Fluvoxamine Dosing Recommendations
Adult Dosing
Start fluvoxamine at 50 mg once daily at bedtime, then increase by 50 mg increments every 4-7 days as tolerated up to a maximum of 300 mg/day, with doses above 100 mg/day split into two divided doses (larger dose at bedtime). 1
Standard Titration Protocol
- Initial dose: 50 mg at bedtime 1
- Titration schedule: Increase by 50 mg every 4-7 days based on tolerability 1
- Therapeutic range: 100-300 mg/day for OCD and anxiety disorders 1
- Dosing frequency: Once daily if ≤100 mg/day; twice daily (unequal split with larger dose at bedtime) if >100 mg/day 1
- Maximum dose: 300 mg/day 1
Special Populations
- Elderly patients: Use lower initial doses and slower titration due to decreased clearance 1
- Hepatic impairment: Modify initial dose and titration schedule due to decreased clearance 1
Pediatric Dosing (Ages 8-17)
Start at 25 mg once daily at bedtime in children and adolescents, then increase by 25 mg increments every 4-7 days, with maximum doses of 200 mg/day for children up to age 11 and 300 mg/day for adolescents. 1
Age-Specific Protocols
- Starting dose: 25 mg at bedtime for all pediatric patients 1
- Titration increments: 25 mg every 4-7 days 1
- Children (ages 8-11): Maximum 200 mg/day due to 2-3 times higher steady-state plasma concentrations compared to adolescents 2, 3
- Adolescents (ages 12-17): Maximum 300 mg/day (similar pharmacokinetics to adults) 2, 3
- Dosing frequency: Twice daily if total dose >50 mg/day, with larger dose at bedtime 1
- Gender consideration: Female children may achieve therapeutic effect at lower doses 1
Clinical Response Timeline
- Initial improvement: Statistically significant improvement may occur within 2 weeks 4
- Clinically meaningful response: Typically by week 6 4
- Maximal benefit: Week 10-12 or later 4
- Trial duration: Continue for at least 10-12 weeks at therapeutic dose before declaring treatment failure 1, 5
Dose-Response Relationship
Higher doses (100-150 mg/day) demonstrate significantly better response rates (73.7%) compared to lower doses (50-75 mg/day, 47.1% response) in depression treatment. 5
- Target therapeutic doses of 100-150 mg/day for optimal efficacy 5
- If no improvement by 6 weeks at adequate dose, consider changing treatment strategy 5
Critical Safety Considerations
Drug Interactions
- Contraindicated with MAOIs: Risk of serotonin syndrome 4
- Extensive CYP450 interactions: Fluvoxamine inhibits CYP1A2, CYP2C19, CYP2C9, CYP3A4, and CYP2D6, creating greater potential for drug-drug interactions compared to other SSRIs 4
- Avoid combining with other serotonergic agents: Including tramadol, dextromethorphan, other SSRIs/SNRIs, and certain opioids 4
Discontinuation Syndrome
- Fluvoxamine carries higher risk: Associated with discontinuation syndrome along with paroxetine and sertraline 4
- Symptoms include: Dizziness, fatigue, myalgias, headaches, nausea, insomnia, sensory disturbances, anxiety, and agitation 4
- Taper gradually: Never discontinue abruptly 1
Common Adverse Effects
- Gastrointestinal: Nausea (most common), abdominal discomfort, diarrhea 2, 3, 6
- CNS effects: Insomnia, sedation, dizziness 2, 3
- Generally mild to moderate severity and often resolve with continued treatment 6
Monitoring Requirements
- Suicidality: Monitor closely during first months and after all dose adjustments, particularly in patients ≤24 years old 4
- Serotonin syndrome: Watch for mental status changes, neuromuscular hyperactivity, autonomic instability, especially within 24-48 hours of dose changes or adding serotonergic agents 4
- Behavioral activation: Monitor for agitation, hypomania, or mania 4
Common Pitfalls to Avoid
- Inadequate dosing: Many patients require 100-300 mg/day for optimal response; 50-75 mg/day is often subtherapeutic 5
- Insufficient trial duration: Must continue for at least 10-12 weeks at therapeutic dose before declaring failure 1, 5
- Forgetting twice-daily dosing: Doses >100 mg/day (adults) or >50 mg/day (pediatrics) require split dosing 1
- Ignoring drug interactions: Fluvoxamine has the most extensive CYP450 interactions among SSRIs 4
- Abrupt discontinuation: High risk of discontinuation syndrome requires gradual taper 4, 1