Total Reports
103
Above-median volume
Breed profile · FDA CVM July 2026 extract
Adverse-event filings for Cattle (unspecified) (Cattle) in the FDA Center for Veterinary Medicine openFDA extract. Browse cattle breeds, reactions, and outcomes below.
By recorded gender -- every report on file for Cattle (unspecified), no filtering.
Data updated September 2026
The verdict
According to the FDA Center for Veterinary Medicine openFDA adverse-event extract, Cattle (unspecified) ranks #229 of 510 by total reports (103) and #15 of 275 by death-coded share (39.8%). National dual: Retriever - Labrador is #1 of 510 by total adverse-event reports (93,675) at death-coded-share rank 195 of 275 breeds with at least 50 reports (3.7%); separately, Atlantic Salmon (Salmo salar) is #1 highest death-coded share at 99.0% (report rank #233).
Report volume reflects how common a breed or drug is and how often owners and vets file — not actual risk. Death-coded share ranks are limited to entries with enough reports to be meaningful. The two maps do not agree at #1.
Release-over-release change
PlainBreed reconstructed the prior snapshot from dated openFDA partitions through 2025 Q4, then compared it with the 2026-07-27 openFDA export. Cattle (unspecified) has 103 reports now versus 102 in that prior snapshot: 1 more (1.0%).
This compares reported-event counts in two source snapshots. It does not establish a change in real-world risk, product safety, or disease incidence.
Subscribe to Cattle (unspecified) changesTotal Reports
103
Above-median volume
Deaths Reported
41
of 103 reports
Death-coded share of reports
39.8%
Highest death-coded share
Avg Age at Report
1.4 yr
268.6 kg avg weight
39.8% of 103 cattle (unspecified) reports involved a death outcome.
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 (4.8%) among breeds with 50 or more reports; values above it suggest higher reporting bias toward severe outcomes, not necessarily higher true mortality.
| Year | Reports | Trend |
|---|---|---|
| 2011 | 2 | |
| 2012 | 1 | |
| 2013 | 5 | |
| 2014 | 27 | |
| 2015 | 9 | |
| 2016 | 7 | |
| 2017 | 4 | |
| 2018 | 5 | |
| 2019 | 8 | |
| 2020 | 6 | |
| 2021 | 7 | |
| 2022 | 9 | |
| 2023 | 7 | |
| 2025 | 6 | |
Signature read: Cattle (unspecified)'s 39.8% death-coded share is in the upper third of the ≥50-report cohort (median 4.8%). According to FDA CVM filings indexed on PlainBreed as of July 2026 extract, Cattle (unspecified) sits at #229 of 510 by report volume among all breeds and #11 of 30 among cattle breeds, with 103 reports and 41 (39.8%) death-coded. On death-coded share among breeds with ≥50 reports, it ranks #15 of 275. Mean age at report: 1.4 years, average weight 268.6 kg (592.3 lbs).
Top reported signs: Lack of efficacy - NOS (34), Death (28), INEFFECTIVE, ESTRUS SYNCHRONIZ (17). Most-referenced drug: Dinoprost Tromethamine (14 reports), followed by Progesterone (12) and Fenbendazol Suspension (11).
Outcome coding on 125 status-recorded reports is dominated by Outcome Unknown (41.6%). Annual submissions ranged 1-2,025 across 14 years on file.
Showing 6 of 29 cattle breeds in our dataset, ranked by closest report volume.
Two openFDA-derived peer sets for Cattle (unspecified), both outside the Cattle family so the neighborhoods are not species containment (the similar-volume list above stays within species).
Nearest other-species breeds with ≥50 reports (39.8% death-coded here).
Nearest other-species breeds by reported average weight (268.6 kg here).
What to do with this cattle
A report does not prove a drug caused the reaction, and popular breeds simply generate more reports.
Compare a breed's report volume against how common the breed is before drawing conclusions. See our methodology for how the death-coded share and rankings are computed, or read breed-specific reporting patterns and FDA CVM reporting.
Source: FDA Center for Veterinary Medicine openFDA Animal & Veterinary Adverse Events (CVM AER) · 2025
Informational only. FDA adverse-event reports are voluntary and do not prove causation; consult a veterinarian before acting on them. Verify with FDA CVM →