The most commonly reported side effects of sodium polystyrene sulfonate include acute kidney injury, hyperkalaemia, and renal failure, based on 5,429 FDA adverse event reports from 2004 to 2025.
Percentages show how often each reaction appears relative to total reports for sodium polystyrene sulfonate.
These are voluntary reports and do not establish that sodium polystyrene sulfonate caused these reactions.
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Other drugs that appear in adverse event reports alongside sodium polystyrene sulfonate. 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.
37.7% of sodium polystyrene sulfonate adverse event reports involve female patients and 55.9% 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 sodium polystyrene sulfonate when the adverse event was reported.
Showing 15 of 128 indications
Sodium Polystyrene Sulfonate is sold under the brand name Kionex.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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