulcers, pressure ulcers, and long-standing acute wounds.
Duration dressing remains on wound before changing
Up to 7 days (recommended to change dressing every 1-2 days at initiation).
Frequency of dressing change
3-7 days
Wounds with high exudate levels may need changing more frequently and may need a secondary dressing.
Caution/contraindications (when not to use the dressing, patient groups to avoid etc.)
Not to be used on infected wounds
Rationale for inclusion in formulary
Cheaper than UrgoStart/UrgoClean combination
Easy to Use
Well tolerated
Positive outcomes on long-standing wounds |
A5.02.03 |
UrgoTul |
A non-adherent flexible wound contact layer containing TLC Healing Matrix. Type of wound product is suitable for Non to low exuding wounds, dermabrasions, traumatic, superficial, blistering. Can be used as a contact layer in cavity wounds with secondary absorbent dressing. Difficult to dress areas – fingers and toes. Duration dressing remains on wound before changing Up to 7 days Frequency of dressing change Depends on clinical needs up to 7 days Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Known sensitivity to any components Rationale for inclusion in formulary Pain free dressing changes. Promotes healing, interactive. Cost effective. Large range of sizes available |
06.01.06 |
Urinalysis Glucose strips Medi-Test Glucose® |
|
06.01.06 |
Urinalysis test strips Diastix® |
|
06.01.06 |
Urine Protein strips Albustix® |
in Primary Care
Secondary care to discuss with Pathology |
06.01.06 |
Urine Protein strips Medi Test Protein 2® |
|
02.10 |
Urokinase |
Hospital only |
01.09 |
Ursodeoxycholic acid |
For specialist initiation only |
01.05 |
Ustekinumab Stelara® |
In line with NICE
Hospital use only |
13.05.03 |
Ustekinumab |
Initiated by hospital consultant only and in line with NICE
For treating moderate to severe psoriasis |
A5.06.01 |
V.A.C. products |
Preferred local option Specialist recommendation only The use of sub atmospheric pressure to promote or assist wound healing or to remove fluids from a site. Required components: Pump, Dressings foam or gauze, tubing and canister. Type of wound product is suitable for Acute, chronic and traumatic wounds. Can be used as a adjunct to surgery and for salvage procedures such as wound dehiscence. Benefits are that it removes excess fluid that may contain bacterial pathogens, reduces soft tissue oedema, promotes granulation and provides a moist wound healing environment. Consider standard interactive dressings first. Duration dressing remains on wound before changing Every three days Frequency of dressing change Determined by exudate levels. Different canister sizes available Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) It should not be used on: Grossly infected or bleeding wounds Malignancy Exposed blood vessels Organs Unexplored fistulae Extensive necrotic wounds Caution with foam, document the number inserted, ensure all pieces are retrieved. Rationale for inclusion in formulary It removes excess fluid that may contain bacterial pathogens, reduces soft tissue oedema, promotes granulation and provides a moist wound healing environment. Both companies products are included due to different contracting arrangements. Can be used on large open wounds to increase speed of wound healing |
07.04.05 |
Vacuum pumps |
Avaiable in line with SLS criteria
If use not in line with SLS criteria Use device with lowest acquisition cost
|
05.03.02.01 |
Valaciclovir |
To be used in exceptional cases only
Least cost effective option
Second line for shingles if compliance is a problem
£££££ |
05.03.02.02 |
Valganciclovir |
|
09.04 |
Valine 1000® |
- Used as an inpatient only
- Used at the time of diagnosis when on haemofiltration and a valine supplement is necessary
|
09.04 |
Valine50® |
- To correct valine deficiency in MSUD
- The only pre-measured sachet of valine that provides 50 mg/dose to correct valine deficiency in MSUD. A pre-measured sachet is particularly important as most of our families with MSUD do not speak English as their first language so require pre-measured products. The dose and frequency of administration will be determined by the specialist dietitian
- Nutritional supplement for the dietary management of inborn errors of amino acid metabolism in adults and children from birth
|
04.02.03 |
Valproic Acid Depakote® |
Use in men and women of non-child bearing potential
Use in women and girls of childbearing potential (all indications). ESCA link below
Contrindiciated in women of childbearing potential unless part of the Pregnancy Prevention Programme. See MHRA guidance |
02.05.05.02 |
Valsartan |
|
05.01.07 |
