Pet Drug Reports

Species

Species

Cat: adverse event reports

148,080 reports, 10.9% of FDA's animal drug adverse event database

148,080reports about cats, 1987–2026
12,477reports, 12 months to March 202614,089 in the 12 months before
16.6%of all reports received in the latest 12 months10.9% over the whole record
35.6%classed serious, as reportedall species: 38.6%

148,080 adverse event reports in FDA's database concern cats: 10.9% of all reports received from January 1987 to March 2026. 12,477 arrived in the 12 months to March 2026, down 11% from 14,089 in the 12 months before. That is 16.6% of all reports received in those 12 months and about 3,773 reports a year over the whole record.

By active ingredient, the drugs named most often are selamectin (14.8% of cat reports), spinosad (7.8% of cat reports), fluralaner (7% of cat reports) and nitenpyram (5.8% of cat reports). Drugs given to the most animals lead the list for that reason; brands are masked in the public data.

The terms listed most often are vomiting (12.5%), lethargy (9.7%) and lack of efficacy (ectoparasite) - flea (7.5%). 35.6% of reports stating seriousness were classed as serious (38.6% across all species), and 9.5% record a death or euthanasia (6.4% overall).

FDA posts reports quarterly with a delay of three to six months, so the newest months are incomplete and usually grow in later releases.

Drugs named most often, by active ingredient

Active ingredients recorded for the drugReportsShare of cat reportsShare of the drug's reports that concern cats
Selamectin21,95614.8%35.3%
Spinosad11,5767.8%15.9%
Fluralaner10,3657%12.2%
Nitenpyram8,6575.8%40.6%
Cefovecin sodium8,5585.8%64.4%
Imidacloprid + Moxidectin8,1295.5%35%
Sarolaner + Selamectin7,9105.3%83.6%
Frunevetmab7,6245.1%97.5%
Emodepside + Praziquantel5,7013.8%93.3%
Buprenorphine5,4453.7%74.9%
Velagliflozin4,2882.9%93.3%
Bexagliflozin3,7702.5%98.3%
Ketamine Hydrochloride3,7072.5%51.5%
Maropitant3,7072.5%22.8%
Insulin3,6272.4%27.2%
Meloxicam3,6242.4%21.1%
Robenacoxib3,1912.2%87.3%
Fluralaner + Moxidectin3,0592.1%81%
Eprinomectin + Esafoxolaner + Praziquantel3,0112%94.3%
Cyclosporine2,9862%13.9%
Butorphanol Tartrate2,2111.5%29.2%
Isoflurane1,9791.3%38.7%
Gabapentin1,8331.2%17.6%
Mirtazapine1,7861.2%63%
Carprofen1,7091.2%3.3%
Praziquantel1,6671.1%42.1%
Amoxicillin1,6161.1%18.7%
Tiletamine Hydrochloride + Zolazepam Hydrochloride1,5651.1%50.1%
Enrofloxacin1,5531%19.4%
Imidacloprid1,5181%21.8%

Ordered by report count, which follows how widely a drug is used. FDA states that these data "cannot be used to estimate the risk associated with the product or compare one drug or device product with another". openFDA masks brand and manufacturer names in adverse event records, so the reports counted here cannot be attributed to a particular brand.

Signs listed in reports

share of cat reports listing the termall species

  1. Vomiting12.5%18,463
  2. Lethargy[unusually tired or inactive]9.7%14,307
  3. Lack of efficacy (ectoparasite) - flea[the product did not have the expected effect: fleas]7.5%11,093
  4. Anorexia[not eating]7.3%10,823
  5. Application site alopecia[hair loss where the product was applied]6.2%9,183
  6. Death5.4%8,042
  7. Application site hair loss[hair loss where the product was applied]5.3%7,802
  8. Diarrhoea[diarrhea]4.8%7,063
  9. Lack of efficacy - NOS[the product did not have the expected effect]4.7%6,951
  10. Behavioural disorder NOS[behaviour change, type not specified]4.6%6,750
  11. Ataxia[unsteady, uncoordinated movement]4.4%6,585
  12. Weight loss4.4%6,521
  13. Hypersalivation[drooling]4.1%6,125
  14. Depression[dull, quiet or withdrawn]4.1%6,123
  15. Emesis[vomiting]3.8%5,681
  16. Death by euthanasia[the animal was euthanized]3.6%5,323
  17. Hyperactivity3.1%4,582
  18. Not eating3%4,431
  19. Vocalisation[crying out or unusual noise]2.9%4,279
  20. Fever2.7%4,006
  21. Accidental exposure[exposure that was not intended]2.6%3,869
  22. Pruritus[itching]2.5%3,759
  23. Elevated blood urea nitrogen (BUN)[a kidney value above the normal range]2.5%3,631
  24. Hiding2.3%3,477
  25. Elevated creatinine[a kidney value above the normal range]2.1%3,058
  26. Ketosis[ketones building up in the body]2.1%3,038
  27. Hyperglycaemia[high blood sugar]1.9%2,805
  28. Panting1.9%2,801

Single ingredients, pooled across combinations

Age and weight

Age of the animal

Under 1 year12.3%18,164
1 to 3 years19.9%29,417
4 to 7 years18.3%27,137
8 to 11 years16.9%25,087
12 years and over19.8%29,336
Age not given12.8%18,939

