How to switch from 20 mg escitalopram (Lexapro) to Pristiq (desvenlafaxine)?

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How to Switch from 20 mg Escitalopram to Desvenlafaxine (Pristiq)

When switching from escitalopram 20 mg to desvenlafaxine (Pristiq), a cross-tapering approach with gradual reduction of escitalopram while introducing desvenlafaxine at 50 mg daily is recommended to minimize discontinuation symptoms and avoid serotonin syndrome.

Cross-Tapering Schedule

Week 1:

  • Reduce escitalopram to 15 mg daily
  • Start desvenlafaxine 50 mg daily (therapeutic starting dose) 1
  • Take both medications at different times of day to minimize risk of serotonin syndrome 2

Week 2:

  • Reduce escitalopram to 10 mg daily
  • Continue desvenlafaxine 50 mg daily 1
  • Monitor for discontinuation symptoms or adverse effects 1

Week 3:

  • Reduce escitalopram to 5 mg daily
  • Continue desvenlafaxine 50 mg daily 1
  • Continue monitoring for adverse effects and therapeutic response 1

Week 4:

  • Discontinue escitalopram completely
  • Continue desvenlafaxine 50 mg daily 1
  • Assess therapeutic response and tolerability 1

Important Considerations

Discontinuation Symptoms

  • Escitalopram can cause discontinuation syndrome characterized by dizziness, fatigue, headaches, nausea, sensory disturbances, anxiety, and irritability 2
  • Gradual tapering reduces risk of discontinuation symptoms 2, 3
  • If severe discontinuation symptoms occur, slow the taper schedule 3

Serotonin Syndrome Risk

  • Both medications affect serotonin levels, creating potential risk for serotonin syndrome during cross-tapering 2, 1
  • Signs of serotonin syndrome include confusion, agitation, tremors, hyperreflexia, tachycardia, diaphoresis, and hyperthermia 2
  • Seek immediate medical attention if these symptoms develop 1

Dosing Considerations

  • Desvenlafaxine 50 mg is both the starting and therapeutic dose 1
  • Take desvenlafaxine at approximately the same time each day with or without food 1
  • Swallow desvenlafaxine tablets whole with fluid; do not divide, crush, chew, or dissolve 1

Special Populations

  • For patients with moderate to severe renal impairment, adjust desvenlafaxine dosing 1
  • For patients with moderate to severe hepatic impairment, maximum dose is 50 mg daily 1
  • For elderly patients, consider a more gradual cross-tapering schedule 2

Monitoring During Transition

  • Monitor blood pressure regularly as desvenlafaxine may increase blood pressure 1
  • Watch for signs of activation of mania/hypomania 1
  • Assess for therapeutic response after 4 weeks on the full desvenlafaxine dose 1
  • Be alert for increased risk of bleeding, especially if patient is taking NSAIDs, aspirin, or anticoagulants 1

Common Side Effects to Expect

  • Nausea (most common with desvenlafaxine, typically resolves within 1-2 weeks) 1
  • Headache 1
  • Dizziness 1
  • Insomnia or somnolence 1
  • Increased sweating 1

Potential Pitfalls and How to Avoid Them

  • Abrupt discontinuation: Never stop escitalopram abruptly as this significantly increases risk of discontinuation syndrome 2, 3
  • Drug interactions: Avoid concomitant use with MAOIs (must wait 14 days after stopping an MAOI before starting desvenlafaxine, and 7 days after stopping desvenlafaxine before starting an MAOI) 1
  • Inadequate cross-tapering: Too rapid transitions increase risk of both discontinuation symptoms and serotonin syndrome 3
  • Overlooking patient factors: Adjust schedule based on individual tolerance and response 2

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Switching and stopping antidepressants.

Australian prescriber, 2016

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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