Viewing nowHyundai Pregabalin Tablet 150mg
Pregabalin 150mg
Tablet · Prescription medication
Hyundai Pharmaceutical Co., Ltd.

MFDS item code 201800512 · Approved 2018.01.29 · Insurance code 642004180
Treatment of peripheral and central neuropathic pain, adjunctive therapy for partial seizures in epilepsy, improvement of fibromyalgia
This medication is used to alleviate peripheral and central neuropathic pain in adults. It is also utilized as an adjunctive therapy for partial seizures in patients with epilepsy to help control symptoms. Additionally, it effectively aids in the treatment of pain in patients with fibromyalgia. Collectively, this drug is used for the treatment of neuropathic pain, epilepsy, and fibromyalgia.
This medication is taken orally twice daily without regard to meals, with the total daily dose divided into two doses. 1. Neuropathic Pain - Peripheral Neuropathic Pain: The initiation dose is 150 mg once daily, and the dose may be increased to 300 mg once daily after 3 to 7 days. If necessary, it can be increased to a maximum of 600 mg at 7-day intervals thereafter. - Central Neuropathic Pain: The initial dose is 150 mg once daily, and 1
Administration is not recommended for children under 12 years and adolescents aged 12 to 17 due to insufficient safety and efficacy data.
This medication is an anticonvulsant, and during treatment, suicidal thoughts, suicidal behaviors, or symptoms of depression may occur or worsen, so both patients and caregivers should closely monitor for these changes. This medication must not be taken by anyone allergic to pregabalin or any of its components. Diabetic patients may experience weight gain while taking this medication, which may require adjustments to their blood sugar control medications. If swelling occurs in the face, mouth, or neck while taking this medication, it should be discontinued immediately and medical consultation sought. Elderly patients may experience symptoms such as dizziness, drowsiness, loss of consciousness, and confusion more frequently when taking this medication, so special caution is required at the start of treatment. This medication may cause blurred vision or changes in eyesight; any symptoms should be discussed with a healthcare professional. Caution is necessary when switching from another anticonvulsant medication to this medication as monotherapy. Abruptly stopping this medication may lead to withdrawal symptoms such as insomnia, headaches, nausea, anxiety, depression, and suicidal thoughts, thus it should be tapered off gradually according to a healthcare professional's instructions. Patients with a history of substance abuse are at higher risk of drug dependence or abuse when taking this medication, so caution is advised. Patients with reduced kidney function should have their doses adjusted, and those with heart failure should use caution as well. When taken with opioid analgesics, there is an increased risk of central nervous system depression; therefore, caution should be exercised. This medication can cause respiratory depression, and special care should be taken in patients with respiratory disorders, kidney issues, and the elderly. In the early stages of pregnancy, there may be a risk of congenital malformations in the fetus, so pregnant women should avoid taking this medication, and women of childbearing age should use effective contraception. Nursing mothers should consider that this medication is excreted in breast milk, thus it is recommended to discontinue nursing or the medication. This medication may cause dizziness and drowsiness, so symptoms should be monitored before performing tasks that require alertness, such as driving or operating hazardous machinery. Rarely, a severe allergic reaction or severe skin disorders may occur; if any skin abnormalities appear, the medication should be discontinued immediately. In the event of overdose, symptoms such as altered consciousness, depression, or seizures may occur; emergency measures such as hemodialysis may be necessary if needed. This medication should be kept out of reach of children and should not be transferred to other containers for safety reasons.
Hives, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, paleness, severe rash with high fever, blisters, peeling skin, mouth/eye mucosal pain, shortness of breath or difficulty breathing, asthma attacks, respiratory abnormalities with cough and fever, yellowing of skin or eyes (jaundice), severe lethargy, sudden and severe headache, thunderclap headache, seizures, confusion, visual disturbances, paralysis, urination
Not everyone experiences these, and they can vary from person to person.
This medication must be stored in a tightly sealed container to protect it from air and moisture exposure. It is advisable to maintain a storage temperature between 1 and 30 degrees Celsius at room temperature.
White or pale yellow round tablet
30 tablets/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.