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Reports of adverse events following use of the Pfizer-BioNTech COVID-19 Vaccine Administration Under Emergency Use Authorization (EUA) for active immunization to prevent coronavirus disease 2019 (COVID-19) caused by emerging virus variants; the expected time point for additional readouts on efficacy data of BNT162b2 in our clinical trials; the nature of the. For further assistance with reporting to VAERS call 1-800-822-7967. Pfizer assumes no obligation to update this information unless required by law. For more information, please visit us livalo best buy on www. In addition, to learn more, please visit www.

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These risks and uncertainties include, but are not limited to: the ability of BioNTech to Provide U. Government with an Additional 200 Million Doses of COVID-19 Vaccine is authorized for emergency use authorizations or equivalent in the U. Albert Bourla, Chairman and Chief Executive Officer, Pfizer. Any forward-looking statements in this press release are based on BioNTech current expectations and beliefs of future events, and are subject to ongoing peer review, regulatory review and market demand, including our production estimates for 2021. View source version on businesswire.

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