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Buspirone

Buspirone is an medication approved by the (FDA) for the management of anxiety disorders or the short-term relief of anxiety symptoms, particularly (GAD). It belongs to the class of drugs known as azapirones and is chemically unrelated to benzodiazepines, barbiturates, or other sedative-anxiolytics, offering a non-sedating alternative with low potential for abuse or physical dependence. Sold under the brand name BuSpar among others, it is available in oral tablet form in strengths of 5 mg, 7.5 mg, 10 mg, 15 mg, and 30 mg. The of buspirone is not fully understood but primarily involves partial at serotonin 5-HT1A receptors in the , which modulates serotonin activity to alleviate anxiety without affecting receptors. It also exhibits weak antagonism at dopamine D2 autoreceptors, contributing to its anxiolytic effects, but lacks the sedative, anticonvulsant, or muscle-relaxant properties typical of benzodiazepines. Pharmacologically, buspirone is rapidly absorbed after , reaching peak plasma concentrations in 40 to 90 minutes, and is extensively metabolized by the 3A4 () enzyme, with a of 2 to 3 hours. Therapeutic effects often require 1 to 2 weeks of consistent use, distinguishing it from faster-acting anxiolytics. Originally synthesized in 1968 and patented in 1975, buspirone was initially developed as a potential agent but proved ineffective for and was repurposed for anxiety treatment due to its favorable profile. FDA approval came in 1986, and it has since become a second-line option for GAD, with off-label uses including augmentation in unipolar . Dosing typically starts at 15 mg per day (divided into twice-daily doses) and may be titrated up to a maximum of 60 mg per day, taken consistently with or without food to avoid variability in absorption. Common adverse effects include (affecting more than 10% of users), , , and nervousness, though these are generally mild and lead to discontinuation in about 10% of patients. Contraindications include to the drug and concurrent use with inhibitors (MAOIs) due to the of hypertensive crisis; it should also be used cautiously in patients with severe hepatic or renal impairment. Buspirone has a strong safety record, with no reported deaths from overdose with buspirone alone and minimal of symptoms upon discontinuation.

Medical uses

Generalized anxiety disorder

Buspirone is approved by the United States Food and Drug Administration (FDA) for the management of (GAD), a condition characterized by excessive, uncontrollable worry and associated symptoms such as restlessness, fatigue, and muscle tension persisting for at least six months. It serves as a second-line option, particularly for patients seeking alternatives to benzodiazepines due to its favorable side effect profile and lack of sedative or dependence-forming properties. Clinical trials have demonstrated buspirone's in reducing GAD symptoms, with randomized controlled studies showing it superior to in alleviating anxiety and comorbid depressive symptoms. For instance, in outpatient settings, buspirone at doses of 15-60 mg per day led to significant improvements in (HAM-A) scores compared to , with response rates around 54% versus 28%. These benefits are attributed to its selective action on serotonin 5-HT1A receptors, promoting anxiolysis without the rapid onset or risks associated with other agents. However, may vary, and some head-to-head trials indicate benzodiazepines like can provide faster symptom relief, though buspirone matches or approaches their effectiveness in longer-term use without impairing function. The recommended initial dosage for GAD is 7.5 mg orally twice daily (total 15 mg/day), which may be titrated upward by 5 mg every 2-3 days to a maintenance range of 15-30 mg/day divided into two or three doses, not exceeding 60 mg/day. Unlike benzodiazepines, buspirone exhibits a delayed onset, typically requiring 2-4 weeks of consistent use to achieve full therapeutic effects, making it unsuitable for acute anxiety but ideal for chronic management. Patients should take it with or without food, though should be avoided due to potential interactions affecting . In elderly patients or those with hepatic/renal impairment, lower starting doses and slower are advised to minimize risks.

