The most commonly reported side effects of mequinol include skin hyperpigmentation, application site reaction, and pneumonia, based on 27 FDA adverse event reports from 2004 to 2019. 7.4% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for mequinol.
These are voluntary reports and do not establish that mequinol caused these reactions.
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Other drugs that appear in adverse event reports alongside mequinol. 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.
66.7% of mequinol adverse event reports involve female patients and 29.6% 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 mequinol when the adverse event was reported.
Mequinol is sold under the brand name Solage.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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