Lucentis
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 | Lucentis |
---|---|
Active Substance | ranibizumab |
Prescription | na recept |
Type of prescription | ograničeni recept |
Distribution | u ljekarni |
ATC Code | S01LA04 |
Medicinal product marketed in the Croatia | Nestašica |
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 |
Vodič za bolesnike - dijabetička retinopatija ili dijabetički makularni edem, verzija 1 Vodič za bolesnike neovaskularizacia žilnice, verzija 4 Vodič za bolesnike neovaskularna senilna makularna degeneracija, verzija 4 Vodič za bolesnike začepljenje vene u pozadini mrežnice, verzija 4 Vodiče za bolesnike dijabetički makularni edem, verzija 4 |