This page is intended for healthcare professionals.
▼ This medicinal product is subject to additional monitoring. This will allow quick identification of new safety information. Reporting forms and information can be found at: www.mhra.gov.uk/yellowcard. Adverse events should also be reported to Takeda at: AE.GBR-IRL@takeda.com.
For Prescribing Information please click GB or NI.
The Summary of Product Characteristics (SmPC) for Qdenga™ (dengue tetravalent vaccine (live, attenuated)) for GB is available on the eMC.
The Summary of Product Characteristics (SmPC) for Qdenga™ (dengue tetravalent vaccine (live, attenuated)) for NI is available on the eMC NI.
Therapeutic indications
QdengaTM▼(dengue tetravalent vaccine (live, attenuated)) is indicated for the prevention of dengue disease in individuals from 4 years of age. The use of Qdenga™ should be in accordance with official recommendations.
Information and resources listed on this page are provided by Takeda UK Ltd.
C-ANPROM/GB/DENV/0251 Date of preparation: September 2024