The most commonly reported side effects of sodium sulfate anhydrous include vomiting, nausea, and abdominal pain, based on 2,086 FDA adverse event reports from 2004 to 2025. 3.8% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for sodium sulfate anhydrous.
These are voluntary reports and do not establish that sodium sulfate anhydrous caused these reactions.
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Other drugs that appear in adverse event reports alongside sodium sulfate anhydrous. 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.
51.7% of sodium sulfate anhydrous adverse event reports involve female patients and 43.0% involve male patients. The largest age group is adult at 50%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking sodium sulfate anhydrous when the adverse event was reported.
Showing 15 of 93 indications
Sodium Sulfate Anhydrous is sold under the brand name Glycoprep.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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