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EMA Product

Vokanamet

Product approved by European Medicines Agency (EU)

Basic Information

Vokanamet

Regulatory Information

EMEA/H/C/002656

Authorised

April 23, 2014

24

December 18, 2024

Company Information

Belgium

Turnhoutseweg 30 B-2340 Beerse

Janssen-Cilag International NV

Active Substances Detail

canagliflozinmetformin hydrochloride

Detailed Information

Therapeutic Indication

### Therapeutic indication Vokanamet is indicated in adults aged 18 years and older with type 2 diabetes mellitus as an adjunct to diet and exercise to improve glycaemic control: - in patients not adequately controlled on their maximally tolerated doses of metformin alone - in patients on their maximally tolerated doses of metformin along with other glucose lowering medicinal products including insulin, when these do not provide adequate glycaemic control. - in patients already being treated with the combination of canagliflozin and metformin as separate tablets For study results with respect to combination of therapies, effects on glycaemic control and cardiovascular events, and the populations studied, see sections 4.4, 4.5 and 5.1.

Overview Summary

This is a summary of the European public assessment report (EPAR) for Vokanamet. It explains how the Agency assessed the medicine to recommend its authorisation in the EU and its conditions of use. It is not intended to provide practical advice on how to use Vokanamet. For practical information about using Vokanamet, patients should read the package leaflet or contact their doctor or pharmacist.

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