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The safety profile of tirzepatide is well-documented through clinical trials involving thousands of participants
Chbili, C
Researchers randomly assigned participants in a 2:1 ratio to once-weekly subcutaneous semaglutide 2.4 mg or placebo for 68 weeks
This method is ideal for breakthrough symptoms or as-needed relief
And those numbers almost certainly underrepresent the real scope of the problem, because state-licensed pharmacies are not required to report adverse events to the FDA
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