The most commonly reported side effects of methyprylon include overdose, drug abuse, and drug interaction, based on 2 FDA adverse event reports from 2014 to 2017.
Percentages show how often each reaction appears relative to total reports for methyprylon.
These are voluntary reports and do not establish that methyprylon caused these reactions.
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Seriousness is determined by the reporter, not by OpenClaim.
Other drugs that appear in adverse event reports alongside methyprylon. 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
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.
0.0% of methyprylon adverse event reports involve female patients and 50.0% involve male patients. The largest age group is adult at 100%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking methyprylon when the adverse event was reported.
Methyprylon is sold under the brand name Noludar.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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