Tiapride
Atypical antipsychotic medication
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Tiapride is an atypical antipsychotic medication primarily used in the treatment of psychosis, dyskinesia, and alcohol withdrawal syndrome. It is known for its selective action on the dopamine D2 and D3 receptors, which contributes to its therapeutic effects.
Pharmacology[edit | edit source]
Tiapride is classified as a benzamide derivative and functions as a selective dopamine antagonist. Its primary mechanism of action involves blocking the dopamine D2 and D3 receptors, which are implicated in the regulation of mood and movement. This selective antagonism helps alleviate symptoms of psychosis and movement disorders without the extensive side effects associated with typical antipsychotics.
Clinical Uses[edit | edit source]
Tiapride is utilized in various clinical settings, including:
- Psychosis: It is effective in managing symptoms of psychosis, particularly in patients who are sensitive to the side effects of other antipsychotic medications.
- Dyskinesia: Tiapride is used to treat movement disorders such as tardive dyskinesia and Huntington's disease.
- Alcohol Withdrawal Syndrome: It helps in managing symptoms associated with alcohol withdrawal, providing a calming effect without significant sedation.
Side Effects[edit | edit source]
While tiapride is generally well-tolerated, it can cause some side effects, including:
Dosage and Administration[edit | edit source]
Tiapride is administered orally, and the dosage varies depending on the condition being treated. It is important to adjust the dosage based on the patient's response and tolerance to the medication.
Chemical Properties[edit | edit source]
Tiapride is a benzamide derivative with a chemical structure that allows it to selectively bind to dopamine receptors. Its molecular formula is C15H24N2O4S, and it has a molecular weight of 328.43 g/mol.
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Contributors: Prab R. Tumpati, MD
