| Formulary Chapter 2: Cardiovascular system - Full Chapter
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| Chapter Links... |
LSCMMG: Atrial Fibrillation Pathway for the prevention of stroke and systemic embolism in AF in the absence of valvular heart disease |
NICE NG196: Atrial fibrillation: diagnosis and management |
NICE NG106: Chronic heart failure in adults: diagnosis and management |
NICE NG187: Acute heart failure: diagnosis and management |
Enoxaparin for Treatment of Venous Thromboembolism **FOR USE IN THE BLACKPOOL REGION ONLY** |
LSC Hypertension in Adults: Diagnosis and Management |
LSC Patient Pathway for Commencing Inclisiran |
LSC Statin Intolerance Pathway |
LSCMMG: Lipid Management Pathway for Primary Prevention of Cardiovascular Disease |
LSCMMG: Lipid Management Pathway for Secondary Prevention of Cardiovascular Disease |
NICE NG136: Hypertension in adults: diagnosis and management |
NICE NG185: Acute Coronary Syndromes |
NICE NG203: Chronic kidney disease: assessment and management |
NICE NG95: Recent-onset chest pain of suspected cardiac origin: assessment and diagnosis |
Policy and procedure for prophylaxis against, and treatment of, VTE in adult patients **FOR USE IN THE CENTRAL LANCS REGION ONLY** |
Prevention of VTE in Medical Surgical Patients (16 years +) and those requiring lower limb plaster casts/immobilisations **FOR USE IN THE BLACKPOOL REGION ONLY** |
Renal: Enhanced Supportive Kidney Care Guideline |
Enoxaparin Shared Care Guideline **FOR USE IN THE MORECAMBE BAY REGION ONLY** |
Low Molecular Weight Heparins - Use in Primary care Best Practice Guideline *FOR USE IN PENNINE REGION ONLY* |
| Details... |
| 02.01.01 |
Cardiac glycosides |
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Digoxin (oral)
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Formulary
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Tablets 62.5 micrograms, 125 micrograms, 250 micrograms Liquid 50 micrograms/1mL
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Digoxin (injection)
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Formulary
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Injection 500 micrograms/2mL
Oral digoxin is the preferred route. Intravenous digoxin should only be used when oral route is unavailable. Digoxin has a narrow therapeutic index and can cause toxicity.
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| 02.01.01 |
Digoxin-specific antibody |
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Digoxin specific antibody fragments (Digifab®)
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Formulary
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Intravenous infusion 40mg
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| 02.01.02 |
Phosphodiesterase type-3 inhibitors |
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Milrinone
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Formulary
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Critical care use only
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Enoximone (injection)
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Formulary
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Critical care use only
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| 02.02.01 |
Thiazides and related diuretics |
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Indapamide
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Formulary
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Tablets 2.5mg
Modified release tablets 1.5mg
First line diuretic for hypertension
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Bendroflumethiazide
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Formulary
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Tablets 2.5mg, 5mg
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Metolazone
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Formulary
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Tablets 2.5mg, 5mg
Treatment of patients with chronic heart failure with resistant volume overload
Must be prescribed by brand
Use the licensed preparation for new patients.
Before requesting primary care prescribing, patients must be established on a stable dose of metolazone for at least 2 weeks, with stable urea and electrolytes (including creatinine) and a stable body weight before discharge.
Ongoing monitoring of urea and electrolytes (including creatinine) should be carried out on a monthly basis and the patients’ weight and blood pressure should be monitored at each clinic visit.
Metolazone has an established role in the treatment of resistant oedema in heart failure where it is combined with a loop diuretic. The combination of metolazone and a loop diuretic is much more potent and needs to be initiated by someone experienced in its use and needs careful monitoring of renal function and electrolytes. It is routinely used in patients with renal impairment who do not respond to a loop diuretic.
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MHRA: Xaqua (metolazone) 5mg tablets: exercise caution when switching patients between metolazone preparations
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| 02.02.02 |
Loop diuretics |
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Furosemide
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First Choice
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Tablets 20mg, 40mg, 500mg Liquid 20mg/5mL, 40mg/5mL, 50mg/5mL
Furosemide 500mg tablets in East Lancashire
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Bumetanide
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Second Choice
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Tablets 1mg, 5mg
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Furosemide (injection)
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Formulary
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Injection
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| 02.02.03 |
Potassium-sparing diuretics and aldosterone antagonists |
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Amiloride Hydrochloride
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Formulary
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Tablets 5mg
Liquid 5mg/5mL
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| 02.02.03 |
Aldosterone antagonists |
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Spironolactone
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Formulary
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Tablets 25mg, 50mg, 100mg
Heart failure
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MHRA: Spironolactone and renin-angiotensin system drugs in heart failure: risk of potentially fatal hyperkalaemia—clarification, December 2016
MHRA: Spironolactone and renin-angiotensin system drugs in heart failure: risk of potentially fatal hyperkalaemia—February 2016 article
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Eplerenone
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Formulary
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Tablets 25mg, 50mg
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MHRA: Spironolactone and renin-angiotensin system drugs in heart failure: risk of potentially fatal hyperkalaemia—clarification, December 2016
MHRA: Spironolactone and renin-angiotensin system drugs in heart failure: risk of potentially fatal hyperkalaemia—February 2016 article
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| 02.02.04 |
Potassium-sparing diuretics with other diuretics |
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Co-amilofruse (amiloride/furosemide)
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Formulary
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Tablets 2.5mg/20mg, 5mg/40mg
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| 02.02.05 |
Osmotic diuretics |
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Mannitol
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Formulary
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Intravenous infusion 10%, 15%, 20%
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| 02.03.02 |
Drugs for arrhythmias |
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Medicines listed in this section should be commenced only on the advice of cardiology and may require specialist supervision. |
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Ajmaline
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Unlicensed
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Injection
Ventricular arrythmias where other options have failed
Cardiology and Critical Care use only
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| 02.03.02 |
Supraventricular arrhythmias |
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Dronedarone
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Formulary
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Tablets 400mg
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LSCMMG Shared Care Protocol: Dronedarone for patients within adult services
MHRA: Dronedarone (Multaq▼): cardiovascular, hepatic and pulmonary adverse events – new restrictions and monitoring requirements
NICE TA197: Dronedarone for the treatment of non-permanent atrial fibrillation
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Adenosine
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Formulary
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Injection 6mg/2mL
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| 02.03.02 |
Supraventricular and ventricular arrhythmias |
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Amiodarone
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Formulary
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Tablets 100mg, 200mg
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LSCMMG Shared Care Protocol: Amiodarone for patients within adult services
MHRA Drug Safety Update March 2022: Amiodarone (Cordarone X): reminder of risks of treatment and need for patient monitoring and supervision
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Disopyramide
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Formulary
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Capsules 100mg
Modified-release tablets 250mg
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Flecainide
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Formulary
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Tablets 50mg, 100mg
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Propafenone
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Formulary
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Tablets 150mg, 300mg
Requires specialist supervision
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Amiodarone (injection)
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Formulary
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Injection 150mg/3mL Injection 300mg/10mL pre-filled syringe
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MHRA Drug Safety Update March 2022: Amiodarone (Cordarone X): reminder of risks of treatment and need for patient monitoring and supervision
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Flecainide
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Formulary
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Injection 150mg/15mL
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| 02.03.02 |
Ventricular arrhythmias |
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Mexiletine
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Formulary
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Capsules 50mg, 100mg, 200mg (as hydrochloride)
Treatment of documented ventricular arrhythmias which, in the judgement of the physician, are considered as life-threatening. For use by specialists in treating arrhythmias only.
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LSCMMG: Mexiletine NMR
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Lidocaine
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Formulary
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Injection
Ventricular arrhythmias.
Cardiology and Critical Care use only.
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| 02.04 |
Beta-adrenoceptor blocking drugs |
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Bisoprolol
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First Choice
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Tablets 1.25mg, 2.5mg, 3.75mg, 5mg, 7.5mg, 10mg
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Carvedilol
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Formulary
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Tablets 3.125mg, 6.25mg, 12.5mg, 25mg
Second line (heart failure)
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Atenolol
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Formulary
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Tablets 25mg, 50mg, 100mg Liquid 25mg/5mL Second line
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Labetalol
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Formulary
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Tablets 100mg, 200mg
Hypertension in pregnancy
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NICE NG133: Hypertension in pregnancy: diagnosis and management
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Metoprolol
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Formulary
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Tablets 50mg
Option when a beta blocker with a short half-life is required
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Nebivolol
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Formulary
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Tablets 5mg Tablets 2.5mg (for dose titration only)
Third line
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Sotalol
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Formulary
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Tablets 40mg, 80mg Arrhythmias (on advice of cardiology only)
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Nadolol
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Formulary
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Tablets 80mg
Long QT syndrome (on advice of cardiology only)
All dose titrations must be carried out by the initiating cardiologist.
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LSCMMG: Nadolol NMR
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Atenolol (injection)
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Formulary
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Injection 5mg/10mL
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Esmolol (injection)
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Formulary
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Injection 100mg/10mL Infusion 2.5g in 250mL
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Labetalol (injection)
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Formulary
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Injection 100mg/20mL Hypertension in pregnancy and hypertensive crisis
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Metoprolol (injection)
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Formulary
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Injection 5mg/5mL
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| 02.05 |
Drugs affecting the renin-angiotensin system and some other antihypertensive drugs |
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| 02.05.01 |
Vasodilator antihypertensive drugs |
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Hydralazine
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Formulary
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Tablets 25mg, 50mg
Hypertension
Heart failure (Initiated in hospital or under specialist supervision)
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NG106: Chronic heart failure in adults: diagnosis and management
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Sildenafil
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Formulary
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Tablets 20mg
Tertiary centre only
Sildenafil and bosentan are licensed for use in pulmonary arterial hypertension (PAH). Treatment of this condition is commissioned nationally through a small number of PAH centres based in hospitals across the UK. All patients should be referred to one of these centres, who carry out all prescribing of these therapies.
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MHRA Drug Safety Update Nov 18: Sildenafil (Revatio and Viagra): reports of persistent pulmonary hypertension of the newborn (PPHN) following in-utero exposure in a clinical trial on intrauterine growth restriction
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Sodium Nitroprusside
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Formulary
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Injection 50mg vials
Specialist use only
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Sotatercept (Winrevair®)
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Formulary

