Viewing nowDivalproez Sodium Extended-Release Tablets 500 mg (Divalproex Sodium)
Divalproex Sodium 538.1mg
Tablet · Prescription medication
Korea Pharma Co., Ltd.

MFDS item code 202303094 · Approved 2023.11.08 · Insurance code 653006910
(Seizures) Treatment of complex partial seizures and absence seizures, (Migraine) Prevention, (Mental illness) Treatment of mania effectiveness
This drug is used as monotherapy or adjunctive therapy for various types of seizures in children aged 10 years and older and adults, such as complex partial seizures and absence seizures. It also helps in the prevention of migraines in adults. However, its effectiveness for the acute treatment of migraines has not been established. Additionally, it is used to treat mania in adults, particularly for acute mania or mixed episodes associated with bipolar disorder, with or without psychotic features. However, if the treatment of mania extends beyond 3 weeks, the patient's condition must be continuously reevaluated. Overall, this drug is effectively used for the prevention of seizures and migraines, as well as the treatment of mania.
This drug is administered once daily in a form that must be swallowed whole without breaking or chewing the tablet. 1. Treatment of seizures - Monotherapy for complex partial seizures: The initial dose is 10-15 mg per kg of body weight per day, and the dose is increased by 5-10 mg per kg of body weight weekly until an optimal clinical response is achieved. Doses exceeding 60 mg per kg of body weight per day are not recommended. - Simple and mixed absence seizures: The initial dose is
This drug can be administered to children aged 10 years and older. 1. Treatment of seizures - Monotherapy for complex partial seizures: The initial dose is 10-15 mg per kg of body weight per day, and the dose is increased by 5-10 mg per kg of body weight weekly until optimal clinical response is achieved.
This drug should not be administered to pregnant women except in special cases. Women of childbearing age must strictly adhere to a pregnancy prevention program, and if not, this drug should not be used. The effectiveness of this drug may be reduced when used with estrogen-containing hormonal contraceptives; therefore, the patient's condition should be carefully monitored at the initiation and termination of therapy. This drug may increase the risk of suicidal thoughts or behavior; thus, mood changes or unusual behavioral signs should be closely monitored during treatment. Because serious liver damage may occur, this drug should be used cautiously, especially in young children or patients with compromised liver function, and liver function tests should be performed regularly during the first 6 months of treatment. If symptoms of pancreatitis appear, such as abdominal pain, nausea, vomiting, or loss of appetite, medical attention should be sought immediately, and the drug should be discontinued if pancreatitis is diagnosed. Patients with urea cycle disorders must confirm the presence of such disorders before taking this drug, as hyperammonemia-related encephalopathy may occur. Elderly patients may experience more pronounced sedation or dehydration symptoms, so the dosage should be increased slowly and their condition should be closely monitored. Thrombocytopenia may occur, thus regular blood tests to check platelet levels before and during treatment are necessary, and any bleeding symptoms should be reported to medical personnel immediately. This drug should be avoided in combination with certain antibiotics (carbapenems) as it may decrease its blood concentration, leading to diminished therapeutic effect. Women of childbearing age must use an effective method of contraception during treatment and consult medical personnel immediately if pregnancy is planned or confirmed. Drowsiness or dizziness may occur during treatment; therefore, it is advisable to avoid driving or operating dangerous machinery. Regular testing of liver function, blood counts, and pancreatic function should be conducted, and if any abnormal symptoms arise, immediate consultation with a physician is recommended. Abruptly discontinuing the drug may worsen symptoms; therefore, when discontinuing, it must be tapered off according to medical personnel's instructions.
Hives, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, pallor, severe rash with fever, blistering, skin peeling, pain in mucous membranes of mouth/eyes, shortness of breath or difficulty breathing, asthma attack, respiratory abnormalities accompanied by cough + fever, yellowing of skin or eyes (jaundice), extreme lethargy, sudden and severe headache, thunderclap headache, seizures, confusion, visual disturbances, paralysis, urine
Not everyone experiences these, and they can vary from person to person.
This drug should be stored in a tightly sealed container to prevent air or moisture from entering. The storage temperature should be maintained between 1 and 30 degrees Celsius at room temperature.
Gray oval-shaped extended-release coated tablets
30 tablets/bottle, 100 tablets/bottle
Even with the same ingredient, strength, dosage form and how it is taken can differ.
Viewing nowDivalproex Sodium 538.1mg
Tablet · Prescription medication
Korea Pharma Co., Ltd.

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Hard capsule · Prescription medication
Abbott Korea LLC

Divalproex Sodium 538.1mg
Tablet · Prescription medication
Abbott Korea, Co., Ltd.

Divalproex Sodium 269.1mg
Tablet · Prescription medication
Abbott Korea Co., Ltd.

Divalproex Sodium 269.05mg
Tablet · Prescription medication
Korea Pharma Co., Ltd.
Divalproex Sodium 538.12mg
Tablet · Prescription medication
Mirae Bio Pharmaceutical Co., Ltd.
Divalproex Sodium 269.06mg
Tablet · Prescription medication
Mirebiopharma Co., Ltd.
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.
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For anything that needs medical judgment, consult a doctor or pharmacist.
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.