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FDA Approves Repatha® In Pediatric Patients Age 10 And Older With Heterozygous Familial Hypercholesterolemia

FDA Approves Repatha® In Pediatric Patients Age 10 And Older With Heterozygous Familial Hypercholesterolemia
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Puerto ricoMichael strapazonTrish rowlandAmgen medinfoKatherine wilemonDavidm reeseKyowa kirin co ltdCenters for diseaseMajor risks to healthFh foundationWorld health organizationDrug administrationBeigene ltdWorld healthExchange commissionTherapeutics inc

FDA Approves Repatha® (evolocumab) In Pediatric Patients Age 10 And Older With Heterozygous Familial Hypercholesterolemia

FDA Approves Repatha® (evolocumab) In Pediatric Patients Age 10 And Older With Heterozygous Familial Hypercholesterolemia
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Pfizer and BioNTech Receive First U S FDA Emergency Use Authorization of a COVID-19 Vaccine Booster

Pfizer and BioNTech Receive First U S FDA Emergency Use Authorization of a COVID-19 Vaccine Booster
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United statesUnited kingdomAlbert bourlaUgur sahinFosun pharmaUs centers for diseaseBayer animal healthPfizer incEuropean unionCenters for diseaseDrug administrationAdvisory committee on immunization practicesExchange commissionRoche groupProducts advisory committeeEmergency use authorization

Pfizer and BioNTech Receive First U S FDA Emergency Use Authorization of Covid Vaccine Booster

Pfizer and BioNTech Receive First U S FDA Emergency Use Authorization of Covid Vaccine Booster
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United statesUnited kingdomAlbert bourlaUgur sahinCenters for diseaseUs centers for diseaseDrug administrationAdvisory committee on immunization practicesPfizer incEuropean unionProducts advisory committeeChief executive officerRelated biological products advisory committeeDisease controlAdvisory committeeImmunization practices

Pfizer and BioNTech Receive First U S FDA Emergency Use Authorization of a COVID-19 Vaccine Booster

Pfizer and BioNTech Receive First U S FDA Emergency Use Authorization of a COVID-19 Vaccine Booster
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United statesUnited kingdomChristopher stevoSylke maasAlbert bourlaAmy roseUgur sahinFosun pharmaCenters for diseaseUs centers for diseaseDrug administrationAdvisory committee on immunization practicesBayer animal healthExchange commissionPfizer incEuropean union