Vancomycin |
|
05.01.07 |
Vancomycin |
|
04.10.02 |
Varenicline Champix® |
|
14.04 |
Varicella Zoster vaccine Zostavax® |
|
14.05.02 |
Varicella-Zoster immunoglobulin |
|
01.09 |
Vasopressin Pitressin® |
|
06.05 |
VASOPRESSIN |
Argipressin - Red
Pitressin - Red |
01.05.03 |
Vedolizumab Entyvio® |
Specialist use only in line with NICE guidance below |
09.08.01 |
Velaglucerase alfa Vpriv® |
NHSE commissioned |
08.01.05 |
Vemurafenib Zelboraf® |
In line with NICE |
08.01.05 |
Venetoclax Venclyxto® |
In line with NICE
Providers are NHS hospital trusts |
04.03.04 |
Venlafaxine |
1st choice = Vensir XL capsules (suggest switching generic prescriptions to this agent) 2nd choice = Venlalic XL tablets |
04.03.04 |
Venlafaxine |
|
02.06.02 |
Verapamil |
Brand prescribe modified release preparations
Follow Optimise Rx advice for new initations
|
11.08.02 |
Verteporfin Visudyne® |
|
04.08.01 |
Vigabatrin |
On specialist advice with an ESCA |
08.01.04 |
Vinblastine Sulphate |
Commissioned by NHSE
Hospital only |
08.01.04 |
Vincristine Sulphate |
Commissioned by NHSE
Hospital only |
08.01.04 |
Vinorelbine |
Commissioned by NHSE Injection-hospital only |
A5.08.09 |
Viscopaste |
Preferred local option Specialist recommendation only Zinc paste bandage. Type of wound product is suitable for Venous leg ulcers. Where venous insufficiency exists, the paste bandage should be used under graduated compression bandaging. Chronic eczema Dermatitis Duration dressing remains on wound before changing Up to 7 days Frequency of dressing change Daily, up to weekly dependant on skin and wound management. Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Do not use in any cases of sensitivity or allergy to ingredients Rationale for inclusion in formulary For treatment of dermatitis and chronic eczema when venous insufficiency is present |
19.49 |
Viscopaste PB7® |
Zinc Paste Bandage has been used with compression bandaging for the treatment of venous leg ulcers. However, paste bandages are associated with hypersensitivity reactions and should be used with caution. |
11.08.01 |
Viscotears eye drops |
|
11.08.01 |
Viscotears Liquid gel single dose units |
|
09.04.02 |
Vital 1.5kcal |
- 200ml size only - for larger volumes use Nutrison Peptisorb Plus HEHP
- 1.5 kcal/mL and 5g (or more) protein/100 mL
- Hydrolysate nutritionally complete in 1 litre
- Standard ACBS indications: Disease-related malnutrition, intractable malabsorption, pre-operative preparation of malnourished patients, dysphagia, proven inflammatory bowel disease, following total gastrectomy, short-bowel syndrome, bowel fistula; except proven inflammatory bowel disease and following total gastrectomy; not recommended for use in children
|
09.06.01 |
Vitamin A |
Paediatric directorate only |
09.06.01 |
Vitamin A 150,000 units |
|
09.06.07 |
Vitamin and mineral supplements Forceval Soluble®and Forceval® |
Specialist recommendation Forceval soluble®-check availability
- Please prescribe as per Chapter 9
- Vitamin and mineral deficiency and as adjunct in synthetic diets
|
09.06.02 |
Vitamin B Tablets, Compound Strong |
Refeeding Syndrome only |
09.06.05 |
Vitamin E Suspension 100mg/ml |
Specialist recommendation
Alpha tocopheryl acetate oral suspension 100mg/ml
£££££ |
09.06.01 |
Vitamins A and D |
Specialist recommendation |
09.04 |
Vitasavoury |
- Protein, fat, and carbohydrate
- Taste fatigue to sweet products
- Disease-related malnutrition, malabsorption states, or other conditions requiring fortification with a high fat or carbohydrate (with protein) supplement
- Not suitable for child under 3 years
|
02.12 |
Volanesorsen |
|
05.02.01 |
Voriconazole |
|
04.03.03 |
Vortioxetine |
In line with NICE Specialist initiation and stabilisation before transfer to Primary Care |
02.08 |
Warfarin |
Sandwell place
Process for continuing prescribing oral anticoagulants in Primary care-Sandwell only |
03.04.02 |
Wasp venom extract |
|
09.02.02.01 |
Water for injections |
|
13.02.01 |
White Soft Paraffin BP |
Most greasy
Over the counter preparation suitable for self-care/purchase if appropriate |
09.04 |
Wysoy® |
- Specialised formulas: Infant and child: Soya-based formula
- Essential for galactosaemia. The only completely lactose free formula, soya based formula suitable for these infants, recommended in international galactosaemia guidelines for feeding infants. The dose and type of product should always be advised by the specialist dietitian according to the needs of the patient
- Proven lactose and associated sucrose intolerance in pre-school children, galactokinase deficiency, galactosaemia, and proven whole cows' milk sensitivity
|
11.08.01 |
Xailin gel |
