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Any potential advantage must be weighed against the well characterised adverse event profile of GLP-1 receptor agonistsincluding gastrointestinal intolerance, gallbladder disease, acute pancreatitis, and other adverse eventswithin a shared, patient centred decision making process that balances individual risk against potential additive gains.1 The observed epidemiological patterns in our study are highly consistent with the known pharmacology and neurobiological mechanisms of GLP-1 receptor agonists

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Liraglutide 3.0 mg and Intensive Behavioral Therapy (IBT) for Obesity in Primary Care: The SCALE IBT Randomized Controlled Trial

Study: Trajectory of weight regain after cessation of GLP-1 receptor agonists: a systematic review and nonlinear meta-regression