What is the use of Buspirone (Buspar)?

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From the Guidelines

Buspirone is a recommended anxiolytic medication, particularly useful for patients with mild to moderate agitation, with a typical starting dose of 5 mg twice daily and a maximum dose of 20 mg three times daily, as supported by the most recent evidence 1.

Key Points

  • Buspirone works differently from benzodiazepines by targeting serotonin receptors in the brain, making it a safer option with no abuse potential.
  • It takes 2-4 weeks to reach full effectiveness, so patience is required when starting treatment.
  • Common side effects include dizziness, headache, nausea, and nervousness, which often diminish over time.
  • Buspirone should not be taken with grapefruit juice or MAO inhibitors, and patients should inform their doctor about all medications they're taking to avoid interactions.
  • The most recent evidence from 2023 1 suggests that buspirone can be used as an augmentation strategy for patients with major depressive disorder who do not respond to initial treatment, with similar efficacy to other pharmacologic switch strategies.

Clinical Considerations

  • Buspirone is particularly useful for generalized anxiety disorder and as an adjunct treatment for depression with anxiety.
  • Unlike sedating anti-anxiety medications, buspirone doesn't significantly impair cognitive function or cause drowsiness, making it suitable for daytime use.
  • The evidence from 2023 1 also highlights the importance of discussing the advantages and disadvantages of each treatment option with patients, including the potential risks and benefits of buspirone.

Dosage and Administration

  • The recommended starting dose of buspirone is 5 mg twice daily, with a maximum dose of 20 mg three times daily, as stated in the 2002 guidelines 1.
  • The dosage may need to be adjusted based on the patient's response to treatment and tolerance to side effects.
  • It's essential to monitor patients for potential side effects and adjust the treatment plan accordingly.

From the FDA Drug Label

Buspirone hydrochloride tablets are indicated for the management of anxiety disorder or the short-term relief of the symptoms of anxiety. The efficacy of buspirone hydrochloride tablets has been demonstrated in controlled clinical trials of outpatients whose diagnosis roughly corresponds to Generalized Anxiety Disorder (GAD). The effectiveness of buspirone hydrochloride tablets in long-term use, that is, for more than 3 to 4 weeks, has not been demonstrated in controlled trials.

Buspirone is indicated for the management of anxiety disorder or the short-term relief of the symptoms of anxiety. The efficacy of buspirone has been demonstrated in controlled clinical trials for Generalized Anxiety Disorder (GAD). However, the effectiveness of buspirone in long-term use (more than 3 to 4 weeks) has not been demonstrated in controlled trials 2.

From the Research

Buspirone Overview

  • Buspirone is an azapirone derivative and a 5-HT1A partial agonist, used for the treatment of generalized anxiety disorder (GAD) 3.
  • It has anxiolytic properties similar to those of benzodiazepines, but with increased safety and lack of dependency-producing aspects 3.

Clinical Uses

  • Buspirone is particularly appropriate for patients with GAD, chronic anxiety, anxious elderly, and those with mixed symptoms of anxiety and depression 3.
  • It has been studied for use in patients with panic disorder, but results have been inconclusive, and it is not recommended for routine treatment of panic disorder 3.
  • Buspirone has also been explored for use in patients with other conditions, including major depressive disorder, obsessive-compulsive disorder, and social phobia 4.

Efficacy and Safety

  • Buspirone has been shown to be effective in reducing anxiety and depressive symptoms in patients with GAD, including those with coexisting mild depressive symptoms 5.
  • It has a generally benign side effect profile, making it a suitable option for patients with certain medical conditions, such as those with Williams syndrome 6.
  • The incidence of adverse events is similar to placebo, but buspirone-treated patients may experience more nausea, dizziness, somnolence, and sweating 5.

Treatment Guidelines

  • Buspirone is considered a second-line treatment for GAD in adults, after selective serotonin reuptake inhibitors (SSRIs) and selective serotonin norepinephrine reuptake inhibitors (SNRIs) 7.
  • In pediatric patients with GAD, SSRIs are considered the first-line pharmacotherapy, and buspirone may be considered as a second-line option 7.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Buspirone in clinical practice.

The Journal of clinical psychiatry, 1990

Research

Buspirone: future directions.

Journal of clinical psychopharmacology, 1999

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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