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EMA Product

Briviact (in Italy: Nubriveo)

Product approved by European Medicines Agency (EU)

Basic Information

Briviact (in Italy: Nubriveo)

Regulatory Information

EMEA/H/C/003898

Authorised

January 13, 2016

25

December 3, 2024

Company Information

Belgium

Allée de la Recherche 60 1070 Bruxelles

UCB PHARMA SA

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Briviact is indicated as adjunctive therapy in the treatment of partial-onset seizures with or without secondary generalisation in adult and adolescent patients from 16 years of age with epilepsy.

Overview Summary

Briviact is an epilepsy medicine used as an add-on to other epilepsy medicines to treat partial-onset seizures (epileptic fits starting in one specific part of the brain). It can be used in patients from the age of 2 years with partial-onset seizures with or without secondary generalisation (where the abnormal electrical activity spreads through the brain). Briviact contains the active substance brivaracetam.

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