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FDA ADE reports for Spectinomycin

ade_spectinomycin_adverse_events

ade en 2026-07-22

Spectinomycin — 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. Spectinomycin is a active ingredient.

Total reports

Spectinomycin: 26

Reports by species (top entries)

  • Cattle 16
  • Human 2

Top reported reactions (VEDDRA terms, top entries)

  • Lack of efficacy (bacteria) - NOS 9
  • Death 6
  • DEATH-TREATMENT FAILURE 3
  • No sign 3
  • Residues in milk 3
  • Accidental exposure 2
  • PR-LUNG(S), LESION(S) 2
  • Seal, Abnormal 2
  • Unclassifiable adverse event 2
  • Application site reaction NOS 1

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b27.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).

Sources

FDA ADE reports for Spectinomycin (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_b27.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