Dulaglutide Trulicity® |
Formulary
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Pre-filled pen 0.75mg/0.5mL, 1.5mg/0.5mL First line GLP-1 agonist |
MHRA Drug Safety Update June 2019: GLP-1 receptor agonists: reports of diabetic ketoacidosis when concomitant insulin was rapidly reduced or discontinued |
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Exenatide prolonged release Bydureon (BCise)® |
Formulary
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prolonged-release suspension for injection in pre-filled pen (BCise) 2mg Third line GLP-1 agonist |
MHRA Drug Safety Update June 2019: GLP-1 receptor agonists: reports of diabetic ketoacidosis when concomitant insulin was rapidly reduced or discontinued |
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Liraglutide Victoza® |
Formulary
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Injection 6mg/mL pre-filled pen |
MHRA Drug Safety Update June 2019: GLP-1 receptor agonists: reports of diabetic ketoacidosis when concomitant insulin was rapidly reduced or discontinued |
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Liraglutide Saxenda |
Formulary
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Managing overweight and obesity. |
MHRA: GLP-1 receptor agonists: reports of diabetic ketoacidosis when concomitant insulin was rapidly reduced or discontinued MHRA: Ozempic▼(semaglutide) and Saxenda (liraglutide): vigilance required due to potentially harmful falsified products NICE TA664: Liraglutide for managing overweight and obesity |
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Semaglutide Ozempic® |
Formulary
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Solution for injection - pre-filled pen 0.25mg, 0.5mg, 1mg First line GLP-1 agonist. Prescribe by brand. |
MHRA: GLP-1 receptor agonists: reports of diabetic ketoacidosis when concomitant insulin was rapidly reduced or discontinued MHRA: Ozempic▼(semaglutide) and Saxenda (liraglutide): vigilance required due to potentially harmful falsified products |
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Semaglutide Rybelsus® |
Formulary
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Tablets 3mg, 7mg, 14mg 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. |
MHRA: GLP-1 receptor agonists: reports of diabetic ketoacidosis when concomitant insulin was rapidly reduced or discontinued National Patient Safety Alert |
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Semaglutide Wegovy® |
Formulary
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Managing overweight and obesity. Prescribe by brand. |
MHRA: GLP-1 receptor agonists: reports of diabetic ketoacidosis when concomitant insulin was rapidly reduced or discontinued NICE TA875: Semaglutide for managing overweight and obesity |
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Tirzepatide |
Formulary
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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).
Managing overweight and obesity |
LSCMMG: Mounjaro® (Tirzepatide) for Type 2 Diabetes Position Statement LSCMMG: Tirzepatide - Managing overweight and obesity NICE TA924: Tirzepatide for treating type 2 diabetes |
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