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Solution for injection 45 mg, 60 mg
Specialist use only
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NICE TA1161: Sotatercept for treating pulmonary arterial hypertension
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Hydralazine
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Formulary
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Injection 20mg/2mL
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| 02.05.02 |
Centrally acting antihypertensive drugs |
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Methyldopa
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Formulary
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Tablets 125mg, 250mg, 500mg
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NG133: Hypertension in pregnancy: diagnosis and management
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Moxonidine
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Formulary
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Tablets 200micrograms, 300micrograms, 400micrograms
Restricted to use in resistant hypertension
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Clonidine Hydrochloride
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Formulary
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Tablets 25 microgram
Vasomotor symptoms (VMS) associated with menopause
Clonidine is considered less suitable for prescribing in hypertension
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LSCMMG: Clonidine for VMS associated with menopause NMR
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| 02.05.04 |
Alpha-adrenoceptor blocking drugs |
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Doxazosin
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Formulary
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Tablets 1mg, 2mg, 4mg
Doxazosin modified-release tablets
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NHSE: Items which should not routinely be prescribed in primary care: policy guidance
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| 02.05.04 |
Phaeochromocytoma |
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Phenoxybenzamine Hydrochloride
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Formulary
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Capsules 10mg
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Phentolamine
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Formulary
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Injection
Critical care and theatre use only
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| 02.05.05 |
Drugs affecting the renin-angiotensin system |
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| 02.05.05 |
Heart Failure |
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Dapagliflozin
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First Choice
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Tablets 5mg, 10mg
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MHRA: SGLT2 inhibitors: reports of Fournier’s gangrene (necrotising fasciitis of the genitalia or perineum)
MHRA: SGLT2 inhibitors: updated advice on increased risk of lower-limb amputation (mainly toes)
MHRA: SGLT2 inhibitors: updated advice on the risk of diabetic ketoacidosis
NICE TA679: Dapagliflozin for treating chronic heart failure with reduced ejection fraction
NICE TA902: Dapagliflozin for treating chronic heart failure with preserved or mildly reduced ejection fraction
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Empagliflozin
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Formulary
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Tablets 10mg, 25mg
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MHRA: SGLT2 inhibitors: reports of Fournier’s gangrene (necrotising fasciitis of the genitalia or perineum)
MHRA: SGLT2 inhibitors: updated advice on increased risk of lower-limb amputation (mainly toes)
MHRA: SGLT2 inhibitors: updated advice on the risk of diabetic ketoacidosis
NICE TA773: Empagliflozin for treating chronic heart failure with reduced ejection fraction
NICE TA929: Empagliflozin for treating chronic heart failure with preserved or mildly reduced ejection fraction
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| 02.05.05.01 |
Angiotensin-converting enzyme inhibitors (ACE inhibitors) |
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Ramipril
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First Choice
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Capsules 1.25mg, 2.5mg, 5mg, 10mg
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Lisinopril
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First Choice
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Tablets 2.5mg, 5mg, 10mg, 20mg
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Perindopril erbumine
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Formulary
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Tablets 2mg, 4mg, 8mg
Perindopril ARGININE is considered ‘Not suitable for prescribing’.
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NHSE: Items which should not routinely be prescribed in primary care: policy guidance
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Enalapril
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Formulary
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Tablets 2.5mg, 5mg, 10mg, 20mg
Restricted to use in post-natal women, in line with NG133.
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NG133: Hypertension in pregnancy: diagnosis and management
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| 02.05.05.02 |
Angiotensin-II receptor antagonists |
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Angiotensin-II receptor antagonists reserved for use when ACE inhibitors are not tolerated. |
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Losartan
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First Choice
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Tablets 12.5mg, 25mg, 50mg, 100mg
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Candesartan
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First Choice
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Tablets 2mg, 4mg, 8mg, 16mg, 32mg
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Irbesartan
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Formulary
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Tablets 75mg, 150mg, 300mg
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Sacubitril/valsartan (Entresto®)
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Formulary
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Film-coated tablets 24.3 mg sacubitril and 25.7 mg valsartan (as sacubitril valsartan sodium salt complex). 48.6 mg sacubitril and 51.4 mg valsartan (as sacubitril valsartan sodium salt complex). 97.2 mg sacubitril and 102.8 mg valsartan (as sacubitril valsartan sodium salt complex).
Entresto® tablets and granules contain sacubitril and valsartan in the form x/y where x and y are the strength in milligrams of sacubitril and valsartan respectively. Doses in BNF Publications are expressed as the total of both drug strengths.
For Entresto® tablets, the 24/26 mg, 49/51 mg, 72/78 mg, and 97/103 mg strengths are referred to as 50 mg, 100 mg, 150 mg, and 200 mg, respectively.
See BNF for more detail.
Ensure that all other ACE inhibitor and/or angiotensin receptor blocker therapy is stopped.
Initiation should be by the heart failure specialist team.
