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This emerged from the work of Janet Mertz, Paul Berg, and Stanley Cohen at Stanford University and Herbert Boyer at the University of California San Francisco

Dulaglutides safety profile is consistent with other GLP-1 receptor agonists, with transient nausea being the most frequently reported adverse event (14.6% incidence). Dose escalation from 0.75 to 1.5 mg is recommended after at least four weeks, based on individual glycemic control needs [57]