The most commonly reported side effects of perflubron include hypersensitivity, blood pressure decreased, and hyperhidrosis, based on 5 FDA adverse event reports from 2004 to 2020.
Percentages show how often each reaction appears relative to total reports for perflubron.
These are voluntary reports and do not establish that perflubron 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 perflubron. 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.
20.0% of perflubron adverse event reports involve female patients and 80.0% involve male patients. The largest age group is adult at 50%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking perflubron when the adverse event was reported.
Perflubron is sold under the brand name Imagent.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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