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FDA ADE reports for Loratidine

ade_loratidine_adverse_events

ade en 2026-07-22

Loratidine — 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. Loratidine is a active ingredient.

Total reports

Loratidine: 156

Reports by species (top entries)

  • Dog 143
  • Human 7
  • Cat 4
  • Monkey 1

Top reported reactions (VEDDRA terms, top entries)

  • Emesis 26
  • Lack of efficacy - NOS 19
  • Lethargy (see also Central nervous system depression in 'Neurological') 18
  • Vomiting 15
  • Diarrhoea 12
  • INEFFECTIVE, ATOPY CONTROL 10
  • Other abnormal test result NOS 10
  • Behavioural disorder NOS 8
  • Seizure NOS 7
  • Anorexia 6

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b19.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).

Sources

FDA ADE reports for Loratidine (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_b19.json

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