Formulary Chapter 9: Nutrition and blood - Full Chapter
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09.01 |
Anaemias and some other blood disorders |
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09.01.01 |
Iron-deficiency anaemias |
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Ferrous fumarate
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Formulary
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Provider notes - NMUH:
- No restriction stated (not Galfer)
- RFL:
- RNOH:
- Oral syrup available as 140 mg/5mL
- UCLH:
- WH:
- Oral syrup available as 140 mg/5mL (ONLY formulation available)
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Ferrous gluconate
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Formulary
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Provider notes - NMUH:
- RFL:
- RNOH:
- UCLH:
- WH:
- Ferrous gluconate contains a lower content of elemental iron and therefore may be better tolerated than ferrous sulphate.
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Ferrous sulphate
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Formulary
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Provider notes - NMUH:
- RFL:
- RNOH:
- First choice for iron-deficiency anaemia
- UCLH:
- WH:
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Ferrous sulphate modified release
(Ferrograd®)
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Formulary
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Provider notes
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Sodium Feredetate
(Sytron®)
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Formulary
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Provider notes - NMUH:
- RFL:
- RNOH:
- UCLH:
- WH:
- Neonatal/paediatrics only
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09.01.01.01 |
Iron and folic acid |
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Ferrous fumarate + Folic acid
(Pregaday®)
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Formulary
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Provider notes
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09.01.01.01 |
Compound iron preparations |
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09.01.01.02 |
Parenteral iron |
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Ferric Carboxymaltose
(Ferinject®)
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Formulary

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See local guidance for iron replacement
Approved for:
- Iron deficient anaemia in Obstetrics (January 2017)
- Iron deficient anaemia in adult outpatients only, not in patients in first trimester of pregnancy or for patient on haemodialysis (March 2017)
Provider notes
- NMUH:
- To be used for day case patients and out patients ONLY
- See link below for parenteral irons prescribing guideline.
- Ferinject must be prescribed on the specific Daycase Ferinject prescription form; see link below
- Note: Parenteral iron is contraindicated in the first trimester of pregnancy. For dose of Ferinject in patients with haemodialysis dependent chronic kidney disease, refer to the summary of prouct characteristics.
- Check MHRA Drug Safety updates
- RFL:
- Approved for use in private patients at RFL
- Approved for use in renal and liver patients at RFH
- RNOH:
- For the optimisation of pre-operative anaemia in patients aged 14 to 17 years.
- UCLH:
- Restricted to outpatients / daycase / facilitate inpatient discharge
- WH:
- Parenteral iron should only be considered if oral therapy has failed due to lack of patient co-operation, severe gastrointestinal side effects, continuing severe blood loss or malabsorption. Provided oral therapy is taken reliably and is absorbed, then the haemoglobin response is not significantly faster with the parenteral route.
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NMUH: The Daycase Ferinject Prescription Form
NMUH: The Trust guidelines on use of parenteral irons for iron deficiency anaemia
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Ferric derisomaltose (previously iron isomaltoside)
(Monofer®)
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Formulary
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See local guidance for iron replacement
Provider notes
- NMUH:
- Check MHRA Drug Safety update
- RFL:
- First-choice of fast infusion product (excluding renal)
- Available to all patient groups at BH and CFH.
- Restricted to specific patient groups at RFH:
- For patients who would otherwise require multiple iron infusions, and there is a documented reason why multiple infusions would impact on patient’s quality of life
- For patients on 2NA in whom a shorter duration iron infusion is indicated, and there is documented reason why a longer infusion would impact on patient’s quality of life
- For patients in whom there is an URGENT need for IV iron e.g. patients planned for Theatre, or for pregnancy
- For patients on a cancer pathway to enable cancer treatment to proceed
- For patients with disabling anaemia who require urgent correction of Hb levels, based on clinical symptoms/clinical need (patient-specific need)
- For patients who have experienced serious / life-threatening allergies or adverse events to other IV iron products
- RNOH:
- For the optimisation of pre-operative anaemia in accordance with local guideline. Oral iron must be used where surgery is not urgent
- UCLH:
- WH:
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Iron Dextran
(CosmoFer®)
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Formulary
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See local guidance for iron replacement
Provider notes
- NMUH:
- See link below to access the Trust guidelines on use of parenteral irons for iron deficiency anaemia
- Check MHRA Drug Safety updates
- RFL:
- RNOH:
- UCLH:
- WH:
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NMUH: The Trust guidelines on use of parenteral irons for iron deficiency anaemia
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Iron Sucrose
(Venofer®)
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Formulary
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See local guidance for iron replacement
Provider notes
- NMUH:
- See Trust guidelines on use of parenteral irons for iron deficiency anaemia; link below
- Check MHRA Drug Safety updates
- RFL:
- Renal anaemia only - Venofer and Cosmofer are preferred choices
- RNOH:
- Preferred parenteral iron preparation for inpatients
- UCLH:
- WH:
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NMUH: The Trust guidelines on use of parenteral irons for iron deficiency anaemia
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09.01.02 |
Drugs used in megaloblastic anaemias |
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Cyanocobalamin
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Restricted
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Provider notes
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Folic Acid
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Formulary
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Provider notes
- NMUH:
- RFL:
- No restriction stated
- When used in combination with oral methotrexate various regimens are used from once-weekly, twice-weekly to daily use (except on day of methotrexate)
- RNOH:
- UCLH:
- WH:
- Folic acid is indicated in confirmed folate deficiency due to dietary lack, gastrointestinal disease, pregnancy, chronic haemolytic states, myeloproliferative disorders, haemodialysis, and parenteral nutrition, intensive care of the very sick patient or in premature infants. Folic acid can be used to correct serious haematological changes caused by dihydrofolate reductase inhibitors (DFRIs), after the DFRI has been discontinued. Examples of DFRIs include trimethoprim and co-trimoxazole.
- Before treating megaloblastic anaemia with folic acid alone, vitamin B12 deficiency MUST be excluded. Folic acid may relieve the haematological features of vitamin B12 deficiency and allow neuropathy to develop undetected. If treatment must be started immediately, both folic acid and hydroxocobalamin should be given.
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Hydroxocobalamin
(Vitamin B12)
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Formulary
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Provider notes
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09.01.03 |
Drugs used in hypoplastic, haemolytic, and renal anaemias |
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Eculizumab infusion
(Haemolytic uraemic syndrome)
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Formulary

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NOTE: There is more than one monograph for this medicine, click here to search for formulary status and its use for other indications.
Provider notes
- NMUH:
- RFL:
- RNOH:
- UCLH:
- WH:
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NICE HST1: Eculizumab for treating atypical haemolytic uraemic syndrome
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Hydroxycarbamide
(Sickle cell)
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Formulary
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NOTE: There is more than one monograph for this medicine, click here to search for formulary status and its use for other indications.
Provider notes
- NMUH:
- Hydroxycarbamide Suspension 50mg/5ml (100 ml) unlicensed preparation is also available
- RFL:
- Restricted to Haematology
- Not prescribed on Chemocare for this indication
- RNOH:
- UCLH:
- WH:
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Darbepoetin alfa
(Aranesp®)
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Restricted

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Provider notes
- NMUH:
- For continuation of supply for those renal patients that have been initiated on treatment by Royal Free Hospital.
- RFL:
- Restricted to Renal team – preferred brand of erythropoietin
- Restricted to Haematology for MDS
- RNOH:
- UCLH:
- WH:
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NICE TA323: Erythropoiesis‑stimulating agents during chemotherapy
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Epoetin alfa
(Eprex®)
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Restricted

