What is the recommended taper schedule for temazepam (Restoril) and how should I discontinue trazodone and initiate low‑dose doxepin for insomnia?

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Tapering Temazepam and Transitioning to Doxepin for Insomnia

Taper temazepam gradually over 2–4 weeks using 25% dose reductions every 1–2 weeks, discontinue trazodone immediately without tapering, and initiate low-dose doxepin 3 mg at bedtime concurrently with Cognitive Behavioral Therapy for Insomnia (CBT-I).

Temazepam Tapering Protocol

Benzodiazepine hypnotics like temazepam require gradual tapering to prevent withdrawal reactions including rebound insomnia, anxiety, seizures, and delirium. 1, 2

Recommended Taper Schedule:

  • Week 1–2: Reduce temazepam dose by 25% (e.g., if taking 15 mg → reduce to 11.25 mg or approximately 10 mg) 1, 2
  • Week 3–4: Reduce by another 25% of the original dose (e.g., 15 mg → 7.5 mg) 1, 2
  • Week 5–6: Reduce to 3.75 mg or discontinue, depending on tolerance 1, 2
  • Monitor closely for withdrawal symptoms (anxiety, tremor, insomnia worsening, irritability); if these occur, pause the taper or slow the reduction rate 1, 2

The FDA explicitly recommends using a gradual taper to discontinue temazepam or reduce dosage, and if withdrawal reactions develop, consider pausing the taper or increasing the dosage to the previous level before decreasing more slowly. 1

Trazodone Discontinuation

Stop trazodone immediately without tapering—it does not require gradual dose reduction when used at hypnotic doses (25–50 mg). 2

  • Trazodone is explicitly NOT recommended for insomnia treatment by the American Academy of Sleep Medicine due to minimal benefit (only ~10 min reduction in sleep latency, ~8 min reduction in wake after sleep onset) with no improvement in subjective sleep quality and harms outweighing benefits 3, 4
  • At low hypnotic doses (25–50 mg), trazodone does not produce significant withdrawal symptoms upon abrupt discontinuation 2
  • There is no need to taper trazodone when discontinuing, unlike benzodiazepines 2

Initiating Low-Dose Doxepin

Start doxepin 3 mg at bedtime immediately, even while tapering temazepam—there is no need to wait for complete benzodiazepine discontinuation. 3, 2

Doxepin Dosing and Titration:

  • Initial dose: 3 mg at bedtime (take within 30 minutes of bedtime with ≥7 hours remaining before planned awakening) 3
  • Mechanism: Selective H₁-histamine receptor antagonism at low doses, with minimal anticholinergic effects and no abuse potential 3
  • Efficacy: Reduces wake after sleep onset by 22–23 minutes, improves sleep efficiency, total sleep time, and sleep quality 3
  • Titration: If 3 mg is insufficient after 1–2 weeks, increase to 6 mg 3
  • No tapering required when discontinuing doxepin 2

Why Doxepin Over Other Options:

  • Low-dose doxepin (3–6 mg) is the preferred first-line agent specifically for sleep-maintenance insomnia according to the American Academy of Sleep Medicine and American College of Physicians 3
  • It has no abuse potential, no DEA scheduling, and minimal side effects compared to benzodiazepines 3
  • Minimal anticholinergic burden at hypnotic doses (3–6 mg), unlike higher antidepressant doses 3

Concurrent Cognitive Behavioral Therapy for Insomnia (CBT-I)

Initiate or optimize CBT-I immediately alongside the medication transition—it is the standard of care and provides superior long-term outcomes compared to medication alone. 3, 2

Core CBT-I Components:

  • Stimulus control therapy: Go to bed only when sleepy; use bed only for sleep and sex; leave bed if unable to sleep within 15–20 minutes 3
  • Sleep restriction therapy: Limit time in bed to actual sleep time + 30 minutes to consolidate sleep 3
  • Relaxation techniques: Progressive muscle relaxation, guided imagery, breathing exercises 3
  • Cognitive restructuring: Address maladaptive beliefs about sleep (e.g., "I must get 8 hours or I'll be dysfunctional") 3
  • Sleep hygiene education: Avoid caffeine/alcohol in evening, maintain consistent sleep-wake times, optimize bedroom environment 3

CBT-I can be delivered via individual therapy, group sessions, telephone, web-based modules, or self-help books—all formats show effectiveness. 3

Monitoring and Reassessment

  • Reassess after 1–2 weeks of doxepin initiation to evaluate efficacy on sleep-onset latency, total sleep time, nocturnal awakenings, and daytime functioning 3
  • Monitor for adverse effects: Morning sedation, headache, cognitive impairment (though rare at low doses) 3
  • Screen for complex sleep behaviors (sleep-driving, sleep-walking) at every visit; discontinue immediately if these occur 3
  • Evaluate for underlying sleep disorders (sleep apnea, restless legs syndrome, circadian rhythm disorders) if insomnia persists beyond 7–10 days despite treatment 3

Common Pitfalls to Avoid

  • Do NOT abruptly stop temazepam—this can precipitate severe withdrawal, including seizures 1, 2
  • Do NOT continue trazodone—it lacks efficacy for insomnia and has an unfavorable risk-benefit profile 3, 4
  • Do NOT use over-the-counter antihistamines (diphenhydramine, doxylamine) as alternatives—they lack efficacy, cause anticholinergic effects, and develop tolerance within 3–4 days 3
  • Do NOT prescribe doxepin without initiating CBT-I—behavioral therapy provides more durable benefits than medication alone 3, 2
  • Do NOT combine multiple sedating agents (e.g., adding another hypnotic to doxepin during the temazepam taper)—this markedly increases risk of respiratory depression, falls, and cognitive impairment 3

Special Population Considerations

  • Elderly patients (≥65 years): Start doxepin at 3 mg and do not exceed 6 mg; monitor closely for falls and cognitive impairment 3
  • Hepatic impairment: Doxepin remains safe at low doses, but monitor for increased sedation 3
  • History of substance use: Doxepin is ideal due to no abuse potential; avoid benzodiazepines entirely 3

References

Guideline

Pharmacotherapy of Insomnia

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Trazodone for Insomnia Treatment

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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