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This website contains promotional content and is intended for Healthcare Professionals based in the United Kingdom only. Some content may only be relevant to HCPs practising in Great Britain (England, Scotland and Wales) according to product availability. This website is optimised for desktop use, and some features may perform differently on mobile devices.

Adverse event reporting can be found at the bottom of the page.

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For your Patients


Discover the post-prescription materials available to support your patients through their TZIELD journey. These comprehensive materials provide key information for both children (ages 8 and over), adults and caregivers about how TZIELD works, what to expect from their treatment, key safety information and their next steps.

Patient Website

The patient website is the go-to digital platform for your patients to explore information about their treatment, what to expect and find additional resources and links. This can be accessed on desktop or on the go, on mobile.

Please note: All of the below resources will be available through the patient website. Any physical copies can only be distributed by you to your patients.

Link to patient website

Patient Guides - Key Safety Information

Risk Minimisation Material - Guide for Patients

Your patients should read this material alongside the Patient Information Leaflet (PIL) before their treatment, as it contains key safety information.

Download Guide for Patients

Patient Information Leaflet

This Patient Information Leaflet contains key safety information about your patient's treatment with Tzield.  You can share this material together with the Guide for Patients.

Download PIL

 

Paediatric Patient Pack

 

Adult Patient Pack

Get in Touch with Us

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INDICATION: TZIELD is indicated to delay the onset of Stage 3 T1D in adult and paediatric patients 8 years of age and older with Stage 2 T1D.1

PIL, patient information leaflet.
 

  1. TZIELD® (teplizumab) UK Summary of Product Characteristics.

MAT-XU-2600466 (v2.0) | June 2026

Adverse events should be reported. 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. Adverse events should also be reported to the Sanofi drug safety department on Tel: +44 (0) 800 0902 314. Alternatively, send via email to UK-drugsafety@sanofi.com