โ† All Topics / ade

FDA ADE reports for Monensin

ade_monensin_adverse_events

ade en 2026-07-22

Monensin 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. Monensin is a active ingredient.

Total reports

Monensin: 2605

Reports by species (top entries)

  • Cattle 1964
  • Turkey 193
  • Horse 117
  • Chicken 95
  • Goat 42
  • Sheep 33

Top reported reactions (VEDDRA terms, top entries)

  • Death 1187
  • Diarrhoea 250
  • Milk production decrease 209
  • Decreased appetite 203
  • Lack of efficacy (protozoa) - Coccidia 197
  • Not eating 187
  • Lack of efficacy - NOS 175
  • NT - Abnormal necropsy finding NOS 155
  • Anorexia 150
  • Recumbency 132

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b9.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).