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FDA ADE reports for potassium gluconate — total reports, species & reaction breakdown

ade_potassium_gluconate_adverse_events

ade 200 tok en 2026-08-16

potassium gluconate — 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. "potassium gluconate" 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

potassium gluconate: 96

Reports by species (top entries)

  • Cat 85
  • Dog 9

Top reported reactions (VEDDRA terms, top entries)

  • Vomiting 21
  • Death by euthanasia 16
  • Dehydration 11
  • Anaemia NOS 10
  • Lack of efficacy - NOS 10
  • Weight loss 10
  • Not eating 9
  • Anorexia 8
  • Decreased appetite 8
  • Lethargy (see also Central nervous system depression in 'Neurological') 8

"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).

Sources

FDA ADE reports for potassium gluconate — 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 2026-08-16

Verification file: pdf-raw/ade/ade_active_ingredients_2026-08-16_b1.json

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