FDA ADE reports for Atorvastatin

ade_atorvastatin_adverse_events

ade en 2026-07-22

Atorvastatin — 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. Atorvastatin is a active ingredient.

Total reports

Atorvastatin: 36

Reports by species (top entries)

Human 35
Monkey 1

Top reported reactions (VEDDRA terms, top entries)

Accidental exposure 24
Diarrhoea 3
Dizziness 3
Feeling anxious 3
Headache 3
Nausea 3
Administration error NOS 2
High blood pressure 2
Local swelling (not application site) 2
Nervousness 2

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b25.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).

Sources

FDA ADE reports for Atorvastatin (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_b25.json

Link points to the issuing authority's site; a direct document link is still being verified.

Machine access

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