Viewing nowPregabalin Capsule 150 mg (Pregabalin)
Pregabalin 150mg
Hard capsule · Prescription medication
Myeongin Pharmaceutical Co., Ltd.

MFDS item code 201109029 · Notified 2011.10.24 · Insurance code 651903590
Relief of peripheral and central neuropathic pain, control of epilepsy (partial seizures), improvement of fibromyalgia
This medication is used to treat peripheral and central neuropathic pain in adults. It is also used as an adjunct therapy in patients with epilepsy who have partial seizures, regardless of whether they have secondary generalization. Additionally, it is effective in treating chronic pain syndromes such as fibromyalgia. In summary, this drug is used in the management of neuropathic pain, as an adjunct treatment for epileptic seizures, and to improve symptoms of fibromyalgia.
The total daily dosage of this medication is administered orally in two divided doses, regardless of food intake. 1. Neuropathic Pain - Peripheral Neuropathic Pain: Starting dosage of 150 mg per day, can be increased to 300 mg per day after 3 to 7 days, with a maximum dosage of up to 600 mg per day. - Central Neuropathic Pain: Starting dosage of 150 mg per day, can be increased to 300 mg per day after one week, after which
Use in children under 12 years and adolescents aged 12-17 is not recommended due to insufficient safety and efficacy data.
This drug may increase the risk of suicidal thoughts or behavior, so if depression or mood changes occur during treatment, consult a doctor immediately. Patients who are allergic to the components of this drug or have specific genetic metabolic disorders should not take it. Diabetic patients should be aware that dosage adjustments may be needed for blood sugar control due to weight gain. If severe allergic reactions such as angioedema occur, discontinue use immediately and inform healthcare personnel. Elderly patients should exercise caution at the beginning of treatment due to the risk of falls from dizziness or drowsiness. Blurry vision or changes in eyesight may occur, and if these symptoms appear, consult a doctor. Abrupt discontinuation of this medication may cause withdrawal symptoms such as insomnia, headache, and anxiety, so the dosage should be gradually adjusted according to the doctor's instructions. Patients with a history of drug abuse may have a higher risk of abusing this medication, so caution is needed during use. Patients with heart or kidney diseases should consult healthcare personnel before taking this drug, especially heart failure patients require careful administration. Caution is necessary when taking this medication in combination with opioid analgesics as it may increase central nervous system depressant effects. Patients with respiratory or neurological disorders, kidney impairment, and the elderly may need dosage adjustments due to the risk of severe respiratory depression. During early pregnancy, there may be a risk of congenital malformation in the fetus, so it is recommended that pregnant women avoid this medication, and women of childbearing age should use effective contraception. Breastfeeding women should consider stopping breastfeeding or discontinuing this medication as it can be passed into breast milk. It is safer to avoid hazardous activities such as driving or operating machinery until dizziness or drowsiness resolves after taking this medication. Severe skin reactions may occur, so if symptoms such as rash, redness, or blisters appear, discontinue use immediately and inform healthcare personnel. Overdose may present symptoms such as drowsiness, confusion, and depression; treatment such as dialysis may be required if necessary. Keep out of reach of children and do not transfer to another container for safety.
Hives, severe swelling, angioedema, chest tightness, difficulty breathing, sweating, pallor, severe rash with fever, blisters, skin peeling, oral/ocular mucosal pain, severe skin abnormal reactions, asthma attacks, respiratory issues accompanied by cough and fever, yellowing of the skin or eyes, extreme lethargy, liver abnormalities, sudden and severe headaches, thunderclap headache, seizures, altered consciousness, vision abnormalities, paralysis, severe complications
Not everyone experiences these, and they can vary from person to person.
This medication may be sensitive to air or moisture, so it should be stored in a sealed container. It is best to maintain the storage temperature between 15 to 30 degrees Celsius. Proper storage can help sustain the effectiveness of the medication over time.
White or light yellow powder contained in a white hard capsule with a white upper and lower part
30 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.