The most commonly reported side effects of temsirolimus include drug dependence, overdose, and death, based on 6,242 FDA adverse event reports from 2004 to 2025.
Percentages show how often each reaction appears relative to total reports for temsirolimus.
These are voluntary reports and do not establish that temsirolimus caused these reactions.
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Seriousness is determined by the reporter, not by OpenClaim.
Other drugs that appear in adverse event reports alongside temsirolimus. 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.
32.2% of temsirolimus adverse event reports involve female patients and 57.4% involve male patients. The largest age group is adult at 47%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking temsirolimus when the adverse event was reported.
Showing 15 of 353 indications
Temsirolimus is sold under the brand name Temsirolimus.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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