Pet Drug Reports

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Breed · Cat

Ragdoll: adverse event reports

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

1,065reports, 1996–20260.7% of cat reports
98reports, 12 months to March 2026111 in the 12 months before
37.8%classed serious, as reportedall cats: 35.6%
14.6%name selamectinall cats: 14.8%

FDA's database holds 1,065 reports where the animal's breed is given as "Ragdoll", shown here as Ragdoll: 0.7% of reports about cats. Reports on crossbred animals are left out of breed pages.

98 reports arrived in the 12 months to March 2026, down 12% from 111 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, cefovecin sodium and nitenpyram. Selamectin is named in 14.6% of this breed's reports, about the same share as in reports about all cats (14.8%).

The terms listed most often are vomiting (14.5%), lethargy (13.6%) and diarrhoea (8.6%). Vomiting appears in 14.5% of reports, about the same share as in all cat reports (12.5%). 37.8% 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 Ragdoll reportsShare of all cat reports
Selamectin15514.6%14.8%
Cefovecin sodium878.2%5.8%
Nitenpyram787.3%5.8%
Sarolaner + Selamectin767.1%5.3%
Spinosad736.9%7.8%
Buprenorphine716.7%3.7%
Fluralaner716.7%7%
Frunevetmab666.2%5.1%
Imidacloprid + Moxidectin575.4%5.5%
Maropitant454.2%2.5%
Meloxicam353.3%2.4%
Robenacoxib333.1%2.2%
Butorphanol Tartrate262.4%1.5%
Eprinomectin + Esafoxolaner + Praziquantel262.4%2%
Mirtazapine262.4%1.2%
Ketamine Hydrochloride242.3%2.5%
Emodepside + Praziquantel212%3.8%
Fluralaner + Moxidectin212%2.1%
Isoflurane201.9%1.3%
Dexmedetomidine191.8%0.8%

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 Ragdoll reports listing the termall cat reports

  1. Vomiting14.5%154
  2. Lethargy[unusually tired or inactive]13.6%145
  3. Diarrhoea[diarrhea]8.6%92
  4. Lack of efficacy (ectoparasite) - flea[the product did not have the expected effect: fleas]8%85
  5. Anorexia[not eating]7.4%79
  6. Behavioural disorder NOS[behaviour change, type not specified]7%75
  7. Application site alopecia[hair loss where the product was applied]5.6%60
  8. Death5%53
  9. Hypersalivation[drooling]4.8%51
  10. Death by euthanasia[the animal was euthanized]4.7%50
  11. Ataxia[unsteady, uncoordinated movement]4.6%49
  12. Application site hair loss[hair loss where the product was applied]4.4%47
  13. Depression[dull, quiet or withdrawn]4%43
  14. Vocalisation[crying out or unusual noise]3.7%39
  15. Fever3.6%38
  16. Lack of efficacy - NOS[the product did not have the expected effect]3.5%37
  17. Panting3.2%34
  18. Hiding2.7%29
  19. Pruritus[itching]2.7%29
  20. Anaphylaxis[sudden severe allergic-type reaction]2.6%28

Age and weight

Age of the animal

Under 1 year16.5%176
1 to 3 years22.4%239
4 to 7 years21.6%230
8 to 11 years17.7%188
12 years and over18.5%197
Age not given3.3%35

Weight of the animal

Under 5 kg (11 lb)55.9%595
5 to 9.9 kg (11–22 lb)36.8%392
10 to 24.9 kg (22–55 lb)0.8%8
25 to 44.9 kg (55–99 lb)0%0
45 kg and over (99 lb+)0%0
Weight not given6.6%70

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

Trend and outcomes

0917Apr 2021: 5May 2021: 4Jun 2021: 6Jul 2021: 2Aug 2021: 3Sep 2021: 6Oct 2021: 6Nov 2021: 2Dec 2021: 6Jan 2022: 52022Feb 2022: 1Mar 2022: 2Apr 2022: 0May 2022: 4Jun 2022: 6Jul 2022: 8Aug 2022: 5Sep 2022: 8Oct 2022: 7Nov 2022: 12Dec 2022: 8Jan 2023: 22023Feb 2023: 7Mar 2023: 8Apr 2023: 7May 2023: 9Jun 2023: 12Jul 2023: 6Aug 2023: 10Sep 2023: 10Oct 2023: 9Nov 2023: 9Dec 2023: 8Jan 2024: 92024Feb 2024: 6Mar 2024: 5Apr 2024: 13May 2024: 16Jun 2024: 7Jul 2024: 10Aug 2024: 17Sep 2024: 10Oct 2024: 7Nov 2024: 5Dec 2024: 10Jan 2025: 52025Feb 2025: 7Mar 2025: 4Apr 2025: 8May 2025: 9Jun 2025: 7Jul 2025: 10Aug 2025: 17Sep 2025: 7Oct 2025: 11Nov 2025: 8Dec 2025: 3Jan 2026: 22026Feb 2026: 6Mar 2026: 10

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/Normal23%245
Recovered with Sequela0.8%9
Ongoing29.2%311
Died6.7%71
Euthanized3.5%37
Outcome Unknown21.6%230

Beside all cats

MeasureRagdollAll cats
Reports1,065148,080
Latest 12 months9812,477
Classed serious, of reports stating it37.8%35.6%
Death or euthanasia recorded, per 1,000 reports101.495

Questions about Ragdoll reports

How many FDA adverse event reports involve Ragdolls?

1,065 reports through March 2026, 0.7% of reports about cats; 98 in the latest 12 months.

Which drugs are named most often in Ragdoll reports?

By active ingredient: selamectin (155), cefovecin sodium (87), nitenpyram (78), sarolaner + selamectin (76) and spinosad (73). Brands are masked in the public data.

What signs are reported most for this breed?

vomiting (14.5%), lethargy (13.6%), diarrhoea (8.6%), lack of efficacy (ectoparasite) - flea (8%) and anorexia (7.4%).

Is the Ragdoll 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 Ragdoll 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 ("Ragdoll" becomes "Ragdoll"). 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.