Drug profile
The FDA adverse-event record for Ponazuril 150 Mg/G Oral Paste
62 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Ponazuril 150 Mg/G Oral Paste. See the species affected, top reactions, and outcomes below.
- 62
- adverse-event reports
- 9.7%
- death-coded share
- Horse
- most-reported species
- 13
- Product Defect, General - top reaction
Active Ingredients
Administration Routes
Species Affected
Most Affected Breeds
Most Reported Reactions
Outcome Breakdown
Ponazuril 150 Mg/G Oral Paste Adverse Event Insights
62 reports name Ponazuril 150 Mg/G Oral Paste; 6 recorded a death outcome (9.7% of reported events, not a population-level mortality rate). Active ingredient: Ponazuril 150 Mg/G Oral Paste. Administration routes: Oral, Unknown.
By species: Horse (27 reports), Unknown (18 reports), Dog (10 reports). By breed: Unknown (20), Quarter Horse (11), Thoroughbred (4).
Leading clinical signs: Product Defect, General (13), Lethargy (see also Central nervous system depression in 'Neurological') (7), Lack of efficacy - NOS (7), Recumbency (5). Outcome, 44 coded reports: Outcome Unknown leads at 61.4%.
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.