EudraVigilance Veterinary

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EudraVigilance Veterinary is the European data-processing network and database management system for the exchange, processing and evaluation of suspected adverse reaction reports (SARs) related to veterinary medicinal products authorised in the European Economic Area (EEA).

The standard terminology for EudraVigilance Veterinary is reviewed on a regular basis, considering comments from all stakeholders.

The Agency is increasing the degree of public access to the information stored in this database. For more information, see the access policy below.

Table of contents


Access policy

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Document(s) Language Status First published Last updated Effective Date
EudraVigilance access policy for medicines for veterinary use (English only) adopted 2011-07-08   2011-07-07
Overview of comments received on draft EudraVigilance access policy for medicines for veterinary use (English only) adopted 2011-07-26    

Data surveillance

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Document(s) Language Status First published Last updated Effective Date
Concept paper for revision of the recommendation for the basic surveillance of EudraVigilance Veterinary data (English only) draft: consultation closed 2015-11-20    
Adopted recommendation for the basic surveillance of Eudravigilance Veterinary data (English only) adopted 2011-03-01    
Draft recommendation for the basic surveillance of EudraVigilance Veterinary data (English only) draft: consultation closed 2010-06-03    
Concept paper for use of data in EudraVigilance veterinary (English only)   2006-06-26    

Veterinary Dictionary for Drug Related Affairs (VeDDRA) terminology

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List of species and breeds

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Document(s) Language Status First published Last updated Effective Date
List of species and breeds for electronic reporting of suspected adverse reactions in veterinary pharmacovigilance (English only) adopted 2006-08-22 2011-06-30 2011-10-10
List of species and breeds for electronic reporting of suspected adverse reactions in veterinary pharmacovigilance (English only) adopted 2004-04-15 2011-06-30  

Controlled terminology and data elements

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