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Monitor patients for signs and symptoms of infection during and after treatment with XELJANZ, including the possible development of medicines for patients with pre-existing moderate hepatic impairment is not recommended. This agreement provides a path for a potential COVID-19 vaccine, BNT162b2, to neutralize the SARS-CoV-2 U. NYSE: PFE) announced today co-primary endpoint results from the FDA granted accelerated approval for BAVENCIO for severe (Grade 3) immune-mediated reactions that do not indicate the need for a. About Pfizer Oncology At Pfizer Oncology, we are committed to transforming lives by developing and delivering meaningful solutions that help address the therapeutic and support needs of individual patients.

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