Janssen-Cilag Ltd, 50–100 Holmers Farm Way, High Wycombe, Buckinghamshire, HP12 4EG.
If you have any questions about your condition, please speak to your doctor or specialist.
Alternatively you could contact NHS Advice Service on 111.
Reporting of side effects
Reporting an Adverse Event will help Janssen monitor the safety of all our healthcare products to ensure they are acceptably safe for patients and those who use them. Reporting adverse events allows Janssen to provide up to date information on our products in the product information leaflets and SmPCs and to help minimise risk and maximise benefit to the patients and consumers.
It is important to report adverse events even if it is a known adverse event as this still provides valuable information for monitoring product safety. Please contact the Drug Safety Team on:
Adverse events can also be reported directly the Medicines and Healthcare products Regulatory Agency. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.
Reporting 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 Yellow Card Scheme at: www.mhra.gov.uk/yellowcard.
By reporting side effects you can help provide more information on the safety of this medicine.
▼This medicine is subject to additional monitoring. This will allow quick identification of new safety information. You can help by reporting any side effects you may get.
See www.mhra.gov.uk/yellowcard for how to report side effects.
We Value Your Privacy
By clicking this link, you are now leaving myTremfya UK patient website. Janssen UK is not responsible for content on the external website.
Please confirm you wish to continue