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Each subject received in a random order a single subcutaneous dose of 1.2 mg liraglutide and placebo at an interval of 48 h, with subsequent clinical follow-up in the metabolic ward, during which blood pressure was monitored for the following 24-h and 24 h urinary samples were collected to assess sodium excretion
Tirzepatide is commonly associated with gastrointestinal issues like nausea, vomiting, and diarrhea, especially during dose titration
Gastroenterology 2013;144:1419-25, 1425.e1-3
Merschel M
Most adults with a BMI over 27 and weight-related health conditions, or a BMI over 30, may qualify for GLP therapy
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