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Gastrointestinal Adverse Reactions In the pool of placebo-controlled trials, gastrointestinal adverse reactions occurred more frequently among patients who received semaglutide tablets than placebo: semaglutide tablets 14 mg once daily (41%), semaglutide tablets 7 mg once daily (32%) and placebo (21%), including severe reactions (semaglutide tablets 14 mg 2.0%, semaglutide tablets 7 mg 0.6%, placebo 0.3%)
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For semaglutide, where the difference between a therapeutic dose and a subtherapeutic dose can be fractions of a milligram, syringe accuracy is not optional
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Building a multidisciplinary framework Implementing tirzepatide in sleep medicine may require a multidisciplinary approach, ideally involving obesity medicine specialists or clinics, registered dieticians, behavioral health professionals and well-trained administrative staff for coverage navigation
