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Empower disclosed most of those cases to the FDA, and an internal investigation determined the drugs did not play a role for at least four of those patients, Empower said in records and statements to the Chronicle

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We invite public comments on whether SUL-DUR meets the cost criterion and our proposal to approve new technology add-on payments for SUL-DUR for FY 2024 for the treatment of HABP/VABP and bloodstream infections due to Acinetobacter baumannii subject to the technology receiving marketing authorization consistent with its QIDP designation by July 1, 2023