What types of problems can be reported using FDA 1932A?
Adverse events can include:
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Side effects in animals, such as vomiting, diarrhea, colic, seizures, and other symptoms.
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Side effects in people exposed to drugs and devices used in animals, such as needle stick injuries, rashes, or headache or nausea secondary to product contact.
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Product defects, such as broken product seals, leaking bottles, and other problems.
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Medication errors, such as giving the wrong drug or dose, giving a drug too frequently, and other scenarios.
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Lack of effectiveness, such as a product not working, a product that stops working, or a product that isn’t working as well as it did.
For unapproved drugs and devices, submit FORM FDA 1932a, "Veterinary Adverse Experience, Lack of Effectiveness or Product Defect Report". This form can be used to report adverse events for any animal drug (FDA-approved or unapproved) or animal device, or even compounded drug products.
What types of problems can be reported using FDA 1932A?
Adverse events can include:
-
Side effects in animals, such as vomiting, diarrhea, colic, seizures, and other symptoms.
-
Side effects in people exposed to drugs and devices used in animals, such as needle stick injuries, rashes, or headache or nausea secondary to product contact.
-
Product defects, such as broken product seals, leaking bottles, and other problems.
-
Medication errors, such as giving the wrong drug or dose, giving a drug too frequently, and other scenarios.
-
Lack of effectiveness, such as a product not working, a product that stops working, or a product that isn’t working as well as it did.
For unapproved drugs and devices, submit FORM FDA 1932a, "Veterinary Adverse Experience, Lack of Effectiveness or Product Defect Report". This form can be used to report adverse events for any animal drug (FDA-approved or unapproved) or animal device, or even compounded drug products.
