Contact us | Qdenga™ ▼

Do you want to know more about Qdenga™▼?

For Adverse Event Reporting, and Product Complaints, please contact us:

For a medical information enquiry please contact: medinfoemea@takeda.com

To report an Adverse Event please contact: AE.GBR-IRL@takeda.com

To report a product quality complaint please contact: complaints.uk.Ireland@takeda.com

Phone

+44 3333 000 181

Takeda UK Limited
1 Kingdom Street
London
W2 6BD
United Kingdom

Registered in England and Wales No. 03362860

Website

https://www.takeda.com/en-gb

▼ This medicinal product is subject to additional monitoring.

GB & NI: Adverse events should be reported. Reporting forms and information can be found at: www.mhra.gov.uk/yellowcard.

ROI: Adverse events should be reported to the Pharmacovigilance Unit at the Health Products Regulatory Authority. Reporting forms and information can be found at: www.hpra.ie.

GB, NI and ROI: Adverse events should also be reported to Takeda UK Ltd at: AE.GBR-IRL@takeda.com

C-APROM/GB/DENV/0074 | Date of preparation: November 2023