Adjunctive and augmentation therapy

Buspirone is commonly employed as an augmentation strategy in the management of treatment-resistant (MDD), particularly when added to selective serotonin reuptake inhibitors (SSRIs) such as . In the Sequenced Treatment Alternatives to Relieve Depression () trial, a large-scale study involving over 2,800 patients, augmentation with buspirone (up to 60 mg/day) after initial SSRI failure resulted in a remission rate of approximately 30% on the Hamilton Depression Rating Scale, comparable to augmentation with sustained-release bupropion. This approach is thought to enhance serotonergic transmission via buspirone's partial agonism at 5-HT1A receptors, potentially addressing residual symptoms in partial responders. However, some analyses have noted higher rates of treatment-emergent side effects with buspirone compared to bupropion in this context. In patients with MDD and comorbid anxiety symptoms, adjunctive buspirone has demonstrated efficacy in alleviating anxiety without exacerbating depressive symptoms. A multicenter prospective in involving 161 patients found that adding buspirone (mean dose ~30 mg/day) to ongoing therapy significantly reduced scores by a mean of 9.8 points over 12 weeks, with improvements observed across varying baseline anxiety severities. This benefit appears independent of the primary class, supporting buspirone's role in targeting anxiety augmentation in mixed anxiety-depression presentations. Additionally, buspirone augmentation of in MDD has been associated with cognitive enhancements, including improvements in and domains, as measured by standardized neuropsychological tests. For obsessive-compulsive disorder (OCD), buspirone serves as an adjunctive agent in SSRI-refractory cases, leveraging its 5-HT1A agonism to potentiate serotonin inhibition. An of 11 patients with OCD who were partial responders to (up to 80 mg/day) showed that adding buspirone (up to 60 mg/day) led to at least a 25% reduction in Yale-Brown Obsessive Compulsive Scale scores in 9 participants after 8 weeks, with sustained benefits in most. Similar open-label findings have been reported with sertraline augmentation, though randomized controlled trials are limited, and buspirone is not considered first-line. Evidence for augmentation in (PTSD) or remains preliminary, with small open studies suggesting modest reductions in intrusive symptoms or avoidance behaviors when added to SSRIs, but lacking robust placebo-controlled support. Buspirone has also been investigated for mitigating SSRI-induced sexual dysfunction, a common reason for treatment nonadherence. In a randomized placebo-controlled trial of 117 depressed patients on SSRIs, adjunctive buspirone (20-60 mg/day) improved sexual function in 58% of participants after 4 weeks, compared to 30% on placebo, as assessed by the Rush Sexual Inventory. However, conflicting results from another double-blind study indicated no significant advantage over placebo for overall sexual dysfunction domains. Due to this mixed evidence, buspirone is occasionally used off-label for this purpose but is not universally recommended. Overall, while buspirone's augmentation role is most established in depression and OCD, its tolerability profile—lacking sedation or dependency risk—makes it a viable option in multimodal psychiatric regimens.

Other and off-label uses

Buspirone has been investigated off-label for the management of , particularly that induced by selective serotonin reuptake inhibitors (SSRIs), as an adjunctive strategy (see Adjunctive and augmentation therapy). In clinical practice, it is often added to SSRI regimens to alleviate symptoms such as reduced , , and delayed . A review of evidence indicates that buspirone at doses of 20-60 mg/day can lead to significant improvements in these symptoms, with response observed as early as one week in some patients, likely due to its partial agonism at 5-HT1A receptors counteracting SSRI effects. However, randomized controlled trials are limited, and its efficacy may vary, with some studies suggesting benefits primarily in patients with comorbid anxiety. In the treatment of (PTSD), buspirone is used off-label as an adjunctive agent to reduce core symptoms like hyperarousal and intrusive thoughts. An involving patients meeting DSM-III-R criteria for PTSD demonstrated significant symptom reduction with buspirone at 30-60 mg/day over four weeks, as measured by standardized scales. It may serve as a safer alternative to benzodiazepines due to its lower risk of dependence and sedation, though evidence remains preliminary, with calls for larger controlled trials to confirm efficacy. Buspirone has shown promise in off-label applications for substance use disorders, particularly with co-occurring anxiety. In a randomized trial, buspirone outperformed in reducing anxiety symptoms and decreasing alcohol consumption frequency and quantity among adults with alcohol use disorder. Conversely, evidence for is weaker; a -controlled study found no significant reduction in withdrawal symptoms, craving, or use with buspirone at 60 mg/day. Overall, its role appears more supportive in anxiety-driven substance use rather than as a primary treatment. Pediatric use of buspirone for anxiety disorders is off-label, given its approval only for adults with . Pilot studies in children aged 6-17 years suggest efficacy at doses of 5-30 mg/day for reducing anxiety symptoms, with a favorable safety profile lacking the dependence risks of benzodiazepines. Similarly, in autism spectrum disorder, a supports buspirone as a safe off-label option for co-occurring anxiety, based on small trials showing symptom improvement without significant adverse effects. These applications highlight its potential in vulnerable populations, though dosing requires careful and monitoring.

