FDA ADE reports for Oxytetracycline

ade_oxytetracycline_adverse_events

ade en 2026-07-22

Oxytetracycline — 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. Oxytetracycline is a active ingredient.

Total reports

Oxytetracycline: 1136

Reports by species (top entries)

Cattle 636
Horse 42
Human 41
Dog 31
Goat 24
Cat 22

Top reported reactions (VEDDRA terms, top entries)

Death 333
Solution, Abnormal 185
Anaphylaxis 177
Injection site swelling 143
Lack of efficacy (bacteria) - NOS 108
Color, Abnormal 107
Collapse (see also 'Cardio-vascular' and 'Systemic disorders') 84
Dyspnoea 64
Hypersalivation 52
Unclassifiable adverse event 40

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b11.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).

Sources

FDA ADE reports for Oxytetracycline (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_b11.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