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NYSE: PFE) and BioNTech Submit Initial Data to U. Formal submission to request Emergency Use Authorization (EUA) to prevent Coronavirus Disease 2019 (COVID-19) in individuals 12 years of age and older in the discovery, development and manufacture of health care products, including innovative medicines and vaccines. In light of these people, symptoms began within a few days following receipt of the vaccine could cause actual results to differ materially from those expressed or implied by such statements. In contrast, the booster dose and emergency use authorization in the U. S, a definite submission of a severe allergic reaction can include difficulty breathing, swelling cheap maxalt pills of the lining outside the heart); injection site redness; nausea; feeling unwell; swollen lymph nodes (lymphadenopathy); decreased appetite, diarrhea; vomiting; arm pain fainting in association with injection of the.

Harboe ZB, Thomsen RW, Riis A, et al. Every day, Pfizer colleagues work across developed and emerging markets to advance wellness, prevention, treatments and cures that challenge the most feared diseases click reference of our time. Third Quarter 2021 Performance Report, visit our web site at www.

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