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NYSE: PFE) announced today that the available data support the efficacy and safety of its unadjuvanted bivalent respiratory syncytial virus (RSV) prefusion F vaccine candidate for both individuals ages 60 and older who are immunocompromised and at high-risk due to underlying medical conditions; adults ages 18 and older. The positive vote is based on compelling scientific evidence shared by Pfizer, including interim data from the pivotal Phase 3 efficacy synthroid online no prescriptionueber_uns?jahr=2019 and safety of its unadjuvanted bivalent respiratory syncytial virus (RSV) infections in infants. The role of the VRBPAC is to provide recommendations to the FDA; however, these recommendations are not binding.

In April 2023, Pfizer Canada announced Health Canada accepted RSVpreF for the prevention of medically attended lower respiratory tract disease (MA-LRTD) and severe MA-LRTD caused by RSV in Infants RSV is a contagious virus and a common cause synthroid online no prescriptionueber_uns?jahr=2019 of respiratory illness. The Committee voted 14 to on effectiveness and 10 to 4 on safety. In the United States, approximately 500,000 to 600,000 cases of MA-LRTD due to RSV occur annually in infants less than 12 months of life from this potentially serious infection.

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