What are the recommended doses for Trintellix (vortioxetine)?

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Last updated: December 15, 2025View editorial policy

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Trintellix (Vortioxetine) Dosing

The recommended starting dose of Trintellix is 10 mg orally once daily, which should then be increased to 20 mg daily as tolerated, with 5 mg daily reserved for patients who cannot tolerate higher doses. 1

Standard Dosing Regimen

  • Starting dose: 10 mg once daily, administered orally without regard to meals 1
  • Target dose: 20 mg once daily, as tolerated 1
  • Lower dose option: 5 mg once daily for patients who do not tolerate higher doses 1

Special Population Adjustments

CYP2D6 Poor Metabolizers

  • Maximum dose: 10 mg daily in known CYP2D6 poor metabolizers 1
  • This is the only population requiring mandatory dose adjustment based on pharmacogenetic considerations 2

Other Populations

  • No dose adjustments required for sex, age, race, body size, renal impairment, or hepatic impairment 2

Dose Titration Strategy

For early optimization: In patients with severe MDD and comorbid generalized anxiety disorder, forced up-titration from 10 mg to 20 mg after 1 week has been shown to be well-tolerated and effective 3

Discontinuation Protocol

  • Abrupt discontinuation is possible 1
  • However, for doses of 15 mg or 20 mg daily: Reduce to 10 mg daily for one week prior to full discontinuation when possible 1

Drug Interaction Dose Modifications

Strong CYP2D6 Inhibitors (e.g., bupropion)

  • Reduce Trintellix dose by half when coadministered 1

Strong CYP Inducers (e.g., rifampin)

  • Consider dose increase when coadministered for more than 14 days 1
  • Maximum dose should not exceed 3 times the original dose 1

Clinical Pharmacology Supporting Dosing

  • Linear pharmacokinetics across the 5-20 mg dose range 2
  • Terminal half-life: Approximately 66 hours 2
  • Time to steady state: Generally achieved within 2 weeks 2
  • Bioavailability: 75% with no food effect 2

Maintenance Therapy

All three doses (5 mg, 10 mg, and 20 mg) are effective for relapse prevention in patients who achieve remission, with cumulative relapse rates of 19.3%, 17.9%, and 17.4% respectively versus 32.5% for placebo over 28 weeks 4

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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