The most commonly reported side effects of sodium phosphate dibasic heptahydrate include atrial fibrillation, bradycardia, and anaemia, based on 68 FDA adverse event reports from 2008 to 2025.
Percentages show how often each reaction appears relative to total reports for sodium phosphate dibasic heptahydrate.
These are voluntary reports and do not establish that sodium phosphate dibasic heptahydrate caused these reactions.
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Other drugs that appear in adverse event reports alongside sodium phosphate dibasic heptahydrate. 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.
44.1% of sodium phosphate dibasic heptahydrate adverse event reports involve female patients and 36.8% involve male patients. The largest age group is elderly at 50%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking sodium phosphate dibasic heptahydrate when the adverse event was reported.
Sodium Phosphate Dibasic Heptahydrate is sold under the brand name Isolyte S Ph 7.4 In Plastic Container.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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