The most commonly reported side effects of voclosporin include therapy interrupted, product dose omission issue, and hypertension, based on 7,261 FDA adverse event reports from 2017 to 2025.
Percentages show how often each reaction appears relative to total reports for voclosporin.
These are voluntary reports and do not establish that voclosporin caused these reactions.
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Other drugs that appear in adverse event reports alongside voclosporin. 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.
82.5% of voclosporin adverse event reports involve female patients and 15.4% involve male patients. The largest age group is adult at 93%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking voclosporin when the adverse event was reported.
Showing 15 of 48 indications
Voclosporin is sold under the brand name Lupkynis.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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