Discover QUVIVIQ™▼ (daridorexant), as a treatment option for adult patients with chronic insomnia1,2
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- NICE recommended for primary care in chronic insomnia3
- SMC accepted for restricted use within NHSScotland4
QUVIVIQ™ (daridorexant) is indicated for the treatment of adult patients with insomnia characterised by symptoms present for at least 3 months and considerable impact on daytime functioning.1
Chronic Insomnia Topics
Diagnosing Chronic Insomnia
Browse Chronic Insomnia Patient Profiles
Discover the Different Chronic Insomnia Patient Profiles
- Explore Patient Profiles
NICE recommends Daridorexant for treating long-term insomnia
Read the evidence-based recommendations on Daridorexant (QUVIVIQ™) for treating long-term insomnia in adults.
Read the evidence-based recommendations on Daridorexant (QUVIVIQ™) for treating long-term insomnia in adults.
- Read NICE Recommendations
Understanding Chronic Insomnia
Deepen Your Understanding of Chronic Insomnia
Explore a self-led course on chronic insomnia through interactive modules and case studies.
- Start E-Learning
Practical Resources
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Discuss key domains to uncover your patients’ insomnia
- Download the Resource
Patient support material from Idorsia Pharmaceuticals UK Ltd.
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Summary of the two Phase 3 studies on daridorexant
- Read the Summary
Promotional material from Idorsia Pharmaceuticals UK Ltd.
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Overactive wake signalling as a cause of chronic insomnia
- Watch the Video
Promotional material from Idorsia Pharmaceuticals UK Ltd.
References
- QUVIVIQ™ Idorsia Pharmaceuticals LTD, Summary of Product Characteristics.
- Mignot E, et al. Lancet Neurol. 2022. 21(2); 125–139.
- NICE. TA922. Daridorexant for treating long-term insomnia, October 2023. Available at: https://www.nice.org.uk/guidance/ta922. Last accessed July 2024.
- SMC. SMC2611. Daridorexant film-coated tablets (Quviviq®). Available at: https://www.scottishmedicines.org.uk/media/8230/daridorexant-quviviq-final-march-2024-for-website.pdf. Last accessed April 2024
Prescribing information can be accessed using the PI button at the side.
This information is intended for UK healthcare professionals.
Adverse events must be reported. Healthcare professionals are asked to report any suspected adverse reactions via http://www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in Google play or Apple App store. Adverse events should also be reported to ds.safety.uk@idorsia.com.
UK-DA-00400 | Date of preparation: August 2024