Medicinal Products


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 Soliris
Active Substance ekulizumab
Prescription na recept
Type of prescription ograničeni recept
Distribution u ljekarni
ATC Code L04AA25
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 7
Educational materials
for patients / caregivers
Vodič za bolesnike ili roditelje skrbnike, verzija 7
Kartica za bolesnike, verzija 5