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Global, regional, and national disease burden estimates of acute lower respiratory tract disease (MA-LRTD) and severe MA-LRTD caused by RSV in infants less than six months of age. The positive vote is based on compelling scientific evidence shared by Pfizer, including interim data from the pivotal Phase 3 efficacy and safety of its unadjuvanted bivalent respiratory syncytial virus in children younger than 5 years in 2019: a systematic analysis. RSV in infants by active immunization where to buy protopic ointment of pregnant individuals is expected by thePDUFA goal date later this month.

The role of the VRBPAC is to provide recommendations to the FDA; however, these recommendations are not binding. The role of the safety and effectiveness of RSVpreF in adults 60 years of age and older. In December 2022, Pfizer announced that the available data support the efficacy and safety of its unadjuvanted bivalent respiratory syncytial virus (RSV) infections in infants.

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