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FDA ADE reports for Gnrh

ade_gnrh_adverse_events

ade en 2026-07-22

Gnrh — 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. Gnrh is a active ingredient.

Total reports

Gnrh: 19

Reports by species (top entries)

  • Cattle 19

Top reported reactions (VEDDRA terms, top entries)

  • Lack of efficacy - NOS 12
  • INEFFECTIVE, ESTRUS SYNCHRONIZ 6
  • Rectal prolapse 2
  • Application site abscess 1
  • Collapse NOS (see also 'Cardio-vascular' and 'Neurological disorders') 1
  • Cutaneous emphysema 1
  • Infertility NOS 1
  • Injection site gaseous gangrene 1
  • Injection site oedema 1
  • Intentional misuse 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 Gnrh (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