Formulary Chapter 4: Central nervous system - Full Chapter
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04.01 |
Hypnotics and anxiolytics |
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04.01.01 |
Non-benzodiazepine hypnotics and sedatives |
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Avoid prescribing hypnotics. Hypnotics licensed for short term use only - If needed, use for 1-3 days only. Do not supply on discharge from hospital. On specialist advice only, some patients with long term psychiatric problems may require long term use.
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Zopiclone
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Formulary
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Tablets 3.75mg, 7.5mg First line short-term hypnotic.
If commenced in hospital, not to be continued at discharge. May have CD status in some hospital Trusts, refer to local policy.
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Daridorexant
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Formulary
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Tablets 25mg, 50mg
Treatment of long-term insomnia
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NICE TA922: Daridorexant for treating long-term insomnia
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Melatonin
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Formulary
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Children with learning disabilities
Children with ADHD
Children and adolescents with Autism Spectrum Disorder (ASD) and / or Smith-Magenis syndrome
Cerebral palsy
Children with complex neurodevelopmental disorders that the specialist considers eligible
Initiation of melatonin must be by a specialist in the indication being prescribed for and have a clear plan for review.
Prescribing and review of melatonin in children must follow the principles outlined in the Melatonin Pathway (Children)
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LSCMMG: Melatonin Pathway (Children)
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Melatonin
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Formulary
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For the Treatment of Rapid Eye Movement (REM) Sleep Behaviour Disorder (RBD) in Parkinson’s Disease and Lewy Body Dementia
Adults with learning disabilities
Sleep disturbance in adults with ADHD
Sleep disorders in the blind
Adults with complex neurodevelopmental disorders that the specialist considers eligible
Initiation of melatonin must be by a specialist in the indication being prescribed for and have a clear plan for review.
Prescribing and review of melatonin in adults must follow the principles outlined in the Melatonin Pathway (adults) **Under development**.
Melatonin is suitable for prescribing for the treatment of REM RBD in PD and LBD when clonazepam is not considered to be appropriate.
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LSCMMG: Melatonin
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Melatonin
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Formulary
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Primary insomnia in those over 55
Sleep problems in patients with dementia associated with Alzheimer’s
Colonis liquid 1mg/ml and 3mg tablets for all indications, including insomnia and jet lag
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LSCMMG: Melatonin
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Zolpidem
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Formulary
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Tablets 5mg, 10mg If commenced in hospital, not to be continued at discharge.
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MHRA: Zolpidem: risk of drowsiness and reduced driving ability
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04.01.01 |
Benzodiazepines |
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Nitrazepam
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Formulary
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Tablets 5mg Liquid 2.5mg/5mL
Insomnia (short term use).
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Temazepam
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Formulary
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Tablets 10mg Liquid 10mg/5mL
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Flurazepam
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Formulary
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Insomnia (short term use).
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Loprazolam
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Formulary
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Lormetazepam
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Formulary
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Insomnia (short term use).
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04.01.01 |
Zaleplon, Zolpidem and Zopiclone |
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04.01.01 |
Chloral and derivatives |
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Chloral Hydrate 500mg in 5mL
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Formulary
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Liquid 500mg/5mL
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MHRA: Chloral hydrate, cloral betaine (Welldorm): restriction of paediatric indication
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04.01.01 |
Clomethiazole (Chlormethiazole) |
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04.01.01 |
Antihistamines |
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Promethazine
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Formulary
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BNF considers promethazine less suitable for prescribing than alternatives for insomnia.
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04.01.01 |
Alcohol |
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04.01.01 |
Sodium oxybate |
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Sodium Oxybate
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Formulary
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Oral solution 500mg/mL
Narcolepsy with cataplexy (under expert supervision)
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04.01.02 |
Anxiolytics |
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Anxiolytics should be used at the lowest possible dose for the shortest possible time. |
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Pregabalin
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Formulary
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Capsules
Generalised Anxiety Disorder (GAD).
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LSCMMG: Pregabalin
MHRA: Pregabalin (Lyrica), gabapentin (Neurontin) and risk of abuse and dependence: new scheduling requirements from 1 April
MHRA: Pregabalin (Lyrica): findings of safety study on risks during pregnancy
MHRA: Pregabalin (Lyrica): reports of severe respiratory depression
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Buspirone
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Formulary
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Anxiety (short term use).
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04.01.02 |
Benzodiazepines |
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Diazepam
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Formulary
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Tablets 2mg, 5mg, 10mg Liquid 2mg/5mL Rectal tubes 5mg/2.5mL, 10mg/2.5mL
Anxiety.
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Lorazepam
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Formulary
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Tablets 1mg
Short term use in anxiety and insomnia.
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Chlordiazepoxide
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Formulary
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Capsules 5mg, 10mg Chlordiazepoxide is also used in a reducing regime for the management of acute alcohol withdrawal. See trust Clinical Guidelines.
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Diazepam
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Formulary
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Injection (solution) 10mg/2mL
Injection (emulsion) (Diazemuls®) 10mg/2mL
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Lorazepam injection
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Formulary
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Oxazepam
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Formulary
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Tablets 10mg, 15mg
Depending on local protocols, Oxazepam may be usedfor in-patient alcohol detoxification of patients with significant hepatic impairment where a short-acting benzodiazepine would be preferred.
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Alprazolam
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Formulary
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Chlordiazepoxide
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Formulary
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Anxiety.
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04.01.02 |
Buspirone |
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04.01.02 |
Beta blockers |
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Propranolol – see section 02.04 |
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Propranolol
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Formulary
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Tablets 10mg, 40mg, 80mg M/R capsules 80mg, 160mg
Anxiety.
Note: significant risks when taken in overdose. Potential for rapid deterioration before medical assistance is received.
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04.01.02 |
Meprobamate |
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Meprobamate
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Formulary
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Short term use in anxiety.
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04.01.03 |
Barbiturates |
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No barbiturates are recommended. For phenobarbital in epilepsy see sections 4.8.1 |
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04.02 |
Drugs used in psychoses and related disorders |
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04.02.01 |
Antipsychotic Drugs |
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04.02.01 |
First-Generation Antipsychotic Drugs |
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Benperidol
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Formulary
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Tablets 250mcg
Control of deviant antisocial sexual behaviour.
LSCFT consultant initiation only.
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Chlorpromazine
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Formulary
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Tablets 10mg, 25mg, 50mg, 100mg Liquid 25mg/5mL, 100mg/5mL
Schizophrenia and other psychoses, mania, anxiety, agitation, violent or dangerously impulsive behaviour, childhood schizophrenia.
Injection
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Flupentixol dihydrochloride tablets
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Formulary
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Tablets 500microgram, 1mg, 3mg
Schizophrenia and psychoses.
for depression
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Haloperidol
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Formulary
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Tablets 1.5mg, 5mg, 10mg Oral liquid 10mg/5mL, 5mg/ 5mL
Schizophrenia and other psychoses, mania, anxiety.
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MHRA: Haloperidol (Haldol): reminder of risks when used in elderly patients for the acute treatment of delirium
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Haloperidol
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Formulary
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Injection 5mg/1mL
Injection for rapid tranquilisation.
Haloperidol injection should be used in combination with promethazine injection for rapid tranquillisation.
This preparation is usually used in hospital for the rapid control of an acute episode and should not be confused with depot preparations of haloperidol decanoate which are usually used in the community or clinics for maintenance treatment.
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MHRA: Haloperidol (Haldol): reminder of risks when used in elderly patients for the acute treatment of delirium
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Promazine Hydrochloride
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Formulary
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Tablets 25mg, 50mg Liquid 25mg/5mL, 50mg/5mL
Short-term management of psychomotor agitation, agitation and restlessness in the elderly.
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Sulpiride
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Formulary
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Tablets 200mg Liquid 200mg/5mL
Schizophrenia.
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MHRA: Clozapine and other antipsychotics: monitoring blood concentrations for toxicity
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Trifluoperazine
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Formulary
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Tablets 1mg Liquid 1mg/5mL, 5mg/5mL
Schizophrenia and other psychoses, short term management of severe anxiety, psychomotor agitation, violent or dangerously impulsive behaviour, severe anxiety.
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Zuclopenthixol
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Formulary
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Tablets 2mg, 10mg, 25mg
Schizophrenia and other psychoses.
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Zuclopenthixol Acetate (Clopixol Acuphase®)
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Formulary
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Injection 50mg/1mL
Short term managementof acute psychosis, mania or exacerbations of chronic psychosis.
This preparation is usually used in hospital for an acute episode and should not be confused with depot preparations which are usually used in the community or clinics for maintenance treatment.
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04.02.01 |
Second-Generation Antipsychotic Drugs |
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The balance of risk and benefit should be considered and discussed with the patient or carers before prescribing antipsychotic drugs for elderly patients. In elderly patients with dementia, the use of antipsychotic drugs are associated with a small increased risk of mortality and an increased risk of stroke or transient ischaemic attack.
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Amisulpride
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Formulary
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Tablets 50mg, 100mg, 200mg, 400mg Liquid 100mg/mL
Schizophrenia.
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LSCMMG: Shared care guideline
MHRA: Clozapine and other antipsychotics: monitoring blood concentrations for toxicity
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Aripiprazole (Abilify®)
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Formulary
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Tablets 5mg,10mg,15mg, 30mg Orodispersible tablets 10mg,15mg Oral solution 1mg/ml
Orodispersible tablets and oral solution for use in swallowing difficulties only.
Consultant psychiatrist initiation only.
When prescribing, dispensing, or administering, check that the correct preparation is used—the preparation usually used in hospital for the rapid control of an acute episode (solution for injection containing aripiprazole 7.5 mg/mL) should not be confused with depot preparations (powder and solvent for prolonged-release suspension for injection), which are usually used in the community or clinics for maintenance treatment.
Alternating hemiplegia under specialist supervision. Bipolar disorder in Adults Bipolar disorder in Adolescents (NICE TA292) Treatment of Schizophrenia in adults. Treatment of Schizophrenia in people aged 15 to 17 years (NICE TA213)
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LSCMMG: Shared care guideline
MHRA: Aripiprazole (Abilify and generic brands): risk of pathological gambling
MHRA: Clozapine and other antipsychotics: monitoring blood concentrations for toxicity
NICE TA213: Aripiprazole for the treatment of schizophrenia in people aged 15 to 17 years
NICE TA292: Aripiprazole for treating moderate to severe manic episodes in adolescents with bipolar I disorder
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Cariprazine (Reagila®)
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Formulary
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Capsules 1.5mg, 3mg, 4.5mg, 6mg
Schizophrenia in adult patients.
