🇪🇺 Anakinra in European Union

EMA authorised Anakinra on 8 March 2002

Marketing authorisation

EMA — authorised 8 March 2002

  • Status: approved

Anakinra in other countries

Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.

Other Immunology approved in European Union

Frequently asked questions

Is Anakinra approved in European Union?

Yes. EMA authorised it on 8 March 2002.

Who is the marketing authorisation holder for Anakinra in European Union?

Biovitrum Ab is the originator. The local marketing authorisation holder may differ — check the official source linked above.