The most commonly reported side effects of rapacuronium include bronchospasm, abdominal pain, and acute hepatic failure, based on 6 FDA adverse event reports from 2007 to 2017.
Percentages show how often each reaction appears relative to total reports for rapacuronium.
These are voluntary reports and do not establish that rapacuronium caused these reactions.
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Other drugs that appear in adverse event reports alongside rapacuronium. 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 rapacuronium adverse event reports involve female patients and 33.3% involve male patients. The largest age group is child at 40%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking rapacuronium when the adverse event was reported.
Rapacuronium is sold under the brand name Raplon.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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