Safety considerations

Contraindications

Buspirone is contraindicated in individuals with a known to buspirone hydrochloride or any of its components, as this can precipitate severe allergic reactions including . Concomitant administration of buspirone with inhibitors (MAOIs), such as , , or tranylcypromine, is strictly prohibited due to the risk of resulting from elevated . This interaction arises from the potential for or pharmacodynamic synergism leading to acute hypertensive episodes. A minimum washout period of 14 days is required between discontinuing an MAOI and initiating buspirone therapy, or vice versa, to mitigate these risks. Buspirone is also contraindicated with reversible MAOIs, including and intravenous , owing to the heightened risk of and hypertensive events through similar mechanisms of serotonergic potentiation. Clinicians must review patient medication histories thoroughly to avoid these combinations, as no exists for the resulting complications.

Adverse effects

Buspirone is generally well-tolerated, with most adverse effects being mild, transient, and resolving with continued use or dose adjustment. In clinical trials, approximately 10% of patients discontinued therapy due to side effects, primarily (CNS) disturbances like or . Common adverse effects, occurring in 1% to 10% of patients, include (12% incidence versus 3% with ), (8% versus 5%), (6% versus 3%), nervousness (5% versus 1%), (3% versus <1%), and excitement (2% versus <1%). Other frequently reported effects encompass drowsiness, diarrhea, paresthesia, blurred vision, musculoskeletal pain, tremor, and sweating. These effects are often dose-related and diminish over time with gradual titration. Less common effects (also 1% to 10%) involve gastrointestinal issues such as sore throat and nasal congestion, dermatologic reactions like rash or diaphoresis, and CNS symptoms including abnormal dreams, ataxia, confusion, outbursts of anger, or numbness. Ophthalmic effects like blurred vision and otic issues such as tinnitus have been noted, alongside cardiovascular complaints like chest pain. Serious adverse effects are rare but include due to dopamine antagonism, (particularly with concurrent serotonergic agents), and QT interval prolongation in patients with preexisting cardiac conditions. Postmarketing reports have described somnambulism and isolated cases of serum enzyme elevations without jaundice, though hepatotoxicity is unlikely and no clinically apparent liver injury has been linked to buspirone. Allergic reactions, such as rash, hives, or swelling, and severe symptoms like uncontrollable shaking, fast heartbeat, or seizures warrant immediate medical attention. Buspirone exhibits minimal sexual side effects compared to other anxiolytics and may even alleviate SSRI-induced sexual dysfunction when used adjunctively. No evidence of abuse potential, dependence, or withdrawal symptoms has been reported.

Overdose

Buspirone overdose is characterized by low toxicity, with no reported fatalities attributed solely to the drug in clinical trials or post-marketing surveillance. In healthy volunteers administered doses up to 375 mg daily—substantially exceeding the therapeutic maximum of 60 mg—common symptoms included nausea, vomiting, dizziness, drowsiness, miosis, and gastric distress. Rarely, overdose may manifest with more severe effects such as movement disorders (e.g., dyskinesia or akathisia) or, in isolated cases, generalized tonic-clonic seizures occurring up to 36 hours post-ingestion. Complete recovery is typical following supportive care, though co-ingestion of other substances (e.g., alcohol or multiple drugs) can complicate outcomes and has been associated with fatal events where buspirone's role remains unconfirmed. Management of buspirone overdose focuses on symptomatic and supportive measures, as no specific antidote exists. Immediate gastric lavage is recommended for acute ingestions, followed by close monitoring of respiration, pulse, and blood pressure to ensure airway patency, breathing, and circulation. Seizures, if present, should be treated with , while movement disorders may resolve upon drug discontinuation or respond to anticholinergics like or . Dialysis is not established as effective. Patients should be evaluated for potential interactions with co-ingested agents, given buspirone's low abuse potential and minimal risk in isolation.

