What is the recommended dosing for Effexor (venlafaxine)?

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Last updated: September 3, 2025View editorial policy

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Venlafaxine (Effexor) Dosing Guidelines

The recommended starting dose for venlafaxine is 75 mg/day, administered in two or three divided doses, taken with food. The dose may be increased to 150 mg/day based on tolerability and clinical need, with further increases up to 225 mg/day if necessary. 1

Initial Dosing

  • Starting dose: 75 mg/day (in 2-3 divided doses with food)
  • Titration: Increase by up to 75 mg/day at intervals of no less than 4 days
  • Target dose range: 75-225 mg/day for most patients
  • Maximum dose: 375 mg/day (generally in three divided doses)

Dosing Considerations Based on Patient Factors

Hepatic Impairment

  • Mild to moderate impairment: Reduce total daily dose by 50%
  • Severe impairment: May require even greater dose reduction
  • Note: Individual variability in clearance makes individualization of dosing advisable 1

Renal Impairment

  • Mild to moderate impairment (GFR 10-70 mL/min): Reduce total daily dose by 25%
  • Hemodialysis patients: Reduce total daily dose by 50%
  • Note: Significant individual variability may require personalized dosing 1

Elderly Patients

  • No specific dose adjustment based on age alone
  • Exercise caution when increasing the dose
  • Start at lower doses and titrate more slowly 1

Extended-Release Formulation

For venlafaxine XR (extended-release):

  • Can be administered once daily
  • Similar efficacy to immediate-release formulation
  • May have better tolerability profile 2

Treatment Duration

  • Acute episodes: Several months of sustained therapy beyond initial response
  • Maintenance treatment: Continued therapy at the same effective dose has demonstrated efficacy in preventing relapse 1

Discontinuation

  • Gradual tapering rather than abrupt cessation is strongly recommended
  • Monitor for discontinuation symptoms (dizziness, nausea, headache, irritability)
  • If intolerable symptoms occur, resume previous dose and decrease more gradually 1

Special Warnings

  • Pregnancy (third trimester): Carefully consider risks/benefits due to potential neonatal complications
  • MAOIs: Allow at least 14 days between discontinuing MAOIs and starting venlafaxine, and at least 7 days between stopping venlafaxine and starting MAOIs 1

Common Side Effects to Monitor

  • Digestive: nausea, dry mouth
  • Nervous system: dizziness, somnolence, insomnia
  • Urogenital: abnormal ejaculation
  • Other: sweating 2
  • Blood pressure increases may occur, particularly at higher doses 3

Clinical Pearls

  • Higher doses (≥375 mg/day) may be beneficial for treatment-resistant depression or severely depressed inpatients 1, 4
  • Therapeutic response may be evident as early as week 2 of treatment 2
  • Venlafaxine at 150 mg/day may be superior to fluoxetine in patients who do not respond early to treatment 5
  • Blood pressure monitoring is recommended, especially at higher doses 3, 4

Common Pitfalls to Avoid

  • Inadequate initial dosing (starting below 75 mg/day may be less effective)
  • Insufficient time for response evaluation (allow at least 2-4 weeks at therapeutic dose)
  • Abrupt discontinuation (always taper gradually)
  • Failure to monitor blood pressure, especially at doses above 225 mg/day
  • Not accounting for renal or hepatic impairment when determining dosage

By following these dosing guidelines and monitoring parameters, venlafaxine can be an effective treatment option for major depression with a manageable side effect profile.

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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