Viewing nowSamsung Pregabalin Capsule 150mg
Pregabalin 150mg
Hard capsule · Prescription medication
Samsung Pharmaceutical Co., Ltd.

MFDS item code 201603280 · Approved 2016.06.08 · Insurance code 642306770
Treatment of peripheral and central neuropathic pain, adjunctive treatment of partial seizures in epilepsy, relief of fibromyalgia
This medication is used for the treatment of peripheral and central neuropathic pain in adults. It is also effective as an adjunct for partial seizures in epilepsy patients, whether or not they have secondary generalized symptoms. Additionally, it is used to improve symptoms of fibromyalgia. In summary, it is used for the treatment of neuropathic pain, partial seizures of epilepsy, and fibromyalgia.
This medication is taken orally, divided into two doses per day without regard to food. 1. Neuropathic Pain 1) Peripheral Neuropathic Pain - Initial dose: 150 mg per day - May increase to 300 mg per day within 3 to 7 days - May further increase to a maximum of 600 mg at intervals of 7 days if necessary 2) Central Neuropathic Pain - Initial dose: 150 mg per day - After one week, increase to 300 mg per day
Safety and efficacy data for children under the age of 12 and adolescents aged 12 to 17 are insufficient, so administration is not recommended.
This medication can increase the risk of suicidal thoughts or actions, so if depression or mood changes occur during treatment, it is essential to inform a healthcare professional. This medication should not be administered to patients with hypersensitivity to this drug or those with genetic problems such as lactose intolerance. Diabetic patients may need to adjust their blood glucose control medications due to weight gain. If symptoms of angioedema, such as swelling of the face or around the mouth, occur, the medication should be discontinued immediately. Elderly patients are at higher risk of accidents such as falls due to side effects like dizziness or drowsiness and should be cautious. Blurred vision or changes in vision may occur, and these symptoms can improve upon discontinuation of the medication. Abrupt cessation of the medication may lead to withdrawal symptoms such as insomnia, headache, and anxiety, so it should be discussed with a healthcare provider. Patients with a history of substance abuse have a higher risk of misuse or dependence on this medication, so caution is advised. Patients with impaired kidney function may require dosage adjustments. Patients with heart disease should be cautious as there may be an increased risk of heart failure when taking this medication. Caution should be exercised since central nervous system depressant effects may occur when taken with opioid analgesics. Patients with compromised respiratory function or elderly patients may face a significant risk of severe respiratory depression, and they should consult their healthcare provider. During early pregnancy, there is a risk of fetal malformations, so women who are pregnant or planning to become pregnant must consult their healthcare provider and use effective contraception. Nursing mothers should discuss with their healthcare provider whether to discontinue breastfeeding, as this medication can be passed through breast milk and may affect the infant. Dizziness or drowsiness may occur while taking this medication, so it is advisable to avoid dangerous activities such as driving or operating machinery. Severe skin reactions may rarely occur, so if any skin abnormalities appear, discontinue the medication and inform a healthcare professional immediately. In cases of overdose, symptoms such as confusion, drowsiness, and seizures may occur, and emergency treatment, including dialysis, may be necessary. This medication should be kept out of reach of children, and it should not be transferred to other containers for safety purposes.
Hives, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, pallor, angioedema, facial swelling, facial flushing, anaphylaxis-like symptoms, severe rash with fever, blisters, skin peeling, mucosal pain in the mouth/eyes, Stevens-Johnson syndrome, toxic epidermal necrolysis, severe allergic reactions, severe skin reactions, shortness of breath or difficulty breathing
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a tightly closed container to prevent air or moisture ingress, and it is best kept at room temperature between 15 and 30 degrees Celsius. Maintaining appropriate storage temperatures will help preserve the medication's effectiveness for a longer duration.
A white to pale yellow powder contained in a white hard capsule with a white upper part and a white 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.