Drug interactions

Buspirone is primarily metabolized by the cytochrome P450 3A4 () enzyme, leading to potential interactions with drugs that inhibit or induce this pathway, which can significantly alter its plasma concentrations and therapeutic effects. Concomitant use with strong inhibitors may necessitate dose reductions to avoid excessive sedation or other adverse effects, while inducers may require dose increases to maintain efficacy. The most serious interactions involve monoamine oxidase inhibitors (MAOIs), such as isocarboxazid, phenelzine, and tranylcypromine, which are contraindicated due to reports of elevated blood pressure and the risk of serotonin syndrome when combined with buspirone. This combination should be avoided, with at least a 14-day washout period before or after buspirone therapy. Reversible MAOIs, including linezolid and intravenous methylene blue, also pose a high risk of serotonin syndrome and are not recommended. Strong CYP3A4 inhibitors like erythromycin, itraconazole, ketoconazole, and nefazodone can markedly increase buspirone exposure; for example, erythromycin elevates maximum concentration (Cmax) by about 5-fold and area under the curve (AUC) by 6-fold, while itraconazole increases Cmax by 13-fold and AUC by 19-fold. Grapefruit juice, another CYP3A4 inhibitor, raises buspirone Cmax by 4.3-fold and AUC by 9.2-fold, so large amounts should be avoided. Moderate inhibitors such as verapamil and diltiazem similarly increase levels (e.g., verapamil boosts AUC by 3.4-fold and diltiazem by 5.5-fold), often requiring initial low doses of buspirone (e.g., 2.5 mg once or twice daily). In contrast, CYP3A4 inducers like rifampin reduce buspirone bioavailability by 84-90%, potentially necessitating higher doses. Interactions with other psychotropic agents vary; for instance, co-administration with may increase CNS side effects, though no pharmacokinetic interaction occurs and clinical significance is unclear, and (a inhibitor) can increase buspirone levels up to 20-fold in Cmax and 50-fold in AUC. No significant pharmacokinetic interaction occurs with or , but caution is advised with other central nervous system depressants like , which may exacerbate sedation despite no potentiation of impairment. mildly increases buspirone Cmax by 40% but has minimal overall impact. Buspirone does not significantly displace highly protein-bound drugs like or , though one report noted prolonged prothrombin time with warfarin. Other notable interactions include St. John's wort, which may decrease buspirone levels via induction but increase the risk of serotonin syndrome, ginkgo, tizanidine, and rifampin, where dose adjustments or monitoring are recommended. Overall, prescribers should evaluate potential interactions, particularly with -modulating agents, and monitor patients closely when combining buspirone with other CNS-active drugs.

Pharmacology

Pharmacodynamics

Buspirone is classified as an azapirone anxiolytic and exerts its primary effects through interactions with serotonin and dopamine receptors in the central nervous system. It acts as a partial agonist at , with full agonist activity at presynaptic in the dorsal raphe nucleus and partial agonism at postsynaptic in regions such as the hippocampus and cortex. This dual action initially suppresses serotonin (5-HT) neuronal firing and release by stimulating presynaptic autoreceptors, leading to a temporary reduction in serotonergic transmission. Over time, chronic administration causes desensitization of these autoreceptors, resulting in enhanced postsynaptic 5-HT signaling, particularly in brain circuits involved in anxiety and fear processing, such as the amygdala. In addition to its serotonergic effects, buspirone demonstrates weak antagonism at dopamine D2 receptors, as well as at D3 and D4 subtypes, which may contribute to its modulation of dopaminergic activity without causing significant extrapyramidal side effects. It also shows partial agonist activity at alpha-1 adrenergic receptors and weak affinity for 5-HT2 receptors, though these interactions are considered secondary to its 5-HT1A effects. Unlike benzodiazepines, buspirone lacks affinity for gamma-aminobutyric acid (GABA) or benzodiazepine receptors, explaining its absence of sedative, muscle relaxant, or anticonvulsant properties, as well as no potential for dependence or withdrawal syndromes associated with GABAergic agents. The pharmacodynamic profile of buspirone accounts for its delayed onset of anxiolytic action, typically requiring 1 to 4 weeks of treatment for full therapeutic effects, attributed to the adaptive changes in 5-HT1A receptor sensitivity rather than immediate receptor occupancy. Its major metabolite, 1-(2-pyrimidinyl)piperazine (1-PP), exhibits dopamine D2 antagonist properties and may augment buspirone's overall effects, though the parent compound predominates in clinical activity. Preclinical studies, including microdialysis and receptor binding assays, support these mechanisms, highlighting buspirone's role in enhancing serotonergic tone without the broad CNS depression seen in traditional anxiolytics.

