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No gastrointestinal adverse events were reported during tirzepatide dose escalation or maintenance, and no patient discontinued therapy due to tolerability issues
It is very common, with a global prevalence of 9.6%, and can have many causes, including infection, post-nasal drip, GORD, asthma and laryngopharyngeal reflux (silent or pharyngeal reflux)
2 Tsapas A, Avgerinos I, Karagiannis T, et al
Ledda C, Cannizzaro E, Cin D, Filetti V, Vitale E, Paravizzini G, et al
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