Second-line therapy in patients where predominantly negative symptoms have been identified as an important feature. Requires prior approval by Lead Pharmacist before initiation.
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LSCFT - Cariprazine medicine request form
LSCMMG: Shared care guideline
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Clozapine
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Formulary
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Tablets 25mg, 100mg
Liquid 100mg/5mL
Injection
Treatment resistant/intolerant schizophrenia Psychosis in Parkinson’s disease.
LSCFT use only - Clinicains to refer to the clozapine procedure.
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LSCFT - Clozapine injection medication request form
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Lurasidone (Latuda®)
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Formulary
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Tablets 18.5mg, 37mg, 74mg
Schizophrenia in adults aged 13 and over.
LSCFT initiated only
Lurasidone will be supplied by the specialist service for the duration of the treatment course. Primary care initiation or continuation of treatment is not recommended unless exceptional circumstances such as specialist GP. Lurasidone may only be prescribed in the following circumstances: 1. The patient has previously had a trial of and has not responded to aripiprazole 2. The patient does not fulfil the treatment resistance criteria as outlined in NICE Clinical Guideline 178 for the initiation of prescribing of clozapine 3. The patient has: a. a metabolic disorder, diabetes or obesity or b. pre-existing risk factors for metabolic disease, diabetes or obesity All requests for lurasidone will be screened by LSCFT
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LSCFT - Lurasidone medicine request form
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Olanzapine
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Formulary
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Tablets 2.5mg, 5mg, 7.5mg, 10mg, 15mg Orodispersible tablets 5mg, 10mg, 15mg, 20mg
Schizophrenia and moderate to severe manic episodes and preventing reoccurrence in bipolar disorder.
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LSCMMG: Shared care guideline
MHRA: Clozapine and other antipsychotics: monitoring blood concentrations for toxicity
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Quetiapine
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Formulary
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Tablets, m/r tablets.
Please prescribe MR tablets by brand.
The XL version is only version licensed as an add-on treatment of major depressive episodes in patients with Major Depressive Disorder who have had sub-optimal response to antidepressant monotherapy.
Brancico XL, Zaluron XL tablets, Sondate XL 150mg, XL 200mg, XL 300mg, XL 400mg tablets [PRESCRIBE BY BRAND].
LSCFT initiated only
Schizophrenia, manic episodes associated with bipolar disorder, major depressive episodes in bipolar disorder, preventing recurrence in bipolar disorder. LSCFT: Approval should be sought from Locality Lead Pharmacist prior to initiation of XL for major depressive disorder.
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LSCFT - Quetiapine XL medicine request form
LSCMMG: Shared care guideline
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Risperidone
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Formulary
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Tablets 500micrograms, 1mg, 2mg, 3mg, 4mg Orodispersible tablets 500micrograms, 1mg, 2mg Oral solution 1mg/mL
Schizophrenia, moderate to severe manic episodes associated with bipolar disorders, shortterm treatment (up to 6 weeks) of persistent aggression in patients with moderate to severe Alzheimer's dementia unresponsive to non-pharmacological approaches and when there is a risk of harm to self or others, short-term symptomatic treatment (up to 6 weeks) of persistent aggression in conduct disorder in children from the age of 5 years and adolescents with subaverage intellectual functioning or mental retardation diagnosed according to DSM-IV criteria, in whom the severity of aggressive or other disruptive behaviours require pharmacologic treatment. May be used for longer periods (off-label) in conduct disorder with autistic spectrum condition or severe learning disability.
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LSCMMG: Shared care guideline
MHRA: Recent drug-name confusion
MHRA: Risperidone and paliperidone: risk of intraoperative floppy iris syndrome in patients undergoing cataract surgery
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Olanzapine Depot Injection
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Formulary
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Schizophrenia.
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04.02.02 |
Antipsychotic depot injections |
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Aripiprazole (Abilify Maintena®)
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Formulary
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Prolonged release suspension for injection 400mg
LSCFT initiation only.
Schizophrenia in adult patients stabilised on oral aripiprazole.
Application from RMO to be sent to Chief Pharmacist and Medical Director requesting its use.
When prescribing, dispensing, or administering, check that the correct preparation is used—the preparation usually used in hospital for the rapid control of an acute episode (solution for injection containing aripiprazole 7.5 mg/mL) should not be confused with depot preparations (powder and solvent for prolonged-release suspension for injection), which are usually used in the community or clinics for maintenance treatment.
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LSCFT - Aripiprazole depot injection medicine request form
MHRA: Aripiprazole (Abilify and generic brands): risk of pathological gambling
MHRA: Clozapine and other antipsychotics: monitoring blood concentrations for toxicity
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Flupentixol Decanoate
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Formulary
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Injection 20mg/1mL, 40mg/2mL Concentrate injection 50mg/0.5mL, 100mg/1mL
Maintenance in schizophrenia and other psychoses.
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Fluphenazine
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Formulary
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Maintenance in schizophrenia and other psychoses.
Licensed product no longer available. Where patients have deteriorated following a switch to an alternative depot antipsychotic a request can be made to use the unlicensed product should be made to the Lead Pharmacist in the locaility.
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Haloperidol decanoate injection
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Formulary
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Injection 50mg/1mL, 100mg/1mL
Maintenance in schizophrenia and other psychoses.
When prescribing, dispensing or administering, check that this is the correct preparation—this preparation is used for maintenance treatment and should not be used for the rapid control of an acute episode.
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MHRA: Haloperidol (Haldol): reminder of risks when used in elderly patients for the acute treatment of delirium
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Paliperidone
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Formulary
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Pre-filled syringes 50mg, 75mg, 100mg, 150mg - monthly injection
Pre-filled syringes 175mg, 263mg, 350mg, 525mg (Trevicta) - 3-monthly injection
Pre-filled syringes 700mg, 1000mg (Byannli) - 6-monthly injection
LSCFT initiation only.
Maintenance treatment of schizophrenia in adult patients.
For the monthly injection (Xeplian) and for Aripiprazole LAI: Application from RMO to be sent to Chief Pharmacist and Medical Director requesting its use.
The three monthly injection (Trevicta) if approval has been given for the monthly paliperidone depot there is no requirement for a further request to be sent to request a move to the three monthly option.
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LSCFT - Paliperidone depot injection medicine request form
LSCMMG: Paliperidone palmitate prolonged release suspension for injection
LSCMMG: Paliperidone palmitate prolonged release suspension for injection (six monthly)
MHRA: Risperidone and paliperidone: risk of intraoperative floppy iris syndrome in patients undergoing cataract surgery
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Pipotiazine Palmitate
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Formulary
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Schizophrenia.
Licensed product no longer available. Where patients have deteriorated following a switch to an alternative depot antipsychotic a request can be made to use the unlicensed product should be made to the Lead Pharmacist in the locaility.
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Risperidone (Risperdal Consta®)
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Formulary
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Injection 25mg, 37.5mg, 50mg
Schizophrenia.
Nonformulary in LSCFT.
Consultant psychiatrist initiation only. Request from doctor must be sent to chief pharmacist and medical director of LSCFT before authorised to prescribe.
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MHRA: Clozapine and other antipsychotics: monitoring blood concentrations for toxicity
MHRA: Recent drug-name confusion
MHRA: Risperidone and paliperidone: risk of intraoperative floppy iris syndrome in patients undergoing cataract surgery
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Zuclopenthixol Decanoate
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Formulary
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Injection 200mg/1mL Concentrate injection 500mg/1mL
Maintenance in schizophrenia and other psychoses.
When prescribing, dispensing, or administering, check that this is the correct preparation—this preparation is used for maintenance treatment and should not be used for the short-term management of an acute episode.
Zuclopenthixol decanoate has been confused with zuclopenthixol acetate; care must be taken to ensure the correct drug is prescribed and dispensed.
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04.02.03 |
Drugs used for mania and hypomania |
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Lamotrigine
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Formulary
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Tablets 25mg, 50mg, 100mg, 200mg Dispersible tablets 5mg, 25mg, 100mg
Bipolar disorder.
Prevention of depressive episodes in adult patients with bipolar I disorder who experience predominantly depressive episodes.
Dose titration required. See BNF/SPC for further information on titration, titration with valproate, and tritration with enzyme inducing drugs. Consider withdrawal if rash or signs of hypersensitivity syndrome develop. See BNF/SPC for more detail.
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MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
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04.02.03 |
Benzodiazepines |
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Clonazepam
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Formulary
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Tablets 500micrograms, 2mg Oral solution 500micrograms/5mL, 2mg/5ml
for use in all forms of epilepsy and in the treatment of mood disorders
for the treatment of anxiety (off-label indication)
Clonazepam has been confused with clobazam; care must be taken to ensure the correct drug is prescribed and dispensed.
Other than epilepsy the use of clonazepam is off-labeL.
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MHRA: Benzodiazepines and opioids: reminder of risk of potentially fatal respiratory depression
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04.02.03 |
Antipsychotic drugs |
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04.02.03 |
Carbamazepine |
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Carbamazepine
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Formulary
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ablets 100mg, 200mg, 400mg Modified-release tablets 200mg, 400mg
Liquid 100mg/5mL Suppositories 125mg, 250mg
Prophylaxis of bipolar disorder unresponsive to lithium.
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MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
MHRA: Carbamazepine, oxcarbazepine and eslicarbazepine: potential risk of serious skin reactions
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04.02.03 |
Valproic acid |
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Sodium valproate
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Formulary
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Mood stabiliser (unlicensed indication)
In November 2023, due to known significant risk of serious harm to a baby after exposure to valproate the MHRA has stipulated that new regulatory measures will be put in place in January 2024 for oral valproate medicines as follows:
- Valproate must not be initiated in patients male or female under the age of 55 years, unless two specialists independently consider and document that there is no other effective or tolerated treatment and any use of valproate in women of childbearing potential should be in accordance with the Pregnancy Prevention Programme.
- At their next annual review females of childbearing potential will require the signature of a second specialist if valproate is to be continued
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MHRA: Antiepileptic drugs in pregnancy: updated advice following comprehensive safety review
MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
MHRA: Full pack dispensing of valproate-containing medicines
MHRA: Valproate use in men: as a precaution, men and their partners should use effective contraception
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Valproic Acid
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Formulary
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E/C tablets 250mg, 500mg
Manic episodes associated with bipolar disorder.
