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Investegate |BioNTech SE Announcements | BioNTech SE: FDA Advisory Committee Votes Unanimously in Favor of COMIRNATY® Booster for Emergency Use in People 65 and Older and Certain High-Risk Populations

Investegate |BioNTech SE Announcements | BioNTech SE: FDA Advisory Committee Votes Unanimously in Favor of COMIRNATY® Booster for Emergency Use in People 65 and Older and Certain High-Risk Populations
investegate.co.uk - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from investegate.co.uk Daily Mail and Mail on Sunday newspapers.

United statesUnited kingdomChristopher stevoSylke maasKathrinu jansenAmy roseFosun pharmaHead of vaccine research developmentIsrael ministry of healthBayer animal healthPfizer incEuropean unionCenters for diseaseFda advisory committee votes unanimously in favorDrug administrationExchange commission

FDA Advisory Committee Votes Unanimously in Favor of COMIRNATY Booster for Emergency Use in People 65 and Older and Certain High-Risk Populations

FDA Advisory Committee Votes Unanimously in Favor of COMIRNATY Booster for Emergency Use in People 65 and Older and Certain High-Risk Populations
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FDA Advisory Committee Votes Unanimously in Favor Of COMIRNATY Booster for Emergency Use in People 65 and Older and Certain High-risk Populations

FDA Advisory Committee Votes Unanimously in Favor Of COMIRNATY Booster for Emergency Use in People 65 and Older and Certain High-risk Populations
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XELJANZ Receives Marketing Authorization in European Union for Treatment of Active Polyarticular Juvenile Idiopathic Arthritis

XELJANZ Receives Marketing Authorization in European Union for Treatment of Active Polyarticular Juvenile Idiopathic Arthritis
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Paula carvalhoPharmacovigilance risk assessment committeeEuropean commissionDrug administrationExchange commissionPfizer incEuropean unionInternational developed markets regionalAna paula carvalhoMedicine productsHuman useEuropean medicines agencyBarr virus associatedNonsteroidal anti inflammatory drugsEnzyme elevationsImportant safety information

Pfizer Inc : XELJANZ (tofacitinib citrate) Receives Marketing Authorization in the European Union for the Treatment of Active Polyarticular Juvenile Idiopathic Arthritis and Juvenile Psoriatic Arthritis

Pfizer Inc : XELJANZ (tofacitinib citrate) Receives Marketing Authorization in the European Union for the Treatment of Active Polyarticular Juvenile Idiopathic Arthritis and Juvenile Psoriatic Arthritis
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Christopher stevoDervila keaneSteve danehyPaula carvalhoPharmacovigilance risk assessment committeeEuropean commissionDrug administrationAmerican college of rheumatologyExchange commissionPfizer incEuropean unionInternational developed markets regionalArthritis foundationAna paula carvalhoInflammation immunologyMedicine products