At its monthly meeting, the European Medicines Agency’s (EMA) Pharmacovigilance Risk Assessment Committee (PRAC) discussed four ongoing safety reviews. More information on all safety reviews currently under evaluation is provided in the table below. The Committee did not initiate or conclude a referral.

The PRAC also focused on the broad spectrum of its responsibilities which cover all aspects of the risk management of the use of medicines. Information on all topics discussed by the PRAC is available below in the agenda for the meeting. A record of the discussions held this week will be provided in the minutes of this meeting, which will be published following the next PRAC meeting at the end of November.

Agenda – PRAC draft agenda of meeting 24-27 October 2016

Posted on the EMA website on 28 October 2016