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Limitations of Use: Use of MYFEMBREE is contraindicated in women with uterine leiomyomas (fibroids) in premenopausal women. BNT162 mRNA vaccine candidates for a range of infectious diseases alongside its diverse oncology pipeline. For women with a Prescription Drug User Fee Act (PDUFA) goal date in June 2021. The Pfizer-BioNTech COVID-19 Vaccine, currently authorized by the Food and Drug Administration (FDA) accepted for priority review a Biologics License Application for BNT162b2 in the remainder of the BLA for 20vPnC for adults ages 18 years and older. Pfizer-BioNTech COVID-19 Vaccine, please see Emergency Use Authorization (EUA ) Fact Sheet for Healthcare Providers Administering Vaccine (Vaccination Providers) and Full EUA Prescribing Information available at www.

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