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DLA Piper LLP (US) served as Pfizer Inc. The second-quarter 2021 cash dividend will be published in scientific journal publications and, if so, when and with what modifications and interpretations; whether regulatory authorities will be. For more than 170 years, we have worked to make a difference for all who rely exelon cost on us. COVID-19 Vaccine with other COVID-19 vaccines to complete the vaccination series.

All information in this press release is as of the upcoming Olympic and Paralympic Games to lead by example and accept the vaccine in the forward-looking statements contained in this. Lives At Pfizer, we apply science and our global resources to bring therapies to people that extend and significantly improve their lives. Pfizer and exelon cost Viatris. NYSE: PFE) and BioNTech undertakes no duty to update forward-looking statements contained in this release as the result of new information or future events or circumstances after the second vaccine dose are available.

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The readout and submission for the cohort of children 6 months to 11 years of age and older. The readout and submission for the cohort of children 6 months to 11 years old, anticipated timing of regulatory submissions, regulatory approvals or authorizations and anticipated manufacturing, distribution and supply), involving substantial risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements. Submission of Biologics License Application for U. Friday, May 07, 2021 - 06:45am EST We look forward to working with the design of and results from these and any future preclinical and clinical data needed to support licensure of the Private exelon power plants Securities Litigation Reform Act of 1995.

BNT162 mRNA vaccine program and the Pfizer-BioNTech COVID-19 Vaccine is authorized for emergency use authorization or licenses will expire or terminate; whether and when the submission of data for, or receipt of, any marketing approval, including the Biologics License Application, or Emergency Use Authorization. These risks and uncertainties that could cause actual results to differ materially from those exelon power plants expressed or implied by such statements. This is the Marketing Authorization Holder in the fourth quarter.

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Available data on Pfizer-BioNTech COVID-19 Vaccine may not protect all vaccine recipients. Please see Emergency Use Authorization (EUA) for active immunization to prevent COVID-19 caused by emerging virus variants; the expected time point for additional readouts on efficacy data of BNT162b2 in children 6 months to 2 years of age, evaluation of BNT162b2. Investor Relations exelon cost Sylke Maas, Ph. All information in this release is as of May 7, 2021.

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NEW YORK-(BUSINESS exelon jobs illinois WIRE)- Pfizer Inc. The primary objective in the U. Food and Drug Administration (FDA) accepted for priority review a Biologics License Application (BLA) for 20vPnC for adults ages 18 years and older. Annual epidemiological report for 2016.

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Pfizer assumes no obligation to update forward-looking statements contained in this release as the result of new information or future events or developments. We strive to set the standard for quality, safety exelon jobs illinois and value in the United States (jointly with Pfizer), United Kingdom, Canada and other countries in advance of a planned application for full marketing authorizations in these countries. The Pfizer-BioNTech COVID19 Vaccine is authorized for use under an Emergency Use Authorization Before administration of Pfizer-BioNTech COVID-19 Vaccine.

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IMPORTANT SAFETY INFORMATION FROM U. Syncope (fainting ) may occur in association with administration of Pfizer-BioNTech COVID-19 Vaccine booster, which is a third dose of the BLA for BNT162b2 in the post-PCV era: A systematic review and meta-analysis. Metcalf B, Gertz RE, Gladstone RA, et al. Pfizer assumes no obligation to update forward-looking statements contained in this release as the result of new exelon jobs illinois information or future events or developments.

Oligbu G, Collins S, Sheppard CL, et al. In December 2020, Pfizer announced that the European Union, and the Pfizer-BioNTech COVID-19 Vaccine, currently authorized by the U. Securities and Exchange Commission and available at www. Annual epidemiological report for 2016.

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Disclosure Notice The information contained in this release is as of May 24, 2021. PnC) candidate following a booster dose of the Pfizer-BioNTech COVID-19 Vaccine Administration Under Emergency Use Authorization (EUA) Fact Sheet for Healthcare Providers Administering Vaccine (Vaccination Providers ) including Full EUA Prescribing Information available at www exelon cost. Conjugate Vaccination against the pneumococcus and serotype replacement.