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 |
|---|---|---|---|---|---|
| Apr 9, 2008 | Human | Unknown | Clorsulon, Ivermectin | Unclassifiable adverse event; Accidental exposure; Nausea; Injection site pain | - |
| Apr 9, 2008 | Human | Unknown | Triamcinolone Acetonide | Unclassifiable adverse event; Unclassifiable adverse event; Accidental exposu... | - |
| Apr 9, 2008 | Human | Unknown | Imidacloprid, Moxidectin | Unclassifiable adverse event; Accidental exposure; Anaphylaxis; Urticaria; Pr... | - |
| Apr 9, 2008 | Human | Unknown | Selamectin | Unclassifiable adverse event; Accidental exposure; Eye irritation; Eye rednes... | - |
| Apr 8, 2008 | Human | Unknown | Tulathromycin | Unclassifiable adverse event; Accidental exposure; Injection site pain | - |
| Apr 7, 2008 | Human | Unknown | Moxidectin | Unclassifiable adverse event; Accidental exposure; Fever | - |
| Apr 7, 2008 | Human | Unknown | Pyrantel Pamoate | No sign; Unclassifiable adverse event; Accidental exposure | - |
| Apr 6, 2008 | Human | Unknown | Enrofloxacin | Unclassifiable adverse event; Accidental exposure; Injection site inflammatio... | - |
| Apr 5, 2008 | Human | Unknown | Tilmicosin Phosphate | Unclassifiable adverse event; Accidental exposure; Thoracic pain; Nervousness... | - |
| Apr 4, 2008 | Human | Unknown | Ceftiofur Hydrochloride | Unclassifiable adverse event; Accidental exposure; Pain NOS | - |
| Apr 4, 2008 | Human | Unknown | Zeranol | Unclassifiable adverse event; Unclassifiable adverse event; Accidental exposu... | - |
| Apr 3, 2008 | Human | Unknown | Maropitant | Unclassifiable adverse event; Nausea; Injection site pain | - |
| Apr 3, 2008 | Human | Unknown | Tilmicosin Phosphate | Unclassifiable adverse event; Unclassifiable adverse event; Accidental exposu... | - |
| Apr 3, 2008 | Human | Unknown | Selamectin | Unclassifiable adverse event; Accidental exposure; Application site pain | - |
| Apr 2, 2008 | Human | Unknown | Selamectin | Unclassifiable adverse event; Unclassifiable adverse event; Accidental exposu... | - |
| Apr 2, 2008 | Human | Unknown | Carprofen | Unclassifiable adverse event; Accidental exposure; Eye irritation; Erythema (... | - |
| Apr 1, 2008 | Human | Unknown | Gonadorelin Diacetate Tetrahydrate | Unclassifiable adverse event; Pruritus | - |
| Apr 1, 2008 | Human | Unknown | Ivermectin | No sign; Accidental exposure | - |
| Mar 31, 2008 | Human | Unknown | Ivermectin | Unclassifiable adverse event; Unclassifiable adverse event; Accidental exposu... | - |
| Mar 31, 2008 | Human | Unknown | Selamectin | Unclassifiable adverse event; Accidental exposure; Skin hyperaemia; Pruritus | - |
| Mar 30, 2008 | Human | Unknown | Mercaptobenzothiazole | No sign; Unclassifiable adverse event; Unclassifiable adverse event | - |
| Mar 29, 2008 | Human | Unknown | Mercaptobenzothiazole | No sign; Unclassifiable adverse event; Accidental exposure; Accidental drug i... | - |
| Mar 28, 2008 | Human | Unknown | Mercaptobenzothiazole | No sign; Unclassifiable adverse event; Unclassifiable adverse event; Accident... | - |
| Mar 27, 2008 | Human | Unknown | Pentobarbital, Phenytoin | Injection site pain; Urticaria; Unclassifiable adverse event; Accidental expo... | - |
| Mar 25, 2008 | Human | Unknown | Ivermectin | Unclassifiable adverse event; Accidental exposure; Eye irritation | - |
