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While the medication itself does not cause bruising, the way it must be delivered—via a needle—is the primary cause
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Safety Profile The adverse-event pattern was the familiar incretin-class signature, gastrointestinal-led, with a dose-dependent discontinuation rate: 4.1% (4 mg), 6.9% (9 mg), and 11.3% (12 mg) discontinued for adverse events, versus 4.9% on placebo
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