In November 2023, due to known significant risk of serious harm to a baby after exposure to valproate the MHRA has stipulated that new regulatory measures will be put in place in January 2024 for oral valproate medicines as follows:
- Valproate must not be initiated in patients male or female under the age of 55 years, unless two specialists independently consider and document that there is no other effective or tolerated treatment and any use of valproate in women of childbearing potential should be in accordance with the Pregnancy Prevention Programme.
- At their next annual review females of childbearing potential will require the signature of a second specialist if valproate is to be continued
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MHRA: Antiepileptic drugs in pregnancy: updated advice following comprehensive safety review
MHRA: Antiepileptic drugs: updated advice on switching between different manufacturers’ products
MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
MHRA: Valproate use in men: as a precaution, men and their partners should use effective contraception
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04.02.03 |
Lithium |
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Due to differences in bioavailability prescribing should be by brand name. For new patients Priadel is recommended. Lithium carbonate 200mg is equivalent to Lithium citrate 509mg.
There are significant interactions with lithium, see BNF. |
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Lithium Carbonate (Camcolit®)
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Formulary
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Modified-release tablets 400mg
Treatment and prophylaxis of mania, bipolar disorder and recurrent depression. Aggressive or self-mutilating behaviour.
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LSCMMG: Shared care guideline
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Lithium Carbonate (Priadel®)
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Formulary
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M/R tablets 200mg, 400mg
Treatment and prophylaxis of mania, bipolar disorder and recurrent depression. Aggressive or self-mutilating behaviour.
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LSCMMG: Shared care guideline
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Lithium Citrate (Priadel®)
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Formulary
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Liquid 520mg/5mL
Treatment and prophylaxis of mania, bipolar disorder and recurrent depression. Aggressive or self-mutilating behaviour.
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LSCMMG: Shared care guideline
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04.03 |
Antidepressant drugs |
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MHRA/CHM advice: SSRI/SNRI antidepressant medicines: small increased risk of postpartum haemorrhage when used in the month before delivery (January 2021)
MHRA: click here for link
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04.03.01 |
Tricyclic and related antidepressant drugs |
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Limited quantities of tricyclic antidepressants should be prescribed at any one time because their cardiovascular and epileptogenic effects are dangerous in overdosage.
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04.03.01 |
Tricyclic antidepressants |
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Amitriptyline
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Formulary
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Tablets 10mg, 25mg, 50mg Liquid 25mg/5mL
Sugar Free oral solution 50mg/5mL
Depression.
Consider overdose risk.
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Clomipramine
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Formulary
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Capsules 10mg, 25mg, 50mg Depressive illness, phobic and obsessional states.
MR tablets are considered by the Joint Formulary Committee for the BNF to be less suitable for prescribing.
Consider overdose risk.
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Imipramine
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Formulary
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Tablets 10mg, 25mg
Depressive illness.
Consider overdose risk.
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Lofepramine
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Formulary
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Tablets 70mg Liquid 70mg/5mL
Depression.
Less cardiotoxicity and lower risk in overdose compared with other tricyclic antidepressants.
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Doxepin
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Formulary
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Capsules 10mg, 25mg, 50mg
Depressive illness.
Consider overdose risk.
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Nortriptyline
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Formulary
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Tablets 10mg, 25mg
Depression.
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Trimipramine (Surmontil®)
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Formulary
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Tablets 10mg, 25mg Capsules 50mg
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Dosulepin
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Formulary
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Tablets and Capsules
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LSCMMG: Guidelines for Primary Care: Review of Dosulepin
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04.03.01 |
Related antidepressants |
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Trazodone
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Formulary
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Capsules 50mg, 100mg Tablets 150mg Liquid 50mg/5mL - for titration/dose reduction and patients with swallowing difficulties.
At the 50mg and 100mg strengths capsules are significantly less expensive than tablets.
Depression, anxiety.
Consider overdose risk.
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04.03.02 |
Monoamine-oxidase inhibitors |
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Phenelzine (Nardil®)
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Formulary
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Tablets 15mg
Depression.
CAUTION: Many interactions with other medication, food and drink. Refer to SPC. Washouts required when changing to and from Phenelzine
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04.03.02 |
Reversible MAOIs |
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Moclobemide
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Formulary
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Tablets 150mg, 300mg
Depression, social phobia.
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04.03.03 |
Selective serotonin re-uptake inhibitors |
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Citalopram
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Formulary
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Tablets (as hydrobromide) 10mg, 20mg Oral drops (as hydrochloride) 40mg/mL (2mg/drop)
8mg oral drops is equivalent to 10mg tablet.
Lower incidence of drug interactions than some other SSRI’s.
First prescribe an SSRI in generic form unless there are interactions with other drugs; consider using citalopram or sertraline because they have less propensity for interactions.
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MHRA: Citalopram and escitalopram: QT interval prolongation
MHRA: Citalopram: suspected drug interaction with cocaine; prescribers should consider enquiring about illicit drug use
MHRA: SSRI/SNRI antidepressant medicines: small increased risk of postpartum haemorrhage when used in the month before delivery
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Escitalopram
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Formulary
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Tablets 5mg, 10mg, 20mg
Generalised Anxiety Disorder, Major depressive illness.
In depression, escitalopram is only licensed for major depressive episodes.
Available for consultant initiation in generalised anxiety disorder but only after sertraline has been tried.
|
LSCMMG: Citalopram and escitalopram: QT interval prolongation
MHRA: SSRI/SNRI antidepressant medicines: small increased risk of postpartum haemorrhage when used in the month before delivery
|
Fluoxetine
|
Formulary
|
Capsules 20mg, Dispersible tablets 20mg (for patients unable to swallow standard capsules), Liquid 20mg/5mL
First line for children and adolescents. Higher propensity for drug interactions.
|
MHRA: SSRI/SNRI antidepressant medicines: small increased risk of postpartum haemorrhage when used in the month before delivery
|
Paroxetine
|
Formulary
|
Tablets 20mg, 30mg
Higher risk of discontinuation reactions. Higher propensity for drug interactions.
|
MHRA: SSRI/SNRI antidepressant medicines: small increased risk of postpartum haemorrhage when used in the month before delivery
|
Sertraline
|
Formulary
|
Tablets 50mg, 100mg NICE advises: First prescribe an SSRI in generic form unless there are interactions with other drugs; consider using citalopram or sertraline because they have less propensity for interactions
LSCFT: Depressive illness, obsessive compulsive disorder (under specialist supervision in children), post traumatic stress disorder, panic disorder, social anxiety disorder. NICE recommend first line for generalised anxiety disorder (unlicensed). Lower incidence of drug interactions than some other SSRI’s.
|
MHRA: SSRI/SNRI antidepressant medicines: small increased risk of postpartum haemorrhage when used in the month before delivery
|
Vortioxetine (Brintellix®)
|
Formulary
|
Tablets 5mg, 10mg, 20mg
Major depressive episodes. Third line use one in line with NICE TA367.
|
MHRA: SSRI/SNRI antidepressant medicines: small increased risk of postpartum haemorrhage when used in the month before delivery
NICE TA367: Vortioxetine for treating major depressive episodes
|
|
04.03.04 |
Other antidepressant drugs |
|
|
Tryptophan
|
Formulary
|
Capsule 500mg Hospital specialist initiation only for long term severe and disabling depressive illness, after trial of standard antidepressant treatment and as an adjunct to other antidepressant medication.
|
|
Agomelatine
|
Formulary
|
Tablets 25mg
Major Depressive Episodes.
with prior approval. LSCFT to approve all applications to use - patients currently on treatment can continue.
|
LSCFT - Agomelatine medicine request form
MHRA: Agomelatine (Valdoxan): risk of liver toxicity
|
Duloxetine (Cymbalta®) (prescribe by brand)
|
Formulary
|
Capsules (Cymbalta®) 30mg, 60mg There can be variation in the licensing of different medicines containing the same drug therefore prescribe by brand name.
Third line use within LSCFT.
CAUTION: available as another brand Yentreve for stress urinary incontinence. Recommended that prescriptions state the brand name Cymbalta.
|
MHRA: Duloxetine: marketed as Cymbalta▼ and Yentreve▼ for different disorders
MHRA: SSRI/SNRI antidepressant medicines: small increased risk of postpartum haemorrhage when used in the month before delivery
|
Reboxetine (Edronex®)
|
Formulary
|
Tablets 4mg
Not licensed in the elderly.
|
|
Venlafaxine
|
Formulary
|
Tablets 37.5mg, 75mg M/R capsules 75mg, 150mg
M/R capsules 225mg - to be prescribed as Vencarm XL in primary care Immediate release tablets are first line.
Third line use only. Consider cardiovascular history e.g. uncontrolled hypertension, and risk of overdose.
Higher propensity for discontinuation.
|
MHRA: SSRI/SNRI antidepressant medicines: small increased risk of postpartum haemorrhage when used in the month before delivery
|
04.03.05 |
Tetracyclic antidepressants |
|
|
Mianserin
|
Formulary
|
Tablets 10mg, 30mg
Depressive illness.
Initiated by LSCFT only.
Due to risks of neutropenia and agranulocytosis a full blood count is recommended every 4 weeks.
|
|
Mirtazapine
|
Formulary
|
Tablets 15mg, 30mg, 45mg
Dispersible tablets 15mg, 30mg, 45mg(only for patients with swallowing difficulties)
|
|
04.04 |
CNS stimulants and other drugs used for attention deficit hyperactivity disorder |
|
|
Atomoxetine
|
Formulary
|
Capsules 10mg, 18mg, 25mg, 40mg, 60mg
ADHD Restricted to initiation by child or adolescent psychiatrists or paediatricians experienced in the management of ADHD.
|
LSCMMG: Shared care guideline
MHRA: Atomoxetine (Strattera▼): increases in blood pressure and heart rate
|
Clonidine hydrochloride
|
Formulary
|
Tablets 25 micrograms
ADHD (unlicensed indication).
|
|
Dexamfetamine
|
Formulary
|
Tablets 5mg, 10mg, 20mg
ADHD
|
LSCMMG: Shared care guideline
|
Guanfacine (Intuniv®)
|
Formulary
|
M/R tablets 1mg, 2mg, 3mg, 4mg For use in children and adolescents 6 - 17 years for whom stimulants are not suitable, not tolerated or have shown to be ineffective.
