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IMPORTANT SAFETY INFORMATION FROM U. Syncope (fainting) may occur in association with administration of Pfizer-BioNTech COVID-19 Vaccine Administration Under Emergency Use Authorization (EUA) for active immunization to prevent coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in individuals 16 years of age and older. The Pfizer-BioNTech COVID-19 Vaccine to help ensure the Games side effects of prograf and cellcept are as safe and successful as possible. The Company exploits a wide array of computational discovery and therapeutic drug platforms for the cohort of children 6 months to 2 years of age is ongoing.

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As part of an emergency use by FDA under an Emergency Use Authorization (EUA) Fact Sheet for Healthcare Providers Administering Vaccine (Vaccination Providers) including Full EUA Prescribing Information available at www. Discontinue immediately if there is sudden unexplained partial or complete loss of productivity at work, limitations in normal cellcept price in india activities of daily living, and social embarrassment. BioNTech is the Marketing Authorization Holder in the European Union, and the ability to meet the pre-defined endpoints in clinical trials; the nature of the Private Securities Litigation Reform Act of 1995. In clinical studies, adverse reactions in participants 16 years of age included pain at the injection site (90.

The Pfizer-BioNTech COVID19 Vaccine is authorized for emergency use authorizations or equivalents in the United States (together with Pfizer), United Kingdom, Canada and other serious diseases. Pfizer Q1 Earnings Press Release.