The most commonly reported side effects of evolocumab include device difficult to use, drug dose omission by device, and wrong technique in product usage process, based on 155,109 FDA adverse event reports from 2014 to 2025.
Percentages show how often each reaction appears relative to total reports for evolocumab.
These are voluntary reports and do not establish that evolocumab caused these reactions.
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Other drugs that appear in adverse event reports alongside evolocumab. 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.
53.9% of evolocumab adverse event reports involve female patients and 38.7% involve male patients. The largest age group is elderly at 63%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking evolocumab when the adverse event was reported.
Showing 15 of 802 indications
Evolocumab is sold under the brand name Repatha.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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