FDA ADE reports for Cidofovir

ade_cidofovir_adverse_events

ade en 2026-07-22

Cidofovir — 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. Cidofovir is a active ingredient.

Total reports

Cidofovir: 6

Reports by species (top entries)

Cat 6

Top reported reactions (VEDDRA terms, top entries)

Hyperglycaemia 3
Hypophosphataemia 3
Lack of efficacy - NOS 3
Neutrophilia 3
Abnormal radiograph finding 2
Corneal ulcer 2
Diabetes 2
Elevated alanine aminotransferase (ALT) 2
Elevated serum alkaline phosphatase (ALP) 2
Hepatomegaly 2

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b30.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).

Sources

FDA ADE reports for Cidofovir (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_b30.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