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Viibryd Tapering Guide

vilazodone

SSRIFDA 2011
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Boxed Warning

Suicidality risk in children, adolescents, and young adults under 25 during initial treatment.

Overview

Vilazodone is a selective serotonin reuptake inhibitor (SSRI) and partial agonist at the 5-HT1A receptor. It is used for the treatment of major depressive disorder.

Common Doses

10mg, 20mg, 40mg

Formulations

Tablets: 10mg, 20mg, 40mg

Pregnancy

Category C (risk cannot be ruled out)

Mechanism of Action

Combined SSRI activity with 5-HT1A receptor partial agonism, providing dual serotonergic modulation. Blocks SERT while partially activating 5-HT1A autoreceptors.

Taper Notes

Unique dual mechanism (SSRI + 5-HT1A partial agonist). Must be taken with food for adequate absorption. Taper slowly — withdrawal can include GI disturbance and dizziness.

Hyperbolic Tapering Guidance

Reduce gradually over months. Consider 10mg steps initially, then smaller reductions at lower doses. No liquid formulation available — tablet splitting may be necessary.

Summary written by TaperCommunity, informed by the Maudsley Deprescribing Guidelines (Horowitz & Taylor) and related literature — see Sources & References below. Not affiliated with or endorsed by the Maudsley.

Common Withdrawal Symptoms

dizzinessnauseadiarrheainsomniaheadacheirritability

Interactions & Safety

Drug Interactions

  • MAOIs — contraindicated (risk of serotonin syndrome)
  • Strong CYP3A4 inhibitors (ketoconazole) — reduce vilazodone dose to 20mg
  • Serotonergic drugs (triptans, tramadol, St. John's Wort) increase serotonin syndrome risk

Food Interactions

  • MUST be taken with food — bioavailability drops ~50% without food
  • No specific food contraindications beyond the requirement to take with food

Contraindications

  • MAOIs within 14 days
  • Known hypersensitivity to vilazodone

Toxicity

Serotonin syndrome risk when combined with serotonergic agents. GI side effects are the most common dose-limiting toxicity.

Pharmacokinetics

ADME Profile

Absorption

Oral bioavailability 72% with food (significantly reduced without food). Tmax ~4–5 hours. Must be taken with food.

Distribution

Not well characterized; extensively distributed.

Metabolism

Hepatic via CYP3A4 (major), CYP2C19, and CYP2D6. Active metabolites are not clinically significant.

Elimination

Primarily fecal (2% unchanged in urine).

Protein Binding

96–99%

Clearance

Apparent clearance ~40 L/hr

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Sources & References

Viibryd (vilazodone) information on this page is sourced from peer-reviewed research, regulatory bodies, clinical guidelines, and patient-advocacy organizations.

Encyclopedic & chemical databases

Neutral, high-authority entity references.

Deprescribing-specific resources

Clinician-facing references on tapering protocols.

Patient-advocacy & lived-experience

Long-running communities documenting withdrawal experience.

TaperCommunity does not provide medical advice. Always consult a qualified prescriber before adjusting psychiatric medication.