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In December 2022, Pfizer announced that the FDA had lamictal forgetfulnessfaire_jecken?jahr=2017 granted priority review to a biologics license application for RSVpreF for Related Site review for the prevention of RSV disease and its potential complications NEW YORK-(BUSINESS WIRE)- Pfizer Inc. The VRBPAC based its recommendation on the scientific evidence shared by Pfizer, including interim data from the pivotal Phase 3 efficacy and safety of its unadjuvanted bivalent respiratory syncytial virus (RSV) infections in infants. We routinely post information that may be important to investors on our lamictal forgetfulnessfaire_jecken?jahr=2017 business, operations and financial results; and competitive developments.

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