The most commonly reported side effects of ramucirumab include malignant neoplasm progression, death, and interstitial lung disease, based on 6,057 FDA adverse event reports from 2010 to 2025. 2.7% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for ramucirumab.
These are voluntary reports and do not establish that ramucirumab caused these reactions.
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Other drugs that appear in adverse event reports alongside ramucirumab. 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.
28.7% of ramucirumab adverse event reports involve female patients and 57.5% involve male patients. The largest age group is elderly at 57%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking ramucirumab when the adverse event was reported.
Showing 15 of 294 indications
Ramucirumab is sold under the brand name Cyramza.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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