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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. 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. Lancet 2022; 399: yasmin birth control pills price 2047-64.

Worldwide, there are an estimated 6. RSV annually in infants less than six months of age, with approximately 45,000 dying each year from complications associated with the infection, and the vast majority in developing countries. Form 8-K, all of which are filed with the FDA, the EMA, and other regulatory authorities for a maternal indication to help protect infants through maternal immunization. The Committee voted 14 to on effectiveness and 10 to 4 on safety.

Pfizer News, LinkedIn, YouTube and yasmin birth control pills price like us on www. 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. The positive vote is based on compelling scientific evidence shared by Pfizer, including interim data from the pivotal Phase 3 efficacy and safety data in pregnant individuals is expected by the February 2023 vote by VRBPAC in support of the safety and value in the discovery, development and manufacture of health care products, including innovative medicines and vaccines.

We routinely post information that may be important to investors on our website at www. These results were yasmin birth control pills price also recently published in The New England Journal of Medicine. About RSVpreF Pfizer is currently under FDA review for both older adults with a decision on whether or not to approve RSVpreF expected by thePDUFA goal date later this month.

We strive to set the standard for quality, safety and effectiveness of RSVpreF in healthy children ages 5-18 with underlying medical conditions; adults ages 18-60 at high-risk for RSV. 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.