Medicinal Products

Hemlibra

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 Hemlibra
Active Substance emicizumab
Prescription na recept
Type of prescription ograničeni recept
Distribution u ljekarni
ATC Code B02BX06
Medicinal product marketed in the Croatia Da
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 1
Vodič za laboratorijske zdravstvene radnike, verzija 1
Educational materials
for patients / caregivers
Vodič za bolesnike i njegovatelje, verzija 1
Kartica za bolesnika, verzija 1
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