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FDA ADE reports for Fexofenadine Hcl

ade_fexofenadine_adverse_events

ade en 2026-07-22

Fexofenadine Hcl 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. Fexofenadine Hcl is a active ingredient.

Total reports

Fexofenadine Hcl: 20

Reports by species (top entries)

  • Dog 13
  • Human 6
  • Cat 1

Top reported reactions (VEDDRA terms, top entries)

  • Vomiting 5
  • Lethargy (see also Central nervous system depression in 'Neurological') 4
  • Accidental exposure 3
  • Anxiety 2
  • Diarrhoea 2
  • Elevated blood urea nitrogen (BUN) 2
  • Elevated serum alkaline phosphatase (SAP) 2
  • Emesis 2
  • INEFFECTIVE, ATOPY CONTROL 2
  • Lack of efficacy (ectoparasite) - flea 2

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b31.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).