What is the recommended starting dose for Trintellix (vortioxetine)?

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Recommended Starting Dose for Trintellix (Vortioxetine)

The recommended starting dose for Trintellix (vortioxetine) is 10 mg administered orally once daily without regard to meals. 1

Dosing Guidelines

  • The initial dose of 10 mg once daily should be increased to 20 mg/day as tolerated 1
  • For patients who do not tolerate higher doses, a lower dose of 5 mg/day can be considered 1
  • Trintellix can be taken without regard to food as no food effect on pharmacokinetics has been observed 2
  • The medication has a mean terminal half-life of approximately 66 hours, with steady-state plasma concentrations generally achieved within 2 weeks of dosing 2

Special Population Considerations

  • For patients who are known CYP2D6 poor metabolizers, the maximum recommended dose is 10 mg/day 1
  • No dose adjustment is needed based on age, gender, or the presence of renal or mild to moderate hepatic impairment 3
  • When co-administered with strong CYP2D6 inhibitors (such as bupropion), the Trintellix dose should be reduced by half 1

Titration and Maintenance

  • After starting at 10 mg/day, if well tolerated, the dose can be increased to the target dose of 20 mg/day 4
  • Some clinical trials have demonstrated that early up-titration to 20 mg/day (after 1 week) can be achieved without compromising tolerability 4
  • For discontinuation, doses of 15 mg/day or 20 mg/day should be reduced to 10 mg/day for one week prior to full discontinuation to avoid potential withdrawal symptoms 1

Efficacy Considerations

  • Clinical trials have shown that 20 mg/day was the effective dose in US studies, while lower doses (5-10 mg/day) were effective in non-US maintenance studies 3
  • Vortioxetine has demonstrated effectiveness in reducing symptoms of both depression and anxiety in patients with major depressive disorder 4, 5
  • The medication has also shown positive effects on cognitive symptoms of major depressive episodes 5

Adverse Effects

  • The most common adverse event is nausea, which is dose-dependent 3
  • Other common adverse reactions (incidence ≥5% and at least twice the rate of placebo) include constipation and vomiting 1
  • Vortioxetine's adverse event profile is generally similar to that of other selective serotonin reuptake inhibitors (SSRIs) 3

By following these dosing recommendations, clinicians can optimize the therapeutic benefits of Trintellix while minimizing potential adverse effects.

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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