Pribacapsule 150 mg (Pregabalin)
Pregabalin 150mg
Hard capsule · Prescription medication
AhnGuk New Pharm Co., Ltd.
MFDS item code 201906644 · Approved 2019.09.23
This product's status changed to Expired on 2024.09.23. It may no longer be sold, so consult a doctor or pharmacist before taking it.
Improvement of peripheral and central neuropathic pain and fibromyalgia, adjunctive treatment for partial seizures in epilepsy
This medication is used in adults for the treatment of peripheral and central neuropathic pain. It is also used as an adjunct for partial seizures in epilepsy, applicable whether or not secondary generalized symptoms are present. Furthermore, it is effective in the treatment of fibromyalgia. In other words, this drug is used to improve neuropathic pain, partial seizures in epilepsy, and fibromyalgia.
This medication is administered orally without regard to meals, divided into two doses per day. 1. Neuropathic pain - Peripheral neuropathic pain: The starting dose is 150 mg per day, which may be increased to 300 mg per day within 3 to 7 days, and if necessary, can be further increased to a maximum of 600 mg per day at 7-day intervals. - Central neuropathic pain: The starting dose is 150 mg per day, which may be increased to 300 mg per day after 1 week.
Administration in children under 12 years of age and in adolescents aged 12 to 17 is not recommended due to insufficient safety and efficacy data.
This medication may increase the risk of suicidal thoughts or behaviors, so if any symptoms of depression or mood changes occur during treatment, patients should immediately inform their healthcare provider. Patients with allergies to any components of this medication or those with certain genetic issues such as lactose intolerance should not take it. Diabetic patients may experience weight gain from this medication, which may require dosage adjustment of blood sugar control medications. If symptoms of angioedema occur, such as swelling around the face or mouth, the use of this medication should be stopped immediately. Elderly patients should be cautious as the risk of dizziness or drowsiness may increase, and symptoms like loss of consciousness or confusion may occur. Some patients may temporarily experience blurred vision or other visual changes, and these symptoms may improve upon discontinuation of the medication. Abruptly stopping this medication may lead to withdrawal symptoms such as insomnia, headache, nausea, and anxiety, so the dosage should be tapered gradually with medical consultation. Patients with a history of substance abuse may have an increased risk of misuse of this medication, so special caution is advised during use. Patients with decreased kidney function may require dose adjustments for this medication. Patients with heart conditions should consult their doctor before taking this medication and should use it cautiously if they have severe heart failure. Using this medication in conjunction with opioid analgesics may increase the risk of central nervous system depression, so strict adherence to the prescriber's instructions is necessary. In patients with respiratory or neurological diseases or those who are elderly, the risk of severe respiratory depression may necessitate dose adjustments. This medication is not recommended for pregnant women in early pregnancy due to the risk of congenital defects in the fetus, and women of childbearing potential should use effective contraceptive methods. Breastfeeding women should consult their healthcare provider regarding the use of this medication, as it can be transmitted in breast milk. This medication can cause dizziness and drowsiness, so patients should confirm their conditions before driving or operating machinery. Rarely, serious allergic reactions may occur on the skin; if symptoms like rash, swelling, or shortness of breath appear, the medication should be stopped immediately and a healthcare provider notified. In case of overdose, symptoms like drowsiness, confusion, or depression may appear, and treatments such as hemodialysis may be required if necessary. This medication should be kept out of reach of children and it is advisable to avoid transferring it to other containers.
Hives, severe swelling (angioedema), tightness in the chest, difficulty breathing, cold sweat, pallor, severe rash accompanied by high fever, blisters, skin peeling, pain in mouth/eye mucous membranes, shortness of breath or difficulty breathing, asthma attack, respiratory abnormalities accompanied by cough and fever, yellowing of skin or eyes (jaundice), severe lethargy, sudden and very severe headache, thunderclap headache, seizures, confusion of consciousness, visual disturbances, paralysis, urination
Not everyone experiences these, and they can vary from person to person.
The medication should be stored in a tightly closed container to prevent exposure to air and moisture. It is important to maintain storage temperatures between 15 to 30 degrees Celsius to safely preserve its efficacy.
A white hard capsule containing a white powder that is white or light yellow in color
30 capsules/bottle, 60 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.