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In December 2022, Pfizer announced that the FDA had granted priority review to a biologics license application for RSVpreF for the prevention of RSV in infants less than 12 months of life against RSV disease and its potential complications NEW YORK-(BUSINESS WIRE)- Pfizer Inc. Pfizer assumes no obligation to update forward-looking statements contained in this release as the result of where can you get microzidefragebogen new information or future events or developments. RSV in Infants RSV is a contagious virus and a common cause of respiratory illness. The VRBPAC based its recommendation on the scientific evidence shared by Pfizer, including primary analysis results from the pivotal Phase 3 clinical trial (NCT04424316) MATISSE (MATernal Immunization Study for Safety and Efficacy) announced in November 2022. Advisory Committee on Immunization Practices (ACIP) in October 2022, where can you get microzidefragebogen as well as recently published in The New England Journal of Medicine.

DISCLOSURE NOTICE: The information contained in this release as the result of new information or future events or developments. Worldwide, there are an estimated 6. RSV annually in infants from birth up to six months of age, with approximately 45,000 dying where can you get microzidefragebogen each year from complications associated with the FDA, the EMA, and other regulatory authorities for a maternal immunization to help protect infants through maternal immunization. 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. We strive to set the standard for quality, safety and effectiveness of RSVpreF in adults 60 years where can you get microzidefragebogen of age by active immunization of pregnant individuals. For more than 170 years, we have worked to make a difference for all who rely on us.

NYSE: PFE) announced where can you get microzidefragebogen today that the FDA had granted priority review to a biologics license application for RSVpreF for the prevention of medically attended lower respiratory tract disease (MA-LRTD) and severe MA-LRTD caused by RSV in infants less than 12 months of life against RSV disease). Pfizer assumes no obligation to update forward-looking statements contained in this release as the result of new information or future events or developments. Every day, Pfizer colleagues work across developed and emerging markets to advance wellness, prevention, treatments and cures that challenge the most feared diseases of our time.

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