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Provider notes
- NMUH:
- For anaemia associated with chronic renal failure only.
- Restricted to renal consultants signature and Dr. Tindall signature only.
- Please note that the CSM has advised that the subcutaneous route is contraindicated in chronic renal failure. Please use the IV route instead. The dialysis unit has changed over to NeoRecormon which is an IV preparation.
- RFL:
- Restricted to Renal team - for patients who cannot tolerate darbepoetin or established patients only
- RNOH:
- UCLH:
- WH:
- Epoetin is available for treatment anaemia of renal disease only
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NICE TA323: Erythropoiesis‑stimulating agents during chemotherapy
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Epoetin beta
(NeoRecormon®)
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Restricted

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Provider notes
- NMUH:
- Positive NICE TA This medicine has a positive NICE Technology Appraisal and is listed in the Trust Medicines Formulary when used in line with NICE recommendations and/or Local Trust Guidelines.
- Restricted to Renal and Haematology Consultants.
- See MHRA drug safety updates
- RFL:
- Restricted to Renal team - for patients who cannot tolerate darbepoetin or established patients only
- Restricted to Haematology for MDS
- RNOH:
- UCLH:
- WH:
- Epoetin is available for treatment anaemia of renal disease only
- Pre-filled syringe 2,000 units, 3,000 units, 4,000 units, 6,000 units, 10,000 units ONLY
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NICE TA323: Erythropoiesis‑stimulating agents during chemotherapy
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Methoxy Polyethylene Glycol-Epoetin Beta
(Mircera®)
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Restricted

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Provider notes
- NMUH:
- RFL:
- Restricted to renal team only - for patients who cannot tolerate darbepoetin or established patients only
- RNOH:
- UCLH:
- WH:
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09.01.03 |
Iron overload |
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Deferasirox
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Restricted

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Provider notes
- NMUH:
- RFL:
- Commissioned as per NHS England policy for haemoglobinopathies.
- Confirm with the commissioning team regarding other indications.
- RNOH:
- UCLH:
- WH:
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NHSE 16070/P: Treatment of iron overload for transfused and non transfused patients with chronic inherited anaemias
NMUH: The formulary awareness bulletin on defersirox (Exjade)
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Deferiprone
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Restricted

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Provider notes
- NMUH:
- To be prescribed by the Haematology Team ONLY.
- See links below
- RFL:
- Commissioned as per NHS England policy for haemoglobinopathies.
- Confirm with the commissioning team regarding other indications.
- RNOH:
- UCLH:
- WH:
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NHSE 16070/P: Treatment of iron overload for transfused and non transfused patients with chronic inherited anaemias
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Desferrioxamine Mesilate
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Restricted

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Provider notes
- NMUH:
- To be prescribed by the Haematology Team ONLY.
- See links below
- RFL:
- Commissioned as per NHS England policy for haemoglobinopathies.
- Confirm with the commissioning team regarding other indications.
- RNOH:
- UCLH:
- WH:
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NHSE 16070/P: Treatment of iron overload for transfused and non transfused patients with chronic inherited anaemias
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09.01.04 |
Drugs used in autoimmune thrombocytopenic purpura |
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Avatrombopag tabs
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Restricted

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See NICE TA for eligibility criteria
Provider notes
- NMUH:
- RFL:
- RNOH:
- UCLH:
- WH:
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NICE TA626: Avatrombopag for treating thrombocytopenia in people with chronic liver disease needing a planned invasive procedure
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Eltrombopag
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Restricted

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Provider notes
- NMUH:
- Positive NICE TA This medicine has a positive NICE Technology Appraisal and is listed in the Trust Medicines Formulary when used in line with NICE recommendations and/or Local Trust Guidelines see link below.
- RFL:
- As per NICE guidance and CCG policy
- RNOH:
- UCLH:
- WH:
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NICE TA293: Eltrombopag for treating chronic ITP
NICE TA382 (not recommended): Eltrombopag for treating severe aplastic anaemia refractory to immunosuppressive therapy (terminated appraisal)
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Lusutrombopag tabs
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Restricted

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See NICE TA for eligibility criteria
Provider notes
- NMUH:
- RFL:
- RNOH:
- UCLH:
- WH:
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NICE TA617: Lusutrombopag for treating thrombocytopenia in people with chronic liver disease needing a planned invasive procedure
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Romiplostim
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Restricted

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Provider notes
- NMUH:
- Positive NICE TA This medicine has a positive NICE Technology Appraisal and is listed in the Trust Medicines Formulary when used in line with NICE recommendations and/or Local Trust Guidelines.
- RFL:
- As per NICE guidance and CCG policy
- RNOH:
- UCLH:
- WH approvals:
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NICE TA221: Thrombocytopenic purpura - romiplostim
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09.01.06 |
Drugs used in neutropenia |
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Filgrastim
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Restricted

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Provider notes
- NMUH:
- Zarzio® is the preferred brand
- Check MHRA Drugs Safety Alerts
- See link below
- RFL:
- Accofil® is the preferred brand (from June 2019)
- RNOH:
- Requires HAEMATOLOGIST approval
- Store in a refrigerator
- UCLH:
- WH:
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NMUH: The Formulary Awareness Bulletin on filgrastim (Zarzio®)
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Lenograstim
(Granocyte®)
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Restricted

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Provider notes
- NMUH:
- Restricted for use in paediatric patients ONLY. For Adult patients, use filgrastim (Zarzio) first line.
- RFL:
- RNOH:
- UCLH:
- WH:
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Lipegfilgrastim
(Patients who cannot inject daily)
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Restricted

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NOTE: There is more than one monograph for this medicine, click here to search for formulary status and its use for other indications.
Alternative to GCSF + district nurse administration at WH only for patients who can receive daily GCSF but cannot self-inject (JFC August 2016)
Provider notes
- NMUH:
- RFL:
- RNOH:
- UCLH:
- WH:
- For use by oncology consultants only in patients unable to receive daily GCSF infections or needle phobic patients (D&TC Sept 2016)
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09.01.07 |
Drugs used to mobilise stem cells |
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09.02 |
Fluids and electrolytes |
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09.02.01 |
Oral preparations for fluid and electrolyte imbalance |
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09.02.01.01 |
Oral potassium |
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Potassium Chloride oral
(Kay-Cee-L®)
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Formulary
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Provider notes
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Potassium Chloride oral
(Sando-K®)
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Formulary
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Provider notes - NMUH:
- RFL:
- RNOH:
- UCLH:
- WH:
- Effervescent potassium is preferred to the modified release preparation as it is associated with less risk of oesophageal ulceration. Effervescent potassium can be administered via a nasogastric tube.
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Potassium Chloride oral
(Slow-K®)
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Formulary
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Provider notes - NMUH:
- RFL:
- RNOH:
- UCLH:
- WH:
- Effervescent potassium is preferred to the modified release preparation as it is associated with less risk of oesophageal ulceration. Effervescent potassium can be administered via a nasogastric tube.
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09.02.01.01 |
Potassium removal |
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Patiromer sorbitex calcium
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Restricted

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See NICE TA for eligibility criteria
Provider notes
- NMUH:
- RFL:
- RNOH:
- UCLH:
- WH:
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NICE TA623: Patiromer for treating hyperkalaemia
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Polystyrene Sulphonate Resins
(Calcium Resonium®)
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Formulary
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Provider notes - NMUH:
- The rectal route should be reserved for patients who are vomiting or have upper gastrointestinal tract problems, including paralytic ileus or it may be used simultaneously with the oral route for more rapid initial results.
- See BNF for instructions on administration. Please consult product literature for further information.
- RFL:
- RNOH:
- UCLH:
- WH:
- 'Calcium Resonium' exchanges potassium ions for calcium ions. It should be avoided in patients with hypercalcaemia, as it further raises calcium levels.
- Adult dose:
- Oral: 15 g PO 6 to 8 hourly in water (not fruit juice which has a high K+ content)
- Rectal: 30g once daily. Made by adding 30g of Calcium Resonium resin to 200ml Methylcellulose 1% solution. The retention enema is left in situ for 9 hours. Although rectal administration may be useful vomiting is a problem, the oral preparation may be preferred by some patients despite some nausea.
- In initial stages, Calcium Resonium may be given both rectally and orally to achieve a more rapid lowering of serum potassium. Administration should be stopped once potassium reaches 5.0 mmol/L. Onset of action is between 2 and 12 hours.
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Polystyrene Sulphonate Resins
(Resonium A®)
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Formulary
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Provider notes - NMUH:
- RFL:
- RNOH:
- UCLH:
- WH:
- 'Resonium A' exchanges potassium ions for sodium. It should be avoided in patients with congestive heart failure, water and salt overload, hypertension or where dietary sodium content is medically restricted.
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Sodium zirconium suspension
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Restricted

