The most commonly reported side effects of ferumoxsil include anaemia, hepatic function abnormal, and interstitial lung disease, based on 481 FDA adverse event reports from 2004 to 2025.
Percentages show how often each reaction appears relative to total reports for ferumoxsil.
These are voluntary reports and do not establish that ferumoxsil caused these reactions.
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Other drugs that appear in adverse event reports alongside ferumoxsil. 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.
44.7% of ferumoxsil adverse event reports involve female patients and 52.6% involve male patients. The largest age group is elderly at 66%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking ferumoxsil when the adverse event was reported.
Showing 15 of 44 indications
Ferumoxsil is sold under the brand name Gastromark.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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