The most commonly reported side effects of florbetaben include amyloid related imaging abnormality-oedema/effusion, injection site pain, and fatigue, based on 18 FDA adverse event reports from 2015 to 2025.
Percentages show how often each reaction appears relative to total reports for florbetaben.
These are voluntary reports and do not establish that florbetaben 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 florbetaben. 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.
61.1% of florbetaben adverse event reports involve female patients and 38.9% involve male patients. The largest age group is elderly at 80%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking florbetaben when the adverse event was reported.
Florbetaben is sold under the brand name Neuraceq.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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