Browse Pet Safety Reports
16,698 FDA adverse event reports for pets.
FDA Veterinary Adverse Event Database
Browse 16,698 adverse event reports collected by the FDA's Center for Veterinary Medicine. Each report includes the animal species, breed, drug or product involved, observed reactions, and outcome. Reports flagged as "serious" involve death, life-threatening conditions, or hospitalization. Use the filters to narrow results by species, outcome severity, or keyword. Note that a higher number of reports does not necessarily indicate a less safe product, widely prescribed drugs naturally accumulate more reports.
Pet Adverse Event Reports
Browse 16,698 FDA veterinary adverse event reports for Human.
| Date | Species | Breed | Drug | Reaction | Outcome |
|---|---|---|---|---|---|
| Aug 25, 2007 | Human | Unknown | Dexamethasone, Neomycin, Thiabendazole | Unclassifiable adverse event; Accidental exposure; Eye irritation | - |
| Aug 24, 2007 | Human | Unknown | Tylosin | Unclassifiable adverse event; Accidental exposure; Cough; Nausea | - |
| Aug 24, 2007 | Human | Unknown | Altrenogest | Unclassifiable adverse event; Accidental exposure; Eye irritation | - |
| Aug 24, 2007 | Human | Unknown | Dexamethasone, Neomycin, Thiabendazole | Unclassifiable adverse event; Accidental exposure; Eye irritation | - |
| Aug 21, 2007 | Human | Unknown | Firocoxib | Unclassifiable adverse event; Accidental exposure; Gastritis | - |
| Aug 17, 2007 | Human | Unknown | Doramectin | Unclassifiable adverse event; Accidental exposure; Injection site swelling | - |
| Aug 17, 2007 | Human | Unknown | Selamectin | Unclassifiable adverse event; Accidental exposure; Digestive tract disorder N... | - |
| Aug 17, 2007 | Human | Unknown | Milbemycin, Lufenuron | Unclassifiable adverse event; Unclassifiable adverse event; Accidental exposu... | - |
| Aug 16, 2007 | Human | Unknown | Firocoxib | Unclassifiable adverse event; Accidental exposure; Vomiting | - |
| Aug 15, 2007 | Human | Unknown | Tilmicosin Phosphate | Unclassifiable adverse event; Accidental exposure; Injection site inflammatio... | - |
| Aug 15, 2007 | Human | Unknown | Imidacloprid, Moxidectin | Unclassifiable adverse event; Accidental exposure; Anaphylaxis; Abnormal brea... | - |
| Aug 14, 2007 | Human | Unknown | Imidacloprid, Moxidectin | Unclassifiable adverse event; Accidental exposure; Rash | - |
| Aug 14, 2007 | Human | Unknown | Dexamethasone, Neomycin, Thiabendazole | Unclassifiable adverse event; Accidental exposure; Eye irritation; Eye pain | - |
| Aug 14, 2007 | Human | Unknown | Selamectin | Unclassifiable adverse event; Accidental exposure; Diarrhoea; Nausea | - |
| Aug 14, 2007 | Human | Unknown | Dexamethasone, Neomycin, Thiabendazole | Accidental exposure; Eye irritation; Unclassifiable adverse event | - |
| Aug 13, 2007 | Human | Unknown | Selamectin | Unclassifiable adverse event; Eye pain; Nasal discharge; Cough; Pruritus | - |
| Aug 13, 2007 | Human | Unknown | Tilmicosin Phosphate | Unclassifiable adverse event; Unclassifiable adverse event; Accidental exposu... | - |
| Aug 13, 2007 | Human | Unknown | Ceftiofur | Malaise | - |
| Aug 10, 2007 | Human | Unknown | Amitraz | Unclassifiable adverse event; Accidental exposure; Balance problem; Feeling d... | - |
| Aug 9, 2007 | Human | Unknown | Imidacloprid, Moxidectin | Unclassifiable adverse event; Accidental exposure; Pain NOS; Hypoaesthesia | - |
| Aug 7, 2007 | Human | Unknown | Milbemycin | Unclassifiable adverse event; Accidental exposure; Nausea | - |
| Aug 6, 2007 | Human | Unknown | Dinoprost Tromethamine | Unclassifiable adverse event; Accidental exposure; Pharyngitis; Vomiting; Nau... | - |
| Aug 6, 2007 | Human | Unknown | Ivermectin | Unclassifiable adverse event; Accidental exposure | - |
| Aug 6, 2007 | Human | Unknown | Tilmicosin Phosphate | Unclassifiable adverse event; Accidental exposure; Injection site pain; Injec... | - |
| Aug 4, 2007 | Human | Unknown | Ivermectin | Unclassifiable adverse event; Unclassifiable adverse event; Accidental exposu... | - |
| Aug 3, 2007 | Human | Unknown | Tilmicosin Phosphate | Unclassifiable adverse event; Accidental exposure; Abdominal pain; Dry mouth;... | - |
