Adverse event reporting is available on the above link or at the bottom of the page
This is intended for HCPs practising in the United Kingdom only.
How many appropriate NovoRapid® patients can switch to Trurapi®?
Number of patients using NovoRapid®
Current annual NovoRapid® spend
Annual spend by switching appropriate patients to Trurapi®
Your annual savings
MAT-GB-2100260 (V1.0) March 2021
What is your current annual
NovoRapid® spend?
Current annual NovoRapid® spend
Annual spend by switching 20% of patients to Trurapi®
Your annual savings
MAT-GB-2100260 (V1.0) March 2021
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
MAT-XU-2305592 (v2.0) Date of Preparation: November 2025