Specialist initiation only.
|
LSCMMG: Shared care guideline
|
Lisdexamfetamine (Elvanse®)
|
Formulary
|
Adult Hard Capsules 30mg, 50 mg and 70mg (Elvanse Adult)
Hard capsules 20mg, 30mg, 40mg, 50mg, 60mg, 70mg (Elvanse)
Lisdexamfetamine (Elvanse) is recommended for use in the treatment of ADHD in children and young adults only in complex patients who meet both of the following criteria. - extenuating circumstances exist which mean that a patient would not reliably receive all the required doses of dexamfetamine throughout the day and requires a once daily dose of lisdexamfetamine to support adherence - treatment has been agreed through the internal governance arrangements of the trust.
|
LSCMMG: Shared care guideline
|
Methylphenidate
|
Formulary
|
Tablets 5mg, 10mg, 20mg M/R tablets 18mg, 27mg, 36mg, 54mg M/R capsules 5mg, 10mg, 20mg, 30mg, 40mg, 50mg, 60mg
All brands are formulary - choice of brand to made by specialist
For adult patients under the care of Psychiatry UK in South Cumbria, please prescribe as Xaggatin XL in primary care
|
LSCMMG: Shared care guideline
MHRA: Methylphenidate long-acting (modified-release) preparations: caution if switching between products due to differences in formulations
|
Modafinil
|
Formulary
|
Tablets 100mg Specialist initiation only.
|
MHRA: Modafinil (Provigil): increased risk of congenital malformations if used during pregnancy
MHRA: Modafinil (Provigil): now restricted to narcolepsy
|
Solriamfetol hydrochloride (Sunosi®)
|
Formulary
|
Tablets 75mg, 150mg
for NICE TA758: Solriamfetol for excessive daytime sleepiness caused by narcolepsy
for NICE TA777: Solriamfetol for treating excessive daytime sleepiness caused by obstructive sleep apnoea
|
NICE TA758: Solriamfetol for treating excessive daytime sleepiness caused by narcolepsy
|
|
04.04 |
Cocaine |
|
|
04.05 |
Drugs used in the treatment of obesity |
|
|
|
04.05.01 |
Anti-obesity drugs acting on the gastro-intestinal tract |
|
|
Liraglutide (Saxenda®)
|
Formulary
|
6mg/ml solution for injection 3ml pre-filled pens
liraglutide is recommended as an option in overweight and obesity as long as it is prescribed in secondary care by a specialist multidisciplinary tier 3 weight management service
for NICE TA749 Liraglutide for managing obesity in people aged 12 to 17 years (terminated appraisal)
|
MHRA: GLP-1 receptor agonists: reports of diabetic ketoacidosis when concomitant insulin was rapidly reduced or discontinued
MHRA: Ozempic▼(semaglutide) and Saxenda (liraglutide): vigilance required due to potentially harmful falsified products
NICE TA664: Liraglutide for managing overweight and obesity
|
Orlistat
|
Formulary
|
Capsules 120mg
|
MHRA: Orlistat: theoretical interaction with antiretroviral HIV medicines
|
Semaglutide (Wegovy®)
|
Formulary
|
Solution for injection in pre filled pen
0.25mg, 0.5mg, 1mg, 1.7mg, 2.4mg
Only available via referral to a Tier 3 Weight Management Service.
for NICE TA910 Semaglutide for managing overweight and obesity in young people aged 12 to 17 years.
|
MHRA: GLP-1 receptor agonists: reports of diabetic ketoacidosis when concomitant insulin was rapidly reduced or discontinued
NICE TA875: Semaglutide for managing overweight and obesity
|
Tirzepatide (Mounjaro®)
|
Formulary
|
Pre-filled pens, solution for injection.
Obesity.
|
LSCMMG: Tirzepatide
|
04.05.02 |
Centrally acting appetite suppressants |
|
|
Naltrexone-Bupropion
|
Formulary
|
Managing overweight and obesity in adults.
|
|
04.06 |
Drugs used in nausea and vertigo |
|
|
|
04.06 |
Vomiting during pregnancy |
|
|
04.06 |
Postoperative nausea and vomiting |
|
|
04.06 |
Motion sickness |
|
|
04.06 |
Other vestibular disorders |
|
|
04.06 |
Cytotoxic chemotherapy |
|
|
Olanzapine
|
Formulary
|
Treatment of post-chemotherapy nausea and vomiting (unlicensed indication). For oncology use only.
|
|
04.06 |
Palliative care |
|
|
04.06 |
Migraine |
|
|
04.06 |
Antihistamines |
|
|
Cyclizine
|
Formulary
|
Tablets 50mg Injection 50mg/mL
|
|
Cinnarizine
|
Formulary
|
Tablets 15mg
|
|
Promethazine Hydrochloride (Phenergan)
|
Formulary
|
Tablets 10mg, 25mg
Nausea and vertigo.
|
|
Doxylamine and pyridoxine (Xonvea®)
|
Formulary
|
Tablets Doxylamine succinate 10 mg, Pyridoxine hydrochloride 10 mg.
Treatment of nausea and vomiting of pregnancy in women who do not respond to conservative management.
|
|
04.06 |
Phenothiazines and related drugs |
|
|
Droperidol
|
Formulary
|
Injection 2.5mg/ml
For the prevention and treatment of post operative nausea and vomiting. Restricted use: Theatre use only, when other treatment options are not suitable.
|
|
Levomepromazine (Methotrimeprazine)
|
Formulary
|
Tablets 25mg Tablets 6.25mg Injection 25mg/1mL
For palliative care use only. Nausea and vomiting and agitation/terminal restlessness in the last days of life.
for schizophrenia (new patients)
|
LSCMMG: Levomepromazine
|
Prochlorperazine
|
Formulary
|
Tablets 5mg Buccal tablets 3mg Injection 12.5mg/1mL
Severe dystonic reactions sometimes occur with phenothiazines, especially in children and young people. Prochlorperazine should be avoided in patients with Parkinson’s disease and should be used cautiously in the elderly.
|
|
04.06 |
Domperidone and metoclopramide |
|
|
Metoclopramide
|
Formulary
|
Tablets 10mg Liquid 5mg/5ml Injection 10mg/2mL
Metoclopramide can induce acute dystonic reactions involving facial and skeletal muscle spasms and oculogyric crises. These dystonic effects are more common in the young (especially girls and young women) and the very old.
Metoclopramide should only be prescribed for short-term use (up to 5 days).
|
MHRA: Metoclopramide: risk of neurological adverse effects
|
Domperidone
|
Formulary
|
Tablets 10mg Liquid 5mg/5mL
Domperidone is no longer indicated for the relief of nausea and vomiting in children aged under 12 years or those weighing less than 35 kg.
Healthcare professionals are advised to adhere to the licensed dose and to use the lowest effective dose for the shortest possible duration (max. treatment duration should not usually exceed 1 week).
|
MHRA: Apomorphine with domperidone: minimising risk of cardiac side effects
MHRA: Domperidone for nausea and vomiting: lack of efficacy in children; reminder of contraindications in adults and adolescents
MHRA: Domperidone: risks of cardiac side effects
|
04.06 |
5HT3 antagonists |
|
|
Ondansetron
|
Formulary
|
Tablets 4mg, 8mg Liquid 4mg/5mL Injection 4mg/2mL, 8mg/4mL
Nausea & vomiting post operatively or chemotherapy induced.
|
MHRA: Ondansetron for intravenous use: dose-dependent QT interval prolongation
MHRA: Ondansetron: small increased risk of oral clefts following use in the first 12 weeks of pregnancy
NICE: Management of vomiting in children and young people with gastroenteritis: ondansetron
|
Granisetron
|
Formulary
|
Tablets 1mg Injection 1mg/1ml, 3mg/3ml
Nausea & vomiting post operatively or chemotherapy induced. Second line 5HT3 anatagonist.
|
|
Ondansetron
|
Formulary
|
Second line for hyperemesis (unlicensed indication) in line with RCOG guidance. Consultant initiation only.
|
MHRA: Ondansetron for intravenous use: dose-dependent QT interval prolongation
MHRA: Ondansetron: small increased risk of oral clefts following use in the first 12 weeks of pregnancy
RCOG: The Management of Nausea and Vomiting of Pregnancy and Hyperemesis Gravidarum (Green-top Guideline No.69)
|
04.06 |
Neurokinin receptor antagonist |
|
|
Aprepitant
|
Formulary
|
Capsules 80mg, 125mg
Adjunct treatment to prevent nausea and vomiting associated with moderately and highly emetogenic chemotherapy.
|
|
Palonosetron with netupitant
|
Formulary
|
Capsules 300 mg/0.5 mg
Prevention of acute and delayed nausea and vomiting associated with highly emetogenic cisplatin-based cancer chemotherapy. Prevention of acute and delayed nausea and vomiting associated with moderately emetogenic cancer chemotherapy. Oncology use only, only when aprepitant is ineffective.
|
|
04.06 |
Cannabinoid |
|
|
04.06 |
Hyoscine |
|
|
Hyoscine Hydrobromide
|
Formulary
|
Tablets 300micrograms Patch 1mg/72hours
|
MHRA: Hyoscine hydrobromide patches (Scopoderm 1.5mg Patch or Scopoderm TTS Patch): risk of anticholinergic side effects, including hyperthermia
|
04.06 |
Other drugs for Ménière's disease |
|
|
Betahistine Dihydrochloride
|
Formulary
|
Tablets 8mg, 16mg
|
|
04.07 |
Analgesics |
|
|
|
|
|
|
|
|
|
|
|
04.07.01 |
Non-opioid analgesics and compound analgesic preparations |
|
|
|
For relief of mild to moderate pain |
|
Co-codamol
|
Formulary
|
Tablets 30/500 (codeine 30mg/paracetamol 500mg), tablets effervescent 30/500
Compound analgesic preparations (containing opioids) should not be used routinely. Patients should be given the individual components where possible to allow titration of dose. Where these preparations are used, they should be for short term use only, for relief of moderate pain.
|
LSCMMG: Over the Counter Items that Should not be Routinely Prescribed in Primary Care Policy
MHRA: Codeine for analgesia: restricted use in children because of reports of morphine toxicity
|
Paracetamol
|
Formulary
|
Tablets 500mg Dispersible tablets 500mg Liquid 120mg/5mL, 250mg/5mL, 1g/10mL
Suppositories
Liquid and dispersible oral preparations reserved for when patients have with swallowing difficulties.
