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Takeda Pharmaceutical Company Limited: Takeda s QDENGA? (Dengue Tetravalent Vaccine [Live, Attenuated]) Approved for Use in European Union

The European Commission Approved QDENGA (TAK-003) for Use in Individuals Four Years of Age and Olderi QDENGA Becomes the Only Dengue Vaccine Approved in the EU for Use in Individuals Regardless of Previous

Sri lankaUnited statesDominican republicGary dubinRachel higginsTomas jelinekJun saitoEuropean commissionWorld health organizationInternational mediaBerlin centre forData monitoring committeeExchange commissionEuropean commission approvedEuropean union eu member statesEuropean union

Takeda s QDENGA (Dengue Tetravalent Vaccine [Live, Attenuated]) Approved for Use in European Union | Vaccines

Takeda’s QDENGA (Dengue Tetravalent Vaccine [Live, Attenuated]) Approved for Use in European Union

United statesSri lankaDominican republicGary dubinTomas jelinekEuropean commission approvedEuropean union eu member statesEuropean unionEuropean commissionBerlin centre forData monitoring committeeDengue tetravalent vaccineIndividuals four yearsOnly dengue vaccine approvedIndividuals regardlessPrevious dengue

Takeda s QDENGA®▼ (Dengue Tetravalent Vaccine [Live, Attenuated]) Approved in Indonesia for Use Regardless of Prior Dengue Exposure - Press Release

Indonesia National Agency for Drug and Food Control, BPOM, Approved QDENGA (TAK-003) for Use in Individuals Six Years to 45 Years of Age1 QDENGA is th

United statesDominican republicSri lankaAnggraini alamGary dubinBadan pengawas obatCenters for diseaseWorld health organizationData monitoring committeeIndonesia national agency for drugExchange commissionEuropean unionTakeda pharmaceutical company limitedEuropean medicines agencyNatural resources defense councilMinistry of health republic indonesia

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