Medication info
Ronaqoo Tablets 4 mg (Blonanserin)

Ronaqoo Tablets 4 mg (Blonanserin)

Prescription medicationTabletOral
Ingredient · strength
Blonanserin›4mg / 1 tablet
Manufacturer / importer
Hanmi Pharmaceutical Co., Ltd.
Appearance
White round tablets
Packaging
30 tablets/bottle, 100 tablets/bottle
Approval status
Active

MFDS item code 201901253 · Approved 2019.02.27 · Insurance code 657203460

Summary

Main use
Treatment of schizophrenia
Who takes it
Adults
Adult dose
Adults: Administer 4 mg per dose twice daily after meals, increasing the dose gradually. The maintenance dose is 8~16 mg per day, divided into 2 doses taken after meals. As the absorption of this drug is readily affected by food, it must be taken after meals. Carefully monitor each patient and adjust the dose to the minimum required; do not exceed the maximum daily dose of 24 mg.

Ingredients

Manufacturer
Hanmi Pharmaceutical Co., Ltd.

Efficacy & effects

Treatment of schizophrenia

  • Schizophrenia
View approved original text

This medication is used to treat symptoms associated with schizophrenia. Schizophrenia is a complex disorder that includes psychotic symptoms, and this medication helps stabilize the patient's mental state and alleviate symptoms.

How to take

Adult dose

Adults: Administer 4 mg per dose twice daily after meals, increasing the dose gradually. The maintenance dose is 8~16 mg per day, divided into 2 doses taken after meals. As the absorption of this drug is readily affected by food, it must be taken after meals. Carefully monitor each patient and adjust the dose to the minimum required; do not exceed the maximum daily dose of 24 mg.

Precautions

Caution is required when using this drug in elderly patients with dementia, as it may increase mortality rates. In particular, patients at high risk of cerebrovascular disease should use this medication with care due to the possibility of stroke. There is a risk of venous thromboembolism, so it is essential to carefully check for thrombotic risk factors before and during the use of this medication and to take preventive measures. This medication should not be administered to patients in a comatose state or those taking central nervous system depressants, as well as patients on specific antifungals or HIV treatments. Patients with hypersensitivity to this medication or genetic issues such as lactose intolerance should also avoid its use. Caution is necessary for patients with a history of cardiovascular disease, Parkinson's disease, epilepsy, suicidal risk, liver impairment, and those with diabetes risk factors. It should be avoided during pregnancy or breastfeeding as its safety has not been established in these populations. This medication may cause side effects such as tremors, movement disorders, insomnia, drowsiness, and anxiety, and, although rare, may also lead to neuroleptic malignant syndrome, tardive dyskinesia, paralytic ileus, and antidiuretic hormone secretion abnormalities. Blood sugar levels may rise, so diabetic patients should monitor their blood sugar closely. If drowsiness or decreased concentration occurs while taking this medication, activities such as driving or operating hazardous machinery should be avoided, and medical advice should be sought if symptoms worsen. This medication is metabolized by the liver, so drug interactions may occur when taken with specific medications; therefore, it is essential to discuss concurrent medications with a physician or pharmacist. Additionally, this medication should be taken after meals, as its effectiveness may decrease when taken on an empty stomach. Elderly patients may be at higher risk for adverse reactions, so careful monitoring is needed. During pregnancy, it should be administered only based on a physician's judgment due to potential fetal impact, and it is recommended to discontinue use while breastfeeding.

Side effects

Tremors, decreased motor activity, excessive saliva secretion, Parkinson's syndrome, inability to sit still, insomnia, elevated prolactin, movement disorders, drowsiness, anxiety, restlessness, irritability, neuroleptic malignant syndrome, akinesia mutism, severe muscle rigidity, dysphagia, tachycardia, blood pressure fluctuations, sweating, altered consciousness, respiratory distress, circulatory collapse, dehydration, acute kidney injury, delayed movement disorder, involuntary muscle movements around the mouth, paralytic ileus, decreased appetite, nausea, vomiting, diarrhea, abdominal distension, lethargy, syndrome of inappropriate antidiuretic hormone secretion, hyponatremia, hypotonicity, urinary sodium overexcretion, high-frequency urination, convulsions, rhabdomyolysis, myalgia, feeling weak, elevated CK, elevated serum myoglobin, elevated urinary myoglobin, agranulocytosis, leukopenia, liver dysfunction, elevated AST, elevated ALT, elevated γ-GTP, elevated ALP, elevated bilirubin, hyperglycemia, diabetic ketoacidosis, diabetic coma, eosinophilia, drug reactions accompanied by systemic symptoms, rash, eczema, pruritus, hypotension, orthostatic hypotension, hypertension, ECG abnormalities, tachycardia, bradycardia, arrhythmia, ventricular ectopic beats, loss of ectopic beats, palpitations, decreased heart rate, symptoms of Parkinson's syndrome, muscle tone abnormalities, elevated AST, elevated ALT, elevated γ-GTP, elevated LDH, elevated ALP, elevated bilirubin, liver dysfunction, control disorders, blurred vision, constipation, decreased appetite, nausea, vomiting, increased appetite, diarrhea, upper abdominal pain, abdominal pain, gastrointestinal disorders, abdominal distension, cheilitis, elevated prolactin, menstrual irregularities, galactorrhea, ejaculation disorders, gynecomastia, erectile dysfunction, dysuria, urinary retention, incontinence, polyuria, insomnia, anxiety, restlessness, anger, drowsiness, dizziness, lightheadedness, dull headache, headache, excitement, tingling in hands and feet, suicide attempt, over-sedation, over-control, depression, hallucinations, auditory hallucinations, delusions, persecutory delusions, sleep disorders, abnormal behavior, hyperactivity, abnormal EEG, manic state, altered consciousness, emotional disturbances, speech disorders, talkativeness, tension, convulsions, leukocytosis, neutrophilia, leukopenia, lymphopenia, erythrocytosis, anemia, decreased red blood cells, decreased hemoglobin, decreased hematocrit, thrombocytosis, thrombocytopenia, atypical lymphocytes, general weakness, thirst, feeling weak, edema, water intoxication, hair loss, sweating, fever, weight gain, weight loss, chest pain, cough, next, facial edema, aspiration pneumonia, hypothermia, elevated CK, increased triglycerides, elevated serum cholesterol, increased serum insulin, increased serum phospholipids, elevated blood sugar, increased BUN, decreased total serum protein, increased serum potassium, decreased serum potassium, decreased serum sodium, positive urinary protein, positive urinary urobilin, positive urinary glucose, epidermal necrolysis, lethargy, thromboembolism, pulmonary embolism, deep vein thrombosis

Not everyone experiences these, and they can vary from person to person.

Storage

This medication should be stored in a tightly closed container to protect it from air and moisture, maintaining a storage temperature between 1 and 30 degrees Celsius. Storing it this way can help preserve the medication's effectiveness for a longer period.

Appearance and packaging

Appearance

White round tablets

Package unit

30 tablets/bottle, 100 tablets/bottle

Same-ingredient medicines

Even with the same ingredient, strength, dosage form and how it is taken can differ.

Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.

Questions about this medicine

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For anything that needs medical judgment, consult a doctor or pharmacist.

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This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.