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See NICE TA for eligibility criteria
Provider notes
- NMUH:
- As per NICE TA599
- See Management of hyperkalaemia guideline
- RFL:
- RNOH:
- UCLH:
- WH:
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NICE TA599: Sodium zirconium cyclosilicate for treating hyperkalaemia
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09.02.01.02 |
Oral sodium and water |
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Sodium Chloride 30% oral
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Formulary
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Provider notes
- NMUH:
- RFL:
- RNOH:
- UCLH:
- WH:
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Sodium Chloride oral
(Slow Sodium®)
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Formulary
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Provider notes
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09.02.01.02 |
Oral rehydration therapy (ORT) |
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Oral Rehydration Salts
(Dioralyte®)
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Formulary
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Provider notes
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Oral Rehydration Salts
(Dioralyte® Relief)
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Formulary
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Provider notes
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Oral Rehydration Salts
(St. Marks’ Solution)
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Formulary
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Provider notes
- NMUH:
- St. Marks’ Solution is not kept at NMUH but all ingredients are available individually (i.e. sodium chloride, sodium bicarbonate and anhydrous glucose).
- RFL:
- St. Marks’ Solution is not kept at RFL but all ingredients are available individually (i.e. sodium chloride, sodium bicarbonate and anhydrous glucose).
- RNOH:
- UCLH:
- WH:
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Oral Rehydration Salts
(WHO Formulation)
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Formulary
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Provider notes
- NMUH:
- RFL:
- WHO Oral Rehydration Powder is not kept at RFL but all ingredients are available individually (i.e. sodium chloride, potassium chloride, sodium citrate and anhydrous glucose).
- RNOH:
- UCLH:
- WH:
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09.02.01.03 |
Oral bicarbonate |
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Sodium Bicarbonate oral
(Electrolyte imbalance)
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Formulary
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NOTE: There is more than one monograph for this medicine, click here to search for formulary status and its use for other indications. Provider notes - NMUH:
- Oral solution - unlicensed preparation, (5mmol / 5mL) also available for correction of acidosis in paediatric patients
- RFL:
- 500mg capsules and 1mmol/mL oral solution stocked
- RNOH:
- UCLH:
- WH:
- The use of sodium bicarbonate capsules is restricted to the Renal team only. Caps 500 mg containing approximately 6 mmol of Na+ and HCO3-
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09.02.02 |
Parenteral preparations for fluid and electrolyte imbalance |
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09.02.02.01 |
Electrolytes and water |
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09.02.02.01 |
Intravenous sodium |
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Ringer's Solution for Injection
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Restricted
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Provider notes
- NMUH:
- RFL:
- Only use if Hartmann’s is unavailable
- RNOH:
- UCLH:
- WH:
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Sodium Chloride + Glucose Intravenous Infusion
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Formulary
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Provider notes
- NMUH:
- RFL:
- RNOH:
- Sodium chloride 0.18% and glucose 4% (500 mL)
- Sodium chloride 0.45% and glucose 5% (500 mL)
- UCLH:
- WH:
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Sodium Chloride intravenous solutions
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Formulary
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Provider notes
- NMUH:
- RFL:
- RNOH:
- Sodium chloride 0.9% (10 mL, 100 mL, 250 mL, 500 mL and 1000 mL)
- Sodium chloride 0.45% (500 mL)
- Sodium chloride 2.7% (500 mL)
- UCLH:
- WH:
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09.02.02.01 |
Intravenous glucose |
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Glucose Intravenous
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Formulary
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Provider notes
- NMUH:
- RFL:
- RNOH:
- Glucose 5% (100 mL, 250 mL, 500 mL and 1000 mL)
- Glucose 10% (500 mL)
- Glucose 20% (500 mL)
- Glucose 50% (50 mL)
- Glucose 1% in compound sodium lactate (Hartmann's) (1000 mL)
- UCLH:
- WH:
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09.02.02.01 |
Intravenous potassium |
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Potassium Chloride + Glucose Intravenous Infusion
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Formulary
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Provider notes
- NMUH:
- RFL:
- Administer according to IV Potassium Policy
- RNOH:
- Potassium chloride 0.15% and glucose 5% (1000 mL)
- Potassium chloride 0.30% and glucose 5% (1000 mL)
- UCLH:
- WH:
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Potassium Chloride + Sodium Chloride + Glucose Intravenous Infusion
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Formulary
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Provider notes
- NMUH:
- RFL:
- Administer according to IV Potassium Policy
- RNOH:
- Potassium chloride 0.15%, sodium chloride 0.18% and glucose 4% (1000 mL)
- Potassium chloride 0.30%, sodium chloride 0.18% and glucose 4% (1000 mL)
- Potassium chloride 0.15%, sodium chloride 0.45% and glucose 5% (500 mL) - for use by ADU/Coxen and CHDU
- Potassium chloride 10mmol with sodium chloride 0.9% and glucose 5% is no longer available. An equivalent fluid can be prepared by adding 50 ml of 50% glucose to 500 mL potassium chloride 0.15% and sodium chloride 0.9%
- UCLH:
- WH:
- Infusion 500 ml (15 mmol Na+ and 10 mmol K+, 80 kcal)
- Infusion 1000 ml (30 mmol Na+ and 20 mmol K+, 160 kcal
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Potassium Chloride + Sodium Chloride Intravenous Infusion
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Formulary
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Provider notes
- NMUH:
- RFL:
- Administer according to IV Potassium Policy
- RNOH:
- Potassium chloride 0.15% and sodium chloride 0.9% (500 mL and 1000 mL)
- Potassium chloride 0.30% and sodium chloride 0.9% (500 mL and 1000 mL)
- Unlicensed: Potassium Chloride 3% in Sodium Chloride 0.9% Intravenous Infusion (40 mmol in 100 mL). Must be ordered and stored as a Controlled Drug. Restricted to ITU only.
- UCLH:
- WH:
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Potassium Chloride 15% Concentrate for Solution for Infusion
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Restricted
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Provider notes
- NMUH:
- RFL:
- Restricted to NICU and Renal Dialysis Wards (for addition to dialysis fluids bags only)
- Must be ordered and stored as a controlled drug.
- Administer according to IV Potassium Policy
- RNOH:
- Must be ordered and stored as a Controlled Drug. Restricted to ITU, Theatres and Recovery only
- UCLH:
- WH:
- The ready-made potassium solutions should cover most requirements and should be used in preference to the strong injection.
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Potassium Chloride 40mmol in 100ml Water For Injection
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Restricted
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Provider notes
- NMUH:
- Restricted to ICU
- Administer according to IV Potassium Policy
- RFL:
- Restricted to ICU and Cardiac Resuscitation Trolleys only
- Administer according to IV Potassium Policy
- RNOH:
- UCLH:
- WH:
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09.02.02.01 |
Bicarbonate and lactate |
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Compound Sodium Lactate (Hartmann's) Intravenous Infusion
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Formulary
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Provider notes
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Sodium Bicarbonate intravenous
(Electrolyte imbalance)
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Formulary
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Provider notes
- NMUH:
- RFL:
- 1.26%, 2.74%, 4.2% and 8.4% polyfusor 500mL
- RNOH:
- 8.4%: 10 mL, 100 mL and 200 mL Polyfusor
- UCLH:
- WH:
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Sodium Bicarbonate intravenous
(Min-I-Jet® Sodium Bicarbonate)
(Electrolyte imbalance)
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Formulary
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Provider notes
- NMUH:
- RFL:
- RNOH:
- UCLH:
- WH:
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Water for Injections
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Formulary
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Provider notes
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Water for Irrigation
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Formulary
|
Provider notes - NMUH:
- RFL:
- RNOH:
- Available as 500 mL and 1000 mL bottles or 1000 mL and 3000 mL bags
- UCLH:
- WH:
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09.02.02.02 |
Plasma and plasma substitutes |
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Albumin Solution
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Restricted
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Provider notes - NMUH:
- RFL:
- Available via the blood bank
- RNOH:
- UCH approvals:
- WH:
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09.02.02.02 |
Plasma substitutes |
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Gelatin intravenous infusion
(Gelaspan®)
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Formulary
|
Provider notes
- NMUH:
- RFL:
- BCF: No restriction stated
- RFH: Non-formulary
- RNOH:
- UCLH:
- WH:
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Gelatin intravenous infusion
(Gelofusine®)
|
Formulary
|
Provider notes
- NMUH:
- RFL:
- BCF: Non-formulary
- RFH: No restriction stated
- RNOH:
- UCLH:
- WH:
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Gelatin intravenous infusion
(Geloplasma®)
|
Formulary
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Provider notes
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Gelatin intravenous infusion
(Volplex®)
|
Formulary
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Provider notes
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Plasma-lyte 148
|
Restricted
|
Provider notes
- NMUH:
- RFL:
- RNOH:
- UCLH:
- WH:
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09.03 |
Intravenous nutrition |
|
|
Parenteral Nutrition (TPN or PN)
|
Formulary
|
Provider notes - RFL:
- Contact Nutrition team for advice
|
|
Supplementary Preparations
(Addiphos®)
|
Formulary
|
Provider notes
|
|
Supplementary Preparations
(Additrace®)
|
Formulary
|
Provider notes
|
|
Supplementary Preparations
(Cernevit®)
|
Formulary
|
Provider notes
|
|
Supplementary Preparations
(Peditrace®)
|
Formulary
|
Provider notes
|
|
Supplementary Preparations
(Solivito N®)
|
Formulary
|
Provider notes
|
|
Supplementary Preparations
(Vitlipid N®)
|
Formulary
|
Provider notes
|
|
09.03 |
Supplementary preparations |
|
|
|
09.04.01 |
Foods for special diets |
|
|
09.04.02 |
Enteral nutrition |
|
|
|
09.05.01 |
Calcium and magnesium |
|
|
09.05.01.01 |
Calcium supplements |
|
|
Calcium Carbonate
(Adcal®)
(Calcium supplement)
|
Formulary
|
NOTE: There is more than one monograph for this medicine, click here to search for formulary status and its use for other indications. Provider notes
|
|
Calcium carbonate
(Cacit®)
|
Formulary
|
Provider notes
- NMUH:
- RFL:
- RNOH:
- For patients requiring effervescent calcium carbonate
- UCLH:
- WH:
|
|
Calcium carbonate
(Calcichew®)
(Calcium supplement)
|
Formulary
|
NOTE: There is more than one monograph for this medicine, click here to search for formulary status and its use for other indications.
Provider notes
- NMUH:
- RFL:
- RNOH:
- UCLH:
- WH:
|
|
Calcium Chloride injection
|
Formulary
|
Provider notes
|
|
Calcium Gluconate 10% injection
|
Formulary
|
Provider notes
|
|
Calcium Gluconate effervescent tablets
|
Formulary
|
Provider notes
- NMUH:
- RFL:
- BCF: No restriction (historical)
- RFH: Non-formulary
- RNOH:
- UCLH:
- WH:
|
|
Sandocal-1000®
|
Formulary
|
Provider notes
- NMUH:
- RFL:
- RNOH:
- UCLH:
- WH:
|
|
09.05.01.02 |
Hypercalcaemia and hypercalciuria |
|
|
Cinacalcet
|
Restricted

