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EMA Product

Aimovig

Product approved by European Medicines Agency (EU)

Basic Information

Aimovig

Regulatory Information

EMEA/H/C/004447

Authorised

July 26, 2018

June 1, 2018

12

August 14, 2023

Company Information

Ireland

Vista Building Elm Park, Merrion Road Dublin 4

NOVARTIS EUROPHARM LIMITED

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Aimovig is indicated for prophylaxis of migraine in adults who have at least 4 migraine days per month when initiating treatment with Aimovig.

Overview Summary

Aimovig is a medicine used to prevent migraine in adults who have migraines at least 4 days a month. Aimovig contains the active substance erenumab.

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