Consider OTC purchase
Some patients may be at increased risk of experiencing toxicity at therapeutic doses, particularly those with a body-weight under 50 kg and those with risk factors for hepatotoxicity. Clinical judgement should be used to adjust the dose of oral and intravenous paracetamol in these patients.
|
LSCMMG: Over the Counter Items that Should not be Routinely Prescribed in Primary Care Policy
|
Paracetamol
|
Formulary
|
Intravenous infusion 1g/100mL
For short term treatment of moderate pain or fever when the oral route is not available.
Some patients may be at increased risk of experiencing toxicity at therapeutic doses, particularly those with a body-weight under 50 kg and those with risk factors for hepatotoxicity. Clinical judgement should be used to adjust the dose of oral and intravenous paracetamol in these patients.
|
|
04.07.01 |
Compound analgesic preparations |
|
|
04.07.02 |
Opioid analgesics |
|
|
|
Strong Opioids: Treatments of choice
Chronic Pain Morphine is the first line strong opioid in management of severe chronic pain, in combination with non-opioid and adjuvant therapies. Oxycodone and topical agents (Fentanyl / Buprenorphine patches) should be considered as second line agents, for patients intolerant or contraindicated of morphine. |
|
Buprenorphine (sublingual)
|
Formulary
|
Sublingual tablets 200micrograms See section 4.10 for products used in opioid dependence.
|
|
Buprenorphine (Transdermal)
|
Formulary
|
Preparations that should be applied every 3 days (72 hours) include Hapoctasin®.
Preparations that should be applied every 4 days (96 hours) include Bupeaze®, Carlosafine®, Relevtec®, and Transtec®.
Preparations that should be applied every 7 days include Bunov®, Bupramyl®, Butec®, BuTrans®, Panitaz®, Rebrikel®, Reletrans®, and Sevodyne®.
Only for use in patients who are unable to take or tolerate oral medicine (including soluble tablets and liquids) OR where use of the low-dose buprenorphine patches may prevent administration problems for frail, elderly patients in the community.
Do not confuse the formulations of transdermal patches which are available in various strengths as 7-day, 4-day and 3-day patches; prescription by brand name is recommended.
|
|
Codeine Phosphate
|
Formulary
|
Tablets 15mg, 30mg Injection 60mg/1mL Syrup 25mg/5mL Linctus, BP 15mg/5mL
|
MHRA: Codeine for analgesia: restricted use in children because of reports of morphine toxicity
MHRA: Codeine for cough and cold: restricted use in children
|
Diamorphine
|
Formulary
|
Injection 5mg, 10mg, 30mg, 100mg, 500mg
**under review**
|
|
Dihydrocodeine
|
Formulary
|
Tablets 30mg
For short term use only.
in MBHT For use only in patients who are breastfeeding or after initiation by the pain team. For short term use only.
|
|
Fentanyl patches
|
Formulary
|
Matrix patches 12, 25, 50, 75, 100micrograms/hour for 72hours
Fentanyl matrix patches should be prescribed by brand name to minimise the risk of reservoir patches being accidentally supplied.
|
MHRA: Transdermal fentanyl patches for non-cancer pain: do not use in opioid-naive patients
MHRA: Transdermal fentanyl patches: life-threatening and fatal opioid toxicity from accidental exposure, particularly in children
|
Meptazinol Meptid
|
Formulary
|
Tablets 200mg Injection 100mg/1mL
MBHT use only: For those women who may need pain relief whilst they await transfer to either RLI or FGH.
|
|
Morphine
|
Formulary
|
Modified-release tablets
Modified-release capsules
Immediate-release tablets
Oral solution
Injection
Orodispersible tablets
Do not confuse modified-release 12-hourly preparations with 24-hourly preparations.
Modified-release tablets and capsules should be prescribed by brand.
Care should be taken to ensure that the correct strength of oral solution is prescribed and dispensed, and the dose stated as both quantity and volume.
|
HSIB: Unintentional overdose of morphine sulfate oral solution
|
Oxycodone oral
|
Formulary
|
Modified-release tablets Immediate-release tablets Immediate-release capsules Oral solution
Refer to Trust guidance and protocols for specific prescribing information.
Do not confuse modified-release 12-hourly preparations with 24-hourly preparations. Modified-release tablets and capsules should be prescribed by brand.
|
|
Pethidine hydrochloride
|
Formulary
|
Injection 50mg/mL, 100mg/2mL
|
|
Tramadol (oral)
|
Formulary
|
Capsules 50mg Dispersible tablets 50mg Modified-release tablets 100mg, 200mg
Do not confuse modified-release 12-hourly preparations with 24-hourly preparations, prescribers and dispensers must ensure that the correct formulation is prescribed and dispensed.
Modified-release formulations should be prescribed by brand.
|
MHRA: Warfarin: be alert to the risk of drug interactions with tramadol
|
Tramadol injection
|
Formulary
|
Injection 100mg/2mL
|
MHRA: Warfarin: be alert to the risk of drug interactions with tramadol
|
Tapentadol modified release
|
Formulary
|
M/R tablets 50mg, 100mg, 150mg, 200mg, 250mg
Chronic severe pain in adults.
|
MHRA: Tapentadol (Palexia): risk of seizures and reports of serotonin syndrome when co-administered with other medicines
|
|
|
|
|
|
|
|
04.07.03 |
Neuropathic pain |
|
|
Amitriptyline
|
Formulary
|
Tablets 10mg, 25mg, 50mg Liquid 25mg/5mL Sugar Free oral solution 50mg/5mL
Use in line with NICE and LSCMMG guidelines.
|
|
Duloxetine
|
Formulary
|
There can be variation in the licensing of different medicines containing the same drug.
|
|
Gabapentin
|
Formulary
|
Capsules 100mg, 400mg, 400mg
|
MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
MHRA: Gabapentin (Neurontin): risk of severe respiratory depression
MHRA: Pregabalin (Lyrica), gabapentin (Neurontin) and risk of abuse and dependence: new scheduling requirements from 1 April
|
Ketamine oral solution
|
Formulary
|
Liquid 50mg/5mL Unlicensed
Fo r chronic pain - Prescribing retained within NHS commissioned specialist pain services in Lancashire and South Cumbria. For palliative care only AMBER0 - under review
|
|
Lidocaine
|
Formulary
|
5% Medicated Plasters
Post Herpetic Neuralgia
For off-label indications.
In UHMB, only indicated (off-label) use endorsed by UHMB acute pain team is for prescribing in rib fractures
Maximum of 4 weeks supply to be given on discharge and not to be continued in primary care.
If required for longer than 4 weeks then GP should refer to chronic pain team for review and not issue a prescription
Any other off label use must be on the advice of the acute pain team and must only be prescribed by secondary care.
For use in Palliative care/EoL settings discuss with the Palliative Care team.
|
LSCMMG: Lidocaine 5% Medicated Plasters
|
Nortriptyline
|
Formulary
|
Tablets 10mg, 25mg
Use in line with NICE and LSCMMG guidelines.
Unlicensed indication.
|
|
Pregabalin
|
Formulary
|
Capsules 25mg, 50mg, 75mg, 100mg, 150mg, 200mg
Use in line with NICE and LSCMMG guidelines.
|
MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
MHRA: Pregabalin (Lyrica), gabapentin (Neurontin) and risk of abuse and dependence: new scheduling requirements from 1 April
MHRA: Pregabalin (Lyrica): findings of safety study on risks during pregnancy
MHRA: Pregabalin (Lyrica): reports of severe respiratory depression
|
04.07.03 |
Trigeminal neuralgia |
|
|
Carbamazepine
|
Formulary
|
Tablets 100mg, 200mg, 400mg Prolonged-release tablets 200mg, 400mg Liquid 100mg/5mL
|
MHRA: Antiepileptic drugs in pregnancy: updated advice following comprehensive safety review
MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
MHRA: Carbamazepine, oxcarbazepine and eslicarbazepine: potential risk of serious skin reactions
|
04.07.03 |
Postherpetic neuralgia |
|
|
04.07.03 |
Chronic facial pain |
|
|
04.07.03 |
NMDA receptor antagonists |
|
|
04.07.04 |
Antimigraine drugs |
|
|
04.07.04.01 |
Treatment of the acute migraine attack |
|
|
04.07.04.01 |
Analgesics |
|
|
04.07.04.01 |
5HT1 agonists |
|
|
Sumatriptan
|
Formulary
|
Tablets 50mg Nasal spray 20mg/0.1mL actuation, 2 unit-dose spray device Injection 6mg/0.5mL, 2 x 0.5mL prefilled syringes and auto-injector
Injection 3mg/0.5ml solution for injection in pre-filled pen
|
|
Zolmitriptan
|
Formulary
|
Orodispersable tablets 2.5mg
Zolmitriptan is recommended by NICE for predictable menstrual-related migraine that does not respond to standard acute treatment (unlicensed indication).
|
|
04.07.04.01 |
Ergot alkaloids |
|
|
04.07.04.01 |
Anti-emetics |
|
|
04.07.04.01 |
Other drugs for migrane |
|
|
04.07.04.02 |
Prophylaxis of migraine |
|
|
Amitriptyline
|
Formulary
|
Tablets 10mg, 25mg, 50mg Liquid 25mg/5mL Sugar Free oral solution 50mg/5mL
|
|
Atogepant (Aquipta®)
|
Formulary
|
Tablets 10mg, 60mg
|
NICE TA973: Atogepant for preventing migraine
|
Botulinum Toxin Type A (botox®)
|
Formulary
|
Powder for solution for injection
Specialist use only
|
NICE TA260: Botulinum toxin type A for the prevention of headaches in adults with chronic migraine
|
Eptinezumab (Vyepti®)
|
Formulary
|
Concentrate for solution for infusion 100mg/1mL
|
NICE TA871: Eptinezumab for preventing migraine
|
Erenumab (Aimovig®)
|
Formulary
|
Pre-filled syringe 70mg, 140mg
Pre-filled pen 70mg, 140mg
|
NICE TA682: Erenumab for preventing migraine
|
Fremanezumab (Ajovy®)
|
Formulary
|
Pre-filled pens/ pre-filled syringes 225mg/1.5ml solution for injection
|
NICE TA764: Fremanezumab for preventing migraine
|
Galcanezumab (Emgality® )
|
Formulary
|
Solution for injection pre-filled pens 120mg/1ml
For NICE TA659: Galcanezumab for preventing migraine
|
NICE TA659: Galcanezumab for preventing migraine
|
Pizotifen
|
Formulary
|
Tablets 500micrograms, 1.5mg
|
|
Propranolol
|
Formulary
|
Tablets 10mg, 40mg, 80mg M/R capsules 80mg, 160mg
Prophylaxis of migraine.
|
HSSIB: Potential under-recognised risk of harm from the use of propranolol
|
Rimegepant (Vydura)
|
Formulary
|
Oral lyophilisate 75mg
Prophylaxis of migraine (in patients who have at least 4 migraine days per month)
** North-West Pathway for Headache being developed **
|
NICE TA906: Rimegepant for preventing migraine
NICE TA919: Rimegepant for treating migraine
|
Topiramate
|
Formulary
|
Tablets 25mg, 50mg, 100mg, 200mg
Migraine Prophylaxis.
