What the label lists and what reports show
Sodium fluoride f 18 side effects
Sodium fluoride f 18's FDA label lists its adverse reactions in its own words. FAERS holds 1,086 reports naming it through July 30, 2026; the reaction reported most often, leaving out the conditions it is used for, product-use terms and outcomes, is pyrexia (172 reports).
- Generic listed
Check it at the source: the sodium fluoride f 18 FDA label on DailyMed (effective January 7, 2026, 3D Imaging Drug Design and Development LLC); the FDA FAERS public dashboard.
What does the label list?
From the label: adverse reactionsNo adverse reactions have been reported for Sodium Fluoride F 18 Injection based on a review of the published literature, publicly available reference sources, and adverse drug reaction reporting systems. However, the completeness of these sources is not known. No adverse reactions have been reported for Sodium Fluoride F 18 Injection based on a review of the published literature, publicly available reference sources, and adverse drug reaction reporting systems (6). To report SUSPECTED ADVERSE REACTIONS, contact 3D Imaging at 1-501-526-5550 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
Source: FDA drug label, 3D Imaging Drug Design and Development LLC, effective January 7, 2026 (SPL set eeaf4f42-e3c6-4e0a-aa79-89722511eaea), via openFDA; the full label on DailyMed
What do FAERS reports show?
1,086 reports list sodium fluoride f 18 among the medicines taken, each a report of something that happened, not proof the medicine caused it; 349 are coded as a death and 388 as a hospital stay. Counts follow how widely a medicine is used and watched, and they are not a measure of how risky it is. Of the 24 reactions below, none is named by the same term (in US spelling) in the label's adverse reactions, warnings or patient leaflet; a reaction the label does not name may still be there under another word, and a report does not show that the medicine caused it.
Reports received each year
The 25 most reported reactions
Source: FDA Adverse Event Reporting System (FAERS) via openFDA, reports through July 30, 2026; reactions as MedDRA preferred terms
What next?
- Sodium fluoride f 18: the full record
- label, generics, price, shortages, recalls
- Report a side effect to the FDA
- MedWatch
- Side effects hub
- the most reported medicines and reactions