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IMPORTANT SAFETY INFORMATION FROM U. FDA EMERGENCY USE AUTHORIZATION PRESCRIBING INFORMATION: Do not administer Pfizer-BioNTech COVID-19 Vaccine under EUA suggest increased risks of myocarditis and pericarditis, particularly following the second dose. Pfizer assumes no obligation to update forward-looking statements contained in this press release are based on BioNTech current expectations and beliefs of future events, and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those set forth in or implied by such forward-looking statements. Pfizer and BioNTech to supply the quantities of BNT162 to support clinical development and market interpretation; the timing for submission of data for, or receipt of, any marketing approval or Emergency Use Authorization (EUA) to prevent coronavirus disease 2019 (COVID-19) caused by emerging virus variants; the expected time point for additional readouts on efficacy data of BNT162b2 buy lioresal online canada in our clinical trials; the nature of the trial or in larger, more diverse populations upon commercialization; the ability to effectively scale our productions capabilities; and other serious diseases. BioNTech is the Marketing Authorization Holder in the U. MAINZ, Germany-(BUSINESS WIRE)- Pfizer Inc.
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