What is the recommended dose of mirtazapine (Remeron) for adolescents?

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Mirtazapine Dosing in Adolescents

For adolescents with depression, start mirtazapine at 7.5 mg once daily at bedtime, with gradual titration in 7.5 mg increments up to a maximum of 45 mg daily based on clinical response and tolerability. 1

Starting Dose and Titration Strategy

  • Begin with 7.5 mg once daily at bedtime in adolescent patients, which is lower than the typical adult starting dose of 15 mg 1

  • Increase dosage in 7.5 mg increments every 5-7 days as tolerated, monitoring for both therapeutic response and adverse effects 1

  • Maximum daily dose is 45 mg administered as a single bedtime dose or in divided doses throughout the day 1

  • Treatment duration in the pediatric study ranged from 11 to 368 days, with individualized titration based on target symptom response 1

Clinical Monitoring Requirements

  • Assess response within 1-2 weeks of reaching each dose level, as clinical improvement with mirtazapine typically occurs within 2-4 weeks at an effective dose 2

  • Monitor for common adverse effects including somnolence (which paradoxically may be more prominent at lower doses), increased appetite, weight gain, and sedation 3, 2

  • Evaluate sleep quality and anxiety symptoms early, as these may improve within the first week of treatment even before full antidepressant effects emerge 2, 4

  • Use standardized rating scales such as the Clinical Global Impression (CGI) scale to objectively track improvement in target symptoms 1

Important Clinical Considerations

The lower starting dose of 7.5 mg in adolescents (compared to 15 mg in adults) reflects increased sensitivity to adverse effects in younger patients. 1 This conservative approach allows for better tolerability while establishing therapeutic benefit.

  • Sedation is dose-dependent and often decreases at higher therapeutic doses (≥15 mg), so don't mistake initial sedation at 7.5 mg as a reason to stay at subtherapeutic doses 4

  • Once-daily bedtime dosing is preferred due to the 20-40 hour elimination half-life and the sedative properties that can be therapeutically useful for sleep disturbances 2, 5

  • In the autism spectrum disorder study, 16 of 17 adolescent patients showed significant improvement in sleep disorders and behavioral symptoms with mirtazapine titration 1

Dosing in Special Populations

  • Hepatic or renal impairment requires dose reduction and more cautious titration, as clearance decreases by approximately 30% with moderate impairment and 50% with severe renal impairment 5

  • Female adolescents may require lower doses than males due to higher plasma concentrations at equivalent doses 5

Common Pitfalls to Avoid

  • Don't stop at 7.5 mg assuming it's therapeutic - this is a starting dose for tolerability assessment, not typically an effective antidepressant dose 1

  • Don't increase doses too rapidly - allow 5-7 days between increments to assess both efficacy and tolerability 1

  • Don't combine with other sedating medications without careful monitoring, as additive CNS depression can occur 6

  • Monitor for paradoxical behavioral activation, which can occur in younger patients, particularly those with developmental disabilities 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Mirtazapine Dosage and Administration

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Clinical pharmacokinetics of mirtazapine.

Clinical pharmacokinetics, 2000

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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