Revlimid
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 | Revlimid |
---|---|
Active Substance | lenalidomid |
Prescription | na recept |
Type of prescription | ograničeni recept |
Distribution | u ljekarni |
ATC Code | L04AX04 |
Medicinal product marketed in the Croatia | 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 |
Direct Healthcare Professional Communication
Name | Date | Download |
---|---|---|
Pismo zdravstvenim radnicima o novim važnim preporukama s obzirom na reaktivaciju virusa uz primjenu lenalidomida (Revlimid) | 08.11.2016 | Celgene Europe Limited |