Rat /
FDA CVM · 2025 release 12 reports on file

Rat (unknown) - FDA Adverse Event Profile

Adverse-event records for Rat (unknown) (Rat) 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 2018 2019 2020 2023 2024 2025 Reports filed Death-coded reports
Annual report volume for Rat (unknown) drawn from FDA CVM filings.

Data updated June 2026

The record at a glance

Rat (unknown)'s FDA record: #423 most-reported rat breed, 12 total reports, 50.0% death-coded (6 reports).

#423
most-reported rat breed
50.0%
death-coded report share
5
Death - top reaction
0.2 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

6

of 12 reports

Death Rate

50.0%

death-coded share

Avg Age at Report

0.2 yr

0.4 kg avg weight

Death-Coded Outcome Share

Rat (unknown) death-coded reports 50.0%
Cross-breed median

50.0% of 12 rat (unknown) 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: 0.4 kg (0.9 lbs)

Top Reported Reactions

Death 5
INEFFECTIVE, ANESTHESIA 3
Product Defect, General 1
Drug administration error 1
Precipitate, Sediment 1

Most Referenced Drugs

Ketamine Hydrochloride 7
Meloxicam 2
Buprenorphine 2
Ketamine 1
Xylazine Hcl 1

Outcome Breakdown

Died
5 (38.5%)
Outcome Unknown
4 (30.8%)
Recovered/Normal
3 (23.1%)
Euthanized
1 (7.7%)

Gender Distribution

Unknown 7 (58.3%)
Mixed 2 (16.7%)
Male 2 (16.7%)
Female 1 (8.3%)

Reports by Year

Year Reports Trend
2018 3
2019 3
2020 3
2023 1
2024 1
2025 1

Rat (unknown) Pet Health Insights

Rat (unknown) accounts for 12 FDA adverse event reports, ranking #423 by volume among rat breeds, with 6 reports (50.0%) coded as a death outcome. Mean age at report: 0.2 years, average weight 0.4 kg (0.9 lbs).

Top reported signs: Death (5), INEFFECTIVE, ANESTHESIA (3), Product Defect, General (1). Most-referenced drug: Ketamine Hydrochloride (7 reports), followed by Meloxicam (2) and Buprenorphine (2).

Outcome coding on 13 status-recorded reports is dominated by Died (38.5%). Annual submissions ranged 2,018-2,025 across 6 years on file.

Frequently Asked Questions

How many FDA adverse event reports involve Rat (unknown)?
There are 12 adverse event reports involving Rat (unknown) in the FDA database, with 6 reports involving death (50.0% death rate). Rat (unknown) ranks #423 by report volume.
What are the most common adverse reactions reported for Rat (unknown)?
The most commonly reported adverse reactions for Rat (unknown) are Death (5 reports), INEFFECTIVE, ANESTHESIA (3 reports), Product Defect, General (1 reports), Drug administration error (1 reports), Precipitate, Sediment (1 reports).
What drugs are most frequently associated with Rat (unknown) adverse events?
The drugs most frequently referenced in Rat (unknown) adverse event reports are Ketamine Hydrochloride (7 reports), Meloxicam (2 reports), Buprenorphine (2 reports), Ketamine (1 reports), Xylazine Hcl (1 reports).
What is the average age of Rat (unknown) in adverse event reports?
The average age of Rat (unknown) at the time of adverse event reports is 0.2 years, with an average weight of 0.4 kg (0.9 lbs).
Does a high number of adverse event reports mean Rat (unknown) 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 Rat (unknown) 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.