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EMA Product

Pregabalin Pfizer

Product approved by European Medicines Agency (EU)

Basic Information

Pregabalin Pfizer

Regulatory Information

EMEA/H/C/003880

Authorised

April 10, 2014

February 20, 2014

35

August 30, 2024

Company Information

Netherlands

Rivium Westlaan 142 Capelle aan den Ijssel 2909 LD

Upjohn EESV

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Neuropathic pain - Pregabalin Pfizer is indicated for the treatment of peripheral and central neuropathic pain in adults. Epilepsy - Pregabalin Pfizer is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation. Generalised Anxiety Disorder - Pregabalin Pfizer is indicated for the treatment of Generalised Anxiety Disorder (GAD) in adults.

Overview Summary

This is a summary of the European public assessment report (EPAR) for Pregabalin Pfizer. 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 Pregabalin Pfizer. For practical information about using Pregabalin Pfizer, patients should read the package leaflet or contact their doctor or pharmacist.

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