The most commonly reported side effects of ferric carboxymaltose include hypophosphataemia, nausea, and pain, based on 4,698 FDA adverse event reports from 2004 to 2025.
Percentages show how often each reaction appears relative to total reports for ferric carboxymaltose.
These are voluntary reports and do not establish that ferric carboxymaltose caused these reactions.
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Other drugs that appear in adverse event reports alongside ferric carboxymaltose. 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.
69.0% of ferric carboxymaltose adverse event reports involve female patients and 15.4% involve male patients. The largest age group is adult at 68%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking ferric carboxymaltose when the adverse event was reported.
Showing 15 of 122 indications
Ferric Carboxymaltose is sold under the brand name Injectafer.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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