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FDA ADE reports for Sulfaquinoxaline

ade_sulfaquinoxaline_adverse_events

ade en 2026-07-22

Sulfaquinoxaline — 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. Sulfaquinoxaline is a active ingredient.

Total reports

Sulfaquinoxaline: 4

Reports by species (top entries)

  • Chicken 2
  • Turkey 2

Top reported reactions (VEDDRA terms, top entries)

  • Death 2
  • Lack of efficacy (bacteria) - NOS 2
  • DEATH-TREATMENT FAILURE 1
  • Depression 1
  • PR-BONE MARROW, LESION(S) 1
  • PR-KIDNEY(S), LESION(S) 1
  • PR-MULTIPLE SITES, BLOOD 1
  • Pallor 1
  • Respiratory distress 1
  • Swelling NOS 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 Sulfaquinoxaline (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