The most commonly reported side effects of telisotuzumab include off label use, pneumonia, and pneumonitis, based on 44 FDA adverse event reports from 2013 to 2025.
Percentages show how often each reaction appears relative to total reports for telisotuzumab.
These are voluntary reports and do not establish that telisotuzumab caused these reactions.
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Other drugs that appear in adverse event reports alongside telisotuzumab. 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.
47.7% of telisotuzumab adverse event reports involve female patients and 40.9% involve male patients. The largest age group is adult at 62%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking telisotuzumab when the adverse event was reported.
Telisotuzumab is sold under the brand name Emrelis.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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