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FDA ADE reports for Cloprostenol Sodium

ade_cloprostenol_adverse_events

ade en 2026-07-22

Cloprostenol Sodium 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. Cloprostenol Sodium is a active ingredient.

Total reports

Cloprostenol Sodium: 221

Reports by species (top entries)

  • Cattle 129
  • Human 19
  • Horse 13
  • Dog 2
  • Pig 1

Top reported reactions (VEDDRA terms, top entries)

  • INEFFECTIVE, ESTRUS SYNCHRONIZ 55
  • Lack of efficacy - NOS 31
  • Death 25
  • Stopper, abnormal 17
  • Accidental exposure 16
  • Unclassifiable adverse event 15
  • INEFFECTIVE, ABORTION 8
  • Abdominal pain 6
  • Emphysema NOS (see 'Respiratory' for pulmonary emphysema) 6
  • Anaphylaxis 5

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b18.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).