Boryeong Buspar Tablets 15mg (Buspirone Hydrochloride)

Adult dose

Administer buspirone hydrochloride 5㎎ orally 3 times daily as the initial dose. 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㎎ daily in divided doses. The total daily dose must not exceed 60㎎. The dose may be adjusted appropriately according to age and symptoms.

This medication should not be administered to certain patients. For example, it should not be used in patients who have allergic reactions to this medication or in patients with severe liver and kidney damage. Additionally, patients with epilepsy, acute glaucoma, and severe myasthenia gravis should not take this medication. This medication contains lactose and should not be administered to patients with lactose intolerance or related genetic issues. Caution is necessary as various side effects may occur while taking this medication. Cardiac-related issues such as chest pain, fainting, blood pressure changes, and rarely heart disease may occur. Neurological and psychiatric symptoms including drowsiness, dizziness, insomnia, hallucinations, and suicidal thoughts may arise from central nervous system effects. Symptoms around the eyes and ears may include tinnitus, itching, and congestion, and eye pressure may increase in rare cases. Gastrointestinal symptoms such as abdominal bloating, changes in appetite, and nausea may occur, while urinary and reproductive systems may experience urination problems or menstrual irregularities. Muscle and joint pain, involuntary movements, respiratory issues, skin rashes, or swelling have also been reported. Liver function abnormalities or blood cell count changes may occur rarely, and in severe cases, a dangerous condition known as neuroleptic malignant syndrome may develop. This medication is not used as an antipsychotic, and its effects on the central nervous system are unpredictable, so caution should be exercised when driving or operating hazardous machinery. In particular, patients who have taken sedatives or sleeping pills for an extended period should taper off their existing medications before starting this treatment. This medication may interact with dopamine receptors and could cause restlessness or movement disorders in some patients. When taken with other medications or alcohol, interactions may occur, so it is essential to consult a doctor. Especially, it should not be taken with MAO inhibitors and it is advisable to avoid alcohol use. Women who are pregnant or breastfeeding should only take this medication if its safety has not been established, and it should be used under a doctor's guidance if absolutely necessary; it is preferable to avoid this medication while breastfeeding. The safety and effectiveness of this medication have not been confirmed in children under 18, so its use in this age group is not recommended. In cases of overdose, symptoms such as nausea, vomiting, dizziness, and drowsiness may occur, but no fatal cases have been reported. In the event of an overdose, gastric lavage and appropriate treatment based on symptoms are necessary. To use this medication safely, it is crucial to inform the doctor of any current medications or alcohol consumption, and consult with a doctor if pregnant or planning to become pregnant. Patients with a history of drug dependence or abuse require even more careful monitoring and evaluation when using this medication.

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

This medication is sensitive to light and should be stored in a container that does not let light in. It should also be stored at a temperature between 1 and 30 degrees Celsius to maintain its efficacy.

Appearance

White, uncoated, dual-sided, flat rectangular tablet

Package unit

30 tablets/bottle, 100 tablets/bottle