Tiserin Tablet 25 mg (Levomepromazine Maleate)

Adult dose

The therapeutic dose of this medicine should be adjusted according to the patient's clinical condition, and the minimum effective dose should be administered whenever possible. Psychosis: The initial dose is 25∼50 mg of levomepromazine per day, administered orally in 2∼4 divided doses, and may be increased to the maximum daily dose of 150∼250 mg. Once symptoms improve, administer a maintenance dose appropriate for the patient's condition. Relief of neurotic anxiety, aggression, and agitation, and pain: The initial dose is 6∼25 mg of this medicine per day, administered in 2∼4 divided doses, and may be increased to 75∼100 mg. Once symptoms improve, administer a maintenance dose appropriate for the patient's condition. Sleep disorders: Administer 10∼25 mg of this medicine once daily at bedtime. Adjust the dose as appropriate according to symptoms.

This medication should be used with caution as it may increase mortality in certain patients, such as elderly patients with dementia. Patients with risk factors for stroke should be especially careful due to potential increased risk of cerebrovascular disease. Venous thrombosis risk factors must be verified and preventative measures taken before and during the use of this drug as it may increase the risk of thromboembolism. Patients with allergies to this medication or similar drugs, those with liver, kidney, or blood-related diseases, and pregnant or nursing women should not use this drug. Patients with severe hypotension, coma, certain neurological disorders, or those taking antihypertensives or specific medications should not be treated with this drug. Caution should be exercised in patients with atherosclerosis, heart disease, asthma, lung disease, the elderly, those in hot environments, or those with seizure disorders such as epilepsy. This medication can cause various neurological adverse reactions such as drowsiness, dizziness, insomnia, and seizures, as well as dry mouth, constipation, hypotension, and heart problems. During treatment, regular monitoring of blood pressure, liver function, blood tests, and electrocardiograms is necessary to check for abnormalities. Drowsiness or decreased concentration may occur after taking this drug; therefore, it is advisable to avoid driving or operating hazardous machinery. Taking this medication with alcohol can exacerbate side effects; therefore, it should never be taken together. Symptoms of blood abnormalities such as leukopenia may occur; if symptoms arise, inform medical personnel immediately. This drug can affect cardiac electrical activity, so patients with heart disease or a family history of heart disease should be cautious. Serious side effects such as tardive dyskinesia or neuroleptic malignant syndrome may occur; if symptoms appear, discontinue use immediately and consult medical personnel. Women who are pregnant or may become pregnant should not use this drug, and nursing mothers should also avoid it. Pediatric patients may easily exhibit extrapyramidal symptoms, so this medication should not be used in children. Elderly patients are more sensitive to side effects, so it is advisable to start with a low dose and gradually increase it while carefully monitoring their condition. In the case of overdose, severe motor disturbances or coma may occur, necessitating immediate medical treatment.

• Drowsiness
• dizziness
• confusion
• insomnia
• headache
• anxiety
• excitement
• easily irritated
• convulsion
• dry mouth

This medication may be sensitive to air or humidity and should be stored in a tightly sealed container. Additionally, to maintain the efficacy of the drug, it is recommended to store it at room temperature, between 1°C and 30°C.

Appearance

White film-coated tablet

Package unit

30 tablets/bottle, 500 tablets/bottle