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Novo Nordisk quoted to The New York Post at the time, “Semaglutide has been extensively examined in robust clinical development programs, large real world evidence studies and has cumulatively over 9.5 million patient years of exposure.” The company also noted that “gastrointestinal (GI) events are well-known side effects of the GLP-1 class.” Lilly told the outlet in a statement, “Patient safety is Lilly’s top priority, and we actively engage in monitoring, evaluating and reporting safety information for all our medicines.” The FDA updated the Ozempic label in September to acknowledge complaints of intestinal blockage in some people who have used the medication.
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