Dog — Chow Chow, Dog (unknown) — Deracoxib
FDA Veterinary Adverse Event Report #N141203 — February 20, 2016 — Serious Event
Animal Information
| Species | Dog |
| Breed | Chow Chow, Dog (unknown) |
| Gender | Female |
| Age | 4.00 Year |
| Weight | 30.708 Kilogram |
Event Summary
| Report ID | N141203 |
| Date | February 20, 2016 |
| Serious | Yes |
| Outcome | Ongoing |
Drug Information
| Active Ingredients | Deracoxib |
| Manufacturer | MSK |
Reported Reactions
Regurgitation; Collapse NOS (see also 'Cardio-vascular' and 'Neurological disorders'); Lateral recumbency; Fever; Nystagmus; Peritonitis; Disseminated intravascular coagulation; Pancreatitis; Icterus; Intestinal perforation; Stomach upset; General illness; Duodenal ulcer; Anaemia NOS; Thrombocytopenia; Leucopenia NOS; Pale mucous membrane; Hypotension; Abdominal pain; Diarrhoea; Digestive tract disorder NOS; Bloody diarrhoea; Vomiting; Haematemesis; Oedema of the extremities (see also other SOCs for most applicable oedema); Acid-base disorder; Hypocalcaemic condition; Ataxia; Epistaxis; Nasal discharge; Anorexia; General pain (see other SOCs for specific pain); Lethargy (see also Central nervous system depression in 'Neurological'); Cutaneous emphysema; Skin petechiae; Dehydration; Other abnormal test result NOS; Bruising; Generalised weakness; Local swelling (not application site); Mental impairment NOS; Skin disorders NOS; Hypoalbuminaemia; Hypoglycaemia; Discoloured urine; Hypoproteinaemia; Shaking; Fluid in abdomen NOS; Head bobbing; Elevated alanine aminotransferase (ALT); Elevated total bilirubin; Elevated serum alkaline phosphatase (SAP); Azotaemia; Weak pulse; Increased coagulation time; Elevated gamma-glutamyl transferase (GGT); Decreased cholesterol (total); Haemoconcentration
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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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