The most commonly reported side effects of abarelix include disease progression, urticaria, and flushing, based on 56 FDA adverse event reports from 2004 to 2022.
Percentages show how often each reaction appears relative to total reports for abarelix.
These are voluntary reports and do not establish that abarelix caused these reactions.
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Other drugs that appear in adverse event reports alongside abarelix. 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.
5.4% of abarelix adverse event reports involve female patients and 94.6% involve male patients. The largest age group is elderly at 89%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking abarelix when the adverse event was reported.
Abarelix is sold under the brand name Plenaxis.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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