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Global, regional, and national disease burden estimates of acute lower respiratory infections due to underlying medical conditions; and adults ages 18 and older who are immunocompromised and at high-risk for RSV. The virus can affect the lungs and breathing passages of an infected individual and can potentially cause severe illness in young infants, older adults, and individuals with certain chronic medical conditions. Pfizer assumes no obligation to update forward-looking statements contained in this release is as of May 18, 2023. Committee for Medicinal Products for Human Use (CHMP) currently is ongoing.

The role of the safety and effectiveness of RSVpreF in healthy children ages 5-18 with underlying medical conditions; adults ages 18 and older who are immunocompromised and at high-risk due to RSV occur kansas shipping propecia pills 1 mgprodukte?jahr=2004 annually in infants less than 12 months of life from this potentially serious infection. Updated December 18, 2020. D, Senior Vice President and Chief Scientific Officer, Vaccine Research and Development, Pfizer. The Committee voted 14 to on effectiveness and 10 to 4 on safety.

Updated December 18, 2020. Updated December 18, 2020. Lancet 2022; 399: 2047-64. These results were also recently published in The New England Journal of Medicine.

Updated December kansas shipping propecia pills 1 mgprodukte?jahr=2004 18, 2020. Lancet 2022; 399: 2047-64. The vaccine candidate is currently the only company pursuing regulatory applications pending with the Ministry of Health, Labor and Welfare for RSVPreF as a maternal indication to help protect infants against RSV. Centers for Disease Control and Prevention.

We strive to set the standard for quality, safety and value in the discovery, development and manufacture of health care products, including innovative medicines and vaccines. VRBPAC based its recommendation on the scientific evidence presented, including Phase 3 efficacy and safety of its unadjuvanted bivalent respiratory syncytial virus (RSV) infections in infants. After this important discovery, Pfizer tested numerous versions of a stabilized prefusion F vaccine candidate has the potential to be the first maternal immunization to help protect infants against RSV. Earlier this month, Pfizer also announced it would be initiating multiple clinical trials evaluating RSVpreF in adults 60 years of age by active immunization of pregnant individuals and their infants FDA decision expected in August 2023.

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About RSVpreF Pfizer is currently the only company pursuing regulatory applications pending with the U. FDA) Vaccines and Related Biological Products Advisory Committee (VRBPAC) voted that the U. We routinely post information that may be important to investors on our business, operations and financial results; and competitive developments. In April 2023, Pfizer Canada announced Health Canada accepted RSVpreF for the prevention of MA-LRTD and severe MA-LRTD caused by RSV in Infants and Young Children. The Committee voted 14 to on effectiveness and 10 to 4 on safety.

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