Atorvastatin
34 adverse event reports submitted to the FDA
Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
34
Total Reports
0
Deaths Reported
0.0%
Death Rate
Active Ingredients
Atorvastatin
Administration Routes
OralUnknown
Species Affected
Human 34
Most Affected Breeds
Unknown 34
Most Reported Reactions
Accidental exposure 23
Diarrhoea 3
Dizziness 3
Feeling anxious 3
Headache 3
Nausea 2
Local swelling (not application site) 2
Vomiting 2
Nervousness 2
High blood pressure 2
Tingling sensation 2
Administration error NOS 2
Outcome Breakdown
Recovered/Normal
16 (47.1%)
Outcome Unknown
15 (44.1%)
Ongoing
2 (5.9%)
Recovered with Sequela
1 (2.9%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.