Veterinary Reporting Form for Animals Injured by Trapping Devices 2025

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For unapproved drugs and devices, submit FORM FDA 1932a, Veterinary Adverse Experience, Lack of Effectiveness or Product Defect Report. You can use this form to report adverse events for any animal drug (FDA-approved or unapproved) or animal device.
You must use the Yellow Card Scheme27 , 28 to inform the MHRA about: serious suspected adverse reactions to a medicine. any suspected adverse reactions to products marked with a Black Triangle symbol (▼).
There are several ways to report: to your vet or retailer: Its a good idea to let your vet know if your animal has experienced a reaction. to the Marketing Authorisation Holder (MAH): Contact details are always given on the product packaging and leaflet.
The AVMA considers it the responsibility of the veterinarian to report suspected cases of animal cruelty when an educational or supportive approach is not appropriate. Knowing the signs consistent with animal maltreatment, cruelty, abuse, and neglect is key to being able to identify it.
Animal foods and FDA-approved products, such as animal medications and devices report the adverse event to the FDA online or by calling 1-888-FDA-VETS (1-888-332-8387).

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Patient initials, age at onset of reaction, reaction term(s), date of onset of reaction, suspected medication(s) reporter information.

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