The most commonly reported side effects of propyliodone include coagulopathy, drug interaction, and pain, based on 2 FDA adverse event reports from 2004 to 2020. 50.0% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for propyliodone.
These are voluntary reports and do not establish that propyliodone 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 propyliodone. 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.
50.0% of propyliodone 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
Propyliodone is sold under the brand name Dionosil Oily.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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