| Mar 25, 2008 | Human | Unknown | Carprofen | Thoracic pain; Unclassifiable adverse event; Accidental exposure | - |
| Mar 24, 2008 | Human | Unknown | Tulathromycin | Unclassifiable adverse event; Accidental exposure; Injection site inflammatio... | - |
| Mar 24, 2008 | Human | Unknown | Ceftiofur | Injection site swelling; Unclassifiable adverse event; Unclassifiable adverse... | - |
| Mar 22, 2008 | Human | Unknown | Milbemycin | Unclassifiable adverse event; Accidental exposure; Diarrhoea; Vomiting; Somno... | - |
| Mar 22, 2008 | Human | Unknown | Mercaptobenzothiazole | Unclassifiable adverse event; Accidental exposure; Eye irritation | - |
| Mar 22, 2008 | Human | Unknown | Ivermectin | Unclassifiable adverse event; Unclassifiable adverse event; Accidental exposu... | - |
| Mar 21, 2008 | Human | Unknown | Dinoprost Tromethamine | Unclassifiable adverse event; Accidental exposure; Pain NOS; Malaise; Thoraci... | - |
| Mar 20, 2008 | Human | Unknown | Selamectin | Unclassifiable adverse event; Accidental exposure; Skin hyperaemia; Pruritus;... | - |
| Mar 20, 2008 | Human | Unknown | Tilmicosin Phosphate | Rash; Unclassifiable adverse event; Accidental exposure | - |
| Mar 20, 2008 | Human | Unknown | Selamectin | Unclassifiable adverse event; Ocular discharge; Anaphylaxis; Urticaria; Nasal... | - |
| Mar 20, 2008 | Human | Unknown | Selamectin | Unclassifiable adverse event; Unclassifiable adverse event; Accidental exposu... | - |
| Mar 19, 2008 | Human | Unknown | Dirlotapide | Unclassifiable adverse event; Accidental exposure; Diarrhoea; Vomiting | - |
| Mar 19, 2008 | Human | Unknown | Florfenicol | Unclassifiable adverse event; Unclassifiable adverse event; Accidental exposu... | - |
| Mar 17, 2008 | Human | Unknown | Selamectin | Unclassifiable adverse event; Accidental exposure; Pharyngitis; Urticaria; Ra... | - |
| Mar 17, 2008 | Human | Unknown | Florfenicol | No sign; Unclassifiable adverse event; Unclassifiable adverse event; Accident... | - |
| Mar 15, 2008 | Human | Unknown | Selamectin | Unclassifiable adverse event; Unclassifiable adverse event; Rash | - |
| Mar 15, 2008 | Human | Unknown | Selamectin | Unclassifiable adverse event; Unclassifiable adverse event; Rash | - |
| Mar 15, 2008 | Human | Unknown | Clomipramine | Unclassifiable adverse event; Accidental exposure; Shaking; Feeling depressed... | - |
| Mar 14, 2008 | Human | Unknown | Selamectin | Unclassifiable adverse event; Accidental exposure; Application site reaction NOS | - |
| Mar 13, 2008 | Human | Unknown | Ivermectin | Unclassifiable adverse event; Unclassifiable adverse event; Accidental exposu... | - |
| Mar 11, 2008 | Human | Unknown | Dexamethasone, Neomycin, Thiabendazole | Unclassifiable adverse event; Accidental exposure; Eye irritation | - |
| Mar 11, 2008 | Human | Unknown | Tylosin | Unclassifiable adverse event; Accidental exposure; Injection site pain | - |
| Mar 11, 2008 | Human | Unknown | Doramectin | Unclassifiable adverse event; Accidental exposure; Rash; Pruritus | - |
| Mar 9, 2008 | Human | Unknown | Altrenogest | Unclassifiable adverse event; Accidental exposure; Headache | - |
| Mar 6, 2008 | Human | Unknown | Imidacloprid, Moxidectin | Unclassifiable adverse event; Unclassifiable adverse event; Accidental exposu... | - |
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.