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EMA Product

Toviaz

Product approved by European Medicines Agency (EU)

Basic Information

Toviaz

Regulatory Information

EMEA/H/C/000723

Authorised

April 20, 2007

30

March 4, 2025

Company Information

Belgium

Boulevard de la Plaine 17 1050 Bruxelles

Pfizer Europe MA EEIG

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Treatment of the symptoms (increased urinary frequency and / or urgency and / or urgency incontinence) that may occur in patients with overactive-bladder syndrome.

Overview Summary

This is a summary of the European public assessment report (EPAR) for Toviaz. 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 Toviaz.

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