Following a full submission
AWMSG advice |
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Status: Recommended with restrictions | |||
Perampanel (Fycompa®) is recommended as an option for restricted use within NHS Wales. This recommendation applies only in circumstances where the approved Wales Patient Access Scheme is utilised. Perampanel (Fycompa®) should be restricted to treatment of patients whose seizures are still uncontrolled with first adjunctive therapy, within its licensed indication as adjunctive treatment of partial-onset seizures with or without secondarily generalised seizures in patients with epilepsy aged 12 years and older. Perampanel (Fycompa®) is not recommended for use within NHS Wales outside of this subpopulation. |
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Medicine details |
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Medicine name | perampanel (Fycompa®) | ||
Formulation | 2 mg, 4 mg, 6 mg, 8 mg, 10 mg, 12 mg film-coated tablet | ||
Reference number | 1219 | ||
Indication | Adjunctive treatment of partial-onset seizures with or without secondarily generalised seizures in patients with epilepsy aged 12 years and older |
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Company | Eisai Ltd | ||
BNF chapter | Central nervous system | ||
Submission type | Full | ||
Status | Recommended with restrictions | ||
Advice number | 1313 | ||
NMG meeting date | 10/04/2013 | ||
AWMSG meeting date | 08/05/2013 | ||
Ratification by Welsh Government | 29/07/2013 | ||
Date of issue | 31/07/2013 | ||
Date of last review | 30/08/2016 | ||
Commercial arrangement | WPAS |