The most commonly reported side effects of cobicistat include bone density decreased, chronic kidney disease, and renal injury, based on 20,703 FDA adverse event reports from 2007 to 2025.
Percentages show how often each reaction appears relative to total reports for cobicistat.
These are voluntary reports and do not establish that cobicistat caused these reactions.
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Other drugs that appear in adverse event reports alongside cobicistat. 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 cobicistat adverse event reports involve female patients and 66.9% involve male patients. The largest age group is adult at 93%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking cobicistat when the adverse event was reported.
Showing 15 of 110 indications
Cobicistat is sold under the brand name Symtuza.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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