Pet Drug Reports

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Breed · Cat

Tonkinese: adverse event reports

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

159reports, 1990–20260.1% of cat reports
9reports, 12 months to March 202611 in the 12 months before
41.8%classed serious, as reportedall cats: 35.6%
18.9%name selamectinall cats: 14.8%

159 adverse event reports received by FDA describe an animal recorded as Tonkinese (FDA breed label "Tonkinese"). That is 0.1% of all reports about cats. Crossbred animals are not counted here, only reports that give this single breed.

9 reports arrived in the 12 months to March 2026, down 18% from 11 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 frunevetmab. Selamectin is named in 18.9% of this breed's reports, a larger share than in reports about all cats (14.8%).

The terms listed most often are anorexia (16.4%), vomiting (15.1%) and lack of efficacy - NOS (10.1%). Anorexia appears in 16.4% of reports, a larger share than in all cat reports (7.3%). 41.8% 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 Tonkinese reportsShare of all cat reports
Selamectin3018.9%14.8%
Cefovecin sodium159.4%5.8%
Frunevetmab148.8%5.1%
Spinosad116.9%7.8%
Cyclosporine106.3%2%
Fluralaner95.7%7%
Insulin95.7%2.4%
Methylprednisolone Acetate85%1%
Prednisone74.4%0.5%
Maropitant63.8%2.5%
Mirtazapine63.8%1.2%
Imidacloprid + Moxidectin53.1%5.5%
Capromorelin42.5%0.5%
Velagliflozin42.5%2.9%
Amoxicillin31.9%1.1%
Amoxicillin Trihydrate + Clavulanate Potassium31.9%0.5%
Buprenorphine31.9%3.7%
Medetomidine31.9%0.3%
Robenacoxib31.9%2.2%
Sarolaner + Selamectin31.9%5.3%

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 Tonkinese reports listing the termall cat reports

  1. Anorexia[not eating]16.4%26
  2. Vomiting15.1%24
  3. Lack of efficacy - NOS[the product did not have the expected effect]10.1%16
  4. Lethargy[unusually tired or inactive]10.1%16
  5. Application site alopecia[hair loss where the product was applied]8.2%13
  6. Death by euthanasia[the animal was euthanized]8.2%13
  7. Depression[dull, quiet or withdrawn]8.2%13
  8. Ataxia[unsteady, uncoordinated movement]6.9%11
  9. Hyperglycaemia[high blood sugar]5%8
  10. Hiding4.4%7
  11. Pruritus[itching]4.4%7
  12. Behavioural disorder NOS[behaviour change, type not specified]3.8%6
  13. Death3.8%6
  14. Lack of efficacy (ectoparasite) - flea[the product did not have the expected effect: fleas]3.8%6
  15. Apnoea[breathing stopped]3.1%5
  16. Diarrhoea[diarrhea]3.1%5
  17. Hypersalivation[drooling]3.1%5
  18. Hypoglycaemia[low blood sugar]3.1%5
  19. Application site erythema[reddened skin where the product was applied]2.5%4
  20. Application site hair loss[hair loss where the product was applied]2.5%4

Age and weight

Age of the animal

Under 1 year11.9%19
1 to 3 years11.9%19
4 to 7 years18.9%30
8 to 11 years19.5%31
12 years and over34%54
Age not given3.8%6

Weight of the animal

Under 5 kg (11 lb)70.4%112
5 to 9.9 kg (11–22 lb)21.4%34
10 to 24.9 kg (22–55 lb)0%0
25 to 44.9 kg (55–99 lb)0%0
45 kg and over (99 lb+)0%0
Weight not given8.2%13

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

Trend and outcomes

035Apr 2021: 0May 2021: 0Jun 2021: 0Jul 2021: 1Aug 2021: 1Sep 2021: 2Oct 2021: 1Nov 2021: 2Dec 2021: 0Jan 2022: 02022Feb 2022: 0Mar 2022: 0Apr 2022: 1May 2022: 0Jun 2022: 0Jul 2022: 0Aug 2022: 0Sep 2022: 0Oct 2022: 4Nov 2022: 1Dec 2022: 1Jan 2023: 02023Feb 2023: 1Mar 2023: 2Apr 2023: 0May 2023: 1Jun 2023: 3Jul 2023: 0Aug 2023: 1Sep 2023: 0Oct 2023: 0Nov 2023: 2Dec 2023: 2Jan 2024: 12024Feb 2024: 1Mar 2024: 0Apr 2024: 0May 2024: 0Jun 2024: 1Jul 2024: 4Aug 2024: 1Sep 2024: 1Oct 2024: 0Nov 2024: 1Dec 2024: 1Jan 2025: 12025Feb 2025: 1Mar 2025: 0Apr 2025: 0May 2025: 1Jun 2025: 0Jul 2025: 0Aug 2025: 0Sep 2025: 0Oct 2025: 1Nov 2025: 0Dec 2025: 0Jan 2026: 22026Feb 2026: 0Mar 2026: 5

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/Normal13.2%21
Recovered with Sequela0%0
Ongoing24.5%39
Died7.5%12
Euthanized5%8
Outcome Unknown17%27

Beside all cats

MeasureTonkineseAll cats
Reports159148,080
Latest 12 months912,477
Classed serious, of reports stating it41.8%35.6%
Death or euthanasia recorded, per 1,000 reports125.895

Questions about Tonkinese reports

How many FDA adverse event reports involve Tonkineses?

159 reports through March 2026, 0.1% of reports about cats; 9 in the latest 12 months.

Which drugs are named most often in Tonkinese reports?

By active ingredient: selamectin (30), cefovecin sodium (15), frunevetmab (14), spinosad (11) and cyclosporine (10). Brands are masked in the public data.

What signs are reported most for this breed?

anorexia (16.4%), vomiting (15.1%), lack of efficacy - NOS (10.1%), lethargy (10.1%) and weight loss (8.8%).

Is the Tonkinese 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 Tonkinese 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 ("Tonkinese" becomes "Tonkinese"). 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.