โ† FDA Adverse-Event Compilations

FDA ADE reports for fortiflora โ€” total reports, species & reaction breakdown

ade_fortiflora_adverse_events

FDA Adverse-Event Compilations derived_from_dataset ade

fortiflora 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 2026-08-16. Counts are report-level: one report may list multiple reactions and multiple animals, so figures are not additive and do not imply causation. "fortiflora" is a name as filed in the drug active-ingredient field of these reports (may be a generic ingredient or a product/brand name as reported).

Total reports

fortiflora: 78

Reports by species (top entries)

  • Dog 58
  • Cat 20

Top reported reactions (VEDDRA terms, top entries)

  • Diarrhoea 21
  • Lethargy (see also Central nervous system depression in Neurological) 17
  • Vomiting 17
  • Death by euthanasia 11
  • Decreased appetite 10
  • Elevated blood urea nitrogen (BUN) 9
  • Anorexia 8
  • Emesis (multiple) 8
  • Urinary tract infection 7
  • Abnormal ultrasound finding 6

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-08-16_b1.json (openFDA animalandveterinary/event.json, pulled 2026-08-16).