Luvox (Fluvoxamine) Dosing for Obsessive-Compulsive Disorder
Adult Dosing
For adults with OCD, 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
Initial Dosing
- Begin with 50 mg as a single daily dose at bedtime 1
- This represents the standard FDA-approved starting dose for adults 1
Titration Schedule
- Increase in 50 mg increments every 4 to 7 days based on tolerability 1
- Continue titration until maximum therapeutic benefit is achieved 1
- The therapeutic dose range in controlled trials was 100-300 mg/day 1
Dose Administration
- Total daily doses exceeding 100 mg should be divided into two doses 1
- When splitting doses unequally, give the larger dose at bedtime 1
- Maximum daily dose is 300 mg 1
Treatment Duration
- Continue treatment for at least 8-12 weeks at an effective dose to assess response 2, 3
- Higher doses of SSRIs are required for OCD compared to depression or other anxiety disorders 2
- After achieving remission, maintain treatment for a minimum of 12-24 months 2
Pediatric Dosing (Ages 8-17 Years)
For children and adolescents with OCD, start fluvoxamine at 25 mg once daily at bedtime, then increase by 25 mg increments every 4-7 days as tolerated, with maximum doses of 200 mg/day for children up to age 11 and 300 mg/day for adolescents. 1
Initial Dosing
- Begin with 25 mg as a single daily dose at bedtime 1
- This lower starting dose accounts for higher plasma concentrations in children 4
Titration Schedule
- Increase in 25 mg increments every 4 to 7 days as tolerated 1
- The therapeutic dose range in controlled trials was 50-200 mg/day 1, 4
Maximum Doses by Age
- Children up to age 11: Maximum 200 mg/day 1
- Adolescents (12-17 years): Maximum 300 mg/day (adult dose) 1
- Female children may achieve therapeutic effect at lower doses 1
Dose Administration
- Total daily doses exceeding 50 mg should be divided into two doses 1
- When splitting doses unequally, give the larger dose at bedtime 1
Special Populations
Elderly and Hepatically Impaired Patients
- Use lower initial doses due to decreased clearance 1
- Titrate more slowly than in younger adults 1
- Monitor closely for adverse effects 1
Pregnant Women (Third Trimester)
- Carefully weigh risks versus benefits when treating during the third trimester 1
- Consider tapering fluvoxamine in the third trimester due to risk of neonatal complications requiring prolonged hospitalization 1
Monitoring and Maintenance
Assessment of Response
- Significant improvement may be observed within the first 2 weeks, with greatest gains occurring early in treatment 2
- However, allow 8-12 weeks at therapeutic doses to fully assess efficacy 2, 3
- Early reduction in symptoms by 4 weeks predicts treatment response at 12 weeks 2
Side Effect Monitoring
- Systematically assess for nausea (most common), somnolence, asthenia, headache, dry mouth, and insomnia 5
- Monitor for gastrointestinal symptoms, which are the most common reason for discontinuation 4, 6
- Abdominal discomfort occurs more frequently with fluvoxamine than placebo 4
Long-Term Management
- Maintain patients on the lowest effective dosage 1
- Periodically reassess the need for continued treatment 1
- Longer treatment beyond 12-24 months may be necessary due to high relapse risk after discontinuation 2
Discontinuation
When stopping fluvoxamine, taper gradually rather than discontinuing abruptly to minimize withdrawal symptoms. 1
- Gradual dose reduction is recommended whenever possible 1
- Monitor for discontinuation symptoms during tapering 1
Treatment-Resistant Cases
Dose Optimization
- In treatment-resistant OCD, doses may occasionally exceed the manufacturer's recommended maximum of 300 mg/day 2, 7
- One case report documented remission with 600 mg/day fluvoxamine, though this is exceptional and requires careful monitoring 7
- Ensure adequate trial duration (at least 8-12 weeks) at maximum tolerated dose before considering treatment failure 2, 3
Alternative Strategies if No Response
- Consider switching to another SSRI or clomipramine 2
- Augment with cognitive-behavioral therapy (CBT), which has larger effect sizes than antipsychotic augmentation 2
- Consider clomipramine augmentation or antipsychotic augmentation if CBT unavailable 2
Important Clinical Considerations
Drug Interactions
- Fluvoxamine is a potent inhibitor of CYP1A2 and moderate inhibitor of CYP2C19 and CYP3A4 5
- Exercise caution when co-administering with alprazolam or triazolam; reduce benzodiazepine doses by 50% 2
- Monitor for drug interactions more carefully than with other SSRIs 5