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FDA ADE reports for Pramoxine Hydrochloride

ade_pramoxine_adverse_events

ade en 2026-07-22

Pramoxine Hydrochloride 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. Pramoxine Hydrochloride is a active ingredient.

Total reports

Pramoxine Hydrochloride: 30

Reports by species (top entries)

  • Dog 25
  • Human 4
  • Cat 1

Top reported reactions (VEDDRA terms, top entries)

  • Pruritus 5
  • Application site pruritus 4
  • Application site erythema 3
  • Erythema (for urticaria see Immune SOC) 3
  • Glaucoma 3
  • Application site reddening 2
  • Behavioural disorder NOS 2
  • Hives (see also 'Skin') 2
  • Lack of efficacy - NOS 2
  • Urticaria 2

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b32.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).