โ† All Topics / ade

FDA ADE reports for Duloxetine

ade_duloxetine_adverse_events

ade en 2026-07-22

Duloxetine 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. Duloxetine is a active ingredient.

Total reports

Duloxetine: 10

Reports by species (top entries)

  • Human 8
  • Dog 2

Top reported reactions (VEDDRA terms, top entries)

  • Accidental exposure 3
  • Stomach upset 3
  • Dry mouth 2
  • Nausea 2
  • Bloody diarrhoea 1
  • Chest discomfort NOS 1
  • Diarrhoea 1
  • Elevated blood urea nitrogen (BUN) 1
  • Facial swelling (see also Skin) 1
  • Heartburn 1

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b30.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).