The most commonly reported side effects of sodium fluoride f-18 include diarrhoea, cerebrovascular accident, and nausea, based on 32 FDA adverse event reports from 2012 to 2025.
Percentages show how often each reaction appears relative to total reports for sodium fluoride f-18.
These are voluntary reports and do not establish that sodium fluoride f-18 caused these reactions.
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Other drugs that appear in adverse event reports alongside sodium fluoride f-18. 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.
25.0% of sodium fluoride f-18 adverse event reports involve female patients and 50.0% involve male patients. The largest age group is adult at 63%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking sodium fluoride f-18 when the adverse event was reported.
Sodium Fluoride F-18 is sold under the brand name Sodium Fluoride F 18.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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