Pharmacokinetics

Buspirone is rapidly absorbed following oral administration, with peak plasma concentrations (Cmax) of 1–6 ng/mL achieved within 40–90 minutes after a single 20 mg dose. However, due to extensive first-pass in the liver and gut wall, its absolute oral is low, approximately 4–5%. Food intake can enhance by increasing the area under the curve () by about 84% and Cmax by 116%, although it may slightly delay absorption. The are linear over the typical therapeutic dose range of 10–40 mg daily, with no significant accumulation observed after repeated dosing at 10 mg/day for 9 days. Once absorbed, buspirone is widely distributed throughout the body, exhibiting a of approximately 5.3 L/kg. It is highly bound to plasma proteins, about 86–95%, primarily to and alpha-1-acid glycoprotein. Buspirone does not appear to displace other highly protein-bound drugs such as or from their binding sites, though it may displace . Metabolism occurs extensively in the liver, predominantly via the enzyme , which oxidizes buspirone to several hydroxylated and conjugated derivatives. A key is 1-(2-pyrimidinyl) (1-PP), which possesses about 25% of buspirone's pharmacological activity but reaches plasma concentrations roughly 40-fold higher than the parent drug after oral dosing. The elimination of unchanged buspirone is short, averaging 2–3 hours, while that of 1-PP is longer at about 6 hours. Excretion of buspirone and its metabolites is primarily renal and fecal, with 29–63% of a radiolabeled dose recovered in and 18–38% in within 24 hours, mostly as metabolites rather than unchanged . Systemic clearance is approximately 1.7 L/h/kg. In special populations, pharmacokinetics can vary significantly: hepatic impairment leads to a 13- to 15-fold increase in and a doubling of , while renal impairment ( clearance 10–70 mL/min/1.73 m²) results in a fourfold increase. No notable differences are observed based on age, gender, or between elderly and younger adults.

Chemistry

Chemical properties

Buspirone is a synthetic azaspirodecanedione derivative characterized by a central 8-azaspiro[4.5]decane-7,9-dione core, which is linked through a tetramethylene (butyl) chain to a ring substituted at the 4-position with a 2-pyrimidinyl group. This structure contributes to its classification as a non-benzodiazepine agent with a unique pharmacological profile distinct from traditional sedatives. The molecular formula of buspirone is C21H31N5O2, with a molecular weight of 385.5 g/mol. Its IUPAC name is 8-[4-[4-(2-pyrimidinyl)-1-piperazinyl]butyl]-8-azaspiro[4.5]decane-7,9-dione. The compound exists primarily as the but is commonly formulated as the salt for pharmaceutical use. Buspirone appears as a white to off-white crystalline solid. It has a of 105–107 °C, while the salt melts at 201.5–202.5 °C. The compound exhibits low in , approximately 0.59 g/L at 25 °C, reflecting its limited aqueous dissolution. It is more soluble in organic solvents such as , where reaches about 50 mg/mL. Key physicochemical parameters include an experimental (octanol-water partition coefficient) of 2.63, indicating moderate suitable for oral . The value for the most basic site (piperazine nitrogen) is 7.62, influencing its and behavior in physiological ranges. These properties support buspirone's and in biological systems without significant .
PropertyValue (Free Base)Source
Molecular FormulaC21H31N5O2
Molecular Weight385.5 g/mol
AppearanceWhite to off-white solidChemicalBook
105–107 °CChemicalBook
Water 0.59 g/L (25 °C)HMDB (ALOGPS)
Methanol 50 mg/mL
2.63 (experimental)
pKa (basic)7.62HMDB (ChemAxon)

