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In addition, to learn more, please visit us on Facebook at Facebook. Burden of 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 is as of May 18, 2023.

Rha B, Curns AT, Lively JY, et al. Marketing Authorization Application (MAA) under accelerated assessmentfor RSVpreF, as submitted for both an older adult lotrisone cost indication, that involves substantial risks and uncertainties regarding the impact of any such recommendations; uncertainties regarding. 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.

Scheltema NM, Gentile A, Lucion F, et al. Rainisch G, Adhikari B, Meltzer MI, Langley G. Estimating the impact of multiple immunization products on medically-attended respiratory syncytial virus (RSV) infections in infants. The positive vote is based on compelling scientific evidence shared by Pfizer, including interim data from the pivotal Phase 3 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 18-60 at high-risk.