The most commonly reported side effects of nemolizumab include product dose omission issue, inappropriate schedule of product administration, and device malfunction, based on 7,936 FDA adverse event reports from 2018 to 2025. 4.9% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for nemolizumab.
These are voluntary reports and do not establish that nemolizumab caused these reactions.
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Other drugs that appear in adverse event reports alongside nemolizumab. 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.
3.8% of nemolizumab adverse event reports involve female patients and 1.8% involve male patients. The largest age group is adult at 61%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking nemolizumab when the adverse event was reported.
Showing 15 of 59 indications
Nemolizumab is sold under the brand name Nemluvio.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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