Adverse reaction reports top a million in 2013
Highest ever figure received by EudraVigilance
EudraVigilance received more than one million post-marketing expedited adverse-drug-reaction (ADR) reports, an increase of 26% over 2012 and its highest ever annual figure, according to the second annual report on EudraVigilance for the European Parliament, the Council and the Commission.
The biggest increase occurred within the European Union (EU), reflecting the combined effort of the EU medicines regulatory network to encourage reporting of suspected adverse reactions to medicines.
The most notable increase was in ADRs reported by patients within the European Economic Area, which was 52% higher than in 2012. This is due to increased awareness among the general public of the importance of adverse reaction reporting, resulting in part from the new EU pharmacovigilance legislation, which introduced direct reporting of adverse reactions by patients and consumers in all Member States.
EudraVigilance is a web-based information system that collects, manages and analyses reports of suspected side effects of medicines. The data held in the database represent an important element in ensuring the continuous safety monitoring of medicines by the European Medicines Agency (EMA) and the Member States of the EU.
The reports received in 2013 were processed and subsequently made available for signal detection and data analysis by the EMA and medicines regulatory authorities in the Member States, which took appropriate regulatory action when necessary.
In 2013, the Agency’s Pharmacovigilance Risk Assessment Committee (PRAC) prioritised and assessed 100 signals, including 43 detected and validated by the EMA and 57 by EU Member States.
