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FDA ADE reports for Ophiopogon Japonicus Root Extract

ade_ophiopogon_japonicus_root_extract_adverse_events

ade en 2026-07-22

Ophiopogon Japonicus Root Extract โ€” FDA Animal & Veterinary Adverse Event (ADE) Reports

Source: openFDA animalandveterinary/event.json, the FDA Center for Veterinary Medicine (CVM) adverse event report database. Data pulled 2026-07-22. Counts are report-level: one report may list multiple reactions and multiple animals, so figures are not additive and do not imply causation. Ophiopogon Japonicus Root Extract is a active ingredient.

Total reports

Ophiopogon Japonicus Root Extract: 56

Reports by species (top entries)

  • Dog 46
  • Cat 7
  • Human 3

Top reported reactions (VEDDRA terms, top entries)

  • Application site erythema 17
  • Application site pruritus 9
  • Lack of efficacy - NOS 6
  • Pruritus 4
  • Application site irritation 3
  • Flaking skin 3
  • Application site itching 2
  • Application site scab 2
  • Hives (see also 'Skin') 2
  • Hot spot (pyotraumatic dermatitis) 2

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b23.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).