Ilaris
The medicinal product has been authorised by the European Commission (EC) via centralised procedure in all EU Member States, based on the European Medicines Agency (EMA) experts' opinion.
| Name | Ilaris |
|---|---|
| Active Substance | kanakinumab |
| Prescription | Medicinal product subject to medical prescription |
| Type of prescription | Medicinal product subject to restricted medical prescription (prašak za otopinu za injekciju, prašak i otapalo za otopinu za injekciju) |
| Distribution | Supply through pharmacies (community) |
| ATC Code | L04AC08 |
| Marketing status | Marketed |
| Shortage status | No shortage |
| Summary of product characteristics (SmPC), labelling and package leaflet (PL) | download |
| Link to the European Medicines Agency's (EMA) product information | download |
| Link to the European Commission's (EC) decisions | download |
| Educational materials for patients / caregivers |
Kartica za bolesnika (Sindrom periodičnih vrućica), verzija 1 Kartica za bolestika (Stillova bolest), verzija 1 |
