The most commonly reported side effects of pravastatin include fatigue, diarrhoea, and nausea, based on 93,920 FDA adverse event reports from 2004 to 2025. 4.2% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for pravastatin.
These are voluntary reports and do not establish that pravastatin caused these reactions.
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Other drugs that appear in adverse event reports alongside pravastatin. Drugs flagged as a suspected cause appear in the first column. Drugs taken at the same time but not suspected appear in the second.
Also suspected
Taken alongside
Co-occurrence in adverse event reports does not establish a drug interaction. Patients often take multiple medications, and these lists reflect prescribing patterns rather than causal relationships. Consult a healthcare provider about potential drug interactions.
52.6% of pravastatin adverse event reports involve female patients and 41.1% involve male patients. The largest age group is elderly at 61%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking pravastatin when the adverse event was reported.
Showing 15 of 547 indications
Pravastatin is sold under the brand name Pravigard Pac (copackaged).
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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