|
Approved for complex primary hyperparathyroidism in adults in line with NHSE clinical commissioning policy (JFC April 2018)
Provider notes
- NMUH:
- This medicine has a positive NICE Technology Appraisal and is listed in the Trust Medicines Formulary when used in line with NICE recommendations and/or Local Trust Guidelines.
- For continuation of supply for those renal patients that have been initiated on treatment by Royal Free Hospital.
- Formulary for treatment of Hypercalcaemia of primary hyperparathyroidism or parathyroid carcinoma - see link below
- RFL:
- Restricted to ‘cinacalcet gatekeeper’ approval only for secondary hyperparathyroidism – see NICE TA.
- Restricted to endocrinology for complex primary hyperparathyroidism – see NHSE commissioning policy
- RNOH:
- WH:
- For primary hyperparathyroidism in line with NHSE policy 16034/P
- For secondary hyperparathyroidism in line with NICE TA 117
|
NHSE 16034/P: Cinacalcet for complex primary hyperparathyroidism in adults
NICE TA117: Hyperparathyroidism - cinacalcet
|
Etelcalcetide
|
Restricted
|
Provider notes
- NMUH:
- RFL:
- Restricted to ‘etelcalcetide gatekeeper’ approval only for secondary hyperparathyroidism – see NICE TA
- RNOH:
- UCLH:
- WH:
|
NICE TA448: Etelcalcetide for treating secondary hyperparathyroidism
|
Calcitriol injection
(Hyperparathyroidism)
|
Restricted

|
Provider notes
- NMUH:
- RFL:
- Approved for percutaneous injection into the parathyroid gland for hyperparathyroidism if intolerant or unresponsive to oral therapy (November 2013)
- RNOH:
- UCLH:
- WH:
|
|
09.05.01.03 |
Magnesium |
|
|
Magnesium Aspartate
(Magnaspartate®)
|
Formulary
|
Approved for magnesium deficiency (JFC March 2017)
Provider notes
- NMUH:
- See link below to access Trust Formulary bulletin on oral Magnesium Aspartate
- RFL:
- RNOH:
- For patients requiring enteral administration i.e. NG/PEG admin or with swallowing difficulties
- UCLH:
- WH:
- First line treatment for hypomagnesaemia (approved by NCL JCF Mar17). Magnesium glycerophosphate only for patients unable to tolerate magnesium aspartate.
|
NMUH: Trust Formulary bulletin on oral Magnesium Aspartate
|
Magnesium glycerophosphate 4mmol/tablet
|
Formulary
|
Provider notes - NMUH:
- RFL:
- RNOH:
- The BNF states that to prevent recurrence of hypomagnesaemia in adults, oral magnesium may be given in a dose of 24 mmol Mg2+ daily in divided doses. In children aged 1 month to 12 years, the BNF for children recommends that the initial dose of oral magnesium for hypomagnesaemia is 0.2 mmol/kg Mg2+ three times daily, with the dose adjusted as needed. In children aged 12 to 18 years, it recommends that the initial dose is 4 to 8 mmol Mg2+ three times daily, adjusted as needed.
- UCLH:
- WH:
- First line treatment for hypomagnesemia is magnesium aspartate. Magnesium glycerophosphate should only be used for patients unable to tolerate magnesium aspartate.
|
|
Magnesium Hydroxide Mixture BP
|
Formulary
|
NOTE: There is more than one monograph for this medicine, click here to search for formulary status and its use for other indications.
Provider notes
- NMUH:
- RFL:
- BCF: No restriction (historical)
- RFH: Non-formulary
- RNOH:
- UCLH:
- WH:
|
|
Magnesium sulfate injection
|
Restricted
|
Provider notes - NMUH:
- RFL:
- Only magnesium sulphate 50% injection stocked
- RNOH:
- UCLH:
- WH:
- The use of magnesium sulphate inj 10% & 20% are restricted to Obstetrics only.
|
|
Magnesium lactate modified-release
(MagTab®)
(Renal tubular disorders)
|
Unlicensed

