

| Dulaglutide Trulicity® |
|
Formulary
|
Pre-filled pen 0.75mg/0.5mL, 1.5mg/0.5mL First line GLP-1 agonist |
|
|
![]()
|
| Liraglutide |
|
Formulary
|
Injection 6mg/mL pre-filled pen Ensure the correct liraglutide product is supplied. Prescribe by brand in accordance with the licensed indications for each product. |
|
|
![]()
|
| Liraglutide |
|
Formulary
|
Managing overweight and obesity. Ensure the correct liraglutide product is supplied. Prescribe by brand in accordance with the licensed indications for each product. |
|
|
![]()
|
| Semaglutide Ozempic® |
|
Formulary
|
Solution for injection - pre-filled pen 0.25mg, 0.5mg, 1mg First line GLP-1 agonist. Prescribe by brand. |
|
|
![]()
|
| Semaglutide Rybelsus® |
|
Formulary
|
First line GLP-1 agonist. Alternative GLP-1 receptor agonist for patients who are unable to use subcutaneous formulations or patients who prefer oral administration. Rybelsus tablets will be replaced with a new formulation with increased bioavailability, which is
bioequivalent to the initial formulation as described below:
• The new formulation has the same efficacy, safety and method of administration as the initial
formulation.
• Rybelsus should always be used as one tablet per day.
• The two formulations will temporarily co-exist on the market, which may cause mix-ups. This
could result in overdosing, which increases the risk of adverse events.
|
|
|
![]()
|
| Semaglutide Wegovy® |
|
Formulary
|
Managing overweight and obesity. Prescribe by brand. |
|
|
![]()
|
| Tirzepatide |
|
Formulary
|
Type 2 Diabetes Preference of agent should be decided based on the clinician’s judgement about patient characteristics. Local specialists have suggested the following: 1. Semaglutide (or other available GLP-1 RAs) may be preferred in patients with lower BMIs e.g. < BMI 35 kg/m2 or patients who have established CVD or are at high risk of CV events and require an agent with proven CV benefit. 2. Tirzepatide may be preferred in patients with higher BMIs e.g. > BMI 40 kg/m2 or who despite optimisation of all other therapies still require further glycaemic control. Careful consideration MUST be given to stopping tirzepatide if ineffective or not tolerated (evidence of poor tolerance as dose escalates). Tirzepatide should be reviewed after 6 months, and the deprescribing of other agents, e.g. sulfonylureas and gliptins, should be considered where possible. As a minimum expectation, it is recommended that tirzepatide is only continued if the adult with type 2 diabetes has had a beneficial metabolic response (a reduction of at least 11 mmol/mol [1.0%] in HbA1c and weight loss of at least 3% of initial body weight in 6 months).
|
|
|
![]()
|
