The most commonly reported side effects of ferric hexacyanoferrate(ii) include crohn^s disease, abdominal pain, and diarrhoea, based on 11 FDA adverse event reports from 2016 to 2025. 9.1% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for ferric hexacyanoferrate(ii).
These are voluntary reports and do not establish that ferric hexacyanoferrate(ii) caused these reactions.
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Other drugs that appear in adverse event reports alongside ferric hexacyanoferrate(ii). 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.
72.7% of ferric hexacyanoferrate(ii) adverse event reports involve female patients and 18.2% involve male patients. The largest age group is adult at 56%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking ferric hexacyanoferrate(ii) when the adverse event was reported.
Ferric Hexacyanoferrate(ii) is sold under the brand name Radiogardase (prussian Blue).
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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