The most commonly reported side effects of lurbinectedin include death, disease progression, and off label use, based on 1,021 FDA adverse event reports from 2013 to 2025.
Percentages show how often each reaction appears relative to total reports for lurbinectedin.
These are voluntary reports and do not establish that lurbinectedin caused these reactions.
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Other drugs that appear in adverse event reports alongside lurbinectedin. 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.
29.8% of lurbinectedin adverse event reports involve female patients and 40.8% involve male patients. The largest age group is elderly at 55%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking lurbinectedin when the adverse event was reported.
Showing 15 of 77 indications
Lurbinectedin is sold under the brand name Zepzelca.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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