Dog — American Pit Bull Terrier — Carprofen
FDA Veterinary Adverse Event Report #A200578 — May 1, 2021 — Serious Event
Animal Information
| Species | Dog |
| Breed | American Pit Bull Terrier |
| Gender | Female |
| Age | 12.00 Year |
| Weight | 17.690 Kilogram |
Event Summary
| Report ID | A200578 |
| Date | May 1, 2021 |
| Serious | Yes |
| Outcome | Ongoing |
Drug Information
| Active Ingredients | Carprofen |
| Manufacturer | MSK |
Reported Reactions
Hyperalbuminaemia; Elevated serum alkaline phosphatase (SAP); Elevated alanine aminotransferase (ALT); Elevated cholesterol (total); Genital tract licking; Inappropriate urination; Urine leakage; Polyuria; Polydipsia; Rubbing; Eyelid erythema; Alopecia local; Crust; Ocular discharge; Conjunctivitis; Stiffness NOS; Abnormal dexamethasone suppression test; Hyperadrenocorticism; Vomiting; Diarrhoea; Unable to stand; Weakness; Falling; Depression; Appetite loss; Dry mucous membrane; Decreased skin turgor; Enophthalmos (see also 'Sunken eyes' in 'Systemic disorders'); Injected sclera; Dental plaque; Swelling around eye; Facial swelling (see also 'Skin'); Elevated temperature; Abnormal ultrasound finding; Gall bladder inflammation; Liver disorder NOS; Lymphopenia; Neutrophilia; Large platelets; Hypoglycaemia; Prolonged activated partial thrombin time (APTT); Elevated blood urea nitrogen (BUN); Elevated creatinine; Elevated aspartate aminotransferase (AST); Other abnormal test result NOS; Elevated total bilirubin; Elevated triglyceride; Anaphylaxis
Related Dog Reports
| Report ID | Breed | Reactions | Outcome | Date |
|---|---|---|---|---|
| N141519 | Terrier - Yorkshire | Lack of efficacy (endoparasite) - hookworm | Ongoing | Dec 29, 2025 |
| A200609 | Shepherd Dog - German | Drooling; Panting; Pacing; Uncomfortable | Ongoing | Dec 29, 2025 |
| N141330 | Pug | Loss of hearing; Ear canal inflammation | Outcome Unknown | Dec 29, 2025 |
| N047956 | Greyhound | Lack of efficacy - NOS; Unrelated death | Euthanized | Dec 29, 2025 |
| N141555 | Pug, Beagle | Bloody stool | Outcome Unknown | Dec 29, 2025 |
Frequently Asked Questions
Stop the medication immediately and call your veterinarian. For severe reactions — seizures, facial swelling, difficulty breathing, extreme lethargy, or collapse — go to an emergency veterinary clinic without waiting. Note the exact time the drug was given and when symptoms first appeared. Do not give any additional medications without guidance. Bring the drug packaging when you go to the vet. After stabilization, ask your vet about reporting the reaction to the FDA CVM, and consider switching to an alternative drug if available.
Not necessarily. Adverse event reports document that a drug was given and that the animal later died — but they do not establish causation. The animal may have died from its underlying condition, from concurrent medications, or from unrelated causes. The FDA applies a structured causality assessment to each report to determine whether the drug was likely, possibly, or unlikely responsible. Still, all death reports are reviewed and tracked because they contribute to safety signal detection, even when individual causality is uncertain.
You can report a suspected adverse drug reaction to the FDA Center for Veterinary Medicine through the FDA Safety Reporting Portal at SafetyReporting.hhs.gov or by calling 1-888-FDA-VETS (1-888-332-8387). You can also contact the drug manufacturer directly — they are required to forward serious adverse event reports to the FDA. Include the drug name and dose, the animal's species, breed, age, and weight, the duration of treatment, and a detailed description of the symptoms observed and their timeline.
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