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EMA Product

Vimpat

Product approved by European Medicines Agency (EU)

Basic Information

Vimpat

Regulatory Information

EMEA/H/C/000863

Authorised

August 29, 2008

June 26, 2008

55

July 24, 2024

Company Information

Belgium

Allée de la Recherche 60 BE-1070 Brussels

UCB PHARMA SA

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Vimpat is indicated as monotherapy and adjunctive therapy in the treatment of partial-onset seizures with or without secondary generalisation in adults, adolescents and children from 4 years of age with epilepsy.

Overview Summary

Vimpat is a medicine used on its own or as an add-on to other epilepsy medicines in the treatment of partial-onset seizures (epileptic fits starting in one specific part of the brain) with or without secondary generalisation (where the abnormal electrical activity spreads through the brain) in patients with epilepsy aged 2 years and older. Vimpat can also be used as add-on to other epilepsy medicines in the treatment of primary generalised tonic-clonic seizures (major fits, including loss of consciousness) in patients from 4 years of age with idiopathic generalised epilepsy (the type of epilepsy that is thought to have a genetic cause). Vimpat contains the active substance lacosamide.

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