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

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Support materials for patients

For your Patients


Discover the materials available to empower your patients through their TZIELD journey. Access comprehensive resources that help patients understand their Type 1 risk,  what TZIELD treatment involves, and how to navigate their care pathway with confidence.

Patient Website

This patient website (www.uk-tzield.com) is the go-to digital platform for your patients to explore their treatment, what to expect, and find additional resources and links.

Link to patient website

Risk Minimisation Materials

Patient Guide

This Patient Guide has been developed for your patients, following their TZIELD prescription. Your patients should read this material before treatment, as it contains key safety information about their treatment with Tzield.

Download Patient Guide

Patient Information Leaflet

This Patient Information Leaflet contains key safety information about their treatment with Tzield.  You can share this material together with Patient Guide.

Download PIL

 

Paediatric patients and caregivers

 

Adult Patients

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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

RMMs, risk minimisation materials; PIL, patient information leaflet.
 

  1. TZIELD® (teplizumab) UK Summary of Product Characteristics. 2025.

MAT-XU-2600466 (v1.0) | March 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