| Aug 3, 2007 | Human | Unknown | Tilmicosin Phosphate | Unclassifiable adverse event; Accidental exposure; Injection site bleeding | - |
| Aug 2, 2007 | Human | Unknown | Atipamezole | Unclassifiable adverse event; Unclassifiable adverse event; Accidental exposu... | - |
| Aug 1, 2007 | Human | Unknown | Selamectin | Unclassifiable adverse event; Dermatitis; Pruritus; Eruption | - |
| Aug 1, 2007 | Human | Unknown | Selamectin | Unclassifiable adverse event; Accidental exposure; Epiphora; Eye irritation; ... | - |
| Jul 30, 2007 | Human | Unknown | Selamectin | Unclassifiable adverse event; Unclassifiable adverse event; Accidental exposu... | - |
| Jul 29, 2007 | Human | Unknown | Tilmicosin Phosphate | No sign; Unclassifiable adverse event; Accidental exposure | - |
| Jul 29, 2007 | Human | Unknown | Ceftiofur | Unclassifiable adverse event; Accidental exposure; Injection site pain | - |
| Jul 28, 2007 | Human | Unknown | Ivermectin | Unclassifiable adverse event; Accidental exposure; Eye irritation | - |
| Jul 27, 2007 | Human | Unknown | Mercaptobenzothiazole | Unclassifiable adverse event; Unclassifiable adverse event; Accidental exposu... | - |
| Jul 27, 2007 | Human | Unknown | Selamectin | Unclassifiable adverse event; Unclassifiable adverse event; Accidental exposu... | - |
| Jul 26, 2007 | Human | Unknown | Imidacloprid, Moxidectin | Unclassifiable adverse event; Unclassifiable adverse event; Headache; Nausea | - |
| Jul 26, 2007 | Human | Unknown | Ivermectin | Unclassifiable adverse event; Accidental exposure; Injection site inflammation | - |
| Jul 25, 2007 | Human | Unknown | Selamectin | Unclassifiable adverse event; Accidental exposure; Dermatitis | - |
| Jul 25, 2007 | Human | Unknown | Flunixin Meglumine | Unclassifiable adverse event; Unclassifiable adverse event; Accidental exposure | - |
| Jul 24, 2007 | Human | Unknown | Tilmicosin Phosphate | Unclassifiable adverse event; Accidental exposure; Injection site oedema; Inj... | - |
| Jul 22, 2007 | Human | Unknown | Selamectin | Unclassifiable adverse event; Accidental exposure; Dermatitis | - |
| Jul 22, 2007 | Human | Unknown | Tilmicosin Phosphate | No sign; Unclassifiable adverse event; Unclassifiable adverse event; Unclassi... | - |
| Jul 21, 2007 | Human | Unknown | Tilmicosin Phosphate | No sign; Unclassifiable adverse event; Accidental exposure | - |
| Jul 21, 2007 | Human | Unknown | Tilmicosin Phosphate | No sign; Unclassifiable adverse event; Accidental exposure | - |
| Jul 21, 2007 | Human | Unknown | Ivermectin, Praziquantel | No sign; Unclassifiable adverse event; Accidental exposure; Accidental drug i... | - |
| Jul 21, 2007 | Human | Unknown | Selamectin | Unclassifiable adverse event; Accidental exposure; Urticaria | - |
| Jul 21, 2007 | Human | Unknown | Mercaptobenzothiazole | No sign; Unclassifiable adverse event; Accidental exposure | - |
| Jul 21, 2007 | Human | Unknown | Nitenpyram | Unclassifiable adverse event; Accidental exposure; Anxious state of mind; Nausea | - |
| Jul 20, 2007 | Human | Unknown | Ractopamine | Unclassifiable adverse event; Cardiac disorder NOS | - |
Frequently Asked Questions
Contact your veterinarian immediately. If the reaction is severe, difficulty breathing, seizures, collapse, or severe swelling, seek emergency veterinary care right away. After your pet is stabilized, report the adverse event to the FDA through safetyreporting.hhs.gov or by calling 1-888-FDA-VETS (1-888-332-8387). Reporting helps the FDA identify safety issues that can lead to label changes or product recalls.
Dogs account for the majority of adverse event reports, followed by cats. This reflects both the larger pet population and wider range of medications for these species. Flea and tick products, pain medications (NSAIDs), and heartworm preventives are among the product categories with the highest report counts across all species.
Not necessarily. A drug used by millions of pets will have more reports in absolute numbers than a niche product, even if the actual rate of adverse events is lower. The FDA uses these reports as one of many tools to evaluate drug safety, looking for patterns and statistical signals rather than raw counts alone. Always consult your veterinarian before changing any medication.