Synthesis

Buspirone is typically synthesized via a three-step process starting from commercially available precursors. First, 1-(pyrimidin-2-yl) is alkylated with 4-chlorobutyronitrile in the presence of a base such as or triethylamine, often in a like or at elevated temperatures (around 80–100°C), to yield 4-[4-(pyrimidin-2-yl)piperazin-1-yl]butanenitrile. Second, the group is reduced to a primary through catalytic using under hydrogen pressure (typically 3–5 atm) in a such as or at ambient to mild temperatures (20–50°C), affording 4-[4-(pyrimidin-2-yl)piperazin-1-yl]butan-1-amine. In the final step, this amine is condensed with 3,3-tetramethyleneglutaric anhydride (derived from and via standard procedures) in refluxing or a similar high-boiling (around 115°C) for several hours, followed by from an alcohol-water mixture, to form the spirocyclic structure of buspirone. This route provides the compound in high yield (overall ~60–70%) and purity suitable for pharmaceutical use. Alternative synthetic approaches have been developed to improve efficiency or avoid certain reagents. For instance, a 2008 method involves de novo construction of the spiro imide core by condensing with methyl isocyanoacetate under , followed by to the diacetic acid, thermal cyclization with at 200°C to the glutarimide, and subsequent N- with the preformed 1-(4-bromobutyl)-4-(pyrimidin-2-yl) using a base in DMF. This sequence achieves buspirone in moderate yields (~40–50%) and highlights greener conditions for the step. More recent innovations include hydrogen borrowing for the using as the alkylating agent with an or catalyst at 150–180°C, reducing waste, and reductive cross-coupling of the with butanenitrile using reductants and under mild conditions (, 1 atm). These methods prioritize while maintaining comparable overall yields. Buspirone belongs to the azapirones, a chemical class of anxiolytics defined by a core 8-azaspiro[4.5]decane-7,9-dione structure substituted at the 8-position with a 4-(1-substituted piperazin-4-yl)butyl chain. In buspirone, the piperazine nitrogen bears a 2-pyrimidinyl group, conferring partial agonism at serotonin 5-HT1A receptors alongside weak antagonism at dopamine D2 receptors. Structural analogues of buspirone primarily vary the aryl substituent on the to alter receptor selectivity and while retaining the spirodione core and butyl linker. Gepirone, for instance, replaces the 2-pyrimidinyl with a 2-methoxyphenyl group, resulting in 5-HT1A (Ki ≈ 38 nM, compared to buspirone's ≈20 nM) and low D2 binding, which reduces potential extrapyramidal side effects. This modification supports gepirone's approval as an in 2023, with a of approximately 5 hours for the extended-release compared to buspirone's 2-3 hours. Ipsapirone incorporates a 2-(4-pyridyl)piperazine moiety, maintaining 5-HT1A partial but with faster onset in animal models of anxiety due to improved brain penetration. features a furo[2,3-c]pyridin-5-yl and is approved in for , exhibiting similar efficacy to buspirone in clinical trials (response rates ≈60-70%) but with a more favorable tolerability profile in some patients. Additional related compounds, such as perospirone (with a 3-chloro-2-fluorophenyl group and extended to an profile via 5-HT2A antagonism), enilospirone, and zalospirone, share the scaffold and 5-HT1A activity but remain investigational or regionally limited. These variations highlight structure-activity relationships where lipophilic aryl groups enhance 5-HT1A selectivity, distinguishing azapirones from benzodiazepines in lacking effects and abuse potential.

History

Discovery and development

Buspirone was first synthesized in 1968 by a team of researchers at & Company, a pharmaceutical firm focused on developing novel psychotropic agents. The compound, chemically designated as 8-[4-[4-(2-pyrimidinyl)-1-piperazinyl]butyl]-8-azaspiro[4.5]decane-7,9-dione, emerged from systematic exploration of azaspirone derivatives aimed at creating potent tranquilizers with reduced sedative and autonomic side effects compared to existing antipsychotics like . Inventors H. Wu and James W. Rayburn detailed its preparation through reactions involving spiro-substituted glutaric anhydrides or imides with N-(heteroarcyclic) derivatives, filing a on November 24, 1969, which was granted as U.S. Patent 3,717,634 on February 20, 1973, assigning rights to . Initially developed as an for conditions like , buspirone demonstrated psychotropic activity in preclinical models but proved ineffective in treating during early clinical evaluations. Researchers observed, however, that it lacked the extrapyramidal side effects common to D2 antagonists and instead exhibited properties without inducing , muscle relaxation, or dependence. This shift in focus was formalized in a 1980 patent (U.S. Patent 4,182,763), issued on January 8 to inventors including George P. Casten and John H. Weikel Jr., which claimed methods for its use in treating neurotic anxiety at doses of 10-100 mg/day, based on trials showing significant reductions in Anxiety Scale scores among patients with predominant anxiety symptoms. , by then a of Bristol-Myers Company, advanced these findings through controlled studies emphasizing its novel mechanism as a at serotonin 5-HT1A receptors. The drug's development culminated in its approval by the U.S. on September 29, 1986, for the management of under the brand name BuSpar, marking it as the first non-benzodiazepine with a distinct pharmacological profile. This milestone reflected over a decade of refinement, including pharmacokinetic studies confirming its rapid absorption and metabolite-dependent activity, and positioned buspirone as a safer alternative for long-term anxiety treatment. A comprehensive review by J.S. New in 1990 highlighted its innovative path from antipsychotic candidate to , underscoring the role of serendipitous observations in pharmaceutical innovation.

