The most commonly reported side effects of mavorixafor include product administration error, product storage error, and hypersomnia, based on 8 FDA adverse event reports from 2014 to 2025.
Percentages show how often each reaction appears relative to total reports for mavorixafor.
These are voluntary reports and do not establish that mavorixafor caused these reactions.
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Other drugs that appear in adverse event reports alongside mavorixafor. 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.
62.5% of mavorixafor adverse event reports involve female patients and 37.5% involve male patients. The largest age group is elderly at 60%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking mavorixafor when the adverse event was reported.
Mavorixafor is sold under the brand name Xolremdi.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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