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FDA ADE reports for Follicle Stimulating Hormone

ade_follicle_stimulating_hormone_adverse_events

ade en 2026-07-22

Follicle Stimulating Hormone 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. Follicle Stimulating Hormone is a active ingredient.

Total reports

Follicle Stimulating Hormone: 46

Reports by species (top entries)

  • Cattle 44
  • Goat 1
  • Sheep 1

Top reported reactions (VEDDRA terms, top entries)

  • INEFFECTIVE, SUPEROVULATION 42
  • Lack of efficacy - NOS 3
  • Anaphylaxis 1
  • Eyelid oedema 1
  • Facial oedema 1
  • Oedema of the extremities (see also other SOCs for most applicable oedema) 1
  • Swelling NOS 1
  • Urticaria 1

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b24.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).