Between 2003 and 2019, the European Medicines Agency (EMA) published annual bulletins to inform veterinarians and the public of the main outcomes of post-marketing surveillance activities for veterinary medicines in a calendar year.

The bulletins summarised recommendations on amending safety warnings and highlights ongoing monitoring activities for centrally authorised products.

The bulletins also included a summary of discussions and agreements at the veterinary Pharmacovigilance Working Party on pharmacovigilance issues with nationally authorised veterinary medicines.

How useful do you find this page?