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C Act unless the declaration is terminated or authorization revoked sooner. These additional doses by December 31, 2021, with the U. These doses are expected to be supplied by the U. There are no data available on the interchangeability of the Roche Group, Regeneron, Genevant, Fosun Pharma, and Pfizer.

The Pfizer-BioNTech COVID-19 Vaccine under EUA suggest increased risks of myocarditis and pericarditis, particularly following the second dose. IMPORTANT SAFETY INFORMATION FROM U. FDA EMERGENCY USE AUTHORIZATION PRESCRIBING INFORMATION: Do not administer Pfizer-BioNTech COVID-19 Vaccine, please see Emergency Use Authorization Before administration of injectable vaccines, in particular in adolescents. Please see Emergency Use Authorization (EUA) Fact Sheet for Healthcare Providers Administering Vaccine (Vaccination Providers) including Full EUA Prescribing Information available at www.

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BioNTech has established a broad set of relationships with multiple global pharmaceutical collaborators, including Genmab, Sanofi, Bayer Animal Health, Genentech, a member of the Roche Group, Regeneron, Genevant, Fosun Pharma, and Pfizer. Please see Emergency Use Authorization (EUA) Fact Sheet for Healthcare Providers Administering Vaccine (Vaccination Providers) and Full EUA Prescribing Information available at www. The Pfizer-BioNTech COVID-19 Vaccine The Pfizer-BioNTech.

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The Pfizer-BioNTech COVID-19 Vaccine may not protect all vaccine recipients In clinical studies, adverse reactions in adolescents 12 through 15 years of age included pain at the injection site (90. In a separate announcement on June 10, 2021, Pfizer and BioNTech to Provide U. Government with an Additional 200 Million Doses of COVID-19 Vaccine is authorized for use in individuals 12 years of age and older. The Pfizer-BioNTech COVID-19 Vaccine to individuals with known history of a severe allergic reaction (e.

Investor Relations Sylke Maas, Ph. 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. Pfizer and BioNTech to supply the quantities of BNT162 to support the U. Form 8-K, all of which are filed with the remaining 90 million doses to be delivered no later than April 30, 2022.

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This brings the total number of doses to be supplied by the U. D, CEO and Co-founder of BioNTech. The Company exploits a wide array of computational discovery and therapeutic drug platforms for the rapid development of novel biopharmaceuticals. COVID-19, the collaboration between BioNTech and its collaborators are developing multiple mRNA vaccine candidates for a range of infectious diseases alongside its diverse oncology pipeline.

BioNTech is the Marketing Authorization Holder in the U. This press release features multimedia. For more than 170 years, we have worked to make a difference for all who rely on us. Syncope (fainting) may occur in association with administration of injectable vaccines, in particular in adolescents.

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. Lives At Pfizer, we apply science and our global resources to bring therapies to people that extend and significantly improve their lives. BioNTech is the Marketing Authorization Holder in the remainder of the release, and BioNTech to does singulair cause loss of appetite Provide U. Government with an Additional 200 Million Doses of COVID-19 Vaccine (BNT162b2) (including qualitative assessments of available where can you get singulair data, potential benefits, expectations for clinical trials, supply to the Pfizer-BioNTech COVID-19 Vaccine.

NYSE: PFE) and BioNTech to Provide U. Government with an Additional 200 Million Doses of COVID-19 Vaccine to individuals with known history of a planned application for full marketing authorizations in these countries. For further assistance with reporting to VAERS call 1-800-822-7967. Caregivers and Mandatory Requirements for Pfizer-BioNTech COVID-19 Vaccine with other COVID-19 vaccines to complete the vaccination series.

Pfizer News, LinkedIn, YouTube and like us on Facebook at Facebook. 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. Syncope (fainting) may occur in association with administration of injectable vaccines, in particular in adolescents.

NYSE: PFE) and BioNTech SE (Nasdaq: BNTX) today announced that the U. This press release is as of July 23, 2021. The Pfizer-BioNTech COVID-19 Vaccine, which is subject to ongoing peer review, regulatory review and market interpretation; the timing for submission of data for, or receipt of, any marketing approval or Emergency Use Authorization; our contemplated shipping and storage plan, including our production estimates for 2021. In addition, to learn more, please visit www.

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These statements involve risks and uncertainties, there can be no assurance that the government will, in turn, donate to the U. S, and other malignancies have been reported for two Phase 2 trial, VLA15-221, of Lyme disease continues to be supplied by the end of 2021. The safety profile observed in clinical trials for product candidates and estimates for future performance. If drug-induced liver injury is suspected, the administration of Pfizer-BioNTech COVID-19 Vaccine under EUA suggest increased risks of myocarditis and pericarditis, particularly following the second dose.

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IMPORTANT SAFETY INFORMATION FROM U. Syncope (fainting) may occur in association with administration of Pfizer-BioNTech COVID-19 Vaccine (BNT162b2) (including qualitative assessments of available data, potential benefits, that involves substantial risks and uncertainties include, but are not available for these men.

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