The most commonly reported side effects of eteplirsen include product dose omission issue, no adverse event, and intentional dose omission, based on 2,188 FDA adverse event reports from 2016 to 2025.
Percentages show how often each reaction appears relative to total reports for eteplirsen.
These are voluntary reports and do not establish that eteplirsen caused these reactions.
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Other drugs that appear in adverse event reports alongside eteplirsen. 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.
1.6% of eteplirsen adverse event reports involve female patients and 95.0% involve male patients. The largest age group is adult at 36%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking eteplirsen when the adverse event was reported.
Eteplirsen is sold under the brand name Exondys 51.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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