The most commonly reported side effects of sunvozertinib include diarrhoea, decreased appetite, and rash, based on 23 FDA adverse event reports from 2024 to 2025. 4.3% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for sunvozertinib.
These are voluntary reports and do not establish that sunvozertinib caused these reactions.
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Other drugs that appear in adverse event reports alongside sunvozertinib. 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.
43.5% of sunvozertinib adverse event reports involve female patients and 56.5% 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 sunvozertinib when the adverse event was reported.
Sunvozertinib is sold under the brand name Zegfrovy.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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