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In a meta-analysis of GLP-1RA use in T1D, all adverse events were significantly higher in the GLP-1RA group, but there was no difference in serious adverse events ( 4.5 Pediatrics Only few small studies have assessed the use of GLP-1RA as adjuvant therapy in pediatric patients with T1D

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From there, the dose can be increased in 2.5 mg increments every four weeks based on tolerability and response, up to a maximum of 15 mg weekly

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