Wegovy cardiovascular risk reduction-EHB
Indications for Prior Authorization
Wegovy (semaglutide)
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For diagnosis of Reduce the risk of major adverse cardiovascular events
Indicated in combination with a reduced calorie diet and increased physical activity to reduce the risk of major adverse cardiovascular events (cardiovascular death, non-fatal myocardial infarction, or non-fatal stroke) in adults with established cardiovascular disease and either obesity or overweight.Limitations of Use: Wegovy contains semaglutide and should not be coadministered with other semaglutide-containing products or with any other GLP-1 receptor agonist. The safety and effectiveness of Wegovy in combination with other products intended for weight loss, including prescription drugs, over-the-counter drugs, and herbal preparations, have not been established. Wegovy has not been studied in patients with a history of pancreatitis.
Criteria
Wegovy
Prior Authorization (Initial Authorization)
Length of Approval: 12 Month(s)
For diagnosis of Reduce the risk of major adverse cardiovascular events
- Treatment is being requested to reduce the risk of major adverse cardiovascular events (cardiovascular death, non-fatal myocardial infarction, or non-fatal stroke) AND
- Patient is 45 years of age or older AND
- Submission of medical records (e.g., chart notes) documenting patient has established cardiovascular disease as evidenced by one of the following:
- Prior myocardial infarction (MI)
- Prior stroke (i.e., transient ischemic attack, ischemic or hemorrhagic stroke)
- Peripheral arterial disease (i.e., intermittent claudication with ankle-brachial index < 0.85, peripheral arterial revascularization procedure, or amputation due to atherosclerotic disease)
- Submission of medical records (e.g., chart notes) documenting that medication is being used in combination with a program supporting a reduced calorie diet of at least 500 kcal/day and patient can be active for at least 150 minutes per week AND
- Submission of medical records (e.g., chart notes) documenting BMI greater than or equal to 27 kg/m2 AND
- Submission of medical records (e.g., chart notes) documenting HbA1c less than 6.5% in the past 12 months AND
- Submission of medical records (e.g., chart notes) documenting patient does not have any of the following:
- Diagnosis of type 1 or type 2 diabetes (excluding gestational diabetes)
- NY Heart Association functional class IV heart failure
- Submission of medical records (e.g., chart notes) or absence of paid claims confirming medication is not being co-administered with any of the following:
- GLP-1 receptor agonists (e.g., Victoza, Ozempic, Rybelsus, Trulicity)
- Tirzepatide-containing products (e.g., Mounjaro)
Wegovy
Prior Authorization (Reauthorization)
Length of Approval: 12 Month(s)
For diagnosis of Reduce the risk of major adverse cardiovascular events
- Submission of medical records (e.g., chart notes) documenting that patient demonstrated medication adherence (e.g., 80% adherence to treatment) over prior 6 months AND
- Submission of medical records (e.g., chart notes) documenting that medication is being used in combination with a program supporting a reduced calorie diet of at least 500 kcal/day and patient can be active for at least 150 minutes per week AND
- Paid claims or submission of medical records (e.g., chart notes) documenting patient is receiving a dose of 1.7mg or 2.4mg per week AND
- Submission of medical records (e.g., chart notes) documenting HbA1c less than 6.5% in the past 12 months AND
- Submission of medical records (e.g., chart notes) documenting patient does not have any of the following:
- Diagnosis of type 1 or type 2 diabetes (excluding gestational diabetes)
- NY Heart Association functional class IV heart failure
- Submission of medical records (e.g., chart notes) or absence of paid claims confirming medication is not being co-administered with any of the following:
- GLP-1 receptor agonists (e.g., Victoza, Ozempic, Rybelsus, Trulicity)
- Tirzepatide-containing products (e.g., Mounjaro)
P & T Revisions
2025-01-03
References
Revision History
- 2025-01-03: New cardiovascular risk reduction program for EHB