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FDA ADE reports for Alendronate Sodium

ade_alendronate_adverse_events

ade en 2026-07-22

Alendronate 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. Alendronate Sodium is a active ingredient.

Total reports

Alendronate Sodium: 8

Reports by species (top entries)

  • Cat 5
  • Human 3

Top reported reactions (VEDDRA terms, top entries)

  • Accidental exposure 3
  • Seizure NOS 3
  • Ataxia 2
  • Other abnormal test result NOS 2
  • Abdominal cramp 1
  • Abdominal pain 1
  • Anorexia 1
  • Appetite loss 1
  • Application site skin scaling 1
  • Death by euthanasia 1

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b33.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).