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Pfizer Inc.: Pfizer and BioNTech Receive Expanded U.S. Emergency Use Authorization for an Additional COVID-19 Vaccine Booster in Individuals Aged 50 Years and Older

FDA also authorizes second booster dose for individuals 12 years of age and older who have certain kinds of immunocompromise Second booster dose is intended to offer increased protection against
Ha Afon United States United Kingdom Sylke Maas Fosun Pharma Emergency Department

Pfizer Inc.: Pfizer and BioNTech Provide Update on Rolling Submission for Emergency Use Authorization of Their COVID-19 Vaccine in Children 6 Months Through 4 Years of Age

Pfizer Inc. (NYSE: PFE) and BioNTech SE (Nasdaq: BNTX) today announced plans to extend their rolling submission to the U.S. Food and Drug Administration (FDA) seeking to amend the Emergency Use Authorization
United States United Kingdom Sylke Maas Fosun Pharma Centers For Disease Drug Administration

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Pfizer Inc.: Pfizer and BioNTech Initiate Rolling Submission for Emergency Use Authorization of Their COVID-19 Vaccine in Children 6 Months Through 4 Years of Age Following Request From U.S. FDA

With pediatric COVID-19 cases surpassing 10 million and at the request of the FDA, the companies have submitted available data on the safety and efficacy of two 3 µg doses as part of a three-dose
United States United Kingdom Sylke Maas Fosun Pharma American Academy Of Pediatrics Centers For Disease

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