|
Provider notes
- NMUH:
- RFL:
- Renal tubular disorders outpatients clinic only (RFL only; JFC September 2018)
- RNOH:
- UCLH:
- WH:
|
|
|
09.05.02.01 |
Phosphate supplements |
|
|
Phosphate Polyfusor®
|
Formulary
|
Provider notes
|
|
Phosphate supplements
(Phosphate-Sandoz®)
|
Formulary
|
Provider notes
|
|
Sodium dihydrogen phosphate oral solution
|
Unlicensed
|
Provider notes
- NMUH:
- For the treatment of hypophosphataemia or premature bone disease in paediatric patients. For further prescribing information, refer to the BNF for Children.
- RFL:
- For neonates & paediatrics
- RNOH:
- UCLH:
- WH:
|
|
09.05.02.02 |
Phosphate-binding agents |
|
|
Calcium acetate + Magnesium carbonate tabs
(Osvaren®)
|
Formulary
|
Provider notes
- NMUH:
- RFL:
- Restricted to renal patients only
- RNOH:
- UCLH:
- WH:
|
|
Calcium acetate tabs
(Phosex®)
|
Restricted
|
Provider notes
- NMUH:
- RFL:
- Restricted to renal patients only
- RNOH:
- UCLH:
- WH:
|
|
Calcium carbonate
(Adcal®)
(Phosphate binder)
|
Formulary
|
NOTE: There is more than one monograph for this medicine, click here to search for formulary status and its use for other indications.
Provider notes
- NMUH:
- RFL:
- RNOH:
- UCLH:
- WH:
|
|
Calcium carbonate
(Calcichew®)
(Phosphate binder)
|
Formulary
|
NOTE: There is more than one monograph for this medicine, click here to search for formulary status and its use for other indications.
Provider notes
- NMUH:
- Calcichew is available on the Formulary for the management of hyperphosphotaemia in renal patients
- RFL:
- RNOH:
- UCLH:
- WH:
|
|
Lanthanum
(Fosrenol ®)
|
Restricted
|
Provider notes - NMUH:
- RFL:
- Restricted to renal patients only
- RNOH:
- UCLH:
- WH:
|
|
Sevelamer carbonate
|
Formulary
|
Provider notes
- NMUH:
- RFL:
- Restricted to renal patients only
- RNOH:
- UCLH:
- WH:
|
|
Sevelamer hydrochloride
|
Restricted
|
Provider notes
- NMUH:
- RFL:
- Restricted to renal patients only - not preferred – use sevelamer carbonate preferentially
- RNOH:
- UCLH:
- WH:
|
|
|
Fluorides
(Duraphat® Toothpaste)
|
Restricted
|
Provider notes - NMUH:
- RFL:
- RNOH:
- UCLH:
- WH:
- 0.619% toothpaste available for Simmons House and Islington community clinics only
|
|
Fluorides
(En-De-Kay® Oral Drops)
|
Restricted
|
Provider notes - NMUH:
- RFL:
- RNOH:
- UCLH:
- WH:
- For Islington community only
|
|
Fluorides
(En-De-Kay® Tablet)
|
Formulary
|
Provider notes - NMUH:
- RFL:
- RNOH:
- UCLH:
- WH:
- For Islington Community Only - direct ward delivery
|
|
09.05.04 |
Zinc |
|
|
Zinc sulfate 125 mg effervescent tablets
|
Formulary
|
Provider notes
- NMUH:
- Only to be used where there is good evidence of deficiency. Therapy to be discontinued when clinical improvement occurs.
- RFL:
- RNOH:
- UCLH:
- WH:
|
|
Zinc sulfate 220 mg capsules
|
Formulary
|
Provider notes
- NMUH:
- RFL:
- RNOH:
- UCLH:
- WH:
|
|
|
|
|
Vitamins A C and D
(Healthy start children’s vitamin drops)
|
Formulary
|
Provider notes - NMUH:
- RFL:
- RNOH:
- UCLH:
- WH:
- For community clinics only
|
|
|
Pabrinex®
|
Formulary
|
Provider notes
|
|
Pyridoxine Hydrochloride
|
Formulary
|
Provider notes - NMUH:
- RFL:
- Only the 50mg tablets kept at the RFH
- RNOH:
- UCLH:
- WH:
|
|
Thiamine tabs
|
Formulary
|
Provider notes
- NMUH:
- RFL:
- RNOH:
- UCLH:
- WH:
|
|
Thiamine Injection 100 mg in 1mL
|
Unlicensed
|
Provider notes
|
|
09.06.02 |
Oral vitamin B complex preparations |
|
|
Vitamin B Tablets, Compound
|
Formulary
|
Provider notes
|
|
Vitamin B Tablets, Compound Strong
|
Formulary
|
Provider notes
|
|
|
|
Ascorbic Acid
(Vitamin C)
(Supplement)
|
Formulary
|
NOTE: There is more than one monograph for this medicine, click here to search for formulary status and its use for other indications. Provider notes - NMUH:
- RFL:
- Tablets 50mg,100mg, 200mg and 500mg
- Injection 500mg
- RNOH:
- UCLH:
- WH:
|
|
|
Alfacalcidol
(One-Alpha®)
|
Formulary
|
Provider notes
|
|
Calcitriol oral
|
Formulary
|
Provider notes
|
|
Calcium and Ergocalciferol
|
Formulary
|
Provider notes
|
|
Colecalciferol + Calcium carbonate
(Adcal-D3®)
|
Formulary
|
Provider notes
|
NCL JFC: Guidelines for Calcium and Vitamin D supplementation for the prevention of osteoporotic fragility fractures
|
Colecalciferol caps/liquid
|
Formulary
|
Provider notes - NMUH:
- RFL:
- RNOH:
- Oral liquid available as 3000 units/mL
- UCLH:
- WH:
|
NCL JFC: Guidelines for Calcium and Vitamin D supplementation for the prevention of osteoporotic fragility fractures
|
Ergocalciferol
|
Formulary
|
Provider notes
- NMUH:
- RFL:
- 300,000 units intramuscular injection only
- RNOH:
- UCLH:
- WH:
- Inj 7.5 mg (300,000 units)/1 ml only
|
|
|
Alpha Tocopheryl Acetate
(Vitamin E)
|
Restricted
|
Provider notes - NMUH:
- RFL:
- Oral suspension and injection 100mg/2ml kept at the RFH.
- RNOH:
- UCLH:
- WH:
|
|
09.06.06 |
Vitamin K |
|
|
Menadiol sodium diphosphate
|
Formulary
|
Provider notes - NMUH:
- RFL:
- RNOH:
- 10 mg tablets stored in the EDC
- UCLH:
- WH:
|
|
Phytomenadione 10 mg in 1 mL injection
(Konakion® MM)
|
Formulary
|
Provider notes - NMUH:
- RFL:
- RNOH:
- Can be given undiluted by slow intravenous injection over at least 30 seconds - see Medusa Injectable Medicines Guide for further information
- UCLH:
- WH:
- Konakion MM may be administered by slow intravenous injection, or by intravenous infusion in glucose 5%, at a rate of not less than 1 mg/minute. It is currently unlicensed for use by intramuscular injection, although it can be given by this route on the prescriber’s responsibility.
|
|
Phytomenadione 2 mg in 0.2 mL
(Konakion® MM Paediatric)
|
Formulary
|
Provider notes
- NMUH:
- RFL:
- RNOH:
- Konakion MM Paediatric can be administered by intramuscular or intravenous injection or by oral administration depending on the indication - see the SPC for further information
- UCLH:
- WH:
- This is the only vitamin K preparation licensed for oral administration. As an alternative there is Phytomenadione 20 mg/ml oral drops (unlicensed).
|
|
Phytomenadione 20 mg in 1 mL oral drugs
|
Unlicensed
|
Provider notes - NMUH:
- RFL:
- RNOH:
- UCLH:
- WH:
- Please note that this preparation is NOT LICENSED for use in the UK
|
|
09.06.07 |
Multivitamin preparations |
|
|
Multivitamin
|
Formulary
|
Provider notes
|
|
Multivitamin liquid
(Abidec®)
|
Formulary
|
Provider notes - NMUH:
- RFL:
- RNOH:
- UCLH:
- WH:
- Discharge prescribing for neonates only
|
|
Multivitamin liquid
(Dalivit®)
|
Formulary
|
Provider notes
|
|
09.06.07 |
Vitamin and mineral supplements and adjuncts to synthetic diets |
|
|
Multivitamin
(Renavit®)
|
Restricted
|
Approved for vitamin deficiency in chronic kidney disease (April 2015)
Provider notes
- NMUH:
- For continuation of treatment. Initiation by the renal team ONLY.
- RFL:
- Preferred multivitamin for CKD - renal team only
- RNOH:
- UCLH:
- WH:
|
|
Vitamin and mineral supplements
(DEKAs® Plus)
|
Restricted
|
Approved for the dietary management of patients with cystic fibrosis on the specific recommendation of a specialist in cystic fibrosis; available as capsules ("Softcaps"), chewable tablets ("Chewables") and liquid ("Liquid") (JFC September 2018).
Provider notes
- NMUH:
- For continuation only. Not stocked but ordered in if patient admitted on supplement as per indication stated above
- RFL:
- RNOH:
- UCLH:
- WH:
|
|
Vitamin and mineral supplements
(Forceval Soluble®)
|
Formulary
|
 (hospital only prescribing) for refeeding syndrome
 for other indications
Approved for prophylaxis of refeeding syndrome (JFC October 2018)
Provider notes
- NMUH:
- For refeeding syndrome ONLY - refer to Trust Guideline
- RFL:
- RNOH:
- UCLH:
- WH:
|
|
Vitamin and mineral supplements
(Forceval®)
|
Formulary
|
Provider notes
|
|
Vitamin and mineral supplements
(Ketovite®)
|
Formulary
|
Provider notes
- NMUH:
- RFL:
- Not preferred – use Renavit preferentially for CKD - renal team only
- RNOH:
- UCLH:
- WH:
|
|
|
09.08 |
Metabolic disorders |
|
|
09.08.01 |
Drugs used in metabolic disorders |
|
|
Eliglustat
|
Formulary

