PecFent
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 | PecFent |
|---|---|
| Active Substance | fentanilcitrat |
| Prescription | na recept |
| Type of prescription | poseban i ograničeni recept |
| Distribution | u ljekarni |
| ATC Code | N02AB03 |
| 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 propisivače lijeka, verzija 1 Vodič za ljekarnike, verzija 1 |
| Educational materials for patients / caregivers |
Vodič za bolesnike ili njegovatelje, verzija 1 Kartica za brojanje doza, verzija 1 Video s uputama za primjenu |
