The most commonly reported side effects of magnesium acetate tetrahydrate include fatigue, nausea, and diarrhoea, based on 79,594 FDA adverse event reports from 2004 to 2025. 6.7% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for magnesium acetate tetrahydrate.
These are voluntary reports and do not establish that magnesium acetate tetrahydrate caused these reactions.
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Other drugs that appear in adverse event reports alongside magnesium acetate tetrahydrate. 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.
65.5% of magnesium acetate tetrahydrate adverse event reports involve female patients and 27.7% 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 magnesium acetate tetrahydrate when the adverse event was reported.
Showing 15 of 868 indications
Magnesium Acetate Tetrahydrate is sold under the brand name Plasma-lyte 56 And Dextrose 5% In Plastic Container.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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