Topiramate is now contraindicated in pregnancy and in women of childbearing potential unless the conditions of a Pregnancy Prevention Programme are fulfilled. This follows a review by the MHRA which concluded that the use of topiramate during pregnancy is associated with significant harm to the unborn child. Harms included a higher risk of congenital malformation, low birth weight and a potential increased risk of intellectual disability, autistic spectrum disorder and attention deficit hyperactivity disorder in children of mothers taking topiramate during pregnancy. |
|
MHRA: Topiramate (Topamax): introduction of new safety measures, including a Pregnancy Prevention Programme
MHRA: Topiramate (Topamax): start of safety review triggered by a study reporting an increased risk of neurodevelopmental disabilities in children with prenatal exposure
|
Zonisamide
|
Formulary
|
Capsules, 25mg. 50mg, 100mg
Approved for use in patients when prior prophylactic treatments have failed and erenumab, galcanezumab and fremanezumab are being considered.
Unlicensed indication.
|
MHRA: Antiepileptic drugs in pregnancy: updated advice following comprehensive safety review
MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
|
Flunarizine
|
Unlicensed
|
Capsules 5mg
Specialist consultant use only
|
|
04.07.04.03 |
Cluster headache |
|
|
04.08 |
Antiepileptics |
|
|
|
|
|
|
|
04.08.01 |
Control of epilepsy |
|
|
Brivaracetam (Briviact®)
|
Formulary
|
Tablets 10mg, 25mg, 50mg, 75mg, 100mg Oral solution 10mg/1ml
Adjunctive therapy in the treatment of partial-onset seizures with or without secondary generalisation.
|
MHRA: Antiepileptic drugs in pregnancy: updated advice following comprehensive safety review
MHRA: Antiepileptic drugs: updated advice on switching between different manufacturers’ products
MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
|
Cannabidiol (Epidyolex®)
|
Formulary
|
Oral solution 100mg/mL
|
MHRA: Antiepileptic drugs in pregnancy: updated advice following comprehensive safety review
MHRA: Antiepileptic drugs: updated advice on switching between different manufacturers’ products
MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
NHSE: Cannabis-based products for medicinal use (CBPMs)
NICE TA614: Cannabidiol with clobazam for treating seizures associated with Dravet syndrome
NICE TA615: Cannabidiol with clobazam for treating seizures associated with Lennox–Gastaut syndrome
NICE TA873: Cannabidiol for treating seizures caused by tuberous sclerosis complex
|
Fenfluramine (Fintepla®)
|
Formulary
|
Oral solution 2.2 mg/mL
|
MHRA: Antiepileptic drugs in pregnancy: updated advice following comprehensive safety review
MHRA: Antiepileptic drugs: updated advice on switching between different manufacturers’ products
MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
NICE TA808: Fenfluramine for treating seizures associated with Dravet syndrome
|
|
|
04.08.01 |
Partial seizures with or without secondary generalisation |
|
|
04.08.01 |
Generalised seizures |
|
|
04.08.01 |
Carbamazepine and Oxcarbazepine |
|
|
Carbamazepine
|
Formulary
|
Tablets 100mg, 200mg, 400mg M/R tablets 200mg, 400mg Liquid 100mg/5mL Suppositories 125mg, 250mg
Epilepsy.
|
MHRA: Antiepileptic drugs in pregnancy: updated advice following comprehensive safety review
MHRA: Antiepileptic drugs: updated advice on switching between different manufacturers’ products
MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
MHRA: Carbamazepine, oxcarbazepine and eslicarbazepine: potential risk of serious skin reactions
|
Eslicarbazepine
|
Formulary
|
Tablets 800mg
Adjunctive therapy in adults with partial onset seizures with or without secondary generalisation.
|
MHRA: Antiepileptic drugs in pregnancy: updated advice following comprehensive safety review
MHRA: Antiepileptic drugs: updated advice on switching between different manufacturers’ products
MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
MHRA: Carbamazepine, oxcarbazepine and eslicarbazepine: potential risk of serious skin reactions
|
Oxcarbazepine (Trileptal®)
|
Formulary
|
Tablets 150mg, 300mg, 600mg Liquid 60mg/ml
Epilepsy.
|
MHRA: Antiepileptic drugs in pregnancy: updated advice following comprehensive safety review
MHRA: Antiepileptic drugs: updated advice on switching between different manufacturers’ products
MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
|
04.08.01 |
Ethosuximide |
|
|
Ethosuximide
|
Formulary
|
Capsules 250mg Liquid 250mg/5mL
Epilepsy.
|
MHRA: Antiepileptic drugs in pregnancy: updated advice following comprehensive safety review
MHRA: Antiepileptic drugs: updated advice on switching between different manufacturers’ products
MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
|
04.08.01 |
Gabapentin and pregabalin |
|
|
Gabapentin
|
Formulary
|
Capsules 100mg, 300mg, 400mg
Epilepsy.
|
MHRA: Antiepileptic drugs in pregnancy: updated advice following comprehensive safety review
MHRA: Antiepileptic drugs: updated advice on switching between different manufacturers’ products
MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
MHRA: Gabapentin (Neurontin): risk of severe respiratory depression
MHRA: Pregabalin (Lyrica), gabapentin (Neurontin) and risk of abuse and dependence: new scheduling requirements from 1 April
|
Pregabalin
|
Formulary
|
Capsules 25mg, 50mg, 75mg, 100mg, 150mg, 300mg
Epilepsy.
|
MHRA: Antiepileptic drugs in pregnancy: updated advice following comprehensive safety review
MHRA: Antiepileptic drugs: updated advice on switching between different manufacturers’ products
MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
MHRA: Pregabalin (Lyrica), gabapentin (Neurontin) and risk of abuse and dependence: new scheduling requirements from 1 April
MHRA: Pregabalin (Lyrica): findings of safety study on risks during pregnancy
MHRA: Pregabalin (Lyrica): reports of severe respiratory depression
|
|
04.08.01 |
Lacosamide |
|
|
Lacosamide
|
Formulary
|
Tablets 50mg, 100mg, 150mg, 200mg Oral solution 50mg/5ml
Epilepsy.
|
MHRA: Antiepileptic drugs in pregnancy: updated advice following comprehensive safety review
MHRA: Antiepileptic drugs: updated advice on switching between different manufacturers’ products
MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
|
Lacosamide IV
|
Formulary
|
200mg/20ml solution for infusion - vials
Epilepsy.
|
MHRA: Antiepileptic drugs in pregnancy: updated advice following comprehensive safety review
MHRA: Antiepileptic drugs: updated advice on switching between different manufacturers’ products
MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
|
04.08.01 |
Lamotrigine |
|
|
Lamotrigine
|
Formulary
|
Tablets 25mg 50mg, 100mg, 200mg Dispersible tablets 2mg, 5mg, 25mg, 100mg
Epilepsy.
|
MHRA: Antiepileptic drugs in pregnancy: updated advice following comprehensive safety review
MHRA: Antiepileptic drugs: updated advice on switching between different manufacturers’ products
MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
|
04.08.01 |
Levetiracetam |
|
|
Levetiracetam
|
Formulary
|
Tablets 250mg, 500mg, 1g Liquid 100mg/mL
Epilepsy.
|
LSCMMG: Position Statement Levetiracetam (Keppra®) prescribing: bioequivalence and antiepileptic drugs
MHRA: Antiepileptic drugs in pregnancy: updated advice following comprehensive safety review
MHRA: Antiepileptic drugs: updated advice on switching between different manufacturers’ products
MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
|
Levetiracetam Concentration for infusion
|
Formulary
|
Concentrate for solution for infusion 500mg/5ml
Specialist use in palliative care.
|
|
04.08.01 |
Perampanel |
|
|
Perampanel
|
Formulary
|
Tablets
Partial-onset seizures with or without secondary generalised seizures.
|
MHRA: Antiepileptic drugs in pregnancy: updated advice following comprehensive safety review
MHRA: Antiepileptic drugs: updated advice on switching between different manufacturers’ products
MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
|
04.08.01 |
Phenobarbital and other barbiturates |
|
|
Phenobarbital (phenobarbitone)
|
Formulary
|
Tablets 15mg, 30mg
|
MHRA: Antiepileptic drugs in pregnancy: updated advice following comprehensive safety review
MHRA: Antiepileptic drugs: updated advice on switching between different manufacturers’ products
MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
|
Primidone
|
Formulary
|
Tablets 250mg
|
MHRA: Antiepileptic drugs in pregnancy: updated advice following comprehensive safety review
MHRA: Antiepileptic drugs: updated advice on switching between different manufacturers’ products
MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
|
04.08.01 |
Phenytoin |
|
|
Phenytoin
|
Formulary
|
Capsules 25mg, 50mg, 100mg Liquid 30mg/5mL
Prescribe by brand.
|
MHRA: Antiepileptic drugs in pregnancy: updated advice following comprehensive safety review
MHRA: Antiepileptic drugs: updated advice on switching between different manufacturers’ products
MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
MHRA: Phenytoin: risk of Stevens-Johnson syndrome associated with HLA-B*1502 allele in patients of Thai or Han Chinese ethnic origin
NHSE: Risk of death and severe harm from error with injectable phenytoin
|
04.08.01 |
Retigaine |
|
|
04.08.01 |
Rufinamide |
|
|
Rufinamide (Inovelon®)
|
Formulary
|
Tablets 100mg, 200mg, 400mg Oral suspension 40mg/ml
Adjunct treatment of seizures in Lennox-Gastaut syndrome.
