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FDA ADE reports for Lactulose

ade_lactulose_adverse_events

ade en 2026-07-22

Lactulose — 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. Lactulose is a active ingredient.

Total reports

Lactulose: 285

Reports by species (top entries)

  • Cat 194
  • Dog 89
  • Human 1
  • Other Birds 1

Top reported reactions (VEDDRA terms, top entries)

  • Vomiting 47
  • Lethargy (see also Central nervous system depression in 'Neurological') 44
  • Anorexia 32
  • Death by euthanasia 32
  • Constipation 30
  • Weight loss 28
  • Diarrhoea 26
  • Other abnormal test result NOS 26
  • Decreased appetite 25
  • Lack of efficacy - NOS 25

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b16.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).

Sources

FDA ADE reports for Lactulose (active ingredient) — total reports, species & reaction breakdown
Source document: FDA FAERS / openFDA Animal & Veterinary Event Reports
US FDA Center for Veterinary Medicine (openFDA animal & veterinary event database)retrieved 2026-07-22

Verification file: pdf-raw/ade/ade_active_ingredients_2026-07-22_b16.json

Link points to the issuing authority's site; a direct document link is still being verified.