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Generic manufacturers must complete FDA approval processes, including demonstrating bioequivalence to the original drug
They transitioned Maria to a different GLP-1 receptor agonist with a lower incidence of gastrointestinal side effects
Of those 10 patients with oral exposures, most ( n = 5, 50%) resulted from inadvertently taking a double dose and only 1 (10%) patient manifested symptoms (fatigue and nausea)
J Biol Chem 288(27):1976019772
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