The most commonly reported side effects of amprenavir include viral mutation identified, virologic failure, and pathogen resistance, based on 1,070 FDA adverse event reports from 2004 to 2025. 2.4% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for amprenavir.
These are voluntary reports and do not establish that amprenavir caused these reactions.
Report severity
Seriousness is determined by the reporter, not by OpenClaim.
Other drugs that appear in adverse event reports alongside amprenavir. 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.
23.6% of amprenavir adverse event reports involve female patients and 59.7% involve male patients. The largest age group is adult at 86%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking amprenavir when the adverse event was reported.
Showing 15 of 33 indications
Amprenavir is sold under the brand name Agenerase.
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.