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EMA Product

Twinrix Adult

Product approved by European Medicines Agency (EU)

Basic Information

Twinrix Adult

Regulatory Information

EMEA/H/C/000112

Authorised

September 19, 1996

24

February 7, 2024

Company Information

Belgium

Rue de l'Institut, 89 B-1330 Rixensart

GlaxoSmithKline Biologicals SA

Active Substances Detail

hepatitis A virus (inactivated)hepatitis B surface antigen

hepatitis A virus (inactivated)

Detailed Information

Therapeutic Indication

### Therapeutic indication Twinrix Adult is indicated for use in non immune adults and adolescents 16 years of age and above who are at risk of both hepatitis A and hepatitis B infection.

Overview Summary

This is a summary of the European public assessment report (EPAR). It explains how the Committee for Medicinal Products for Human Use (CHMP) assessed the studies performed, to reach their recommendations on how to use the medicine. If you need more information about your medical condition or your treatment, read the package leaflet (also part of the EPAR) or contact your doctor or pharmacist. If you want more information on the basis of the CHMP recommendations, read the scientific discussion (also part of the EPAR).

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