Hexacima, cjepivo protiv difterije, tetanusa, pertutisa (nestanično, komponentno), hepatitisa B (rDNA), poliomijelitisa (inaktiviranog) i hemofilusa tip b (konjugirano), adsorbirano
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 | Hexacima, cjepivo protiv difterije, tetanusa, pertutisa (nestanično, komponentno), hepatitisa B (rDNA), poliomijelitisa (inaktiviranog) i hemofilusa tip b (konjugirano), adsorbirano |
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Active Substance | toksoid difterije toksoid tetanusa toksoid pertusisa filamentozni hemaglutinin pertusisa površinski antigen virusa hepatitisa B poliovirus tip 1, soj Mahoney (inaktiviran) poliovirus tip 2, soj MEF-1 (inaktiviran) poliovirus tip 3, soj Saukett (inaktiviran) polisaharid hemofilusa influence tip b (poliribozilribitolfosfat) |
Prescription | na recept |
Type of prescription | ograničeni recept |
Distribution | u ljekarni |
ATC Code | J07CA09 |
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 |