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Legal Basis for the Claims Failure to warn the label and marketing did not adequately disclose the risk of ileus and bowel obstruction Negligent design and testing semaglutide was not adequately evaluated for long-term gastrointestinal safety before release Off-label promotion marketing for weight loss to patients without diabetes, raising informed consent questions Strict product liability the drug was unreasonably dangerous given the warnings provided Note that in California, prescription drug manufacturers are not strictly liable for design defect under Brown v

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Each cuvette was inverted three times to ensure complete mixing and the initial rate of product formed was followed by spectrofluorimetric measurement of increase in fluorescence per minute at wavelength 475nm.The rate represented the non enzymatic rate of product formed