Myalepta
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 | Myalepta |
|---|---|
| Active Substance | metreleptin |
| Prescription | Medicinal product subject to medical prescription |
| Type of prescription | ograničeni recept |
| Distribution | Supply through pharmacies (community) |
| ATC Code | A16AA07 |
| 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 healthcare professionals |
Vodič za zdravstvene radnike, verzija 2 |
| Educational materials for patients / caregivers |
Vodič za bolesnike, verzija 2 Kartica za bolesnike, verzija 2 Upute za upotrebu bočica od 3 mg, verzija 2 Upute za upotrebu bočica od 5,8 mg, verzija 2 Upute za upotrebu bočica od 11,3 mg, verzija 2 |
