The most commonly reported side effects of alvimopan include hospitalisation, no adverse event, and myocardial infarction, based on 273 FDA adverse event reports from 2006 to 2025.
Percentages show how often each reaction appears relative to total reports for alvimopan.
These are voluntary reports and do not establish that alvimopan caused these reactions.
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Other drugs that appear in adverse event reports alongside alvimopan. 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.
33.3% of alvimopan adverse event reports involve female patients and 38.1% involve male patients. The largest age group is elderly at 50%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking alvimopan when the adverse event was reported.
Showing 15 of 34 indications
Alvimopan is sold under the brand name Alvimopan.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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