vericiguat — Blue Cross Blue Shield of Kansas
symptomatic chronic heart failure (NYHA Class II-IV) with left ventricular ejection fraction <45% following hospitalization for heart failure or use of outpatient intravenous diuretics
Initial criteria
- ONE of the following:
 - A. The requested agent is eligible for continuation of therapy AND ONE of the following:
 - 1. The patient has been treated with the requested agent (not samples) within the past 90 days OR
 - 2. The prescriber states the patient has been treated with the requested agent (not samples) within the past 90 days and is at risk if therapy is changed OR
 - B. BOTH of the following:
 - 1. ONE of the following:
 - A. The patient has symptomatic chronic heart failure (NYHA Class II–IV) AND left ventricular ejection fraction <45% AND ONE of the following:
 - i. Hospitalization for heart failure within the past 6 months OR
 - ii. Use of outpatient intravenous diuretics for heart failure within the past 3 months OR
 - B. The patient has another FDA labeled indication for the requested agent and route of administration
 - 2. If the patient has an FDA labeled indication, ONE of the following:
 - A. The patient’s age is within FDA labeling for that indication OR
 - B. There is support for use of the requested agent for the patient’s age and indication OR
 - C. The patient has another indication supported in compendia (AHFS or DrugDex 1 or 2a level of evidence)
 - The prescriber is a specialist in the area of the patient’s diagnosis (e.g., cardiologist) OR has consulted with such a specialist
 - The patient does NOT have any FDA labeled contraindications to the requested agent
 
Reauthorization criteria
- The patient was previously approved for the requested agent through the plan’s prior authorization process
 - The patient has had clinical benefit with the requested agent
 - The prescriber is a specialist in the area of the patient’s diagnosis (e.g., cardiologist) OR has consulted with such a specialist
 - The patient does NOT have any FDA labeled contraindications to the requested agent
 
Approval duration
12 months