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Volume 28, Issue 2
April 2005
Pages 185-201

Veterinary pharmacovigilance. Part 4. Adverse reactions

in humans to veterinary medicinal products
K. N. WOODWARD  
First published: 13 April 2005 | https://doi.org/10.1111/j.1365-2885.2005.00648.x | Related Information

Citations: 12

 Dr K. N. Woodward, Schering-Plough Animal Health, Breakspear Road Recommended

South, Harefield, Uxbridge, Middlesex UB9 6LS, UK. E-mail:
Veterinary Pharmacovigilance – the
kevin.woodward@spcorp.com
UK Experience

K. N. Woodward BA, BSc (Jt Hons), MSc

PDF  TOOLS  SHARE (Exp Pathol/Toxicol), MSc
(Pharmacovigilance), PhD, CBiol, FIBiol,
EurProBiol, CChem, FRSC, DipRCPath
(Tox), MTOPRA, FBTS

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Pharmacovigilance in veterinary
medicine in Chile: a pilot study

D. IRAGÜEN, S. URCELAY, B. SAN MARTÍN

Abstract
Journal of Veterinary Pharmacology
and Therapeutics
Although seemingly rare, adverse reactions to veterinary products do occur.
These may arise from inadvertent exposure during use or as a result of
occupational accidents. They are often mild in nature and include adverse Veterinary pharmacovigilance. Part
e ects such as minor skin reactions. However, more serious reactions may 3. Adverse e ects of veterinary
occur, and they are not restricted to the e ects of the veterinary medicines medicinal products in animals and
themselves. For example, high-pressure injection injuries may occur as a on the environment

result of accidents occurring during animal vaccination operations. This K. N. WOODWARD

paper reviews some of these events, mentions where appropriate the Journal of Veterinary Pharmacology
regulatory actions taken, and describes some of the measures used to and Therapeutics
minimise such e ects in the future, and serves to bring the issues discussed
here to the attention of pharmacologists, pharmacoepidemiologists and
others who train those who use veterinary medicinal products.

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