Vfend
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 | Vfend |
|---|---|
| Active Substance | vorikonazol |
| Prescription | Medicinal product subject to medical prescription |
| Type of prescription | neponovljivi recept (tableta, prašak za oralnu suspenziju) ograničeni recept (prašak za otopinu za infuziju, prašak i otapalo za otopinu za infuziju) |
| Distribution | Supply through pharmacies (community) |
| ATC Code | J02AC03 |
| Marketing status | trajni prekid opskrbe |
| 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, ver 2 |
