The most commonly reported side effects of chlophedianol include febrile neutropenia, enterobacter bacteraemia, and off label use, based on 22 FDA adverse event reports from 2007 to 2025. 4.5% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for chlophedianol.
These are voluntary reports and do not establish that chlophedianol caused these reactions.
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Other drugs that appear in adverse event reports alongside chlophedianol. 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.
81.8% of chlophedianol adverse event reports involve female patients and 18.2% involve male patients. The largest age group is adult at 68%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking chlophedianol when the adverse event was reported.
Chlophedianol is sold under the brand name Ulo.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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