The most commonly reported side effects of elvitegravir include bone density decreased, renal injury, and chronic kidney disease, based on 16,371 FDA adverse event reports from 2005 to 2025.
Percentages show how often each reaction appears relative to total reports for elvitegravir.
These are voluntary reports and do not establish that elvitegravir caused these reactions.
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Other drugs that appear in adverse event reports alongside elvitegravir. 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.
23.3% of elvitegravir adverse event reports involve female patients and 68.7% involve male patients. The largest age group is adult at 94%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking elvitegravir when the adverse event was reported.
Showing 15 of 88 indications
Elvitegravir is sold under brand names including Stribild, Elvitegravir, Cobicistat, Emtricitabine And Tenofovir Alafenamide.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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