The most commonly reported side effects of bictegravir include bone density decreased, chronic kidney disease, and bone loss, based on 17,632 FDA adverse event reports from 2017 to 2025.
Percentages show how often each reaction appears relative to total reports for bictegravir.
These are voluntary reports and do not establish that bictegravir caused these reactions.
Report severity
Seriousness is determined by the reporter, not by OpenClaim.
Other drugs that appear in adverse event reports alongside bictegravir. 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.
24.7% of bictegravir adverse event reports involve female patients and 69.4% involve male patients. The largest age group is adult at 92%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking bictegravir when the adverse event was reported.
Showing 15 of 113 indications
Bictegravir is sold under brand names including Bictegravir, Emtricitabine And Tenofovir Alafenamide, Biktarvy.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
Ask OpenClaim about your specific drug combination. Get a sourced report using FDA data, drug labels, and medical literature.