What is the recommended dosing for Viibryd (vilazodone)?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: September 4, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Vilazodone (Viibryd) Dosing Recommendations

The recommended dosing for Viibryd (vilazodone) is to start with 10 mg once daily with food for 7 days, then increase to 20 mg once daily with food, with the option to increase to 40 mg once daily with food after a minimum of 7 days between dosage increases. 1

Initial Dosing and Titration Schedule

  • Starting dose: 10 mg once daily with food for 7 days
  • Week 2: Increase to 20 mg once daily with food
  • Week 3 or later: May increase to 40 mg once daily with food (if needed)
  • Target therapeutic dose range: 20-40 mg once daily 1

Administration Requirements

  • Must be taken with food to ensure adequate plasma concentrations 1, 2
  • If a dose is missed, it should be taken as soon as remembered, unless it's almost time for the next dose
  • Do not take two doses at the same time 1

Special Dosing Considerations

Drug Interactions

  • When used with strong CYP3A4 inhibitors (e.g., itraconazole, clarithromycin, voriconazole):

    • Dose should not exceed 20 mg once daily 1
    • Original dose can be resumed when the inhibitor is discontinued
  • When used with strong CYP3A4 inducers (e.g., carbamazepine, phenytoin, rifampin):

    • Consider increasing dosage by 2-fold, up to maximum 80 mg once daily, over 1-2 weeks
    • Gradually reduce back to original dose over 1-2 weeks when inducer is discontinued 1

Discontinuation Protocol

To minimize discontinuation symptoms, taper gradually rather than stopping abruptly:

  • From 40 mg: Reduce to 20 mg once daily for 4 days, then 10 mg once daily for 3 days
  • From 20 mg: Reduce to 10 mg once daily for 7 days 1

Efficacy Timeline

  • Initial improvement in depressive symptoms may be observed as early as 1-2 weeks 3, 4
  • Full therapeutic effect typically observed at 4-6 weeks of therapy 3
  • In clinical trials, significant reductions in depression scores were seen from week 1, week 2, or week 6, depending on the study 5

Common Side Effects

  • Diarrhea (most common)
  • Nausea
  • Vomiting
  • Insomnia 3, 6

Other reported effects include:

  • Dizziness
  • Dry mouth
  • Fatigue
  • Decreased libido 3

Clinical Advantages

Vilazodone has a unique mechanism as both a selective serotonin reuptake inhibitor and a 5-HT1A receptor partial agonist, which may offer:

  • Potentially faster onset of action compared to some other antidepressants
  • Limited adverse effects on sexual function
  • Minimal effect on body weight 5, 3

Important Monitoring Considerations

  • Screen for bipolar disorder before initiating treatment 1
  • Monitor for emergence of suicidal thoughts and behaviors, particularly in young adults 1
  • Allow at least 14 days between discontinuing MAOIs and starting vilazodone, and vice versa 1

Vilazodone represents an effective option for treating major depressive disorder with a unique pharmacological profile that may provide advantages for certain patients, though direct comparative studies with other antidepressants are limited 4.

References

Research

Other Antidepressants.

Handbook of experimental pharmacology, 2019

Research

A review of current evidence for vilazodone in major depressive disorder.

International journal of psychiatry in clinical practice, 2013

Research

Vilazodone: a novel antidepressant.

American journal of health-system pharmacy : AJHP : official journal of the American Society of Health-System Pharmacists, 2012

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.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.