Neurobalin Capsule 300 Milligrams (Pregabalin)
Pregabalin 300mg
Hard capsule · Prescription medication
White Life Sciences Co., Ltd.
MFDS item code 202009425 · Approved 2020.12.31
This product's status changed to Expired on 2025.12.31. It may no longer be sold, so consult a doctor or pharmacist before taking it.
Treatment of peripheral and central neuropathic pain, adjunct for partial seizures, improvement of fibromyalgia.
This medication is used to relieve peripheral and central neuropathic pain in adults. It is also utilized as an adjunct for partial seizures with or without secondary generalized symptoms in epilepsy patients. Additionally, it is effective in alleviating pain caused by fibromyalgia. It is widely used for the treatment of various nerve and muscle-related symptoms.
This medication is to be taken orally in divided doses twice a day, regardless of food. 1. Neuropathic pain - Peripheral neuropathic pain: Starting dose of 150mg once a day, can be increased to 300mg once a day after 3-7 days, and subsequently can be increased to a maximum of 600mg at intervals of 7 days. - Central neuropathic pain: Starting dose of 150mg once a day, can be increased to 300mg once a day after 1 week, with further adjustments as needed.
Administration is not recommended for children under 12 years of age and adolescents aged 12 to 17 due to insufficient safety and efficacy data.
This medication contains an anticonvulsant component, and while taking it, there may be mental changes such as suicidal thoughts, suicidal behavior, or depression, which should be closely monitored for any changes in symptoms. Patients allergic to pregabalin or any components of this medication, as well as those with certain genetic lactose intolerance, should not take this medication. Diabetic patients may require adjustment of blood sugar control medication dosage due to weight gain, and if symptoms of edema appear, consumption should be stopped immediately. Elderly patients should be cautious as dizziness or drowsiness may increase with this medication, and one should be careful until accustomed to its effects. This medication may cause transient blurred vision or changes in eyesight, and consultation with a doctor is necessary if symptoms appear. Abrupt cessation may result in withdrawal symptoms such as insomnia, headache, nausea, and anxiety; therefore, dosage should be gradually adjusted according to a doctor's instructions. Patients with a history of substance abuse should take this medication carefully due to the risk of misuse or abuse, and signs of drug dependence should be closely monitored. Patients with impaired kidney function may require dose adjustments, and those with heart disease should use caution while taking the medication. Co-administration with opioid analgesics may increase the risk of central nervous system depression; therefore, caution is advised, particularly in patients with respiratory disease or kidney impairment, as there is a risk of severe respiratory depression necessitating dosage adjustments. In early pregnancy, there may be a risk of congenital malformations to the fetus, so pregnant women should not take this medication unless in special circumstances, and women of childbearing age should utilize effective contraceptive methods. Breastfeeding women should consult with a doctor about stopping breastfeeding or discontinuing the medication, as this medication can pass into breast milk and affect the baby. Before driving or operating dangerous machinery, it is necessary to verify whether this medication causes dizziness or drowsiness. If severe rash, swelling, or difficulty breathing occurs while taking this medication, one should stop taking it immediately and inform healthcare personnel. In case of overdose, symptoms may include drowsiness, confusion, depression, seizures, and immediate medical treatment should be sought, and blood dialysis may be performed if necessary. Children and the elderly should keep this medication in a safe place out of reach. This medication has few drug interactions; however, caution is warranted when used in conjunction with central nervous system depressants as effects may be enhanced.
Hives, severe swelling (edema), facial, oral and upper airway swelling, chest tightness, difficulty breathing, cold sweat, pallor, severe rash with high fever, blisters, skin peeling, mucosal pain in mouth/eyes, severe skin reactions, difficulty breathing or breathlessness, asthma attacks, respiratory issues accompanied by cough and fever, jaundice (yellowing of skin or eyes), extreme and sudden headache, confusion.
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a tightly sealed container to prevent exposure to air or moisture. Additionally, it is important to store it at a cool temperature between 15 degrees and 30 degrees Celsius to maintain its efficacy.
A hard capsule with a reddish-brown upper part and white lower part containing a white powder that is white or light yellow.
30 capsules/bottle, 100 capsules/bottle
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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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.