The most commonly reported side effects of secukinumab include psoriasis, pain, and arthralgia, based on 157,280 FDA adverse event reports from 2014 to 2025. 18.3% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for secukinumab.
These are voluntary reports and do not establish that secukinumab caused these reactions.
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Other drugs that appear in adverse event reports alongside secukinumab. 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.
57.6% of secukinumab adverse event reports involve female patients and 35.2% involve male patients. The largest age group is adult at 81%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking secukinumab when the adverse event was reported.
Showing 15 of 585 indications
Secukinumab is sold under the brand name Cosentyx.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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