The specialist team must titrate, prescribe, and monitor until the patient is stabilised on an optimised dose (2-3 weeks on optimised dose).
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NICE TA388 Sacubitril valsartan for treating symptomatic chronic heart failure with reduced ejection fraction
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Valsartan
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Formulary
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tablets and capsules
Existing patients only
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| 02.05.05.03 |
Renin inhibitors |
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Aliskiren
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Formulary
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NHSE: Items which should not routinely be prescribed in primary care: policy guidance
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| 02.06.01 |
Nitrates |
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Isosorbide Mononitrate
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Formulary
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Tablets 10mg, 20mg M/R tablets 60mg LA capsules 25mg, 50mg
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Glyceryl Trinitrate
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Formulary
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Aerosol spray 400micrograms/dose Patches 5mg/24h, 10mg/24h
Patches should only be considered in patients unable to comply with or tolerate oral isosorbide mononitrate.
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Glyceryl Trinitrate
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Formulary
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Infusion
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| 02.06.02 |
Calcium-channel blockers |
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Amlodipine (as maleate or mesilate)
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First Choice
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Tablets 5mg, 10mg
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Lercanidipine
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Second Choice
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Tablets 10mg, 20mg
Option when amlodipine is not tolerated (e.g. where patients develop significant ankle oedema)
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Felodipine
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Formulary
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M/R tablets 2.5mg, 5mg, 10mg
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Nifedipine
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Formulary
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Modified-release tablets 10mg, 20mg (prescribe by brand)
Capsules 5mg, 10mg, 20mg (use of immediate-release capsules may be associated with large variations in blood pressure and reflex tachycardia)
Capsules: Nifedipine immediate-release capsules are no longer recommended for the treatment of angina or hypertension.
Pregnancy: Refer to the individual SPC of each nifedipine preparation for further details on use in pregnancy.
Raynaud's syndrome: Nifedipine is used in Raynaud's syndrome (modified-release preparations - unlicensed use).
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NICE NG133: Hypertension in pregnancy: diagnosis and management
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Lacidipine
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Formulary
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A second line dihydropyridine calcium channel blocker when amlodipine is not tolerated (e.g. where patients develop significant ankle oedema).
For existing patients only
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Nimodipine (Nimotop®)
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Formulary
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Tablets 30mg Intravenous infusion 10mg/50mL Prevention and treatment of ischaemia following subarachnoid haemorrhage
For use only within licensed indications following aneurysmal subarachnoid haemorrhage.
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Verapamil
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Formulary
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Tablets 40mg, 80mg, 120mg M/R tablets 120mg, 240mg Liquid 40mg/5mL
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Diltiazem oral
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Formulary
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Prescribe diltiazem modified-release preperations by brand name.
There may be variation in brands between hospital Trusts. Follow local Trust policy regarding brand switches.
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Verapamil
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Formulary
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Injection 5mg/2mL
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Nicardipine
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Formulary
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Injection 10mg/10mL
Specialist use only
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| 02.06.03 |
Other anitanginal drugs |
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Nicorandil
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Formulary
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Tablets 10mg, 20mg
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MHRA: Nicorandil (Ikorel): now second-line treatment for angina - risk of ulcer complications
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Ranolazine
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Formulary
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M/R tablets 375mg, 500mg, 750mg
Restricted to use in line with CG126.
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Ivabradine
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Formulary
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Tablets 5mg, 7.5mg
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LSCMMG - Ivabradine prescribing information sheet
LSCMMG: Ivabradine POTS NMR
NICE TA267: Ivabradine for treating chronic heart failure
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| 02.06.04 |
Peripheral vasodilators and related drugs |
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Naftidrofuryl oxalate
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Formulary
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Capsules 100mg
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NICE TA223- Cilostazol, naftidrofuryl oxalate, pentoxifylline and inositol nicotinate for the treatment of intermittent claudication in people with peripheral arterial disease
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Iloprost injection
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Formulary
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Severe Raynaud's phenomena
Specialist use only
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Iloprost nebuliser solution
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Formulary
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Pulmonary hypertension
For use by specialist centres only.
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Sildenafil
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Formulary
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Tablets 25mg
Digital ulceration 
