The most commonly reported side effects of ferric pyrophosphate citrate include thrombosis in device, fatigue, and dialysis, based on 416 FDA adverse event reports from 2004 to 2025. 4.6% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for ferric pyrophosphate citrate.
These are voluntary reports and do not establish that ferric pyrophosphate citrate caused these reactions.
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Other drugs that appear in adverse event reports alongside ferric pyrophosphate citrate. 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.
45.0% of ferric pyrophosphate citrate adverse event reports involve female patients and 41.8% involve male patients. The largest age group is adult at 39%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking ferric pyrophosphate citrate when the adverse event was reported.
Showing 15 of 53 indications
Ferric Pyrophosphate Citrate is sold under the brand name Triferic Avnu.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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