Viewing nowLyrica Capsule 150 mg (Pregabalin)
Pregabalin 150mg
Hard capsule · Prescription medication
Viatris Korea Co., Ltd.

MFDS item code 200511058 · Approved 2005.06.14 · Insurance code 073400210
Treatment of peripheral and central neuropathic pain, adjunctive therapy for partial seizures in epilepsy, improvement of fibromyalgia
This medication is used to treat peripheral and central neuropathic pain in adults. It is also used as an adjunctive treatment for partial seizures in patients with epilepsy, whether or not they are accompanied by secondary general symptoms. Additionally, it is effective in the treatment of fibromyalgia. It is used to improve multiple nerve-related disorders and pain.
The total daily dosage of this medication should be divided into two doses taken orally with or without food. 1. Neuropathic Pain 1) Peripheral Neuropathic Pain - Starting dose of 150 mg per day - Can increase to 300 mg per day after 3 to 7 days - After that, can be increased to a maximum of 600 mg per day at intervals of 7 days 2) Central Neuropathic Pain - Starting dose
This medication may increase the risk of suicidal thoughts or behaviors, so if there are changes in mood or behavior during treatment, healthcare providers should be notified immediately. Individuals with allergies to any of the ingredients of this medication or those with genetic conditions such as galactose intolerance, lactase deficiency, and glucose-galactose malabsorption should not take this medication. Patients with diabetes may experience weight gain while taking this medication, necessitating adjustments in their blood sugar controlling medications. If severe allergic reactions such as angioedema occur, the medication should be discontinued immediately. Elderly patients may experience symptoms such as dizziness, drowsiness, loss of consciousness, and confusion while taking this medication and should exercise caution. When such symptoms arise, they should avoid driving or operating dangerous machinery. Temporary blurring or changes in vision may occur, and if symptoms are severe, it may be necessary to discontinue the medication. Suddenly stopping this medication may lead to withdrawal symptoms such as insomnia, headache, nausea, and anxiety; thus, it should be tapered off gradually according to a physician's guidance. Due to the potential for drug abuse or dependence, caution is advised for patients with a history of drug abuse, and they should consult healthcare professionals if unusual behavior occurs. Patients with impaired renal function may need dosage adjustments. Patients with cardiovascular diseases should be careful when taking this medication, especially patients with congestive heart failure who should take it cautiously. Care should be taken when using this medication in combination with opioids, as it may enhance central nervous system depression. Patients with respiratory diseases, neurological disorders, renal impairment, and elderly patients are at higher risk of severe respiratory depression and may need dose adjustments. During early pregnancy, there is a risk of fetal malformations, so it is best not to take this medication during pregnancy, and women of childbearing age should use effective contraception. This medication is excreted in breast milk, so breastfeeding should be avoided or a consultation with a physician should be obtained. This medication can cause dizziness and drowsiness, so it is safer to refrain from driving or operating dangerous machinery after taking it. Severe skin reactions are rare but can occur; if symptoms such as rash or swelling appear, the medication should be stopped immediately and healthcare providers notified. This medication has minimal pharmacokinetic interactions with other drugs; however, caution is advised as its effects may increase if taken with alcohol or central nervous system depressants. In cases of overdose, symptoms such as drowsiness, confusion, depression, and seizures may occur, requiring immediate treatment at a hospital. Children, the elderly, and patients with impaired renal function need special care when taking this medication. Keep this medication out of the reach of children, and do not transfer it to another container.
Hives, severe swelling (angioedema), chest tightness, difficulty breathing, cold sweat, paleness, severe rashes with fever, blisters, skin peeling, pain in oral/ocular mucosa, shortness of breath or breathing difficulties, asthma attacks, respiratory abnormalities accompanied by cough and fever, jaundice (yellowing of skin or eyes), extreme drowsiness throughout the body, sudden and very severe headaches, thunderclap headache, seizures, altered consciousness, visual disturbances, paralysis, urination issues
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 tightly closed container. Additionally, it is advisable to store it at room temperature between 15 to 30 degrees Celsius to maintain its effectiveness.
A hard capsule with a white upper part and a white lower part containing white powder that is white or light yellow.
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.