Specialist initiation only
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MHRA: Sildenafil (Revatio and Viagra): reports of persistent pulmonary hypertension of the newborn (PPHN) following in-utero exposure in a clinical trial on intrauterine growth restriction
NICE ESUOM42: Digital ulcers: sildenafil
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Epoprostenol
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Formulary
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Injection 500micrograms
Specialist initiation only
Digital ulcers  Pulmonary arterial hypertension 
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MHRA: Veletri (epoprostenol) powder for solution for infusion: incompatibilities with some models of administration devices
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Cilostazol
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Formulary
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NICE TA223- Cilostazol, naftidrofuryl oxalate, pentoxifylline and inositol nicotinate for the treatment of intermittent claudication in people with peripheral arterial disease
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Pentoxifylline
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Formulary
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NICE TA223- Cilostazol, naftidrofuryl oxalate, pentoxifylline and inositol nicotinate for the treatment of intermittent claudication in people with peripheral arterial disease
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| 02.07.01 |
Inotropic sympathomimetics |
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Dobutamine
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Formulary
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Infusion
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Dopamine
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Formulary
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Injection
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Isoprenaline
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Formulary
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Unlicensed
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| 02.07.02 |
Vasoconstrictor sympathomimetics |
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Midodrine
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Formulary
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Tablets 2.5mg, 5mg
Postural hypotension
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Noradrenaline (Norepinephrine)
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Formulary
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Intravenous infusion
Critical care and theatre use only
Healthcare professionals should be aware of the differences in strength and presentation between noradrenaline products.
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Phenylephrine
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Formulary
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Injection
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Metaraminol
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Formulary
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Injection 2.5mg/5mL, 10mg/1mL
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| 02.07.03 |
Cardiopulmonary resuscitation |
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Adrenaline (epinephrine) (1 in 10 000)
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Formulary
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Injection 1mg/10mL amp, 1mg/10mL pre-filled syringe
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| 02.08.01 |
Parenteral anticoagulants |
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Argatroban monohydrate
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Formulary
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Solution for infusion 50mg/50ml
Concentrate for solution for infusion 250mg/2.5ml
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Bivalirudin
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Formulary
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Infusion 250mg
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NICE NG185: Acute coronary syndromes
|
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| 02.08.01 |
Heparin |
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Heparin
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Formulary
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Injection 1000units/1mL, 10 000units/10mL, 20 000units/20mL
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| 02.08.01 |
Low molecular weight heparins |
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Refer to local Trust guidance for advice on the prescribing and monitoring of low molecular weight heparins. |
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Dalteparin
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Formulary
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Refer to local Trust guidance for advice on the prescribing and monitoring of low molecular weight heparins.
Care when prescribing/selecting strength of syringes - Different strengths available.
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Enoxaparin
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Formulary
|
Refer to local Trust guidance for advice on the prescribing and monitoring of low molecular weight heparins.
Due to the differences in injectable device, all enoxaparin prescribing should be by brand name. In addition, due to the availability of biosimilar versions of enoxaparin, MHRA guidance to prescribe by brand name should be followed.
Switching between brands should be as a last resort after full training in the use of the new device has taken place.
Care when prescribing/selecting strength of syringes - Different strengths available.
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Tinzaparin
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Formulary
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Refer to local Trust guidance for advice on the prescribing and monitoring of low molecular weight heparins.
Care when prescribing/selecting strength of syringes - Different strengths available
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| 02.08.01 |
Heparinoids |
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Danaparoid sodium injection
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Formulary
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Anticoagulation where standard options are contra-indicated. Use only following haematologist advice.
|
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| 02.08.01 |
Heparin flushes |
|
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Heparin flush
|
Formulary
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Flush 50units/5mL
Arterial line patency
Critical care use only
|
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|
| 02.08.01 |
Epoprostenol |
|
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Epoprostenol
|
Formulary
|
Injection 500micrograms
Specialist initiation only
Renal dialysis when heparins are unsuitable or contra-indicated
|
MHRA: incompatibilities between Veletri and some administration devices
|
| 02.08.01 |
Fondaparinux |
|
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Fondaparinux
|
Formulary
|
Injection 1.5mg in 0.3mL, 2.5mg in 0.5mL, 5mg in 0.4mL, 7.5mg in 0.6mL, 10mg in 0.8mL
|
NICE NG185: Acute coronary syndromes
|
| 02.08.02 |
