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[Article] [PubMed]7

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In its Complete Response Letter (CRL), the FDA cited undisclosed product quality and master filing issues for the infusion device, which is proprietary to the device manufacturer, according to Supernus announcement

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ZhangXPengNZhangXZhuZMiaoYWuYet alAssociation of glucagon-like peptide-1 receptor agonists with atrial fibrillation, cardiac arrest, and ventricular fibrillation: casual evidence from a drug target Mendelian randomization

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