The most commonly reported side effects of sutilains include coma, convulsion, and necrosis ischaemic, based on 4 FDA adverse event reports from 2009 to 2019.
Percentages show how often each reaction appears relative to total reports for sutilains.
These are voluntary reports and do not establish that sutilains caused these reactions.
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Other drugs that appear in adverse event reports alongside sutilains. 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.
75.0% of sutilains adverse event reports involve female patients and 25.0% involve male patients. The largest age group is elderly at 67%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Sutilains is sold under the brand name Travase.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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