โ† FDA Adverse-Event Compilations

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

ade_loratadine_adverse_events

FDA Adverse-Event Compilations derived_from_dataset ade

loratadine 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. "loratadine" 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

loratadine: 102

Reports by species (top entries)

  • Dog 89
  • Cat 7
  • Human 6

Top reported reactions (VEDDRA terms, top entries)

  • Vomiting 16
  • Diarrhoea 15
  • Lethargy (see also Central nervous system depression in 'Neurological') 15
  • Panting 9
  • Death by euthanasia 8
  • Lack of efficacy - NOS 8
  • Emesis 7
  • Other abnormal test result NOS 7
  • Polydipsia 7
  • Elevated alanine aminotransferase (ALT) 6

"Lack of efficacy" terms denote product-performance reports, not adverse reactions.

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