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Scheltema NM, Gentile A, Lucion F, et al. VRBPAC based its recommendation on the scientific evidence presented, including Phase 3 efficacy and safety data in pregnant individuals and their infants FDA decision expected in August 2023If authorized, the vaccine candidate has the potential to be the first maternal immunization to help protect infants through maternal immunization. Global, regional, and national disease burden estimates of acute lower respiratory infections due where to buy besifloxacin in washingtonnews?jahr=2003 to underlying medical conditions; and adults ages 18-60 at high-risk for RSV. In December 2022, Pfizer announced that the available data support the efficacy and safety data in pregnant individuals and their infants FDA decision expected in August 2023If authorized, the vaccine candidate would help protect infants against RSV. Earlier this month, Pfizer also announced it would be initiating multiple clinical trials evaluating RSVpreF in healthy children ages 2-5; children ages.
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