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[14] However, anecdotal reports from patients and post-marketing surveillance data in the FDA Adverse Event Reporting System (FAERS) suggest that some individuals taking semaglutide do experience dry mouth symptoms
The US has placed no ban
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But the same industry group that sued the FDA for the tirzepatide change also just sued the agency for removing semaglutide from its shortage list on essentially the same groundsthat they had dismissed evidence that the drug is still in short supply
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