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International Diabetes Federation Guideline Development, Global guideline for type 2 diabetes, Diabetes research and clinical practice, 104 (2014) 152

Discontinuation because of gastrointestinal reactions climbed with the dose: 1.9 percent at 5 mg, 3.3 percent at 10 mg, and 4.3 percent at 15 mg, versus 0.5 percent on placebo

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Per-component dose ranges in the published clinical-trial program centred on a 1:1 fixed-ratio framework with weekly subcutaneous administration

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