The most commonly reported side effects of lactitol include acute kidney injury, fall, and hyponatraemia, based on 331 FDA adverse event reports from 2004 to 2025. 3.6% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for lactitol.
These are voluntary reports and do not establish that lactitol caused these reactions.
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Other drugs that appear in adverse event reports alongside lactitol. 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.
42.0% of lactitol adverse event reports involve female patients and 51.4% involve male patients. The largest age group is elderly at 55%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking lactitol when the adverse event was reported.
Showing 15 of 26 indications
Lactitol is sold under the brand name Pizensy.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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