What is the recommended starting dose of Prozac (fluoxetine)?

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Prozac (Fluoxetine) Starting Dose

The recommended starting dose of Prozac (fluoxetine) for adults with major depressive disorder is 20 mg once daily, administered in the morning. 1

Standard Adult Dosing for Depression

  • Start with 20 mg/day in the morning for most adult patients with major depressive disorder 1
  • This 20 mg dose is sufficient to obtain a satisfactory response in most cases, as demonstrated in controlled trials 1
  • Dose increases may be considered after several weeks if insufficient clinical improvement is observed, with a maximum of 80 mg/day 1
  • The full therapeutic effect may be delayed until 4 weeks of treatment or longer 1

Pediatric Dosing (Children and Adolescents)

  • Start with 10 mg/day for pediatric patients with depression 1
  • After 1 week at 10 mg/day, increase to 20 mg/day 1
  • For lower weight children, the starting and target dose may remain at 10 mg/day due to higher plasma levels 1

Special Population Considerations

Elderly Patients

  • Use 10 mg every other morning as the initial dose for elderly patients with dementia and depression 2
  • Maximum dose is 20 mg every morning in this population 2, 3
  • Fluoxetine should generally be avoided in older adults due to greater risk of agitation and overstimulation 2, 3
  • The drug is activating with a very long half-life, making it particularly problematic in geriatric populations 2

Hepatic Impairment

  • A lower or less frequent dosage should be used in patients with hepatic impairment 1

Renal Impairment

  • Dosage adjustments for renal impairment are not routinely necessary 1

Other Indications with Different Starting Doses

Obsessive-Compulsive Disorder (OCD)

  • Adults: Start with 20 mg/day in the morning 1
  • Adolescents and higher weight children: Start with 10 mg/day, increase to 20 mg/day after 2 weeks 1
  • Lower weight children: Start with 10 mg/day, with a target range of 20-30 mg/day 1

Bulimia Nervosa

  • Start with 60 mg/day administered in the morning 1
  • For some patients, titrate up to this target dose over several days 1
  • Only the 60 mg dose was statistically superior to placebo in controlled trials 1

Panic Disorder

  • Start with 10 mg/day 1
  • After 1 week, increase to 20 mg/day 1
  • The most frequently administered dose in clinical trials was 20 mg/day 1

Important Clinical Considerations

Activation and Side Effects

  • Fluoxetine tends to be activating and may cause initial anxiety or agitation 2
  • Common adverse events at the 20 mg/day dose include nausea, nervousness, insomnia, and headache 4, 5
  • These side effects are dose-related and more common at higher doses 4

Long Half-Life

  • Fluoxetine has a half-life of 1-3 days, with its active metabolite (norfluoxetine) having a half-life of 7-15 days 5
  • This long half-life essentially precludes withdrawal phenomena 4
  • At least 5 weeks should be allowed after stopping fluoxetine before starting an MAOI 1

Drug Interactions

  • Fluoxetine is an inhibitor of cytochrome P450 2D6 and other CYP enzymes 4
  • Use with caution in patients with conditions predisposing to QT prolongation, including CYP2D6 poor metabolizers 3

References

Guideline

Fluoxetine Dosing Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Fluoxetine Dosing Considerations for Special Populations

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Safety and side effect profile of fluoxetine.

Expert opinion on drug safety, 2004

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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