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This clinical oversight matches the safety process for any prescription medication, minus the insurance bureaucracy
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Additionally, the company is asking for the associated lawsuits to be dismissed, under a 702 judgment, “based on the adequacy of the FDA-approved product labeling and the lack of admissible expert testimony on general causation.” This is a common defense tactic in mass litigation, like this MDL for Ozempic and other GLP-1 drugs