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Maine Coon: adverse event reports

FDA breed label "Maine Coon" · single-breed animals only

2,217reports, 1989–20261.5% of cat reports
169reports, 12 months to March 2026192 in the 12 months before
37.5%classed serious, as reportedall cats: 35.6%
14.5%name selamectinall cats: 14.8%

2,217 adverse event reports received by FDA describe an animal recorded as Maine Coon (FDA breed label "Maine Coon"). That is 1.5% of all reports about cats. Crossbred animals are not counted here, only reports that give this single breed.

169 reports arrived in the 12 months to March 2026, down 12% from 192 in the 12 months before. A breed's count mostly mirrors how common the breed is; registration and ownership figures by breed are not public data, so no per-animal rate can be given.

By active ingredient, the drugs named most often are selamectin, spinosad and nitenpyram. Selamectin is named in 14.5% of this breed's reports, about the same share as in reports about all cats (14.8%).

The terms listed most often are vomiting (13.4%), lethargy (11.3%) and lack of efficacy (ectoparasite) - flea (8.6%). Vomiting appears in 13.4% of reports, about the same share as in all cat reports (12.5%). 37.5% of reports stating seriousness were classed as serious, against 35.6% for cats overall.

Drugs named most often, by active ingredient

Active ingredients recorded for the drugReportsShare of Maine Coon reportsShare of all cat reports
Selamectin32114.5%14.8%
Spinosad25311.4%7.8%
Nitenpyram2139.6%5.8%
Fluralaner1878.4%7%
Imidacloprid + Moxidectin1315.9%5.5%
Sarolaner + Selamectin1195.4%5.3%
Cefovecin sodium1165.2%5.8%
Frunevetmab1014.6%5.1%
Buprenorphine843.8%3.7%
Maropitant703.2%2.5%
Insulin693.1%2.4%
Cyclosporine612.8%2%
Robenacoxib572.6%2.2%
Fluralaner + Moxidectin522.3%2.1%
Meloxicam472.1%2.4%
Velagliflozin421.9%2.9%
Emodepside + Praziquantel391.8%3.8%
Bexagliflozin371.7%2.5%
Butorphanol Tartrate311.4%1.5%
Gabapentin311.4%1.2%

Ordered by report count. Differences from the species column often come from body size (which drugs a breed is prescribed) and from how common the breed was in the years a drug sold most. FDA states that these data cannot be used to estimate risk or to compare one product with another. Brand and manufacturer names are masked by FDA in these records.

Signs listed in reports

share of Maine Coon reports listing the termall cat reports

  1. Vomiting13.4%296
  2. Lethargy[unusually tired or inactive]11.3%250
  3. Lack of efficacy (ectoparasite) - flea[the product did not have the expected effect: fleas]8.6%190
  4. Anorexia[not eating]7.8%172
  5. Application site alopecia[hair loss where the product was applied]6%134
  6. Diarrhoea[diarrhea]5.6%124
  7. Emesis[vomiting]5.3%117
  8. Application site hair loss[hair loss where the product was applied]5.1%113
  9. Behavioural disorder NOS[behaviour change, type not specified]5.1%112
  10. Panting4.8%106
  11. Lack of efficacy - NOS[the product did not have the expected effect]4.4%97
  12. Death4.2%94
  13. Hypersalivation[drooling]3.9%86
  14. Pruritus[itching]3.6%80
  15. Death by euthanasia[the animal was euthanized]3.6%79
  16. Vocalisation[crying out or unusual noise]3.6%79
  17. Depression[dull, quiet or withdrawn]3.4%76
  18. Ataxia[unsteady, uncoordinated movement]3.3%74
  19. Fever2.8%62
  20. Agitation2.4%54
  21. Hiding2.3%52

Age and weight

Age of the animal

Under 1 year11%243
1 to 3 years22.5%498
4 to 7 years20.9%464
8 to 11 years20.4%453
12 years and over21.7%480
Age not given3.6%79

Weight of the animal

Under 5 kg (11 lb)31.6%701
5 to 9.9 kg (11–22 lb)59.5%1,319
10 to 24.9 kg (22–55 lb)4.1%90
25 to 44.9 kg (55–99 lb)0%0
45 kg and over (99 lb+)0%0
Weight not given4.8%107

Coloured bar: Maine Coon reports. Grey bar: all cat reports.

Trend and outcomes

01733Apr 2021: 7May 2021: 7Jun 2021: 5Jul 2021: 13Aug 2021: 20Sep 2021: 8Oct 2021: 6Nov 2021: 5Dec 2021: 2Jan 2022: 32022Feb 2022: 4Mar 2022: 3Apr 2022: 3May 2022: 6Jun 2022: 7Jul 2022: 8Aug 2022: 13Sep 2022: 7Oct 2022: 10Nov 2022: 12Dec 2022: 5Jan 2023: 52023Feb 2023: 10Mar 2023: 7Apr 2023: 6May 2023: 15Jun 2023: 8Jul 2023: 14Aug 2023: 21Sep 2023: 16Oct 2023: 33Nov 2023: 17Dec 2023: 13Jan 2024: 82024Feb 2024: 19Mar 2024: 12Apr 2024: 15May 2024: 13Jun 2024: 18Jul 2024: 22Aug 2024: 21Sep 2024: 14Oct 2024: 15Nov 2024: 13Dec 2024: 21Jan 2025: 172025Feb 2025: 9Mar 2025: 14Apr 2025: 18May 2025: 19Jun 2025: 15Jul 2025: 17Aug 2025: 14Sep 2025: 14Oct 2025: 9Nov 2025: 14Dec 2025: 14Jan 2026: 112026Feb 2026: 15Mar 2026: 9

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

Outcome recorded in the report

Recovered/Normal24.5%543
Recovered with Sequela0.8%17
Ongoing26.7%593
Died5.8%128
Euthanized2.5%55
Outcome Unknown23.4%518

Beside all cats

MeasureMaine CoonAll cats
Reports2,217148,080
Latest 12 months16912,477
Classed serious, of reports stating it37.5%35.6%
Death or euthanasia recorded, per 1,000 reports82.595

Questions about Maine Coon reports

How many FDA adverse event reports involve Maine Coons?

2,217 reports through March 2026, 1.5% of reports about cats; 169 in the latest 12 months.

Which drugs are named most often in Maine Coon reports?

By active ingredient: selamectin (321), spinosad (253), nitenpyram (213), fluralaner (187) and imidacloprid + moxidectin (131). Brands are masked in the public data.

What signs are reported most for this breed?

vomiting (13.4%), lethargy (11.3%), lack of efficacy (ectoparasite) - flea (8.6%), anorexia (7.8%) and application site alopecia (6%).

Is the Maine Coon more sensitive to certain drugs?

Report counts cannot answer that. They show what was reported, not what a drug did, and they are not adjusted for how many Maine Coon animals exist or were treated. Breed-related drug sensitivities that are established are described on FDA-approved labels; a veterinarian is the person to ask about an individual animal.

Why are crossbreds not included?

FDA records crossbred animals with one or more component breeds. Counting them under each component would double count, so breed pages use single-breed reports only. Crossbreds remain in the species totals.

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 1 Oct 2026. Breed names are FDA's labels rearranged into everyday order ("Maine Coon" becomes "Maine Coon"). 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.