The most commonly reported side effects of perfluoropolymethylisopropyl include acute kidney injury, insomnia, and fatigue, based on 84 FDA adverse event reports from 2005 to 2025. 4.8% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for perfluoropolymethylisopropyl.
These are voluntary reports and do not establish that perfluoropolymethylisopropyl caused these reactions.
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Other drugs that appear in adverse event reports alongside perfluoropolymethylisopropyl. 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.
48.8% of perfluoropolymethylisopropyl adverse event reports involve female patients and 41.7% involve male patients. The largest age group is adult at 59%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking perfluoropolymethylisopropyl when the adverse event was reported.
Showing 15 of 17 indications
Perfluoropolymethylisopropyl is sold under the brand name Skin Exposure Reduction Paste Against Chemical Warfare Agents.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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