Pet Safety Statistics

Data and trends from 1,320,423 FDA veterinary adverse event reports. Drug reactions, outcomes, and species breakdown.

0 Total Reports
0 Serious Events
0 Fatalities
0 Recovered

Adverse Event Reports by Year

Number of FDA veterinary adverse event reports filed per year.

Most Reported Drugs

Active ingredients with the highest number of adverse event reports.

#Active IngredientReports
1 Spinosad; Milbemycin Oxime 133,770
2 Ivermectin; Pyrantel As Pamoate Salt 80,972
3 Spinosad 70,969
4 Selamectin 59,875
5 Moxidectin 52,066
6 Pyrantel Pamoate;Sarolaner 46,238
7 Afoxolaner 46,081
8 Carprofen 43,401
9 Ivermectin, Pyrantel 39,299
10 Fluralaner Chew Tablets 35,404
11 Milbemycin Oxime; Praziquantel 27,304
12 Fluralaner 13.64% 12-Week Chew 24,847
13 Oclacitinib Maleate 23,505
14 Milbemycin 23,037
15 Nitenpyram 18,725

Most Common Reactions

Most frequently reported adverse reactions in animals.

#ReactionReports
1 Vomiting 210,445
2 Depression 132,102
3 Lethargy 90,713
4 Death 81,504
5 Anorexia 59,467
6 Seizure 33,829
7 Ataxia 33,010
8 Pruritus 29,351
9 Salivation 16,232
10 Trembling/Tremor 12,845
11 Dermatitis 8,506
12 Diarrhea 0

Most Reported Breeds

Animal breeds with the highest number of adverse event reports.

#BreedReports
1 Retriever - Labrador 96,860
2 Crossbred Canine/dog 94,685
3 Domestic Shorthair 61,077
4 Dog (unknown) 54,982
5 Shepherd Dog - German 34,255
6 Retriever - Golden 32,804
7 Chihuahua 27,795
8 Domestic (unspecified) 27,275
9 Terrier - Yorkshire 24,541
10 Shih Tzu 23,628
11 Boxer (German Boxer) 20,059
12 Beagle 17,998
13 Pit Bull 16,555
14 Cat (unknown) 15,990
15 Dachshund (unspecified) 15,623

Reports by Species

Adverse event reports filed per animal species.

SpeciesReports
Dog 960,599
Cat 141,763
Cattle 30,889
Horse 17,908
Human 16,621
Pig 2,590
Other 1,488
Sheep 1,064
Chicken 1,056
Goat 819
Turkey 516
Rabbit 499
Ferret 367
Other Birds 208
Fish 208
Rat 142
Donkey 139
Mouse 123
Guinea Pig 119
Other Deer 87

About This Data

All pet adverse event data comes from the FDA's Center for Veterinary Medicine through the openFDA public data program. The FDA publishes quarterly data files containing reports from veterinarians, pet owners, and drug manufacturers. Our database contains 1,320,423 reports.

Not necessarily. Popular drugs prescribed to millions of animals will naturally accumulate more reports than niche products, even if the rate of adverse events is lower. Reporting is voluntary in many cases. These reports are a signal for further investigation, not a verdict on drug safety. Always consult your veterinarian.

An adverse event is classified as "serious" when it results in death, a life-threatening condition, hospitalization, disability, or a congenital anomaly. In our database, 328,345 reports (25%) are classified as serious. Of these, 65,727 resulted in death and 19,161 in euthanasia.