|
See NICE HST for eligibility criteria
Provider notes
- NMUH:
- RFL:
- Gaucher disease in line with NICE HST
- RNOH:
- UCLH:
- Gaucher disease in line with NICE HST
- WH:
|
NICE HST5: Eliglustat for treating type 1 Gaucher disease
|
Idursulfase
|
Restricted

|
Provider notes
- NMUH:
- RFL:
- Restricted to the lysosomal storage disorders unit
- RNOH:
- UCLH:
- WH:
|
|
Ubiquinone
|
Formulary
|
Provider notes
- NMUH:
- RFL:
- RNOH:
- UCLH:
- Primary mitochondrial deficiency in patients with confirmed mitochondrial defect or defined respiratory chain deficiency (August 2016)
- WH:
|
|
Biotin
|
Unlicensed
|
Provider notes
- NMUH:
- RFL:
- Restricted to paediatrics and neonates
- RNOH:
- UCLH:
- WH:
|
|
|
Penicillamine
(Metabolic disorders)
|
Formulary

|
NOTE: There is more than one monograph for this medicine, click here to search for formulary status and its use for other indications. Provider notes
|
|
Trientine Dihydrochloride
(Metabolic disorders)
|
Formulary
|
Provider notes
- NMUH:
- RFL:
- Restricted for Wilson’s specialist use only
- See NHSE clinical commissioning policy
- RNOH:
- UCLH:
- WH:
|
NHSE 170094P: Trientine for Wilson disease (all ages)
|
Zinc acetate
(Wilzin®)
(Metabolic disorders)
|
Formulary
|
Provider notes
- NMUH:
- RFL:
- RNOH:
- UCLH:
- WH:
|
|
09.08.01 |
Carnitine deficiency |
|
|
Levocarnitine
(l-carnitine)
|
Formulary

|
Provider notes
- NMUH:
- RFL:
- Non-formulary for paediatrics (GOSH specialist service)
- For peritoneal dialysis patients (levocarnitine deficiency)
- RNOH:
- UCLH:
- WH:
|
|
|
Agalsidase alfa and beta
(Fabrazyme®)
|
Restricted

|
Provider notes
- NMUH:
- RFL:
- Restricted to the lysosomal storage disorders unit
- RNOH:
- UCLH:
- WH:
|
|
Agalsidase alfa and beta
(Replagal®)
|
Restricted

|
Provider notes
- NMUH:
- RFL:
- Restricted to the lysosomal storage disorders unit
- RNOH:
- UCLH:
- WH:
|
|
Elosulfase alfa
|
Restricted
|
See NICE HST for eligibility criteria
Provider notes
- NMUH:
- RFL:
- Morquio A Syndrome in line with NICE HST
- RNOH:
- UCLH:
- WH:
|
NICE HST2: Elosulfase alfa for treating mucopolysaccharidosis type IVa (Morquio A Syndrome)
|
Migalastat caps
|
Restricted

|
See NICE HST for eligibility criteria
Provider notes
- NMUH:
- RFL:
- Fabry disease in line with NICE HST
- RNOH:
- UCLH:
- WH:
|
NICE HST4: Migalastat for treating Fabry disease
|
09.08.01 |
Gaucher's disease |
|
|
Imiglucerase
|
Restricted

|
Provider notes
- NMUH:
- RFL:
- Restricted to the lysosomal storage disorders unit
- RNOH:
- UCLH:
- WH:
|
|
Miglustat
|
Restricted

|
Provider notes
- NMUH:
- RFL:
- Restricted to the lysosomal storage disorders unit
- RNOH:
- UCLH:
- WH:
|
|
Velaglucerase alfa
|
Restricted

|
Provider notes
- NMUH:
- RFL:
- Restricted to the lysosomal storage disorders unit
- RNOH:
- UCLH:
- WH:
|
|
09.08.01 |
Mucopolysaccharidosis I |
|
|
Galsulfase
|
Formulary

|
Provider notes
- NMUH:
- RFL:
- Restricted to the lysosomal storage disorders unit
- RNOH:
- UCLH:
- WH:
|
|
Laronidase
|
Restricted

|
Provider notes
- NMUH:
- RFL:
- Restricted to the lysosomal storage disorders unit
- RNOH:
- UCLH:
- WH:
|
|
|
Alglucosidase Alfa
|
Restricted
|
Provider notes
- NMUH:
- RFL:
- Restricted to the lysosomal storage disorders unit
- RNOH:
- UCLH:
- WH:
|
|
09.08.01 |
Nephropathic cystinosis |
|
|
Mercaptamine
(Cystagon®, Procysbi®)
(Cystinosis)
|
Restricted

|
Provider notes
- NMUH:
- RFL:
- RNOH:
- UCLH:
- WH:
|
|
09.08.01 |
Urea cycle disorders |
|
|
Arginine
|
Formulary
|
Provider notes
- NMUH:
- RFL:
- For peritoneal dialysis patients only (arginine deficiency)
- Non-formulary for other indications (inc. paediatrics)
- RNOH:
- UCLH:
- WH:
|
|
Sodium benzoate
|
Restricted
|
Provider notes
- NMUH:
- RFL:
- Non-formulary (inc. paediatrics)
- RNOH:
- UCLH:
- WH:
|
|
09.08.02 |
Acute porphyrias |
|
|
Haem Arginate
(Normosang®)
(human hemin)
|
Formulary

