Horse /
FDA CVM · 2025 release 5 reports on file

Selle Français - FDA Adverse Event Profile

Adverse-event records for Selle Français (Horse) 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. 78k 59k 39k 20k 0 2018 2019 2020 2021 2022 2023 Reports filed Death-coded reports
Annual report volume for Selle Français drawn from FDA CVM filings.

Data updated June 2026

The record at a glance

Selle Français's FDA record: #505 most-reported horse breed, 5 total reports, 0.0% death-coded (0 reports).

#505
most-reported horse breed
0.0%
death-coded report share
2
Colic - top reaction
14.7 yr
average age at report

Read report counts next to breed popularity: a bigger number often just means more owners and more vet visits.

Total Reports

5

FDA CVM filings

Deaths Reported

0

of 5 reports

Death Rate

0.0%

death-coded share

Avg Age at Report

14.7 yr

no age data

Death-Coded Outcome Share

Selle Français death-coded reports 0.0%
Cross-breed median

0.0% of 5 selle français 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.

Top Reported Reactions

Colic 2
Injection site swelling 2
Malaise 1
Fever 1
Faecal impaction 1

Most Referenced Drugs

Pentosan Polysulfate Sodium 3
Fenbendazol Oral Paste 1
Pyrantel Pamoate (Pyrantel Embonate) 1
Clostridium Tetani Seed Lot #18 H-1 Massachusetts Strain;Eastern Equine Encephal 1
Flu/Rhino 1

Outcome Breakdown

Recovered/Normal
4 (80.0%)
Ongoing
1 (20.0%)

Gender Distribution

Male 4 (80.0%)
Female 1 (20.0%)

Reports by Year

Year Reports Trend
2020 1
2025 4

Selle Français Pet Health Insights

Selle Français accounts for 5 FDA adverse event reports, ranking #505 by volume among horse breeds, with 0 reports (0.0%) coded as a death outcome. Mean age at report: 14.7 years.

Top reported signs: Colic (2), Injection site swelling (2), Malaise (1). Most-referenced drug: Pentosan Polysulfate Sodium (3 reports), followed by Fenbendazol Oral Paste (1) and Pyrantel Pamoate (Pyrantel Embonate) (1).

Outcome coding on 5 status-recorded reports is dominated by Recovered/Normal (80.0%). Annual submissions ranged 2,020-2,025 across 2 years on file.

Horse Breeds With a Similar Report Volume

Frequently Asked Questions

How many FDA adverse event reports involve Selle Français?
There are 5 adverse event reports involving Selle Français in the FDA database, with 0 reports involving death (0.0% death rate). Selle Français ranks #505 by report volume.
What are the most common adverse reactions reported for Selle Français?
The most commonly reported adverse reactions for Selle Français are Colic (2 reports), Injection site swelling (2 reports), Malaise (1 reports), Fever (1 reports), Faecal impaction (1 reports).
What drugs are most frequently associated with Selle Français adverse events?
The drugs most frequently referenced in Selle Français adverse event reports are Pentosan Polysulfate Sodium (3 reports), Fenbendazol Oral Paste (1 reports), Pyrantel Pamoate (Pyrantel Embonate) (1 reports), Clostridium Tetani Seed Lot #18 H-1 Massachusetts Strain;Eastern Equine Encephal (1 reports), Flu/Rhino (1 reports).
What is the average age of Selle Français in adverse event reports?
The average age of Selle Français at the time of adverse event reports is 14.7 years.
Does a high number of adverse event reports mean Selle Français 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 Selle Français 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.