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The three vials that arrived failed visual authenticity checks on 59 to 63 percent of packaging criteria, exceeded labeled semaglutide content by 28.56 to 38.69 percent on quantitative LC-MS analysis, measured only 7.7 to 14.37 percent purity against a 99 percent label claim, and tested positive for bacterial endotoxin in every sample at 2.1645 to 8.9511 endotoxin units per milligram
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