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solriamfetol (Sunosi®)

 

Status: Excluded due to NICE appraisal

Product meets AWMSG exclusion criteria due to NICE appraisal TA777: Solriamfetol for treating excessive daytime sleepiness caused by obstructive sleep apnoea

Medicine details

Medicine name solriamfetol (Sunosi®)
Formulation 75 mg, 150 mg film-coated tablet
Reference number 4434
Indication

To improve wakefulness and reduce excessive daytime sleepiness (EDS) in adult patients with obstructive sleep apnoea (OSA) whose EDS has not been satisfactorily treated by primary OSA therapy, such as continuous positive airway pressure (CPAP)

Company Jazz Pharmaceuticals plc
BNF chapter Central nervous system
Submission type N/A
Status Excluded due to NICE appraisal
Date of issue 22/01/2020
NICE guidance

TA777: Solriamfetol for treating excessive daytime sleepiness caused by obstructive sleep apnoea

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