Buspirone (BuSpar) Dosing for Generalized Anxiety Disorder
For treating generalized anxiety disorder (GAD) in adults, start buspirone at 15 mg daily (either 7.5 mg twice daily or 5 mg three times daily), then titrate to a target dose of 30 mg daily (15 mg twice daily or 10 mg three times daily), with a maximum dose of 60 mg daily if needed. 1
Initial Dosing Strategy
- Start with 15 mg/day divided doses: Begin with either 7.5 mg twice daily or 5 mg three times daily 1, 2
- The lower starting dose minimizes initial side effects while establishing tolerability 3
Titration Schedule
- Increase gradually over 2-4 days: Titrate from the initial 15 mg/day to the target dose of 30 mg/day 1
- The standard therapeutic dose is 30 mg daily, administered as either:
- Both BID and TID regimens show equivalent efficacy and safety, though BID dosing may improve compliance 2, 4
Maximum Dosing
- Maximum dose: 60 mg/day (20 mg three times daily or 30 mg twice daily) 5, 1
- Most patients respond adequately to 15-30 mg/day without requiring maximum doses 6
Critical Timing Considerations
- Onset of effect: 2-4 weeks - Patients must understand that buspirone does not provide immediate anxiety relief like benzodiazepines 5, 7
- This delayed onset makes buspirone inappropriate for patients requiring rapid symptom control 7
- A full therapeutic trial requires maintaining the target dose for at least 2-4 weeks before assessing efficacy 5
Special Populations
Elderly Patients
- Use the same starting dose (5 mg twice daily) as in younger adults 5
- Maximum dose remains 20 mg three times daily (60 mg/day) 5
- Pharmacokinetics are similar in elderly patients, though individual sensitivity may vary 1
Hepatic or Renal Impairment
- Avoid buspirone in severe hepatic or renal impairment - the drug shows increased plasma levels and prolonged half-life in these patients 1
- If mild-to-moderate impairment, use lower doses with careful monitoring 1
Important Clinical Caveats
Drug Interactions
- CYP3A4 inhibitors (e.g., ketoconazole, erythromycin, grapefruit juice): Significantly increase buspirone levels; reduce buspirone dose and monitor closely 1
- CYP3A4 inducers (e.g., rifampin): May require higher buspirone doses to maintain efficacy 1
- MAO inhibitors: Contraindicated due to risk of elevated blood pressure 1
Laboratory Interference
- Discontinue buspirone 48 hours before urine catecholamine testing - it interferes with metanephrine/catecholamine assays and can cause false-positive results for pheochromocytoma 1
Patient Selection
- Buspirone is most appropriate for patients with chronic GAD who can tolerate gradual symptom improvement 7
- Not recommended for panic disorder - studies have been inconclusive 7
- Ideal for patients where benzodiazepine dependence is a concern 7, 3
Long-Term Use
- Buspirone can be safely used for up to 12 months when clinically indicated 6
- No withdrawal syndrome occurs with abrupt discontinuation, even after prolonged use 6
- Periodically reassess the need for continued therapy when used beyond several months 6
Common Adverse Effects
- Most frequent: dizziness, headache, nausea, nervousness, and lightheadedness 3, 4
- Palpitations occur more frequently with BID dosing (5%) versus TID dosing (1%) 4
- Overall adverse event incidence is low and similar between dosing regimens 2, 4
- No sedation, psychomotor impairment, abuse potential, or dependence reported 3