suvorexant
Brands: BELSOMRA
Last reviewed 2025-12-28
Reviewed by PsychMed Editorial Team.
Quick answers
What is suvorexant?
Suvorexant (brand Belsomra) is a dual orexin receptor antagonist (DORA) approved for insomnia (sleep onset and sleep maintenance).
What is BELSOMRA?
BELSOMRA is a brand name for suvorexant.
What is BELSOMRA (suvorexant) used for?
Label indications include: Insomnia (label).
What drug class is BELSOMRA (suvorexant)?
Dual orexin receptor antagonist (DORA); orexin OX1R/OX2R antagonist.
What strengths does BELSOMRA (suvorexant) come in?
Tablets: 5 mg, 10 mg, 15 mg, 20 mg.
Snapshot
- Class: Adjunctive therapy
- Common US brands: BELSOMRA
- Therapeutic drug monitoring not routinely recommended.
- Last reviewed: 2025-12-28
Clinical Highlights
Suvorexant (brand Belsomra) is a dual orexin receptor antagonist (DORA) approved for insomnia (sleep onset and sleep maintenance). DORAs target orexin-mediated wake drive and do not rely on GABA-A modulation; this can be useful when avoiding GABAergic hypnotics, but next-day impairment and additive sedation risks still apply.
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- Key safety issues are next-day impairment, additive sedation with other CNS depressants, and uncommon “REM intrusion” symptoms (sleep paralysis, hypnagogic hallucinations, cataplexy-like symptoms) (label).
- Suvorexant is contraindicated in narcolepsy and is a Schedule IV controlled substance; screen for misuse risk and avoid open-ended refills.
- The compare view and the suvorexant evidence feed can help weigh alternatives, and the suvorexant print page can support safety counseling.
- Approved for insomnia (sleep onset and sleep maintenance); treat as a time-limited adjunct to CBT-I and sleep hygiene rather than a chronic nightly default.
- Not available generically (brand only); ensure benefit is meaningful before continuing, and avoid long-term continuation without periodic deprescribing attempts.
Dosing & Formulations
Tablets: 5 mg, 10 mg, 15 mg, 20 mg. Typical dose is 10 mg once nightly within 30 minutes of bedtime, with at least 7 hours remaining before planned awakening; maximum 20 mg nightly (label).
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- Time to effect may be delayed if taken with or soon after a meal (label).
- With moderate CYP3A inhibitors, recommended dose is 5 mg (generally do not exceed 10 mg); avoid strong CYP3A inhibitors (label).
- Avoid “middle of the night” redosing; if awakenings persist, reassess the diagnosis and consider alternatives rather than increasing hypnotic burden.
Monitoring & Risks
Daytime somnolence and impaired driving can occur; risk rises with dose and if taken with less than a full night of sleep remaining (label). Sleep paralysis, hypnagogic hallucinations, and rare complex sleep behaviors can occur; discontinue if dangerous behaviors occur (label).
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- In patients with depression, worsening depression and suicidal thoughts have been reported with sedative-hypnotics; monitor closely (label).
- If there is no meaningful benefit after a reasonable trial, stop rather than continuing indefinitely; ongoing hypnotic use should have explicit goals and periodic deprescribing attempts.
Drug Interactions
Strong CYP3A inhibitors increase exposure—avoid combination; moderate inhibitors require dose reduction (label). Strong CYP3A inducers (e.g., rifampin, carbamazepine) can reduce effect (label).
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- Avoid alcohol and other CNS depressants when possible.
Practice Notes
Favor CBT-I first and use suvorexant as a time-limited adjunct; reassess benefit and safety at each refill decision. Avoid in narcolepsy and be cautious in polypharmacy or older adults where fall and driving risks are high.
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- If insomnia persists, assess for untreated sleep apnea, circadian rhythm disorders, stimulant use, alcohol/cannabis use, and mood episodes before adding additional sedatives.
References
- Belsomra (suvorexant) prescribing information — DailyMed (2025)
- Clinical Practice Guideline for the Pharmacologic Treatment of Chronic Insomnia in Adults: An American Academy of Sleep Medicine Clinical Practice Guideline — Journal of Clinical Sleep Medicine (2017)
- Efficacy and Acceptability of Pharmacological Interventions for Insomnia in Patients With Severe Mental Illness — Acta Psychiatrica Scandinavica (2025)
- Residual effects of medications for sleep disorders on driving performance — European Neuropsychopharmacology (2024)