|
Provider notes
|
|
09.08.02 |
Drugs unsafe for use in acute porphyrias |
|
|
09.09 |
Unlicensed Medicines / Significant off-label use |
|
|
Azathioprine
(Haematology)
|
Formulary
|
NOTE: There is more than one monograph for this medicine, click here to search for formulary status and its use for other indications.
Provider notes
- NMUH:
- RFL:
- Approved for Immune thrombocytopenia (ITP) and Autoimmune Haemolytic Anaemia (AIHA)
- RNOH:
- UCLH:
- WH:
|
|
Ciclosporin
(Haematology)
|
Formulary
|
NOTE: There is more than one monograph for this medicine, click here to search for formulary status and its use for other indications.
Provider notes
- NMUH:
- RFL:
- Approved for Immune thrombocytopenia (ITP) and Autoimmune Haemolytic Anaemia (AIHA)
- RNOH:
- UCLH:
- WH:
|
|
Cyclophosphamide tablets
(Haematology)
|
Formulary
|
NOTE: There is more than one monograph for this medicine, click here to search for formulary status and its use for other indications.
Provider notes
- NMUH:
- RFL:
- Approved for Immune thrombocytopenia (ITP) and Autoimmune Haemolytic Anaemia (AIHA)
- RNOH:
- UCLH:
- WH:
|
|
Danazol
(Haematology)
|
Formulary
|
NOTE: There is more than one monograph for this medicine, click here to search for formulary status and its use for other indications.
Provider notes
- NMUH:
- RFL:
- Approved for Immune thrombocytopenia (ITP) and Autoimmune Haemolytic Anaemia (AIHA)
- RNOH:
- UCLH:
- WH:
|
|
Eculizumab infusion
(Hyperhaemolysis)
|
Formulary

|
NOTE: There is more than one monograph for this medicine, click here to search for formulary status and its use for other indications.
Approved for 2nd line management of Delayed Haemolytic Transfusion Reactions [DHTRs] hyperhaemolysis in adult Sickle Cell and β-thalassaemia patients who have not responded to IVIG and steroids (pending internal funding approval; JFC July 2019)
Provider notes
- NMUH:
- RFL:
- RNOH:
- UCLH:
- Restricted to haematology. UMC to be informed of each patient. Funding agreed for 1 patient per annum.
- WH:
|
|
Mycophenolate mofetil
(Haematology)
|
Formulary
|
NOTE: There is more than one monograph for this medicine, click here to search for formulary status and its use for other indications.
Provider notes
- NMUH:
- RFL:
- Approved for Immune thrombocytopenia (ITP) and Autoimmune Haemolytic Anaemia (AIHA)
- RNOH:
- UCLH:
- WH:
|
|
.... |
Non Formulary Items |
Alpha Tocopherol
(Vedrop®)

|
Non Formulary
|
|
|
Asfotase alfa injection

|
Non Formulary
|
See NICE HST for eligibility criteria
Provider notes
- NMUH:
- RFL:
- RNOH:
- UCLH:
- WH:
|
NICE HST6: Asfotase alfa for treating paediatric-onset hypophosphatasia
|
Babiven start up

|
Non Formulary
|
|
|
Betaine
(Homocystinuria)

|
Non Formulary

|
|
|
Calcium acetate tabs
(Renacet®)
|
Non Formulary
|
|
|
Calcium carbonate
(Calcium-500®)
(Calcium supplement)

|
Non Formulary
|
NOTE: There is more than one monograph for this medicine, click here to search for formulary status and its use for other indications. |
|
Calcium carbonate
(Calcium-500®)
(Phosphate binder)

|
Non Formulary
|
NOTE: There is more than one monograph for this medicine, click here to search for formulary status and its use for other indications. |
|
Calcium Lactate tablets

|
Non Formulary
|
|
|
Carglumic acid

|
Non Formulary

|
|
|
Cerliponase alfa

|
Non Formulary
|
See NICE HST for eligibility criteria
Provider notes
- NMUH:
- RFL:
- RNOH:
- UCLH:
- WH:
|
NICE HST12: Cerliponase alfa for treating neuronal ceroid lipofuscinosis type 2
|
Chenodexoycholic acid
(Xenbilox®)

|
Non Formulary
|
|
|
Citrulline

|
Non Formulary
|
Provider notes
- NMUH:
- RFL:
- RNOH:
- UCLH:
- Approved for adult Inherited Metabolic Disorders (UCLH only; JFC October 2020).
- WH:
|
|
Colecalciferol + Calcium carbonate
(Accrete D3®)

|
Non Formulary
|
|
|
Colecalciferol + Calcium carbonate
(Cacit® D3)

|
Non Formulary
|
|
|
Colecalciferol + Calcium carbonate
(Calceos®)

|
Non Formulary
|
|
|
Colecalciferol + Calcium carbonate
(Calchichew-D3 Once Daily)

|
Non Formulary
|
|
|
Colecalciferol + Calcium carbonate
(Calcichew-D3®)

|
Non Formulary
|
|
|
Colecalciferol + Calcium carbonate
(Calcichew-D3® Forte)

|
Non Formulary
|
Provider notes |
|
Colecalciferol + Calcium carbonate
(Calci-D®)

|
Non Formulary
|
|
|
Colecalciferol + Calcium carbonate
(Kalcipos-D®)

|
Non Formulary
|
|
|
Colecalciferol + Calcium carbonate
(Natecal D3®)

|
Non Formulary
|
|
|
Colecalciferol + Calcium carbonate
(TheiCal- D3)

|
Non Formulary
|
|
|
Colecalciferol with Calcium phosphate
(Calfovit D3®)

|
Non Formulary
|
|
|
Creatine

|
Non Formulary
|
Provider notes
- NMUH:
- RFL:
- RNOH:
- UCLH:
- Approved for adult Inherited Metabolic Disorders (UCLH only; JFC October 2020).
- WH:
|
|
Dextran 40 ®

|
Non Formulary
|
|
|
Dextran 70 + Sodium chloride hypertonic intravenous

|
Non Formulary
|
|
|
Dextran 70 intravenous

|
Non Formulary
|
|
|
Dihydrotachysterol
(AT 10®)

|
Non Formulary
|
|
|
Eculizumab infusion
(Paroxysmal nocturnal haemoglobinuria)

|
Non Formulary

|
NOTE: There is more than one monograph for this medicine, click here to search for formulary status and its use for other indications.
Not approved for the treatment of paroxysmal nocturnal haemoglobinuria (PNH); see UCLH DTC minutes October 2007. |
|
Efmoroctocog alfa
(Elocta®)

|
Non Formulary
|
|
|
Epoetin alfa
(Binocrit®)

|
Non Formulary

|
Approved to treat anaemia (and prevent ribavirin dose reduction) in patients treated for hepatitis C virus (October 2013) |
|
Epoetin theta
(Eporatio®)

|
Non Formulary

|
|
NICE TA323: Erythropoiesis‑stimulating agents during chemotherapy
|
Epoetin zeta
(Retacrit®)

|
Non Formulary

|
|
NICE TA323: Erythropoiesis‑stimulating agents during chemotherapy
|
Etherified Starch
(HAES-steril®)

|
Non Formulary
|
|
|
Etherified Starch
(Hemohes®)

|
Non Formulary
|
|
|
Etherified Starch
(Infukoll®)

|
Non Formulary
|
|
|
Ferric maltol caps

|
Non Formulary
|
|
|
Ferrous fumarate + Folic acid
(Galfer FA®)

|
Non Formulary
|
|
|
Ferrous sulfate + Folic acid
(Fefol®)

