FDA Moves to Remove Prescription Fluoride Products for Children Amid Health Concerns
The FDA is evaluating prescription fluoride drops and tablets for children, citing potential health risks including altered gut microbiome and decreased IQ.
Overview
The FDA announced its intent to phase out prescription fluoride tablets and drops for children, citing studies linking ingestion to altered gut microbiomes and possible health issues. Commissioner Dr. Marty Makary emphasized a precautionary approach, while Health Secretary Robert F. Kennedy Jr. called the decision long overdue. Dentists contest claims against fluoride's efficacy, touting its role in preventing cavities, especially for children in low-fluoride areas. States like Utah have halted fluoride water treatment, increasing the demand for supplements, which may soon be unavailable if FDA removes them from the market. A review is due by October 31.
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Analysis
- The FDA is reviewing the safety of prescription fluoride supplements, noting potential risks such as altering gut microbiota and associations with thyroid disorders and decreased IQ.
- Health Secretary Robert F. Kennedy Jr. supports the discontinuation of ingestible fluoride, claiming it poses significant health risks, while some health experts defend the long-standing benefits of fluoride in preventing cavities.
- Although the move to remove fluoride supplements is framed as a precaution, it raises concerns among dental health professionals about diminishing options for children at risk of cavities.
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The FDA has noted that ingestible fluoride can alter the gut microbiome and has been linked to thyroid disorders, weight gain, and possibly decreased IQ.
Dentists are concerned because fluoride is crucial for preventing tooth decay, especially in low-income families without access to other fluoride sources like fluoridated water.
Health Secretary Robert F. Kennedy Jr. has been a vocal critic of fluoride, calling the decision to remove ingestible fluoride products 'long overdue' and previously questioning its safety.
The FDA plans to complete its safety review and public comment period by October 31, with the aim of removing ingestible fluoride products from the market.
History
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