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"This is part of the agency's decisive steps to safeguard consumers from illegal GLP-1 active ingredients imported from overseas to ensure patient safety and a secure drug supply chain," the FDA said in a news release
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This cohort was composed of patients who started and continued on either a GLP-1 receptor agonist or an SGLT-2 inhibitor (canagliflozin, dapagliflozin, empagliflozin, ertugliflozin) for the first time between 1 January 2013 (the year that SGLT-2 inhibitors entered the UK market) and 31 December 2020
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