Drug profile
The FDA adverse-event record for Ophiopogon Japonicus Root Extract
63 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Ophiopogon Japonicus Root Extract. See the species affected, top reactions, and outcomes below.
- 63
- adverse-event reports
- 0.0%
- death-coded share
- Dog
- most-reported species
- 19
- Application site erythema - top reaction
Active Ingredients
Administration Routes
Species Affected
Most Affected Breeds
Most Reported Reactions
Outcome Breakdown
Ophiopogon Japonicus Root Extract Adverse Event Insights
63 reports name Ophiopogon Japonicus Root Extract; 0 recorded a death outcome (0.0% of reported events, not a population-level mortality rate). Active ingredient: Ophiopogon Japonicus Root Extract. Administration routes: Topical, Unknown.
By species: Dog (51 reports), Cat (9 reports), Human (3 reports). By breed: Crossbred Canine/dog (7), Shih Tzu (5), Terrier - Yorkshire (4).
Leading clinical signs: Application site erythema (19), Application site pruritus (9), Lack of efficacy - NOS (7), Flaking skin (4). Outcome, 63 coded reports: Ongoing leads at 36.5%.
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.