It should be used as a fourth line adjunctive therapy, usually in a combination with one or more of the following medicines; sodium valproate (unlicensed), topiramate or lamotrigine.
|
MHRA: Antiepileptic drugs in pregnancy: updated advice following comprehensive safety review
MHRA: Antiepileptic drugs: updated advice on switching between different manufacturers’ products
MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
|
04.08.01 |
Rufinamide |
|
|
04.08.01 |
Tiagabine |
|
|
Tiagabine
|
Formulary
|
Tablets 5mg, 10mg, 15mg
Epilepsy.
Only to be considered in line with NICE as a third line add-on treatment option in people with focal seizures.
|
MHRA: Antiepileptic drugs in pregnancy: updated advice following comprehensive safety review
MHRA: Antiepileptic drugs: updated advice on switching between different manufacturers’ products
MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
|
04.08.01 |
Topiramate |
|
|
Topiramate
|
Formulary
|
Tablets 25mg,50mg, 100mg, 200mg Sprinkle capsules 15mg, 25mg, 50mg
Epilepsy.
Topiramate oral suspension - Restricted for paediatric use only, when sprinkle capsules are unsuitable. Prescribers should be cautious when selecting the strength of suspension as multiple strengths are available.
Topiramate is now contraindicated in pregnancy and in women of childbearing potential unless the conditions of a Pregnancy Prevention Programme are fulfilled. This follows a review by the MHRA which concluded that the use of topiramate during pregnancy is associated with significant harm to the unborn child. Harms included a higher risk of congenital malformation, low birth weight and a potential increased risk of intellectual disability, autistic spectrum disorder and attention deficit hyperactivity disorder in children of mothers taking topiramate during pregnancy.
|
|
MHRA: Antiepileptic drugs in pregnancy: updated advice following comprehensive safety review
MHRA: Antiepileptic drugs: updated advice on switching between different manufacturers’ products
MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
MHRA: Topiramate (Topamax): introduction of new safety measures, including a Pregnancy Prevention Programme
MHRA: Topiramate (Topamax): start of safety review triggered by a study reporting an increased risk of neurodevelopmental disabilities in children with prenatal exposure
|
04.08.01 |
Valproate |
|
|
|
In November 2023, due to known significant risk of serious harm to a baby after exposure to valproate the MHRA has stipulated that new regulatory measures will be put in place in January 2024 for oral valproate medicines as follows:
- Valproate must not be initiated in patients male or female under the age of 55 years, unless two specialists independently consider and document that there is no other effective or tolerated treatment and any use of valproate in women of childbearing potential should be in accordance with the Pregnancy Prevention Programme.
- At their next annual review females of childbearing potential will require the signature of a second specialist if valproate is to be continued
|
|
|
Sodium Valproate (Epilim®)
|
Formulary
|
Crushable tablets 100mg e/c tablets 200mg, 500mg Liquid 200mg/5mL
Episenta® capsules (prolonged release sodium valproate) are also available for use, and are especially helpful for those patients with swallowing difficulties. They are given once daily as capsules or sachets which can be opened and put on soft food if required, without chewing. Like other valproate preparations when used for epilepsy, they should be prescribed by brand name.
In November 2023, due to known significant risk of serious harm to a baby after exposure to valproate the MHRA has stipulated that new regulatory measures will be put in place in January 2024 for oral valproate medicines as follows:
- Valproate must not be initiated in patients male or female under the age of 55 years, unless two specialists independently consider and document that there is no other effective or tolerated treatment and any use of valproate in women of childbearing potential should be in accordance with the Pregnancy Prevention Programme.
- At their next annual review females of childbearing potential will require the signature of a second specialist if valproate is to be continued
|
|
MHRA: Antiepileptic drugs in pregnancy: updated advice following comprehensive safety review
MHRA: Antiepileptic drugs: updated advice on switching between different manufacturers’ products
MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
MHRA: Valproate use in men: as a precaution, men and their partners should use effective contraception
|
Sodium Valproate Intravenous
|
Formulary
|
Injection 400mg with 4mL water for injections
400mg/4ml solution ampoules
Epilepsy. Different preparations may vary in bioavailability and are therefore not interchangeable, prescriptions should include the brand name.
In November 2023, due to known significant risk of serious harm to a baby after exposure to valproate the MHRA has stipulated that new regulatory measures will be put in place in January 2024 for oral valproate medicines as follows:
- Valproate must not be initiated in patients male or female under the age of 55 years, unless two specialists independently consider and document that there is no other effective or tolerated treatment and any use of valproate in women of childbearing potential should be in accordance with the Pregnancy Prevention Programme.
- At their next annual review females of childbearing potential will require the signature of a second specialist if valproate is to be continued
|
|
MHRA: Antiepileptic drugs in pregnancy: updated advice following comprehensive safety review
MHRA: Antiepileptic drugs: updated advice on switching between different manufacturers’ products
MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
MHRA: Valproate use in men: as a precaution, men and their partners should use effective contraception
|
|
04.08.01 |
Vigabatrin |
|
|
Vigabatrin
|
Formulary
|
Tablets 500mg Powder sachet 500mg
Epilepsy.
|
MHRA: Antiepileptic drugs in pregnancy: updated advice following comprehensive safety review
MHRA: Antiepileptic drugs: updated advice on switching between different manufacturers’ products
MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
|
04.08.01 |
Zonisamide |
|
|
Zonisamide
|
Formulary
|
Capsules 25mg, 50mg, 100mg
Epilepsy.
|
MHRA: Antiepileptic drugs in pregnancy: updated advice following comprehensive safety review
MHRA: Antiepileptic drugs: updated advice on switching between different manufacturers’ products
MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
|
04.08.01 |
Benzodiazepines |
|
|
Clobazam
|
Formulary
|
Tablets 10mg
|
MHRA: Antiepileptic drugs in pregnancy: updated advice following comprehensive safety review
MHRA: Antiepileptic drugs: updated advice on switching between different manufacturers’ products
MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
MHRA: Benzodiazepines and opioids: reminder of risk of potentially fatal respiratory depression
|
04.08.01 |
Other Drugs |
|
|
Cenobamate (Ontozry®)
|
Formulary
|
Tablets 12.5mg*, 25mg* (*initiation pack) 50mg, 100mg, 150mg, 200mg
|
MHRA: Antiepileptic drugs in pregnancy: updated advice following comprehensive safety review
MHRA: Antiepileptic drugs: updated advice on switching between different manufacturers’ products
MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
NICE TA753: Cenobamate for treating focal onset seizures in epilepsy
|
Stiripentol (Diacomit® )
|
Formulary
|
Capsules 250mg, 500mg
Powder for oral suspension in sachet 250mg, 500mg
RED RAG (for all ages) for continuation of treatment of patients who have previously received the drug during childhood under the NHSE standard contract for paediatric neurosciences - neurology. Not to be newly initiated in adults
|
MHRA: Antiepileptic drugs in pregnancy: updated advice following comprehensive safety review
MHRA: Antiepileptic drugs: updated advice on switching between different manufacturers’ products
MHRA: Antiepileptics: risk of suicidal thoughts and behaviour
|
04.08.02 |
Drugs used in status epilepticus |
|
|
Clonazepam
|
Formulary
|
Injection 1mg/1mL with 1mL water for injections
Status epilepticus.
|
|
Diazepam
|
Formulary
|
Injection (solution) 10mg/2mL Injection (emulsion) (Diazemuls®)10mg/2mL
|
MHRA: Benzodiazepines and opioids: reminder of risk of potentially fatal respiratory depression
|
Diazepam rectal tubes
|
Formulary
|
Rectal solution tube 5mg/2.5ml, 10mg/2.5ml
Status epilepticus.
|
MHRA: Benzodiazepines and opioids: reminder of risk of potentially fatal respiratory depression
|
Lorazepam
|
Formulary
|
Injection 4mg/1mL
Status epilepticus.
|
MHRA: Benzodiazepines and opioids: reminder of risk of potentially fatal respiratory depression
|
Midazolam (Epistatus ®)
|
Formulary
|
Oromucosal solution pre-filled oral syringes (Buccolam®) 2.5mg/0.5ml, 5mg/1ml, 7.5mg/1.5ml, 10mg/2ml
Buccal liquid (Epistatus ®) 10mg/1mL
Status epilepticus.
When an oral midazolam preparation is prescribed, a licensed product should be prescribed.
Buccal midazolam is available as both a 5mg/ml and 10mg/ml solution. To avoid confusion prescribe midazolam buccal solution using the brand name and state the dose in milligrams (mg) and millilitres (ml).
|
CEWT: Epilepsy-to-go
MHRA: Benzodiazepines and opioids: reminder of risk of potentially fatal respiratory depression
MHRA: Buccal midazolam (Buccolam▼): new authorised medicine for paediatric use
|
Paraldehyde
|
Formulary
|
Rectal solution 50% in olive oil
Status epilepticus. Unlicensed
|
|
Phenytoin sodium
|
Formulary
|
Injection 250mg/5mL
Status epilepticus.
|
|
04.08.03 |
Febrile convulsions |
|
|
04.09 |
Drugs used in parkinsonism and related disorders |
|
|
|
It is recommended that all patients with suspected Parkinson’s disease are referred to a neurologist or geriatrician with a special interest in Parkinson’s disease, before treatment is initiated. |
|
|
04.09.01 |
Dopaminergic drugs used in Parkinsons disease |
|
|
|
Treatment with levodopa and dopamine-receptor agonists are associated with impulse control disorders, including pathological gambling, binge eating, and hypersexuality. Patients and their carers should be informed about the risk of impulse control disorders.
|
|
|
|
|
|
04.09.01 |
Dopamine receptor agonists |
|
|
Pramipexole
|
Formulary
|
Tablets 88micrograms, 180micrograms, 350 micrograms, 700micrograms pramipexole base (equivalent to 125micrograms, 250micrograms, 500micrograms and 1mg pramipexole salt) Modified-release tablets 260 micrograms, 520 micrograms 1.05mg, 1.57mg, 2.1mg, 2.62mg, 3.15mg base (equivalent to 375micrograms, 750micrograms, 1.5mg, 2.25mg, 3mg, 3.75mg, 4.5mg salt)
Parkinson's disease.
|
|
Pramipexole
|
Formulary
|
Tablets 88micrograms, 180micrograms, 350 micrograms, 700micrograms pramipexole base (equivalent to 125micrograms, 250micrograms, 500micrograms and 1mg pramipexole salt)
Restless leg syndrome. Recommended as the first line pharmacological treatment for restless leg syndrome, in line with the LSCMMG Restless Legs Syndrome Guidance.
|
LSCMMG: The Management of Restless Legs Syndrome in Adults in Primary Care
|
Ropinirole
|
Formulary
|
Tablets 250micrograms, 500micrograms, 1mg, 2mg Modified-release tablets 2mg, 3mg, 4mg, 6mg, 8mg
Parkinson's disease.
|
MHRA: Recent drug-name confusion
|
Ropinirole
|
Formulary
|
Tablets 250micrograms, 500micrograms, 1mg, 2mg
Restless leg syndrome.
