Skip to main content

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.

Want to rewatch the webinar? Jump to the recording here

Levemir is being discontinued with stock expected to run out by end of 2026. As the only basal insulin licensed for twice-daily use, there's no direct alternative — a planned, proactive approach to switching is essential.¹

Sanofi have been supporting the switch efforts by running webinars and talks at Diabetes UK 2026. We were joined by three leading speakers, each with hands-on experience in managing insulin switches:

Phil Newland-Jones

Consultant Pharmacist 
Diabetes & Endocrinology and Clinical Director Diabetes & Endocrinology UHS

Tamsin Fletcher-Salt

Lead Diabetes and Endocrinology Nurse for the University Hospital of North Midlands. Clinical Inpatient Diabetes Lead NHS Midlands Network.

Anne Goodchild

Diabetes Specialist Nurse, director of DIME square Ltd and Founder of PITstop and Pre-PITstop.

You can find the key takeaways and speaker insights from these events below:


What do I need to consider before the switch is made?

The Association of British Clinical Diabetologists (ABCD) and Primary Care Diabetes & Obesity (PCDO) Society have published the below guidance¹:

  • Do not initiate new patients on Levemir¹
  • A planned and proactive approach is essential¹
  • Alternative insulins need to be chosen after individual clinical review with clinical blood glucose (CBG)/CGM data and an aim to optimise the individual’s treatment regimen¹
  • Local plans should aim to diversify prescribing across available options¹
  • People living with diabetes should be reviewed at 2-3 weeks to support with dose titration, as necessary.¹
  • For those at higher risk of dysglycaemia aim for close clinical review within 1-2 weeks of change where possible, including those with the below attributes:
    ◦ Impaired hypoglycaemia awareness
    ◦ History of severe hypoglycaemia or recurrent diabetic ketoacidosis (DKA)
    ◦ Evidence of lipohypertrophy at injection sites
    ◦ Frailty and/or older age
    ◦ Children and Adolescents
    ◦ Renal or severe hepatic impairment
    ◦ High glucose variability on CGM
    ◦ Cognitive or functional impairment
    ◦ Learning difficulties or low health literacy
    ◦ Those with visual impairment and manual dexterity problems
    ◦ High alcohol intake or binge drinking
    ◦ High level of physical activity

When considering options to change insulins, consider:

  • Type of diabetes
  • Local formularies and guidance
  • Product availability, via the SPS tool
  • Product cost
  • Device availability and suitability for the patient

When optimising the treatment regimen, you may want to consider:

  • physical and mental ability to manage current regimen
  • injection technique, injection sites, insulin storage
  • renal and ASCVD protection within treatment regimen
  • how is the individual currently living their life (e.g. shift work, flexible eating pattern, activity, sleep)
  • hypoglycaemia and current glucose profile, including variability
  • retinopathy screening results
  • concordance with all medication
  • HbA1c trajectory
  • time in range and percentages either side

What clinical considerations need to be made when making the switch?

The ABCD PCDOS guidance states that “when switching between insulins, there can be differences between absorption, potency, and action profile, therefore consider reducing doses by 10-20% to avoid the initial risk of hypoglycaemia.” ¹

Close monitoring is required:²,³ where possible, people with diabetes should be encouraged to self-adjust insulin doses according to their blood glucose concentrations after switching to alternative insulins whilst awaiting a further review.¹

Read the guidance below to see specific guidance and case studies for patients with Type 1 and Type 2 Diabetes

Switching patients with type 1 diabetes requires careful consideration — it's an opportunity to review the full treatment regimen, not just change the insulin to optimise and agree time in range targets, based on the patients’ co-mobordities.

Want more support? Download fictional case studies for managing the switch:

Managing the switch with Toujeo (insulin glargine 300U/mL) or  Lantus (insulin glargine 100U/mL)

Switching patients with type 1 diabetes requires careful consideration — it's an opportunity to review the full treatment regimen, not just change the insulin to optimise and agree time in range targets, based on the patients’ co-mobordities.

Want more support? Download fictional case studies for managing the switch:

Managing the switch with Toujeo (insulin glargine 300U/mL) or  Lantus (insulin glargine 100U/mL)

What were the highlights?

Watch the reel below for the standout moments from each speaker and the Q&A.

Looking for more support?

Get in touch with the Diabetes Team

Related content:

The BRIGHT Study: Comparing Toujeo® (insulin glargine 300 U/mL) and Insulin Degludec 100 U/mL

Efficacy and safety considerations are essential for effective Type 2 diabetes management.

Sanofi's Commitment to Diabetes

Toujeo®

MAT-XU-2601506 (v1.0) Date of Preparation: 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