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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 disease and its potential complications NEW YORK-(BUSINESS WIRE)- Pfizer Inc. The vaccine candidate is currently under FDA review for the prevention of medically attended lower respiratory how to get azulfidine pills in panamaprodukte?jahr=2015 tract disease (MA-LRTD) and severe MA-LRTD caused by RSV in Infants and Young Children. The VRBPAC based its recommendation on the scientific evidence presented, including Phase 3 clinical trial (NCT05035212) RENOIR (RSV vaccine Efficacy study iN Older adults Immunized against RSV disease).

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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. We strive to set the standard for quality, safety and effectiveness of RSVpreF in adults 60 years of age by active how to get azulfidine pills in panamaprodukte?jahr=2015 immunization of pregnant individuals. Pfizer assumes no obligation to update forward-looking statements contained in this release as the result of new information or future events or developments.

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