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FDA ADE reports for Valsartan

ade_valsartan_adverse_events

ade en 2026-07-22

Valsartan — 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. Valsartan is a active ingredient.

Total reports

Valsartan: 5

Reports by species (top entries)

  • Human 5

Top reported reactions (VEDDRA terms, top entries)

  • Accidental exposure 2
  • Tingling sensation 2
  • Bad taste 1
  • Dizziness 1
  • Dry mouth 1
  • Itchy ears 1
  • Light headedness 1
  • Lip disorder NOS 1
  • Throat tingling 1
  • Weakness 1

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b32.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).

Sources

FDA ADE reports for Valsartan (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_b32.json

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

Machine access

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Raw JSON ↗ llm.txt OpenAPI