|
Non Formulary
|
|
|
Ferrous sulphate + Folic acid
(Ferrograd Folic®)

|
Non Formulary
|
|
|
Ferrous sulphate modified release
(Feospan®)

|
Non Formulary
|
|
|
Ferrous sulphate oral drops
(Ironorm® drops)

|
Non Formulary
|
|
|
Fluorides
(Duraphat® Mouthwash)

|
Non Formulary
|
|
|
Fluorides
(En-De-Kay® Mouthwash)

|
Non Formulary
|
|
|
Fluorides
(Flour-a-day® Tablet)

|
Non Formulary
|
|
|
Fluorides
(FlouriGard® Gel)

|
Non Formulary
|
|
|
Fluorides
(FlouriGard® Mouthwash)

|
Non Formulary
|
|
|
Fluorides
(FluoriGard® Tablet)

|
Non Formulary
|
|
|
Gelatin intravenous infusion
(Haemaccel®)

|
Non Formulary
|
|
|
Glycerol phenylbutyrate

|
Non Formulary

|
Provider notes
- NMUH:
- RFL:
- RNOH:
- UCLH:
- Approved for urea cycle disorders for patients who cannot be managed by dietary protein restriction and/or amino acid supplementation alone (UCLH only; JFC October 2018)
- WH:
|
|
Hypertonic Solution
(HyperHAES®)

|
Non Formulary
|
|
|
Intralipid 20%

|
Non Formulary
|
|
|
Iron Isomaltoside
(Diafer®)

|
Non Formulary
|
|
|
Lipegfilgrastim
(Patients with a history of severe neutropenia despite prophylactic daily GCSF)

|
Non Formulary

|
NOTE: There is more than one monograph for this medicine, click here to search for formulary status and its use for other indications. Not approved for patients with a history of severe neutropenia despite prophylactic daily GCSF (August 2016) |
|
Magnesium oxide tabs/caps

|
Unlicensed
|
|
|
Mercaptamine eye drops
(Cystadrops®)
(Cystinosis)

|
Non Formulary

|
|
|
Methionine

|
Non Formulary
|
Provider notes
- NMUH:
- RFL:
- RNOH:
- UCLH:
- Approved for adult Inherited Metabolic Disorders (UCLH only; JFC October 2020).
- WH:
|
|
Molgramostim

|
Unlicensed

|
|
|
Multivitamin eye supplement
(MaculEH Light®)

|
Non Formulary
|
|
|
Multivitamin including lutein
(PreserVision®, Vitalux Plus®)

|
Non Formulary
|
|
|
Multivitamin including lutein
(Vitalux Plus®)

|
Non Formulary
|
|
|
Multivitamin including lutein and zeaxanthin
(ICaps®, Macushield®, Ocuvite®)

|
Non Formulary
|
|
|
Multivitamin including lutein and zeaxanthin
(Macushield®)

|
Non Formulary
|
|
|
Multivitamin including lutein and zeaxanthin
(Ocuvite®)

|
Non Formulary
|
|
|
Nitisinone

|
Non Formulary

|
|
|
Nutryelt ®

|
Non Formulary
|
|
|
Oral Rehydration Salts
(Electrolade®)

|
Non Formulary
|
|
|
Oral Rehydration Salts
(Rapolyte®)

|
Non Formulary
|
|
|
Other Compounds
(Potaba®)

|
Non Formulary
|
|
|
Oxymetholone

|
Non Formulary
|
|
|
Paricalcitol

|
Non Formulary
|
|
|
Pegfilgrastim
(Patients with a history of severe neutropenia despite prophylactic daily GCSF)

|
Non Formulary

|
NOTE: There is more than one monograph for this medicine, click here to search for formulary status and its use for other indications. Not approved for patients with a history of severe neutropenia despite prophylactic daily GCSF (August 2016) |
|
Pegfilgrastim
(Patients who cannot inject daily)

|
Non Formulary

|
NOTE: There is more than one monograph for this medicine, click here to search for formulary status and its use for other indications.
Provider notes
- NMUH:
- RFL:
- RNOH:
- UCLH:
- WH:
|
|
Phytomenadione capsules

|
Non Formulary
|
|
|
Plasma-lyte 148 with Glucose 5%

|
Non Formulary
|
|
|
Plerixafor

|
Non Formulary
|
Provider notes
- NMUH:
- RFL:
- RNOH:
- UCLH:
- WH:
|
|
Polysaccharide Iron Complex
(Miferex®)

|
Non Formulary
|
|
|
Potasium Chloride
(Klofer®)

|
Non Formulary
|
|
|
Potassium Bicarbonate
(Effervescent tablets)

|
Non Formulary
|
|
|
Potassium Chloride 20mmol in 20ml Water For Injection

|
Non Formulary
|
|
|
Potassium Chloride 40mmol in 50ml Water For Injection

|
Non Formulary
|
|
|
Potassium Chloride 50mmol in 50mL Sodium Chloride 0.9% prefilled syringe

|
Non Formulary
|
|
|
Potassium dihydrogen phosphate
(Potassium acid phosphate)
|
Non Formulary
|
|
|
Preparations
(Forceval Protein Powder®)

|
Non Formulary
|
|
|
Riboflavin (Vitamin B2)

|
Non Formulary
|
|
|
Sapropterin dihydrochloride

|
Non Formulary

|
|
|
Sebelipase alfa

|
Non Formulary
|
|
|
Selenium
(Selenase®)

|
Non Formulary
|
|
|
Sodium Dichloroacetate
|
Non Formulary
|
|
|
Sodium phenylbutyrate
(Ammonaps®, Pheburane®)
|
Non Formulary

|
|
|
Sucroferric oxyhydroxide
(Velphoro®)

|
Non Formulary
|
|
|
Supplementary Preparations
(Decan®)

|
Non Formulary
|
|
|
Supplementary Preparations
(Dipeptiven®)

|
Non Formulary
|
|
|
Supplementary Preparations
(Glycophos® Sterile Concentrate)

|
Non Formulary
|
|
|
Supplementary Preparations
(Tracutil®)

|
Non Formulary
|
|
|
Tetrastarch intravenous infusion
(Tetraspan®)

|
Non Formulary
|
|
|
Tetrastarch intravenous infusion
(Venofundin®)

|
Non Formulary
|
|
|
Tetrastarch intravenous infusion
(Volulyte®)

|
Non Formulary
|
|
|
Tetrastarch intravenous infusion
(Voluven®)

|
Non Formulary
|
|
|
Vitamin B complex preparations
(Vigranon B®)

|
Non Formulary
|
|
|
Vitamins C, D and folic acid
(Healthy start vitamins for women)

|
Non Formulary
|
|
|
|
Key |
Traffic Light Status Information
Status |
Description |
 
|
Medicines that should be initiated by a specialist. Prescribing can be transferred to primary care once the patient has been stabilised.
Shared care: For drugs with regular, ongoing need for monitoring and/or assessment of efficacy or toxicity. Prior agreement must be obtained by the specialist from the primary care provider before prescribing responsibility is transferred. The shared care protocol must have been agreed by the relevant secondary care trust Drugs and Therapeutics Committee(s) (DTC) and approved by the North Central London JFC.
Fact sheet: For drugs with some concerns surrounding safety or efficacy but do not require regular monitoring and/or monitoring of effectiveness/toxicity. |
 
|
Medicines which should normally be prescribed by specialists only (hospital only).
For patients already receiving prescriptions in primary care - continue. No new patients to receive prescriptions in primary care.
See link for the complete NCL Red List https://www.ncl-mon.nhs.uk/wp-content/uploads/2017/08/ncl_red_list.pdf |
 
|
Medicines not recommended for routine use in primary or secondary care.
Medicines, which the North Central London JFC has actively reviewed and does not recommend for use at present due to limited clinical and/or cost effective data. |
|
|
|