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Creation and maintenance of GLP-1RA audit rules The information pharmacists create GLP-1RA drug audit rules in combination with the actual situation of the hospital, including standardization of indications, dosage, medication for special populations, special pathological states, co-medication, interactions, and other audit judgment criteria, in order to warn the patients of prudent use, prohibited use, and ADEs
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Plaintiffs allege that these companies: Failed to adequately warn patients and doctors about serious risks Did not fully disclose the severity or frequency of complications Marketed the drugs without sufficient safety transparency Continued aggressive promotion despite emerging safety concerns At the center of these cases is the claim that patients were not given the information they needed to make fully informed medical decisions
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