The most commonly reported side effects of golodirsen include product dose omission issue, no adverse event, and poor venous access, based on 431 FDA adverse event reports from 2020 to 2025.
Percentages show how often each reaction appears relative to total reports for golodirsen.
These are voluntary reports and do not establish that golodirsen caused these reactions.
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Other drugs that appear in adverse event reports alongside golodirsen. 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.
0.0% of golodirsen adverse event reports involve female patients and 97.9% involve male patients. The largest age group is adolescent at 40%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking golodirsen when the adverse event was reported.
Golodirsen is sold under the brand name Vyondys 53.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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