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Current 2024 multi-society guidance suggests most patients can continue GLP-1 agonist therapy with appropriate risk stratification rather than routine holds
Although underlying mechanisms are still not completely explained, the interaction with RAAS seems to play a relevant role
The Core Issue: Failure to Warn Patients of Severe Risks The central argument in the GLP-1 lawsuits is that manufacturers like Novo Nordisk and Eli Lilly knew, or should have known, about the risk of severe side effects like stomach paralysis and bowel obstruction but failed to adequately warn doctors and patients
However, the emergence of numerous online pharmacies and telemedicine companies selling off-brand drugs has made it difficult to determine which facilities are properly following safety regulations
It has been proven safe and effective and has been shown to be relatively well tolerated among test patients according to a study published in the US National Library of Medicine/National Institutes of Health
