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While GLP-1 medications have FDA-approved dosing schedules, microdosing itself has not been specifically studied or approved by the FDA

GLP-1 activation can reduce the pathological process of amyloid- plaque aggregation/deposition and tau hyperphosphorylation enhanced by neuroinflammation, thus preventing age-related neurodegenerative changes, such as decline of learning and memory (Li et al., 2012)

Solution: Make sure to hydrate

Side effects, safety, and the boxed warning All GLP-1 agonists (and tirzepatide, a GIP/GLP-1 dual agonist) share a well-characterized profile: nausea, vomiting, diarrhea, constipation, abdominal pain, and headache are common, especially during the first 48 weeks and after each dose escalation

To investigate the potential barriers to and strategies for the optimal use of GLP-1 RAs in people with T2D with high CV risk or established CVD in the Spanish setting, a two-round Delphi consultation was conducted among primary care physicians, endocrinologists, cardiologists, and internal medicine specialists