Medicinal Products

Soliris

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
aHUS Vodič za propisivace, verzija 5
gMG Vodič za propisivače, verzija 4
NMSOD Vodič za propisivače, verzija 1
PNH Vodič za propisivače, verzija 5
Educational materials
for patients / caregivers
aHUS Brošura za roditelje, verzija 3
aHUS Brošura za bolesnike roditelje, verzija 5
gMG Brošura za bolesnike, verzija 4
NMOSD Brošura za bolesnike, verzija 1
PNH Brošura za bolesnike roditelje, verzija 5
PNH Brošura za roditelje, verzija 3
Kartica sa sigurnosnim informacijama za bolesnika, verzija 4
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