The most commonly reported side effects of alectinib include death, fatigue, and constipation, based on 9,586 FDA adverse event reports from 2009 to 2025. 3.1% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for alectinib.
These are voluntary reports and do not establish that alectinib caused these reactions.
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Other drugs that appear in adverse event reports alongside alectinib. 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.
54.1% of alectinib adverse event reports involve female patients and 36.6% involve male patients. The largest age group is adult at 57%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking alectinib when the adverse event was reported.
Showing 15 of 429 indications
Alectinib is sold under the brand name Alecensa.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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