Pet Drug Reports

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Breed · Cat

Manx: adverse event reports

FDA breed label "Manx" · single-breed animals only

323reports, 1988–20260.2% of cat reports
17reports, 12 months to March 202623 in the 12 months before
42.3%classed serious, as reportedall cats: 35.6%
18%name selamectinall cats: 14.8%

323 adverse event reports received by FDA describe an animal recorded as Manx (FDA breed label "Manx"). That is 0.2% of all reports about cats. Crossbred animals are not counted here, only reports that give this single breed.

17 reports arrived in the 12 months to March 2026, down 26% from 23 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 cefovecin sodium. Selamectin is named in 18% of this breed's reports, about the same share as in reports about all cats (14.8%).

The terms listed most often are vomiting (16.4%), lethargy (13%) and anorexia (10.5%). Vomiting appears in 16.4% of reports, a larger share than in all cat reports (12.5%). 42.3% 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 Manx reportsShare of all cat reports
Selamectin5818%14.8%
Spinosad3912.1%7.8%
Cefovecin sodium288.7%5.8%
Fluralaner257.7%7%
Imidacloprid + Moxidectin247.4%5.5%
Frunevetmab226.8%5.1%
Sarolaner + Selamectin195.9%5.3%
Nitenpyram154.6%5.8%
Maropitant103.1%2.5%
Meloxicam103.1%2.4%
Insulin92.8%2.4%
Robenacoxib92.8%2.2%
Buprenorphine72.2%3.7%
Emodepside + Praziquantel72.2%3.8%
Eprinomectin + Esafoxolaner + Praziquantel61.9%2%
Bexagliflozin51.5%2.5%
Fluralaner + Moxidectin51.5%2.1%
Mirtazapine51.5%1.2%
Butorphanol Tartrate41.2%1.5%
Carprofen41.2%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 Manx reports listing the termall cat reports

  1. Vomiting16.4%53
  2. Lethargy[unusually tired or inactive]13%42
  3. Anorexia[not eating]10.5%34
  4. Depression[dull, quiet or withdrawn]8.7%28
  5. Death8.4%27
  6. Application site alopecia[hair loss where the product was applied]7.4%24
  7. Emesis[vomiting]7.4%24
  8. Diarrhoea[diarrhea]6.5%21
  9. Death by euthanasia[the animal was euthanized]6.2%20
  10. Application site hair loss[hair loss where the product was applied]5.9%19
  11. Lack of efficacy (ectoparasite) - flea[the product did not have the expected effect: fleas]5.9%19
  12. Hypersalivation[drooling]5%16
  13. Ataxia[unsteady, uncoordinated movement]4.3%14
  14. Lack of efficacy - NOS[the product did not have the expected effect]4.3%14
  15. Elevated blood urea nitrogen (BUN)[a kidney value above the normal range]4%13
  16. Anaemia NOS[low red blood cell count]3.7%12
  17. Adipsia[not drinking]3.4%11
  18. Behavioural disorder NOS[behaviour change, type not specified]3.4%11
  19. Pruritus[itching]3.4%11
  20. Fever3.1%10
  21. Hyperglycaemia[high blood sugar]2.8%9
  22. Hypothermia[low body temperature]2.8%9

Age and weight

Age of the animal

Under 1 year12.7%41
1 to 3 years20.1%65
4 to 7 years21.7%70
8 to 11 years19.2%62
12 years and over24.1%78
Age not given2.2%7

Weight of the animal

Under 5 kg (11 lb)54.2%175
5 to 9.9 kg (11–22 lb)36.5%118
10 to 24.9 kg (22–55 lb)0.9%3
25 to 44.9 kg (55–99 lb)0%0
45 kg and over (99 lb+)0%0
Weight not given8.4%27

Coloured bar: Manx reports. Grey bar: all cat reports.

Trend and outcomes

036Apr 2021: 2May 2021: 0Jun 2021: 2Jul 2021: 0Aug 2021: 2Sep 2021: 3Oct 2021: 2Nov 2021: 0Dec 2021: 1Jan 2022: 12022Feb 2022: 0Mar 2022: 1Apr 2022: 0May 2022: 0Jun 2022: 0Jul 2022: 1Aug 2022: 0Sep 2022: 2Oct 2022: 0Nov 2022: 1Dec 2022: 6Jan 2023: 12023Feb 2023: 1Mar 2023: 1Apr 2023: 0May 2023: 3Jun 2023: 2Jul 2023: 2Aug 2023: 1Sep 2023: 2Oct 2023: 4Nov 2023: 1Dec 2023: 2Jan 2024: 02024Feb 2024: 3Mar 2024: 2Apr 2024: 3May 2024: 5Jun 2024: 2Jul 2024: 3Aug 2024: 0Sep 2024: 0Oct 2024: 4Nov 2024: 0Dec 2024: 2Jan 2025: 22025Feb 2025: 1Mar 2025: 1Apr 2025: 1May 2025: 1Jun 2025: 1Jul 2025: 1Aug 2025: 2Sep 2025: 2Oct 2025: 0Nov 2025: 2Dec 2025: 0Jan 2026: 42026Feb 2026: 3Mar 2026: 0

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/Normal18.6%60
Recovered with Sequela0.6%2
Ongoing26.3%85
Died10.5%34
Euthanized4%13
Outcome Unknown18.6%60

Beside all cats

MeasureManxAll cats
Reports323148,080
Latest 12 months1712,477
Classed serious, of reports stating it42.3%35.6%
Death or euthanasia recorded, per 1,000 reports145.595

Questions about Manx reports

How many FDA adverse event reports involve Manxs?

323 reports through March 2026, 0.2% of reports about cats; 17 in the latest 12 months.

Which drugs are named most often in Manx reports?

By active ingredient: selamectin (58), spinosad (39), cefovecin sodium (28), fluralaner (25) and imidacloprid + moxidectin (24). Brands are masked in the public data.

What signs are reported most for this breed?

vomiting (16.4%), lethargy (13%), anorexia (10.5%), depression (8.7%) and death (8.4%).

Is the Manx 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 Manx 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 ("Manx" becomes "Manx"). 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.