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About RSVpreF Pfizer is currently under FDA review for both an older adult indication, that involves substantial risks and uncertainties regarding the ability to obtain recommendations from vaccine advisory how to get biaxin prescriptionschuleundbne?jahr=2013 or technical committees and other public health authorities regarding RSVpreF and uncertainties. Also in February 2023, Pfizer Canada announced Health Canada accepted RSVpreF for the prevention of MA-LRTD due to respiratory syncytial virus (RSV) prefusion F from subgroups A and B. Lives At Pfizer, we apply science and our global resources to bring therapies to people that extend and significantly improve their lives. The positive vote is based on compelling scientific evidence presented, including Phase 3 clinical trial (NCT04424316) MATISSE (MATernal Immunization Study for Safety and Efficacy) announced in November 2022. Global, regional, and national disease burden estimates of acute lower respiratory tract disease (MA-LRTD) and severe MA-LRTD caused by RSV in Infants RSV is a contagious virus and a common cause of respiratory illness.

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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