Babron Tablet 10mg (Buspirone Hydrochloride)

Adult dose

Adults: The initial dose is 5㎎ of buspirone hydrochloride per dose, taken orally 3 times daily. If necessary, to achieve an adequate therapeutic response, it is preferable to increase the daily dose by 5㎎ at intervals of 2-3 days and administer 20-30㎎ per day in divided doses. The total daily dose should not exceed 60㎎. The dose may be adjusted as appropriate according to age and symptoms.

This medication should not be used in certain patients. For example, individuals who are allergic to this medication, those with severe liver or kidney impairment, patients with epilepsy, those with acute glaucoma, patients with myasthenia gravis, and individuals taking MAO inhibitors should not take this medication. Additionally, this medication contains lactose and should not be administered to patients with lactose intolerance or certain genetic disorders. Caution is necessary while taking this medication as various side effects may occur. It may affect the heart and blood vessels, potentially leading to chest pain, fainting, or blood pressure changes. In the central nervous system, drowsiness, dizziness, anxiety, hallucinations, and in severe cases, symptoms of psychosis may occur. Patients may also experience unusual symptoms in the eyes, ears, and throat, and rare endocrine side effects such as thyroid abnormalities or milk secretion have been reported. In the gastrointestinal tract, changes in appetite, abdominal bloating, or nausea may be observed, and side effects can occur in various body areas including the genitourinary system, musculoskeletal system, skin, liver, and blood. This medication is not definitively recognized as an antipsychotic and is not used for the treatment of mental disorders, thus patients should avoid driving or operating dangerous machinery while taking it. Furthermore, patients who have previously taken sedatives or sleeping pills for an extended period should taper off their existing medications slowly before changing to this medication, paying attention to withdrawal symptoms due to sudden discontinuation. This medication may affect dopamine receptors, leading to restlessness or movement disorders in some patients, so monitoring is necessary. When used with other psychiatric medications, there may be potential interactions, so caution is advised, particularly against concurrent use with MAO inhibitors due to the risk of increased blood pressure. It is also safer to avoid concurrent use with alcohol. Women who are pregnant or may become pregnant should carefully consider the risks and benefits of using this medication, and breastfeeding mothers should preferably avoid taking it. It is advisable not to use this medication in children under the age of 18 as its safety and efficacy have not been established. In case of overdose, symptoms may include nausea, vomiting, dizziness, and drowsiness; there is no specific antidote, so immediate medical treatment is necessary. Lastly, while taking this medication, patients must inform their doctor about any other medications they are currently taking or alcohol consumption and should consult their doctor if they are pregnant or breastfeeding. The risk of drug abuse cannot be completely ruled out, and patients with a history of substance abuse require particularly careful monitoring.

• Non-specific chest pain
• syncope
• hypertension
• hypotension
• cerebrovascular disease
• congestive heart failure
• myocardial infarction
• cardiomyopathy
• bradycardia
• sleep disturbances

This medication can be sensitive to air and moisture, so it must be stored in a tightly closed container. It is important to maintain room temperature between 1 degree and 30 degrees Celsius. This will help preserve the efficacy and safety of the medication for an extended period.

Appearance

White oval-shaped tablet

Package unit

30 tablets/bottle, 300 tablets/bottle