Oral anticoagulants |
|
|
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Apixaban
|
Formulary
|
Tablets 2.5mg, 5mg Apixaban for preventing stroke and systemic embolism in people with non-valvular atrial fibrillation (NICE TA275)
Apixaban for the prevention of venous thromboembolism after total hip or knee replacement in adults (NICE TA245)
Apixaban for the treatment and secondary prevention of deep vein thrombosis and/or pulmonary embolism (NICE TA341)
Use in patients with limb casts. Use according to Trust protocols.
|
NICE TA245: Apixaban for the prevention of venous thromboembolism after total hip or knee replacement in adults
NICE TA275: Apixaban for preventing stroke and systemic embolism in people with non-valvular atrial fibrillation
NICE TA341: Apixaban for the treatment and secondary prevention of deep vein thrombosis and/or pulmonary embolism
|
Rivaroxaban
|
Formulary
|
Tablets 2.5mg, 10mg, 15mg, 20mg
Rivaroxaban for the prevention of stroke and systemic embolism in people with atrial fibrillation (NICE TA256)
Rivaroxaban for the prevention of venous thromboembolism after total hip or total knee replacement in adults (NICE TA 170)
Rivaroxaban for preventing adverse outcomes after acute management of acute coronary syndrome (NICE TA335)
Rivaroxaban for the treatment of deep vein thrombosis and prevention of recurrent deep vein thrombosis and pulmonary embolism (NICE TA261)
Rivaroxaban for treating pulmonary embolism and preventing recurrent venous thromboembolism (NICE TA287)
*10mg tablets* Treatment of DVT and PE, and extended prevention of recurrent DVT and PE in adults
Use in patients with limb casts. Use according to Trust protocols.
|
LSCMMG: Rivaroxaban 10mg NMR
MHRA: Rivaroxaban (Xarelto▼) after transcatheter aortic valve replacement: increase in all-cause mortality, thromboembolic and bleeding events in a clinical trial
MHRA: Rivaroxaban (Xarelto▼): reminder that 15 mg and 20 mg tablets should be taken with food
NICE TA170: Rivaroxaban for the prevention of venous thromboembolism after total hip or total knee replacement in adults
NICE TA256: Rivaroxaban for the prevention of stroke and systemic embolism in people with atrial fibrillation
NICE TA261: Rivaroxaban for the treatment of deep vein thrombosis and prevention of recurrent deep vein thrombosis and pulmonary embolism
NICE TA287: Rivaroxaban for treating pulmonary embolism and preventing recurrent venous thromboembolism
NICE TA335: Rivaroxaban for preventing adverse outcomes after acute management of acute coronary syndrome
|
Edoxaban
|
Formulary
|
tablets 15mg, 30mg, 60mg Edoxaban for preventing stroke and systemic embolism in people with non-valvular atrial fibrillation (NICE TA355)
Edoxaban for treating and for preventing deep vein thrombosis and pulmonary embolism (NICE TA354)
Use in patients with limb casts. Use according to Trust protocols.
|
NICE TA354: Edoxaban for treating and for preventing deep vein thrombosis and pulmonary embolism
NICE TA355: Edoxaban for preventing stroke and systemic embolism in people with non-valvular atrial fibrillation
|
Dabigatran
|
Formulary
|
Capsules 110mg, 150mg Dabigatran etexilate for the prevention of stroke and systemic embolism in atrial fibrillation (NICE TA249)
Dabigatran etexilate for the prevention of venous thromboembolism after hip or knee replacement surgery in adults (NICE TA157)
Dabigatran etexilate for the treatment and secondary prevention of deep vein thrombosis and/or pulmonary embolism (NICE TA327)
Use in patients with limb casts. Use according to Trust protocols.
|
MHRA: Dabigatran (Pradaxa): contraindicated in patients with prosthetic heart valve(s) requiring anti-coagulant treatment
NICE TA157: Dabigatran etexilate for the prevention of venous thromboembolism after hip or knee replacement surgery in adults
NICE TA249: Dabigatran etexilate for the prevention of stroke and systemic embolism in atrial fibrillation
NICE TA327: Dabigatran etexilate for the treatment and secondary prevention of deep vein thrombosis and/or pulmonary embolism
|
Rivaroxaban with aspirin
|
Formulary
|
Tablets 2.5mg
Prevention of cardiac events in patients with coronary (CAD) or peripheral artery Disease (PAD)
East Lancashire only
|
MHRA: Rivaroxaban (Xarelto▼) after transcatheter aortic valve replacement: increase in all-cause mortality, thromboembolic and bleeding events in a clinical trial
MHRA: Rivaroxaban (Xarelto▼): reminder that 15 mg and 20 mg tablets should be taken with food
NICE TA607: Rivaroxaban for preventing atherothrombotic events in people with coronary or peripheral artery disease
|
Warfarin
|
Formulary
|
Tablets 1mg, 3mg, 5mg
Treatment of venous thromboembolism
Prevention of stroke and systemic embolism in non-valvular atrial fibrillation
|
LSCMMG: Atrial Fibrillation Pathway for the prevention of stroke and systemic embolism in AF in the absence of valvular heart disease
MHRA: Direct-acting antivirals to treat chronic hepatitis C: risk of interaction with vitamin K antagonists and changes in INR
MHRA: Warfarin: be alert to the risk of drug interactions with tramadol
MHRA: Warfarin: reports of calciphylaxis
|
Acenocoumarol (Sinthrome®)
|
Formulary
|
Tablets 1mg
Second line vitamin K antagonist
|
|
|
Andexanet alfa (Ondexxya ®)
|
Formulary
|
Powder for solution for infusion 200mg
|
NICE TA697- Andexanet alfa for reversing anticoagulation from apixaban or rivaroxaban
|
Idarucizumab® (Praxbind)
|
Formulary
|
Solution for injection/infusion 2.5 g/50 mL
Rapid reversal of anticoagulant effects of dabigatran
|
LSCMMG: Idarucizumab NMR
|
|
|
|
|
|
|
|
|
|
|
|
|
| 02.08.03 |
Protamine sulphate |
|
|
Protamine
|
Formulary
|
Injection 50mg/5mL
|
|
|
| 02.09 |
Antiplatelet drugs |
|
|
Aspirin
|
Formulary
|
Dispersible tablets 75mg, 300mg
The use of enteric coated aspirin 75mg is not recommended
|
|
|
Clopidogrel
|
Formulary
|
Tablets 75mg
|
MHRA: Clopidogrel and proton pump inhibitors: interaction—updated advice
MHRA: Clopidogrel: risk of acquired haemophilia
NICE TA210: Clopidogrel and modified-release dipyridamole for the prevention of occlusive vascular events
|
Dipyridamole
|
Formulary
|
Tablets 25mg, 100mg Modified-release capsules 200mg
|
NICE NG128: Stroke and transient ischaemic attack in over 16s: diagnosis and initial management
NICE TA210: Clopidogrel and modified-release dipyridamole for the prevention of occlusive vascular events
|
Prasugrel
|
Formulary
|
Tablets 5mg, 10mg
|
MHRA: Prasugrel (Efient▼): rare but serious hypersensitivity reactions
MHRA: Prasugrel (Efient): increased risk of bleeding
NICE TA317: Prasugrel with percutaneous coronary intervention for treating acute coronary syndromes
|
Ticagrelor
|
Formulary
|
Tablets 60mg, 90mg
|
NICE NG185: Acute coronary syndromes
NICE TA236: Ticagrelor for the treatment of acute coronary syndromes
NICE TA420: Ticagrelor for preventing atherothrombotic events after myocardial infarction
|
Tirofiban
|
Formulary
|
Infusion
Emergency use - Initiated under specialist supervision. Follow local protocol.
|
|
|
|
|
|
|
|
|
|
|
| 02.10.02 |
Fibrinolytic drugs |
|
|
Alteplase
|
Formulary
|
Follow local policy
|
NICE TA264: Alteplase for treating acute ischaemic stroke
|
Streptokinase
|
Formulary
|
Follow local policy
|
|
|
Tenecteplase (Metalyse®)
|
Formulary
|
Follow local policy
|
NICE TA990: Tenecteplase for treating acute ischaemic stroke
|
Urokinase
|
Formulary
|
Follow local policy
|
|
|
|
|
|
|
|
|
| 02.11 |
Antifibrinolytic drugs and haemostatics |
|
|
Tranexamic Acid
|
Formulary
|
Tablets 500mg
|
|
|
Efanesoctocog alfa
|
Formulary