|
11.08.01 |
Xailin Night® |
|
A5.05.01 |
Xupad range |
Preferred local option Latex free absorbent dressing pad Type of wound product is suitable for Low exuding closed surgical wounds only Duration dressing remains on wound before changing 1 – 7 days depending on exudate Frequency of dressing change 1 – 7 days depending on exudate Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Not for moderate or highly exuding wounds. Always consider an interactive dressing. Not suitable for any wound type except for closed surgical wounds Rationale for inclusion in formulary Cost effective Various sizes available |
12.02.02 |
Xylometazoline |
Short Term Use Only
Do not exceed 7 days treatment. Rebound congestion may occur on withdrawal. Maximum of 5 days in children aged 6-12 years. Do not use in children under 6 years. |
05.03.04 |
Zanamivir Relenza® |
For Primary Care-Green only during Flu season and on authorisation by NHS England/Department of Health & Social Care or via commissioned service for out of season supply |
05.03.04 |
Zanamivir Injection Dectova ® |
|
13.02.01.01 |
ZeroAQS |
SLS free
Over the counter preparation suitable for self-care/purchase if appropriate |
13.02.01 |
ZeroAQS ® |
Least greasy option Use as a soap substitute in eczema, not emollient
Over the counter preparation suitable for self-care/purchase if appropriate |
A5.13 |
ZeroAQS cream |
Preferred local option Emollient cream that occludes and moisturises the skin. Type of wound product is suitable for For external application for use as an emollient and as a skin cleanser/soap substitute in the management for dry skin conditions. Frequency of use Daily or more frequently if required Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Allergy or hypersensitivity to any of the ingredients Rationale for inclusion in formulary Dermatology approved Does not contain sodium lauryl sulphate (SLS) |
A5.13 |
Zerobase |
Preferred local option Emollient cream containing liquid paraffin, to moisturise dry or chapped skin Type of wound product is suitable for Symptomatic treatment of dry or chapped skin Can be used as a pre bathing emollient for dry skin to alleviate drying effects Frequency of use Daily or more frequently if required Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Allergy or hypersensitivity to any of the ingredients Rationale for inclusion in formulary Dermatology approved |
13.02.01 |
Zerobase® |
Least greasy
Preferred alternative to Diprobase |
A5.13 |
Zerocream |
Preferred local option Emollient cream containing liquid paraffin and soft white paraffin, to moisturise dry skin Type of wound product is suitable for Symptomatic treatment of flaking, dry skin, sunburn, dry eczema and dry cases of psoriasis Frequency of use Daily or more frequently if required Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Allergy or hypersensitivity to any of the ingredients Rationale for inclusion in formulary Dermatology approved |
13.02.01 |
Zerocream® |
More greasy Preferred alternative to E45 cream |
13.02.01 |
Zeroderm Ointment |
CCG preffered alternative to Epaderm and Hydromol |
A5.13 |
Zeroderm ointment |
Preferred local option Emollient ointment containing liquid paraffin and white soft paraffin to assist the skin in retaining moisture Type of wound product is suitable for For use on all dry skin conditions including eczema and psoriasis Can be used as a soap substitute/skin cleanser Frequency of use Daily or more frequently if required Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Allergy or hypersensitivity to any of the ingredients Rationale for inclusion in formulary Treatment of dry skin conditions. Dermatology approved Free from fragrance and colours, sodium lauryl sulphate, additives and preservatives |
A5.13 |
Zeroguent |
Preferred local option Rich emollient cream containing light liquid paraffin, white soft paraffin and soya bean oil To assist the skin in retaining moisture Type of wound product is suitable for For use as a barrier and moisturiser for symptomatic treatment of dermatitis, ichthyosis, eczema and psoriasis Can be used as a pre bathing emollient for dry skin to alleviate drying effects Frequency of use Daily or more frequently if required Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Allergy or hypersensitivity to any of the ingredients Rationale for inclusion in formulary Dermatology approved |
13.02.01 |
Zeroguent® |
More greasy Preferred alternative to Unguentum M |
19.05 |
Zetuvit®E |
Absorbent cellulose pad with fluid repellent backing
*only sterile to be used for wound care*
Type of wound product is suitable for
Moderate exuding wounds . Secondary dressing.
