Pharmacovigilance & Reporting Adverse Events
If you suspect an adverse event either in animals or humans that may be associated with the use of a Norbrook product or if you believe there is a a product quality issue with a Norbrook product, please report the details immediately by completing the form below.
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What is an adverse event?
An adverse event is a report of a harmful and unintended outcome which is due to exposure to a veterinary medicine administered to an animal. In other words it is any harmful or unexpected side effect to a veterinary medicine. Adverse reactions can occur in animals treated with veterinary medicines, or people who are exposed to veterinary medicines or treated animals. Adverse events also include instances where a veterinary medicine does not work as intended (lack of efficacy), adverse environmental effects and problems with residues of veterinary medicines in human food (milk and meat).
- What happens to reports when they are received?
- How can I report an adverse event?
- Reporting
Pharmacovigilance Adverse Event Reporting Form
This report should be completed when a suspected adverse event or lack of efficacy is suspected in animals or humans during, or after the use of one of Norbrook’s Veterinary Medicines. Upon receipt of this report, a member of the Pharmacovigilance department will contact the reporter to investigate the adverse event. The contact details of the reporter will be treated as confidential and will not be passed to anyone outside of Norbrook without permission.