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ing to the World Health Organization, in pharmacovigilance there are considered to be four main elements to every case of an adverse event. These four elements are an identifiable patient, an identifiable reporter, a drug in question, and the actual adverse event.

Pharmacovigilance is the process and science of monitoring the safety of medicines and taking action to reduce the risks and increase the benefits of medicines. It is a key public health function.

Pharmacovigilance is a process by which information is collected to detect and prevent unexpected or unwanted adverse effects following the use of medicinal products. The scope of veterinary pharmacovigilance is mainly the safety and efficacy in animals and safety in people.

32. Veterinary Dictionary for Drug Regulatory Activities (VeDDRA) A list of standard clinical terms to be used in reporting suspected adverse events in animals or humans after exposure to veterinary medicinal products.

Veterinary pharmacovigilance involves closely monitoring the safety and efficacy of veterinary medicines on the European Union (EU) market.

Pharmacovigilance is the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other medicine/vaccine related problem. All medicines and vaccines undergo rigorous testing for safety and efficacy through clinical trials before they are authorized for use.