Available in non sterile and sterile.
Duration dressing remains on wound before changing
1-7 days
Frequency of dressing change
Usually 1-2 days or when wet. If using daily consider Zetuvit® Plus
Caution/contraindications (when not to use the dressing, patient groups to avoid etc.)
Known product or component sensitivity
Do not cut or tear
Rationale for inclusion in formulary
Required for absorbency, for moderately exuding wounds
Step down from Zetuvit® Plus |
19.05 |
Zetuvit®Plus |
Super absorbent dressing
Type of wound product is suitable for
Moderate to heavily exuding acute and chronic wounds. Secondary dressing only
Duration dressing remains on wound before changing
1-7 days
Frequency of dressing change
1-3 days, if changing daily, review if needs more highly absorbent dressing, if lasting 7
days step down to Zetuvit®E
Caution/contraindications (when not to use the dressing, patient groups to avoid etc.)
Do not use if sensitivity to dressing or components
Do not cut or tear
Rationale for inclusion in formulary
Moderate to heavily exuding wounds, higher absorbency than Zetuvit®E. Cost effective. |
A5.01.02 |
Zetuvit® E sterile: 10x10cm, 10x20cm, 20x20cm, 20x40cm non sterile: 10x10cm, 10x20cm, 20x20cm, 20x40cm |
Preferred local option Absorbent cellulose pad with fluid repellent backing *Only STERILE to be used for wound care* Type of wound product is suitable for Moderate exuding wounds . Secondary dressing. Available in non sterile and sterile. Duration dressing remains on wound before changing 1-7 days Frequency of dressing change Usually 1-2 days or when wet. If using daily consider Zetuvit® Plus Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Known product or component sensitivity Do not cut or tear Rationale for inclusion in formulary Required for absorbency, for moderately exuding wounds Step down from Zetuvit® Plus |
A5.01.02 |
Zetuvit® Plus |
Preferred local option Super absorbent dressing Type of wound product is suitable for Moderate to heavily exuding acute and chronic wounds. Secondary dressing only Duration dressing remains on wound before changing 1-7 days Frequency of dressing change 1-3 days, if changing daily, review if needs more highly absorbent dressing, if lasting 7 days step down to Zetuvit®E Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Do not use if sensitivity to dressing or components Do not cut or tear Rationale for inclusion in formulary Moderate to heavily exuding wounds, higher absorbency than Zetuvit®E. Cost effective. |
05.03.01 |
Zidovudine Retrovir® |
|
05.03.01 |
Zidovudine |
|
05.03.01 |
Zidovudine and Lamivudine |
|
13.14.06 |
Zinc & salicylic acid paste (Lassar’s paste) half-strength |
|
13.02.02 |
Zinc and Caster Oil Ointment BP |
Over the counter preparation suitable for self-care/purchase if appropriate |
A5.15 |
Zinc and castor oil ointment |
Barrier cream Type of wound product is suitable for For relief of the symptoms of nappy rash and as a protective water resistant cream for dry, chapped skin Frequency of use As required, up to four times daily or at each nappy change. Caution/contraindications (when not to use the dressing, patient groups to avoid etc.) Not to be used on adults in conjunction with containment products for incontinence due to the inclusion of peanut oil in the ingredients, which will repel urine/faeces back onto the skin. Any allergy to the listed ingredients May mask x-ray images Rationale for inclusion in formulary Dermatology approved |
09.05.04 |
Zinc Sulphate Solvazinc® |
|
06.06 |
Zoledronic acid |
Red - Aclasta
Red - Zometa |
04.07.04.01 |
Zolmitriptan |
|
04.01.01 |
Zolpidem |
|
04.08.01 |
Zonisamide Zonegran® |
On specialist advice with an ESCA
MHRA Advice When prescribing for epilepsy the patient should be assessed to make a clinical judgement if the same manufacturer's product/brand is necessary taking into account factors such as seizure frequency and treatment history. Also take into account patient/carer related factors such as their negative perceptions about alternative products and/or other issues related to the patient such as co-morbid autism, mental health issues or learning disability |
04.01.01 |
Zopiclone |
Licensed for short-term use only (4 weeks). |
04.02.01 |
Zuclopenthixol |
Supported by ESCA |
04.02.02 |
Zuclopenthixol Decanoate |
The APC's view is that, on clinical grounds, the status of antipsychotic depot injections should be amber with a framework in place in Primary Care before transfer
HOWEVER, until the commissioning arrangements have been agreed to allow safe transfer of patient care, the status will remain RED |
06.04.01.01 |
Zumenon® |
|