The most commonly reported side effects of hexafluorenium include diarrhoea, abdominal pain upper, and febrile neutropenia, based on 5 FDA adverse event reports from 2015 to 2025. 20.0% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for hexafluorenium.
These are voluntary reports and do not establish that hexafluorenium caused these reactions.
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Other drugs that appear in adverse event reports alongside hexafluorenium. 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.
60.0% of hexafluorenium adverse event reports involve female patients and 20.0% 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 hexafluorenium when the adverse event was reported.
Hexafluorenium is sold under the brand name Mylaxen.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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