The most commonly reported side effects of rilpivirine include bone density decreased, renal injury, and skeletal injury, based on 23,811 FDA adverse event reports from 2008 to 2025.
Percentages show how often each reaction appears relative to total reports for rilpivirine.
These are voluntary reports and do not establish that rilpivirine caused these reactions.
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Other drugs that appear in adverse event reports alongside rilpivirine. 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.
23.2% of rilpivirine adverse event reports involve female patients and 55.9% involve male patients. The largest age group is adult at 91%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking rilpivirine when the adverse event was reported.
Showing 15 of 121 indications
Rilpivirine is sold under brand names including Cabenuva Kit, Edurant Ped.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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