Nuedexta — Blue Cross Blue Shield of Oklahoma
pseudobulbar affect (PBA) associated with traumatic brain injury
Initial criteria
- The patient has a diagnosis of pseudobulbar affect (PBA) AND
 - The patient has ONE of the following: amyotrophic lateral sclerosis (ALS) OR multiple sclerosis (MS) OR dementia OR stroke OR traumatic brain injury AND
 - The prescriber has assessed the patient's PBA episodes (laughing and/or crying episodes) prior to therapy with the requested agent AND
 - The prescriber is a specialist in the area of the patient’s diagnosis (e.g., neurologist, neuropsychologist, psychiatrist) or the prescriber has consulted with a specialist in the area of the patient’s diagnosis AND
 - The patient does NOT have any FDA labeled contraindications to the requested agent
 
Reauthorization criteria
- The patient has been previously approved for the requested agent through the plan’s Prior Authorization process AND
 - The patient has had clinical benefit with the requested agent AND
 - The prescriber is a specialist in the area of the patient’s diagnosis (e.g., neurologist, neuropsychologist, psychiatrist) or the prescriber has consulted with a specialist in the area of the patient’s diagnosis AND
 - The patient does NOT have any FDA labeled contraindications to the requested agent
 
Approval duration
12 months (BCBSIL); 3 months initial for other plans, then 12 months renewal