EMA to make public side-effects in EudraVigilance database by end of 2011

The European Medicines Agency by the end of 2011 plans to start granting public access to information in its EudraVigilance database on potential side-effects of certain human drugs1.

The European Medicines Agency by the end of 2011 plans to start granting public access to information in its EudraVigilance database on potential side-effects of certain human drugs1.

The EMA says monthly summary reports of suspected adverse drug reactions information held in the database for all human medicines authorised through the centralised procedure will be made available to...

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