Medicinal Products

Soliris

Name Soliris
Active Substance eculizumab
Prescription na recept
Type of prescription ograničeni recept
Distribution u ljekarni
ATC Code L04AA25
Medicinal product marketed in the Croatia Da
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 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

Note

The medicinal product has been authorised via centralised procedure in all Member States of the European Union based on the European Medicines Agency's expert opinion. Additional information on the medicinal product can be found under the following link:https://www.ema.europa.eu/en/medicines/human/EPAR/soliris

The marketing authorisation has been granted by the European Commission. All marketing authorisations of the European Commission can be found under the following link: http://ec.europa.eu/health/documents/community-register/html/index_en.htm

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