This information is for people in the UK and Republic of Ireland who are prescribed Dupixent® (dupilumab).

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Reporting of side effects

If you get any side effects talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in the package leaflet. You can also report side effects directly via the national reporting systems. By reporting adverse drug reactions (ADRs), you can help provide more information on the safety of this medicine.

In the UK

Please report suspected adverse drug reactions (ADRs) Through the MHRA Yellow Card scheme, via the Yellow Card website www.mhra.gov.uk/yellowcard, the free Yellow Card app available in Apple App Store or Google Play Store.

Alternatively, you can call 0800 731 6789 for free, Monday to Friday between 9am and 5pm.

Adverse drug reactions (ADRs) should also be reported to Sanofi: Tel: 0800 0902314. email: uk-drugsafety@sanofi.com.

In Ireland

Suspected side effects should be reported to the Health Products Regulatory Authority (HPRA) at www.hpra.ie.

You can also report side effects directly to Sanofi on IEPharmacovigilance@sanofi.com or + 353 1 403 5600.

Alternatively, contact Sanofi on

UK: +44 (0)800 0902314
uk-drugsafety@sanofi.com

Ireland: +353 1 403 5600
iepharmacovigilance@sanofi.com

Health information contained herein is provided for general educational purposes only. Please consult your healthcare professional if you have any questions about your health or treatment

The contents of this website have been developed and funded by Sanofi and Regeneron

MAT-XU-2303364 (v4.0)

Date of preparation: December 2024

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