The most commonly reported side effects of relugolix include hot flush, fatigue, and therapy interrupted, based on 23,465 FDA adverse event reports from 2005 to 2025.
Percentages show how often each reaction appears relative to total reports for relugolix.
These are voluntary reports and do not establish that relugolix caused these reactions.
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Other drugs that appear in adverse event reports alongside relugolix. 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.
6.5% of relugolix adverse event reports involve female patients and 48.1% involve male patients. The largest age group is elderly at 75%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking relugolix when the adverse event was reported.
Showing 15 of 157 indications
Relugolix is sold under the brand name Myfembree.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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