Recommended as the second line pharmacological treatment for restless leg syndrome, in line with the LSCMMG Restless Legs Syndrome Guidance.
|
MHRA: Recent drug-name confusion
|
Rotigotine
|
Formulary
|
Patches 2mg/24 hours, 4mg/24 hours, 6mg/24 hours, 8mg/24 hours
Parkinson's Disease.
Rotigotine has shown inferiority to ropinirole and should not be used in preference to other dopamine agonists unless such alternative are not suitable (e.g. compliance issues, need for social care to administer other oral therapies, dysphagia), not tolerated (GI disturbance), or ineffective.
|
|
Rotigotine
|
Formulary
|
Patches 1mg/24 hours, 2mg/24 hours, 3mg/24 hours
Restless Legs Syndrome.
Recommended for restricted use in line with the LSCMMG Restless Legs Syndrome Guidance.
|
|
Apomorphine (Dacepton®)
|
Formulary
|
Injection 50mg/5mL
Pre-filled pen 30mg/3mL
|
LSCMMG: Shared care guideline
MHRA: Apomorphine with domperidone: minimising risk of cardiac side effects
|
Amantadine
|
Formulary
|
Capsules 100mg Liquid 50mg/5mL
Parkinson's disease (but not drug-induced extrapyramidal symptoms).
|
|
04.09.01 |
Levodopa |
|
|
Co-Beneldopa
|
Formulary
|
Capsules 62.5mg (12.5/50), 125mg (25/100), 250mg (50/200) Dispersible tablets 62.5mg (12.5/50), 125mg(25/100) Modified-release capsules 125mg (25/100)
Parkinson's disease.
|
|
Co-Careldopa
|
Formulary
|
Tablets 62.5mg (12.5/50), 110mg (10/100), 125mg (25/100), 275mg (25/250) Modified-release tablets 125mg (25/100), 250mg (50/200)
Parkinson's disease.
|
|
Co-Careldopa and Entacapone
|
Formulary
|
Tablets (multiple strength combinations available).
Parkinson's disease.
|
|
Foslevodopa–Foscarbidopa (Produodopa®)
|
Formulary
|
Solution for infusion 240mg/ml + 12mg/ml
Parkinson's disease.
|
NICE TA934: Foslevodopa–foscarbidopa for treating advanced Parkinson’s with motor symptoms
|
Levodopa-Carbidopa- Entacapone Intestinal Gel (LECIG)
|
Formulary
|
Treatment with LECIG for Parkinson’s Disease may be delivered and managed through any acute provider trust which treats patients with Parkinson’s disease under either neurology or elderly care services. Eligibility must be determined through a specialist Parkinson’s clinician in an agreed networked approach with a specialist Parkinson's service in a regional specialised neurology centre. This may be through direct clinical assessment by clinicians with appropriate expertise within the network or through a Parkinson’s disease MDT arrangement managed through a specialised neurology centre.
|
|
Levodopa-Carbidopa Intestinal Gel (LCIG)
|
Formulary
|
Treatment with LCIG for Parkinson’s Disease may be delivered and managed through any acute provider trust which treats patients with Parkinson’s disease under either neurology or elderly care services. Eligibility must be determined through a specialist Parkinson’s clinician in an agreed networked approach with a specialist Parkinson's service in a regional specialised neurology centre. This may be through direct clinical assessment by clinicians with appropriate expertise within the network or through a Parkinson’s disease MDT arrangement managed through a specialised neurology centre.
|
|
04.09.01 |
Monoamine-oxidase-B inhibitors |
|
|
Rasagiline (Azilect®)
|
Second Choice
|
Tablets 1mg
Parkinson's disease.
|
|
Selegiline Hydrochloride
|
Formulary
|
Tablets 5mg, 10mg
Parkinson's disease.
See BNF for information on dose equivalence and conversion between tablet and lyophilisate formulations.
|
|
04.09.01 |
Catachol-O-methyltransferase inhibitors |
|
|
Entacapone (Comtess®)
|
Formulary
|
Tablets 200mg
Adjunct to co-beneldopa or co-careldopa in Parkinson's disease.
|
|
Opicapone (Ongentys®)
|
Formulary
|
Capsules 50mg
Adjunctive therapy in adults with end-of-dose motor fluctuations who cannot be stabilised on preparations of levodopa/DOPA decarboxylase inhibitors.
|
|
Tolcapone (Tasmar®)
|
Formulary
|
Tablets 100mg
Tolcapone as an adjunct to co-beneldopa or co-careldopa in Parkinson's disease with 'end-of-dose' motor fluctuations if another inhibitor of peripheral catechol-O-methyltransferase is inappropriate.
Third Line.
|
|
04.09.01 |
Amantadine |
|
|
04.09.02 |
Antimuscarinic drugs used in parkinsonism |
|
|
Orphenadrine
|
Formulary
|
Liquid 50mg/5mL
|
|
Procyclidine
|
Formulary
|
Tablets 5mg
Liquid 5mg/5mL
|
|
Procyclidine
|
Formulary
|
Injection 10mg/2mL
|
|
Trihexyphenidyl hydrochloride
|
Formulary
|
Tablets 2mg, 5mg Liquid 5mg/5mL
|
|
04.09.03 |
Drugs used in essential tremor, chorea, tics, and related disorders |
|
|
Piracetam
|
Formulary
|
Tablets 800mg, 1200mg
|
|
Primidone
|
Formulary
|
See section 4.8.1
|
|
Propranolol
|
Formulary
|
See section 2.4
|
|
Riluzole (Rilutek®)
|
Formulary
|
Tablets 50mg
Suspension 5mg/1ml
Amyotrophic Lateral Sclerosis form of Motor Neurone Disease. Consultant neurologist initiation only.
|
LSCMMG: Riluzole
LSCMMG: Shared care guideline
NICE TA20: Guidance on the use of riluzole (Rilutek) for the treatment of motor neurone disease
|
Tetrabenazine (Xenazine® 25)
|
Formulary
|
Tablets 25mg
|
|
04.09.03 |
Torsion dystonias and other involuntary movements |
|
|
Botulinum Toxin Type A (Xeomin®)
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First Choice
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Injection 100 units Preferred preparation. Consultant use only. Brands are not interchangeable.
Focal Spasticity in Multiple Sclerosis, Contracture of the joint in Multiple Sclerosis. Focal spasticity, Hand and wrist disability associated with stroke, Blepharospasm, Hemifacial spasm, Spasmodic torticollis.
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Botulinum Toxin Type A (Botox®)
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Formulary
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Injection 100units For existing patients Consultant use only Brands are not interchangeable
Focal Spasticity in Multiple Sclerosis, Contracture of the joint in Multiple Sclerosis. Focal spasticity, Hand and wrist disability associated with stroke, Blepharospasm, Hemifacial spasm, Spasmodic torticollis.
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04.09.04 |
Restless leg syndrome |
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04.10 |
Drugs used in substance dependence |
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Please refer to local pathway/protocols for guidance on use of drugs for dependency. This section is currently under development. |
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04.10 |
Alcohol dependence |
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These products should normally only be initiated by the community drug and alcohol team, or other specialist |
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04.10 |
Cigarette smoking |
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Patients wishing to quit should be referred to smoking cessation services for advice and support. Hospital pharmacies stock patches only for use by in-patients (or COPD homecare) |
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04.10 |
Opioid dependence |
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04.10.01 |
Alcohol dependence |
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These products should normally only be initiated by the community drug and alcohol team, or other specialist |
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04.10.02 |
Nicotine dependence |
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Varenicline (Champix®)
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Formulary
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Tablets 0.5mg, 1mg
Prescribed only as part of a programme of behavioural support for patients in England through NHS Stop Smoking Services.
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NICE TA123: Varenicline for smoking cessation
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04.10.03 |
Opioid dependence |
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04.10.03 |
Opioid substitution therapy |
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04.10.03 |
Adjunctive therapy and symptomatic treatment |
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04.10.03 |
Opioid-receptor antagonists |
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04.11 |
Drugs for dementia |
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Donepezil
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Formulary
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Tablets 5mg, 10mg Orodispersible tablet 5mg, 10mg
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Galantamine
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Formulary
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m/r capsules 8mg, 16mg, 24mg Oral liquid 4mg/1ml
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Memantine
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Formulary
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Tablets 10mg, 20mg Oral solution 10mg/mL
Primary care prescribers may start treatment with memantine without taking advice from a specialist clinician where an AChEI is already prescribed.
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MHRA: Memantine pump device (Ebixa): risk of medication errors
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Rivastigmine
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Formulary
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Capsules 1.5mg, 3mg, 4.5mg, 6mg Patches 4.6mg/24hours, 9.5mg/24hours, 13.3mg/24 hours Liquid 2mg/mL
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MHRA: Rivastigmine (Exelon) transdermal patch: risk of medication errors
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04.12 |
Other Nervous System medicines |
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Patisiran (Onpattro®)
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Formulary
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For treating hereditary transthyretin amyloidosis in line with NICE HST10 guidance via Specialist Centre
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Tafamidis
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Formulary
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NICE TA984: Tafamidis for treating transthyretin amyloidosis with cardiomyopathy
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.... |
Key |
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Restricted Drug |
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Unlicensed |
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Link to adult BNF
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Link to children's BNF
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Link to SPCs
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Scottish Medicines Consortium |
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Cytotoxic Drug |
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Controlled Drug |
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High Cost Medicine |
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Cancer Drugs Fund |
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NHS England |
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Homecare |
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ICB |
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Low carbon footprint |
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Medium carbon footprint |
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High carbon footprint |
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Status |
Description |
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Green:
Appropriate for initiation and ongoing prescribing in both primary and secondary care.
Generally, little or no routine drug monitoring is required. |
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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.
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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. |
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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. |
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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. |
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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). |
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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. |
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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.
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Refer to local guidance. |
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