Pet Drug Reports

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Breed · Cat

Siamese: adverse event reports

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

2,912reports, 1987–20262% of cat reports
156reports, 12 months to March 2026209 in the 12 months before
39.8%classed serious, as reportedall cats: 35.6%
16%name selamectinall cats: 14.8%

FDA's database holds 2,912 reports where the animal's breed is given as "Siamese", shown here as Siamese: 2% of reports about cats. Reports on crossbred animals are left out of breed pages.

156 reports arrived in the 12 months to March 2026, down 25% from 209 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 16% of this breed's reports, about the same share as in reports about all cats (14.8%).

The terms listed most often are vomiting (15.3%), lethargy (10.9%) and anorexia (9.5%). Vomiting appears in 15.3% of reports, about the same share as in all cat reports (12.5%). 39.8% 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 Siamese reportsShare of all cat reports
Selamectin46516%14.8%
Spinosad2889.9%7.8%
Cefovecin sodium2167.4%5.8%
Fluralaner2037%7%
Imidacloprid + Moxidectin1645.6%5.5%
Frunevetmab1184.1%5.1%
Nitenpyram1153.9%5.8%
Buprenorphine1143.9%3.7%
Meloxicam1053.6%2.4%
Maropitant973.3%2.5%
Sarolaner + Selamectin953.3%5.3%
Emodepside + Praziquantel873%3.8%
Insulin752.6%2.4%
Cyclosporine632.2%2%
Robenacoxib592%2.2%
Amoxicillin561.9%1.1%
Velagliflozin551.9%2.9%
Bexagliflozin511.8%2.5%
Ketamine Hydrochloride491.7%2.5%
Enrofloxacin471.6%1%

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 Siamese reports listing the termall cat reports

  1. Vomiting15.3%446
  2. Lethargy[unusually tired or inactive]10.9%317
  3. Anorexia[not eating]9.5%277
  4. Lack of efficacy (ectoparasite) - flea[the product did not have the expected effect: fleas]6.7%194
  5. Application site alopecia[hair loss where the product was applied]6%176
  6. Ataxia[unsteady, uncoordinated movement]5.9%171
  7. Depression[dull, quiet or withdrawn]5.7%167
  8. Death5.5%159
  9. Emesis[vomiting]5.5%159
  10. Behavioural disorder NOS[behaviour change, type not specified]5.4%156
  11. Diarrhoea[diarrhea]4.7%137
  12. Hypersalivation[drooling]4.5%132
  13. Death by euthanasia[the animal was euthanized]4.2%122
  14. Lack of efficacy - NOS[the product did not have the expected effect]4.1%120
  15. Application site hair loss[hair loss where the product was applied]3.8%112
  16. Elevated blood urea nitrogen (BUN)[a kidney value above the normal range]3.4%99
  17. Pruritus[itching]2.9%83
  18. Elevated creatinine[a kidney value above the normal range]2.8%82
  19. Accidental exposure[exposure that was not intended]2.6%75
  20. Hiding2.4%70

Age and weight

Age of the animal

Under 1 year12.1%353
1 to 3 years20.9%608
4 to 7 years21.3%619
8 to 11 years19.7%575
12 years and over23.4%682
Age not given2.6%75

Weight of the animal

Under 5 kg (11 lb)59.5%1,734
5 to 9.9 kg (11–22 lb)33.6%979
10 to 24.9 kg (22–55 lb)0.3%10
25 to 44.9 kg (55–99 lb)0%0
45 kg and over (99 lb+)0%0
Weight not given6.5%189

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

Trend and outcomes

01326Apr 2021: 13May 2021: 8Jun 2021: 9Jul 2021: 9Aug 2021: 18Sep 2021: 7Oct 2021: 9Nov 2021: 12Dec 2021: 7Jan 2022: 62022Feb 2022: 7Mar 2022: 9Apr 2022: 5May 2022: 5Jun 2022: 10Jul 2022: 8Aug 2022: 16Sep 2022: 19Oct 2022: 9Nov 2022: 10Dec 2022: 9Jan 2023: 92023Feb 2023: 6Mar 2023: 14Apr 2023: 13May 2023: 8Jun 2023: 13Jul 2023: 20Aug 2023: 25Sep 2023: 9Oct 2023: 17Nov 2023: 7Dec 2023: 10Jan 2024: 62024Feb 2024: 21Mar 2024: 19Apr 2024: 10May 2024: 20Jun 2024: 16Jul 2024: 23Aug 2024: 26Sep 2024: 25Oct 2024: 17Nov 2024: 16Dec 2024: 16Jan 2025: 132025Feb 2025: 12Mar 2025: 15Apr 2025: 11May 2025: 12Jun 2025: 19Jul 2025: 14Aug 2025: 13Sep 2025: 14Oct 2025: 14Nov 2025: 12Dec 2025: 15Jan 2026: 112026Feb 2026: 13Mar 2026: 8

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/Normal21%612
Recovered with Sequela0.8%23
Ongoing22.2%646
Died7.1%206
Euthanized2.8%81
Outcome Unknown20.9%609

Beside all cats

MeasureSiameseAll cats
Reports2,912148,080
Latest 12 months15612,477
Classed serious, of reports stating it39.8%35.6%
Death or euthanasia recorded, per 1,000 reports98.695

Questions about Siamese reports

How many FDA adverse event reports involve Siameses?

2,912 reports through March 2026, 2% of reports about cats; 156 in the latest 12 months.

Which drugs are named most often in Siamese reports?

By active ingredient: selamectin (465), spinosad (288), cefovecin sodium (216), fluralaner (203) and imidacloprid + moxidectin (164). Brands are masked in the public data.

What signs are reported most for this breed?

vomiting (15.3%), lethargy (10.9%), anorexia (9.5%), lack of efficacy (ectoparasite) - flea (6.7%) and application site alopecia (6%).

Is the Siamese 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 Siamese 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 ("Siamese" becomes "Siamese"). 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.