The most commonly reported side effects of voxelotor include sickle cell anaemia with crisis, product dose omission issue, and diarrhoea, based on 22,285 FDA adverse event reports from 2010 to 2025.
Percentages show how often each reaction appears relative to total reports for voxelotor.
These are voluntary reports and do not establish that voxelotor caused these reactions.
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Seriousness is determined by the reporter, not by OpenClaim.
Other drugs that appear in adverse event reports alongside voxelotor. 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.
58.8% of voxelotor adverse event reports involve female patients and 39.0% involve male patients. The largest age group is adult at 75%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking voxelotor when the adverse event was reported.
Showing 15 of 126 indications
Voxelotor is sold under the brand name Oxbryta.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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