The most commonly reported side effects of magnesium sulfate anhydrous include hypotension, pyrexia, and premature delivery, based on 37 FDA adverse event reports from 2005 to 2025.
Percentages show how often each reaction appears relative to total reports for magnesium sulfate anhydrous.
These are voluntary reports and do not establish that magnesium sulfate anhydrous caused these reactions.
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Other drugs that appear in adverse event reports alongside magnesium 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.
37.8% of magnesium sulfate anhydrous adverse event reports involve female patients and 51.4% involve male patients. The largest age group is elderly at 47%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking magnesium sulfate anhydrous when the adverse event was reported.
Magnesium Sulfate Anhydrous is sold under the brand name Magnesium Sulfate Anhydrous; Potassium Sulfate; Sodium Sulfate.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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