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Of first major adverse CV events reported, 11.2% occurred during the first 20 weeks, favoring the semaglutide group (HR = 0.58

Some batches showed weight discrepancies of up to -32.4%, meaning a vial labeled 10mg might contain as little as 6.76mg

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The retinal damage procedure included L-NAME administration in a total dose of 5 mg/kg, which was given by retrobulbar application in each eye, with 0.5 mg/0.1 ml saline per eye

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