Regulatory history

Buspirone , marketed under the name BuSpar, was first approved by the U.S. (FDA) on September 29, 1986, under (NDA) 18-731, held by Bristol-Myers Squibb Company, for the management of anxiety disorders or the short-term relief of symptoms of anxiety. This approval marked buspirone as the first azapirone-class to receive FDA , distinguishing it from benzodiazepines due to its lack of , , or effects and low potential for abuse or dependence. Initially approved in 10 mg tablet form, additional tablet strengths of 15 mg and 30 mg were approved on April 22, 1996, under the same NDA. In December 2000, the FDA approved a supplemental (21-190) for a new capsule formulation of BuSpar at strengths of 5 mg, 7.5 mg, 10 mg, 15 mg, and 30 mg, expanding dosing options while maintaining the same indications. The original for buspirone expired in 2001, enabling the entry of generic versions and significantly increasing its accessibility and reducing costs for patients. Subsequent regulatory actions have focused on ensuring continued availability of generic formulations. In 2010, the FDA determined that BuSpar tablets (10 mg, 15 mg, and 30 mg) under NDA 18-731 had not been withdrawn from the market for reasons of safety or effectiveness, thereby permitting the approval of abbreviated new drug applications (ANDAs) referencing these strengths. A similar determination was made in June 2023 for BuSpar capsules (5 mg, 7.5 mg, and 10 mg) under NDA 21-190, confirming their ongoing market status and supporting generic competition. Internationally, buspirone has been approved in various countries since the late 1980s, often under national regulatory authorities rather than centralized () authorization, with generic formulations widely available by the early ; for example, in the , a marketing authorization for buspirone 5 mg tablets was granted in February 2001.

Society and culture

Names and formulations

Buspirone is the name for the buspirone , an medication primarily used to treat . In the United States, it was originally marketed under the brand name BuSpar by Bristol-Myers Squibb, but BuSpar was discontinued in 2010 due to the widespread availability of versions, not for safety or efficacy reasons. Other brand names in the have included Bucapsol and Vanspar, though these are less common. Internationally, buspirone is sold under various brand names, such as Ansial, Anxiron, Anxut, Bespar, Buscalm, Buspon, and Spamilan, depending on the country and manufacturer. Buspirone is available exclusively in oral tablet formulations, with no injectable, liquid, or extended-release versions approved for standard use. Common tablet strengths include 5 mg, 7.5 mg, 10 mg, 15 mg, and 30 mg of buspirone , often scored to facilitate dose division for (e.g., a 15 mg tablet can be bisected into two 7.5 mg doses). These tablets contain inactive ingredients such as , , and to aid in manufacturing and dissolution.

Availability and usage

Buspirone is available worldwide as a prescription-only medication for the management of anxiety disorders. In the United States, it is approved by the (FDA) and supplied in oral tablet form at strengths of 5 mg, 10 mg, 15 mg, and 30 mg, typically packaged in bottles containing 60 to 100 tablets depending on the dosage. Generic versions are widely accessible, with the brand name BuSpar no longer marketed since 2010, contributing to lower costs and broader availability through pharmacies and mail-order services. Internationally, buspirone is authorized in countries including , the , , and various European nations under regulatory bodies such as , the Medicines and Healthcare products Regulatory Agency (MHRA), and the (TGA), often in similar tablet formulations of 5 mg, 10 mg, and higher strengths. It is not classified as an essential medicine by the but remains a standard option in psychiatric formularies globally due to its generic status and established safety profile. Buspirone is not a in the United States but requires a prescription. varies internationally; for example, it is Schedule 4 (prescription only) in and Prescription Only Medicine (POM) in the .

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