|
Specialist use only
|
NICE TA1051: Efanesoctocog alfa for treating and preventing bleeding episodes in haemophilia A in people 2 years and over
|
Emicizumab (Hemlibra®)
|
Formulary

|
Solution for injection
Specialist use only
|
NHSE: Emicizumab for prophylaxis of bleeding episodes in people with moderate haemophilia A without inhibitors
|
Marstacimab (Hympavzi®)
|
Formulary

|
Solution for injection pre-filled pen 150mg/ml
Specialist use only
|
NICE TA1073: Marstacimab for treating severe haemophilia A or B in people 12 years and over without anti-factor antibodies
|
Tranexamic Acid
|
Formulary
|
Injection 500mg/5mL
|
NICE NG39: Major trauma: assessment and initial management
|
| 02.12 |
Lipid-regulating drugs |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
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|
|
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|
| 02.12 |
Statins |
|
|
Atorvastatin
|
First Choice
|
Tablets 10mg, 20mg, 40mg, 80mg
Chewable tablets 10mg, 20mg (Restricted for use in patients for whom the standard tablets are not suitable who would otherwise require a liquid)
|
MHRA: Statins: interactions, and updated advice for atorvastatin
|
Simvastatin
|
Formulary
|
Tablets 10mg, 20mg, 40mg
|
|
|
Rosuvastatin
|
Formulary
|
Tablets 5mg, 10mg, 20mg
|
|
|
Pravastatin
|
Formulary
|
Tablets 10mg, 20mg, 40mg
Restricted to use in patients who cannot tolerate other statins.
|
|
|
Simvastatin with ezetimibe
|
Formulary
|
|
|
|
| 02.12 |
Bile acid sequestrants |
|
|
Colestyramine
|
Formulary
|
Powder 4g/sachet
|
|
|
Colesevelam hydrochloride
|
Formulary
|
Tablets 625 mg Cardiovascular Disease prevention in hyperlipidaemia when the patient is intolerant of all other options.
|
LSCMMG: Colesevelam for Cardiovascular Disease (CVD) prevention NMR
|
| 02.12 |
Ezetimibe |
|
|
Ezetimibe
|
Formulary
|
Tablets 10mg
|
NICE TA385: Ezetimibe for treating primary heterozygous-familial and non-familial hypercholesterolaemia
|
| 02.12 |
Fibrates |
|
|
Bezafibrate
|
Formulary
|
Tablets 200mg Modified-release tablets 400mg
|
MHRA: Fibrates: first-line treatment not recommended
|
Fenofibrate
|
Formulary
|
Capsules (micronised) 200mg, 267mg Tablets (micronised) 160mg
To reduce the progression of diabetic retinopathy for people with non-proliferative retinopathy and type 2 diabetes (unlicensed indication). Ophthalmologist recommendation or initiation only. The GP should contact the patient’s endocrinologist for advice if serum transaminases and/or serum creatinine levels are of concern.
|
LSCMMG: Fenofibrate NMR
MHRA: Fibrates: first-line treatment not recommended
NICE NG242: Diabetic retinopathy: management and monitoring
|
| 02.12 |
PCSK9 inhibitors |
|
|
Alirocumab (Praluent®)
|
Formulary
|
Pre-filled pen 75mg, 150mg, 300mg
|
NICE TA393: Alirocumab for treating primary hypercholesterolaemia and mixed dyslipidaemia
|
Evolocumab (Repatha®)
|
Formulary
|
Solution for injection pre-filled pen 140mg
|
NICE TA394: Evolocumab for treating primary hypercholesterolaemia and mixed dyslipidaemia
|
Evolocumab (Repatha®)
|
Formulary
|
Prevention of cardiac events in patients with CHD and a history of ACS, in combination with a statin
|
LSCMMG: Evolocumab NMR
|
| 02.12 |
Other lipid modifying agents |
|
|
Bempedoic acid with Ezetimibe (Nustendi®)
|
Formulary
|
Tablets 180mg/10mg
|
NICE TA694: Bempedoic acid with ezetimibe for treating primary hypercholesterolaemia or mixed dyslipidaemia
|
Bempedoic acid (Nilemdo®)
|
Formulary
|
Tablets 180mg
Where ezetimibe is not tolerated, Bempedoic acid may be used as monotherapy.
|
|
|
Icosapent ethyl (Vazkepa®)
|
Formulary
|
Capsules 998 mg
|
NICE TA805: Icosapent ethyl with statin therapy for reducing the risk of cardiovascular events in people with raised triglycerides
|
Inclisiran (Leqvio®)
|
Formulary
|
Solution for injection pre-filled syringes 284mg/1.5ml
Restricted to use in line with LSCMMG: Lipid Management Pathway for Secondary Prevention of Cardiovascular Disease (CVD).
Included in NHS England HCD list to facilitate prescribing in secondary care until primary care prescribing is established.
NHSE has introduced funding arrangements to allow prescribing in Primary Care for a nominal amount, see link below.
|
LSC Patient Pathway for Commencing Inclisiran
NHSE: Funding and supply of inclisiran (Leqvio®)
NICE TA733: Inclisiran for treating primary hypercholesterolaemia or mixed dyslipidaemia
|
Lomitapide capsules (Lojuxta®)
|
Formulary

