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Suspected adverse events, 2015.

S Cooles¹, G Diesel¹, J Blenkinsop¹

¹Pharmacovigilance Unit, Veterinary Medicines Directorate, Woodham Lane, New Haw, Surrey KT15 3LS;

The Veterinary Record

|May 14, 2017

Summary

This summary is machine-generated.

Veterinary Medicines Directorate (VMD) surveillance in 2015 showed fewer reports for food animals but more for pets. A notable trend included dogs experiencing adverse events from large animal medications.

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Area of Science:

Veterinary pharmacology
Animal health surveillance
Pharmacovigilance

Background:

The Veterinary Medicines Directorate (VMD) conducts ongoing surveillance of animal medicines.
Understanding trends in adverse event reporting is crucial for animal safety.

Purpose of the Study:

To summarize key findings from the VMD's 2015 pharmacovigilance surveillance work.
To identify shifts in reporting patterns for different animal groups.

Main Methods:

Analysis of pharmacovigilance reports submitted to the VMD in 2015.
Categorization of reports by species and medication type.

Main Results:

A decrease in the number of adverse event reports for food-producing animal species was observed.
An increase in the number of adverse event reports for pet animals was noted.
Specific reports detailed dogs experiencing adverse effects from medications intended for large animals.

Conclusions:

The VMD's 2015 surveillance data indicates a changing landscape in animal medicine adverse event reporting.
Increased vigilance is required for pet animal pharmacovigilance.
Potential risks associated with off-label or incorrect use of veterinary medicines, particularly in mixed-species contexts, need further investigation.