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FDA CVM · 2025 release 16 reports on file

Korat - FDA Adverse Event Profile

Adverse-event records for Korat (Cat) from the FDA Center for Veterinary Medicine.

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Annual adverse-event report trend Yearly FDA CVM adverse-event report counts for this breed. 5 3.75 2.5 1.25 0 2014 2015 2016 2020 2021 2022 2023 2024 Reports filed Death-coded reports
Annual report volume for Korat drawn from FDA CVM filings.

Data updated June 2026

The record at a glance

Korat's FDA record: #390 most-reported cat breed, 16 total reports, 6.3% death-coded (1 reports).

#390
most-reported cat breed
6.3%
death-coded report share
3
Other abnormal test result NOS - top reaction
9.5 yr
average age at report

Higher volume usually means a more popular breed, not a riskier one, compare against how common the breed is.

Total Reports

16

FDA CVM filings

Deaths Reported

1

of 16 reports

Death Rate

6.3%

death-coded share

Avg Age at Report

9.5 yr

4.7 kg avg weight

Death-Coded Outcome Share

Korat death-coded reports 6.3%
Cross-breed median

6.3% of 16 korat reports involved a death outcome.

How to read this number

Read alongside breed popularity, veterinary access, and owner awareness, these shape how many events ever reach the FDA. The comparison line marks the cross-breed median death-coded share (about 4.8%) among breeds with 50 or more reports; values above it suggest higher reporting bias toward severe outcomes, not necessarily higher true mortality.

Average weight at time of report: 4.7 kg (10.4 lbs)

Top Reported Reactions

Other abnormal test result NOS 3
Vomiting 3
Application site pruritus 2
Head shake - ear disorder 2
Application site hair loss 2

Most Referenced Drugs

Spinosad 3
Selamectin 2
Robenacoxib 2
Genta/Momet/Clotrim Ear Oint 2
Selamectin;Sarolaner 2

Outcome Breakdown

Recovered/Normal
7 (43.8%)
Ongoing
4 (25.0%)
Outcome Unknown
3 (18.8%)
Recovered with Sequela
1 (6.3%)
Euthanized
1 (6.3%)

Gender Distribution

Male 10 (62.5%)
Female 5 (31.3%)
Unknown 1 (6.3%)

Reports by Year

Year Reports Trend
2012 2
2014 5
2015 1
2016 1
2020 1
2021 1
2022 1
2023 3
2024 1

Korat Pet Health Insights

Korat accounts for 16 FDA adverse event reports, ranking #390 by volume among cat breeds, with 1 reports (6.3%) coded as a death outcome. Mean age at report: 9.5 years, average weight 4.7 kg (10.4 lbs).

Top reported signs: Other abnormal test result NOS (3), Vomiting (3), Application site pruritus (2). Most-referenced drug: Spinosad (3 reports), followed by Selamectin (2) and Robenacoxib (2).

Outcome coding on 16 status-recorded reports is dominated by Recovered/Normal (43.8%). Annual submissions ranged 2,012-2,024 across 9 years on file.

Cat Breeds With a Similar Report Volume

Frequently Asked Questions

How many FDA adverse event reports involve Korat?
There are 16 adverse event reports involving Korat in the FDA database, with 1 reports involving death (6.3% death rate). Korat ranks #390 by report volume.
What are the most common adverse reactions reported for Korat?
The most commonly reported adverse reactions for Korat are Other abnormal test result NOS (3 reports), Vomiting (3 reports), Application site pruritus (2 reports), Head shake - ear disorder (2 reports), Application site hair loss (2 reports).
What drugs are most frequently associated with Korat adverse events?
The drugs most frequently referenced in Korat adverse event reports are Spinosad (3 reports), Selamectin (2 reports), Robenacoxib (2 reports), Genta/Momet/Clotrim Ear Oint (2 reports), Selamectin;Sarolaner (2 reports).
What is the average age of Korat in adverse event reports?
The average age of Korat at the time of adverse event reports is 9.5 years, with an average weight of 4.7 kg (10.4 lbs).
Does a high number of adverse event reports mean Korat is unhealthy?
No. FDA adverse event reports are voluntarily submitted and do not prove causation. Popular breeds with more veterinary visits tend to have more reports. The data reflects reporting patterns, not actual incidence rates. Always consult a veterinarian for health decisions.
Where does this Korat safety data come from?
All data comes from the FDA Center for Veterinary Medicine's adverse event reporting system. Pet owners, veterinarians, and manufacturers voluntarily submit reports about adverse events potentially linked to animal drugs and other products.

Every figure on PlainBreed is rendered directly from FDA openFDA adverse event data, no number is typed in by an editor. Breed figures are computed directly from FDA openFDA data, no figure is typed in by an editor. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.