Cat /
FDA CVM · 2025 release 12 reports on file

Chartreuse - FDA Adverse Event Profile

Adverse-event records for Chartreuse (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. 3 2.25 1.5 0.75 0 2012 2013 2014 2015 2019 2020 2025 Reports filed Death-coded reports
Annual report volume for Chartreuse drawn from FDA CVM filings.

Data updated June 2026

The record at a glance

Among cat breeds, Chartreuse is #418 by FDA report volume; 16.7% of its 12 reports (2) were death-coded.

#418
most-reported cat breed
16.7%
death-coded report share
3
Vomiting - top reaction
7.1 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

12

FDA CVM filings

Deaths Reported

2

of 12 reports

Death Rate

16.7%

death-coded share

Avg Age at Report

7.1 yr

5.5 kg avg weight

Death-Coded Outcome Share

Chartreuse death-coded reports 16.7%
Cross-breed median

16.7% of 12 chartreuse 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: 5.5 kg (12.1 lbs)

Top Reported Reactions

Vomiting 3
Hyperpigmentation 1
Tongue disorder NOS 1
Inappetence 1
Dehydration 1

Most Referenced Drugs

Maropitant Citrate 2
Selamectin 2
Cefovecin 1
Cyclosporine A 1
Amoxicillin/ Clavulanic Acid 1

Outcome Breakdown

Outcome Unknown
5 (41.7%)
Recovered/Normal
4 (33.3%)
Ongoing
1 (8.3%)
Euthanized
1 (8.3%)
Died
1 (8.3%)

Gender Distribution

Female 6 (50.0%)
Male 6 (50.0%)

Reports by Year

Year Reports Trend
2012 1
2013 3
2014 2
2015 2
2019 2
2020 1
2025 1

Chartreuse Pet Health Insights

Chartreuse accounts for 12 FDA adverse event reports, ranking #418 by volume among cat breeds, with 2 reports (16.7%) coded as a death outcome. Mean age at report: 7.1 years, average weight 5.5 kg (12.1 lbs).

Top reported signs: Vomiting (3), Hyperpigmentation (1), Tongue disorder NOS (1). Most-referenced drug: Maropitant Citrate (2 reports), followed by Selamectin (2) and Cefovecin (1).

Outcome coding on 12 status-recorded reports is dominated by Outcome Unknown (41.7%). Annual submissions ranged 2,012-2,025 across 7 years on file.

Cat Breeds With a Similar Report Volume

Frequently Asked Questions

How many FDA adverse event reports involve Chartreuse?
There are 12 adverse event reports involving Chartreuse in the FDA database, with 2 reports involving death (16.7% death rate). Chartreuse ranks #418 by report volume.
What are the most common adverse reactions reported for Chartreuse?
The most commonly reported adverse reactions for Chartreuse are Vomiting (3 reports), Hyperpigmentation (1 reports), Tongue disorder NOS (1 reports), Inappetence (1 reports), Dehydration (1 reports).
What drugs are most frequently associated with Chartreuse adverse events?
The drugs most frequently referenced in Chartreuse adverse event reports are Maropitant Citrate (2 reports), Selamectin (2 reports), Cefovecin (1 reports), Cyclosporine A (1 reports), Amoxicillin/ Clavulanic Acid (1 reports).
What is the average age of Chartreuse in adverse event reports?
The average age of Chartreuse at the time of adverse event reports is 7.1 years, with an average weight of 5.5 kg (12.1 lbs).
Does a high number of adverse event reports mean Chartreuse 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 Chartreuse 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.