|
Capsules 5mg, 10mg, 20mg
Under expert supervision
|
NHSE: Clinical Commissioning Policy: Lomitapide for treating homozygous familial hypercholesterolaemia (adults) [1679]
|
Evinacumab (Evkeeza®)
|
Formulary

|
Concentrate for solution for infusion vials 345mg/2.3ml
|
NICE TA1002: Evinacumab for treating homozygous familial hypercholesterolaemia in people 12 years and over
|
Omega-3 acid ethyl esters
|
Formulary
|
|
|
|
| 02.13 |
Local sclerosants |
|
|
Sodium Tetradecyl Sulphate (Fibrovein®)
|
Formulary
|
Solution for Injection 3%, 1%, 0.5%, 0.2%
|
|
|
| .... |
Key |
 |
Restricted Drug |
 |
Unlicensed |
|
|
Link to adult BNF
|
|
|
Link to children's BNF
|
|
|
Link to SPCs
|
|
Scottish Medicines Consortium |
|
Cytotoxic Drug |
|
Controlled Drug |
|
|
High Cost Medicine
|
|
Cancer Drugs Fund
|
|
Homecare |
|
ICB commissioned |
|
NHS England commissioned |
|
Blueteq form needed |
|
Low carbon footprint |
|
Medium carbon footprint |
|
High carbon footprint |
|
| Status |
Description |

