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The LSMS called it detrimental to put our patients health at risk to achieve exorbitant profits for a corporation. That language sounds populist until you remember the people saying it were also, technically, the people selling

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]

Without discrediting developing research into semaglutides alternative benefits, not everybody is as unquestioningly accepting of its adoption beyond regulated treatment for diabetes and obesity

Thank you BrainMD! I was really starting to get concerned about memory problems