Drug profile
The FDA adverse-event record for Zilpaterol Oral Powder
11 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Zilpaterol Oral Powder. See the species affected, top reactions, and outcomes below.
- 11
- adverse-event reports
- 72.7%
- death-coded share
- Cattle
- most-reported species
- 5
- Death by euthanasia - top reaction
Active Ingredients
Administration Routes
Species Affected
Most Affected Breeds
Most Reported Reactions
Outcome Breakdown
Zilpaterol Oral Powder Adverse Event Insights
11 reports name Zilpaterol Oral Powder; 8 recorded a death outcome (72.7% of reported events, not a population-level mortality rate). Active ingredient: Zilpaterol Oral Powder. Administration routes: Oral, Unknown.
By species: Cattle (7 reports), Dog (2 reports), Human (1 reports). By breed: Cattle (other) (3), Crossbred Bovine/Cattle (3), Unknown (1).
Leading clinical signs: Death by euthanasia (5), Death (3), Unclassifiable adverse event (2), Other abnormal test result NOS (2). Outcome, 14 coded reports: Euthanized leads at 42.9%.
Read these counts as reporting volume, not risk: per our methodology, a widely-prescribed drug will rack up more raw FDA reports in a given year than a rarely-used one at an identical true rate, so we recommend comparing within similar-exposure products rather than across the full 2025 catalog.
Source: FDA Center for Veterinary Medicine openFDA Animal & Veterinary Adverse Events (CVM AER) · 2025
Every figure on PlainBreed is rendered directly from FDA openFDA adverse event data, no number is typed in by an editor. This page draws directly on 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.