Welcome to EudraVigilance Veterinary

EudraVigilance Veterinary is the European data-processing network and database management system for the exchange, processing, and evaluation of Suspected Adverse Events related to veterinary medicinal products authorised in the European Economic Area (EEA) this is the European Union, Norway, Iceland and Liechtenstein.

Pharmacovigilance concerns the surveillance of veterinary medicinal products, with particular reference to adverse reactions in animals and human beings related to the use of veterinary medicinal products.

Pharmacovigilance also comprises available information related to the lack of expected efficacy, off-label use, investigation into the validity of the withdrawal period, and any potential environmental problems arising from the use of the product.

EudraVigilance is a key component in supporting the Member States and the European Medicines Agency within its scientific committees in the co-ordination of the supervision, under practical conditions of use, of veterinary medicinal products which have been authorised within the EEA and the provision of advice on the measures to ensure the safe and effective use of these products.

This website provides further information, and access to the tools available to report adverse events.


As of 1.2.2020, the UK is no longer an EU Member State. However, EU law still applies to the UK during the transition period.