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EMA Product

Karvezide

Product approved by European Medicines Agency (EU)

Basic Information

Karvezide

Regulatory Information

EMEA/H/C/000221

Authorised

October 16, 1998

50

February 11, 2025

Company Information

France

82 Avenue Raspail 94250 Gentilly

SANOFI WINTHROP INDUSTRIE

Active Substances Detail

irbesartanhydrochlorothiazide

Detailed Information

Therapeutic Indication

### Therapeutic indication Treatment of essential hypertension. This fixed-dose combination is indicated in adult patients whose blood pressure is not adequately controlled on irbesartan or hydrochlorothiazide alone.

Overview Summary

This is a summary of the European public assessment report (EPAR) for Karvezide. It explains how the Committee for Medicinal Products for Human Use (CHMP) assessed the medicine to reach its opinion in favour of granting a marketing authorisation and its recommendations on the conditions of use for Karvezide. 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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