|
Green:
Appropriate for initiation and ongoing prescribing in both primary and secondary care.
Generally, little or no routine drug monitoring is required. |

|
Green (Restricted):
Appropriate for initiation and ongoing prescribing in both primary and secondary care provided:
Additional criteria specific to the medicine or device are met, or
The medicine or device is used following the failure of other therapies as defined by the relevant LSCMMG pathway.
Generally, little or no routine drug monitoring is required.
|

|
Red medicines:
Medicine is supplied by the hospital for the duration of the treatment course.
Primary care initiation or continuation of treatment is not recommended unless exceptional circumstances such as specialist GP.
Red medicines are those where primary care prescribing is not recommended. These treatments should be initiated by specialists only and prescribing retained within secondary care. They require specialist knowledge, intensive monitoring, specific dose adjustments or further evaluation in use. If however, a primary care prescriber has particular specialist knowledge or experience of prescribing a particular drug for a particular patient it would not always be appropriate for them to expect to transfer that prescribing responsibility back to secondary care. There should be a specific reason and a specific risk agreement, protocol and service set up to support this.
Primary care prescribers may prescribe RED medicines in exceptional circumstances to patients to ensure continuity of supply while arrangements are made to obtain ongoing supplies from secondary care. |

|
Amber level 0:
Suitable for prescribing in primary care following recommendation or initiation by a specialist.
Little or no specific monitoring required.
Patient may need a regular review, but this would not exceed that required for other medicines routinely prescribed in primary care.
Brief prescribing document or information sheet may be required.
Primary care prescribers must be familiar with the drug to take on prescribing responsibility or must get the required information.
When recommending or handing over care, specialists should ask primary care prescribers to take over prescribing responsibility, and should give enough information about the indication, dose, monitoring requirements, use outside product licence and any necessary dose adjustments to allow them to confidently prescribe. |

|
Amber level 1 (with shared care):
Suitable for prescribing in primary care following recommendation or initiation by a specialist.
Minimal monitoring required.
Patient may need a regular review, but this would not exceed that required for other medicines routinely prescribed in primary care.
Full prior agreement about patient’s on-going care must be reached under the shared care agreement.
Primary care prescribers are advised not to take on prescribing of these medicines unless they have been adequately informed by letter of their responsibilities with regards monitoring, side effects and interactions and are happy to take on the prescribing responsibility. A copy of locally approved shared care guidelines should accompany this letter which outlines these responsibilities. Primary care prescribers should then tell secondary care of their intentions as soon as possible by letter so that arrangements can be made for the transfer of care. |

|
Amber level 2 (with shared care and enhanced service):
Initiated by specialist and transferred to primary care following a successful initiation period.
Significant monitoring required on an on-going basis.
Full prior agreement about patient’s on-going care must be reached under the shared care agreement.
Suitable for enhanced service.
These medicines are considered suitable for GP prescribing following specialist initiation of therapy, as per shared care document which will be sent out with the request to prescribe, with on-going communication between the primary care prescriber and specialist. Amber Level 2 medicines require significant monitoring for which an enhanced service may be suitable. (Subject to local commissioning agreements). |

|
Do not prescribe: NOT recommended for use by the NHS in Lancashire and South Cumbria.
Includes medicines that NICE has not recommended for use and terminated technology appraisals, unless there is a local need. |

|
Grey medicines:
Medicines which have not yet been reviewed or are under the review process.
GPs and specialists are recommended not to prescribe these drugs.
This category includes drugs where funding has not yet been agreed.
|

|
Refer to local guidance. |
|
|
|