The most commonly reported side effects of sulopenem include wrong dose, product use in unapproved indication, and lactic acidosis, based on 2 FDA adverse event reports from 2019 to 2021. 50.0% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for sulopenem.
These are voluntary reports and do not establish that sulopenem 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 sulopenem. 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 sulopenem 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 sulopenem when the adverse event was reported.
Sulopenem is sold under the brand name Orlynvah.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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