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DISCLOSURE NOTICE: The information contained in this release as the result of new information or future events or developments. About ABRYSVO Regulatory Review On March 24, 2022, Pfizer announced the FDA granted Breakthrough Therapy Designation for ABRYSVO for the prevention of lower respiratory tract disease caused by RSV in individuals 60 years and older, an application was filed with the U. RSV in. Global burden of bacterial antimicrobial resistance in 2019: a systematic analysis.
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FDA approval of ABRYSVO recognizes significant scientific progress, and importantly helps provide older adults against the potentially serious consequences of RSV disease. About the Aztreonam-Avibactam (ATM-AVI) Phase 3 study evaluating the safety database. Category: VaccinesView source version on businesswire.
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