Weight of the animal

Under 5 kg (11 lb)50.4%74,657
5 to 9.9 kg (11–22 lb)33.9%50,256
10 to 24.9 kg (22–55 lb)0.5%796
25 to 44.9 kg (55–99 lb)0%12
45 kg and over (99 lb+)0%24
Weight not given15.1%22,335

Outcomes and report types

Outcome recorded in the report

Recovered/Normal20.5%30,291
Recovered with Sequela0.5%726
Ongoing23.5%34,790
Died6.9%10,228
Euthanized2.6%3,841
Outcome Unknown26.1%38,703

What kind of report it was

Safety issue84.1%124,537
Lack of expected effectiveness8.6%12,735
Both safety and lack of expected effectiveness5.2%7,651
Manufacturing or product defect2%3,003
Other0.1%154

Coloured bar: cat reports. Grey bar: all 1,357,245 reports. Outcomes are as stated by the reporter.

Trend

06931,386Apr 2021: 534May 2021: 537Jun 2021: 581Jul 2021: 600Aug 2021: 600Sep 2021: 558Oct 2021: 549Nov 2021: 476Dec 2021: 384Jan 2022: 4062022Feb 2022: 386Mar 2022: 488Apr 2022: 385May 2022: 437Jun 2022: 439Jul 2022: 531Aug 2022: 728Sep 2022: 687Oct 2022: 651Nov 2022: 692Dec 2022: 584Jan 2023: 7142023Feb 2023: 659Mar 2023: 731Apr 2023: 758May 2023: 892Jun 2023: 969Jul 2023: 1,018Aug 2023: 1,184Sep 2023: 923Oct 2023: 1,130Nov 2023: 1,053Dec 2023: 886Jan 2024: 9892024Feb 2024: 1,100Mar 2024: 1,059Apr 2024: 1,211May 2024: 1,280Jun 2024: 1,286Jul 2024: 1,386Aug 2024: 1,375Sep 2024: 1,306Oct 2024: 1,254Nov 2024: 1,124Dec 2024: 1,070Jan 2025: 1,0082025Feb 2025: 965Mar 2025: 824Apr 2025: 1,135May 2025: 1,063Jun 2025: 1,137Jul 2025: 1,109Aug 2025: 1,103Sep 2025: 1,166Oct 2025: 1,197Nov 2025: 980Dec 2025: 961Jan 2026: 1,0222026Feb 2026: 911Mar 2026: 693

Reports by month FDA received them. The newest months are incomplete because FDA posts reports with a delay of three to six months.

07,22014,4401987: 5519871988: 891989: 1351990: 1301991: 19719911992: 1861993: 2511994: 2521995: 36219951996: 4711997: 4631998: 7141999: 92619992000: 2,4292001: 2,1982002: 1,5362003: 1,20020032004: 1,5292005: 1,5922006: 2,0152007: 2,56320072008: 3,2202009: 4,1422010: 4,4292011: 4,15020112012: 5,5472013: 6,7172014: 6,0672015: 6,15420152016: 6,4192017: 7,3912018: 7,2222019: 7,38220192020: 6,7312021: 6,1712022: 6,4142023: 10,91720232024: 14,4402025: 12,6482026: 2,626
MeasureCatAll reports
Reports148,0801,357,245
Classed serious, of reports stating it35.6%38.6%
Death or euthanasia recorded, per 1,000 reports94.963.8
Filed as lack of expected effectiveness (wholly or partly)13.8%23%

Breeds with their own page

Single-breed labels with at least 100 reports. Crossbred animals count in the species total only.

Questions about cat reports

How many adverse event reports involve cats?

148,080 reports through March 2026, 10.9% of the database; 12,477 in the latest 12 months.

Which drugs are reported most often for cats?

By active ingredient: selamectin (21,956), spinosad (11,576), fluralaner (10,365), nitenpyram (8,657) and cefovecin sodium (8,558). The order tracks how widely each is used; brands are masked in the public data.

What signs are reported most in cats?

vomiting (12.5%), lethargy (9.7%), lack of efficacy (ectoparasite) - flea (7.5%), anorexia (7.3%) and application site alopecia (6.2%).

What ages are the cats in these reports?

1 to 3 years (19.9%), 12 years and over (19.8%) and 4 to 7 years (18.3%); age is not given in 12.8% of reports.

Do more reports mean more risk for this species?

No. Counts follow how many animals are treated and how readily their owners and veterinarians report. FDA states that "there is no certainty that the reported drug or device caused the adverse event" and that the event "may have been related to an underlying disease, other drugs used at the same time or other non-drug related sources."

How do I report a problem?

Call the drug company using the number on the label, or send Form FDA 1932a to FDA. See the guide on how to report.

Where this comes from. Counts are built from the openFDA Animal & Veterinary adverse event bulk files released 28 Sep 2026, which hold reports FDA's Center for Veterinary Medicine received through 31 Mar 2026. openFDA masks brand and manufacturer names in these files, so drugs are counted by the active ingredients each record discloses and no figure is attributed to a brand, application or company. Ingredient names, and the separate reference lists of approved products, follow the FDA Green Book as of 30 Sep 2026. No report text, lot numbers or reporter details are published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.