Lecapri Capsule 150mg (Pregabalin)

Adult dose

This medication should be taken orally, divided into two doses per day, regardless of food. 1. Neuropathic pain - Peripheral neuropathic pain: initial dose 150 mg per day, may be increased to 300 mg per day 3 to 7 days later, may be further increased to a maximum of 600 mg per day at intervals of 7 days if needed. - Central neuropathic pain: initial dose 150 mg per day, may be increased to 300 mg after one week

This drug, as an anticonvulsant, may increase the risk of suicidal thoughts or behaviors, so patients should inform their healthcare provider if they experience depression or mood changes during treatment. Patients with known allergies to any of the ingredients in this drug or those with lactose intolerance should not take it. Diabetic patients may experience weight gain after taking this drug, and dosage adjustments may be necessary for blood sugar control. If symptoms of a severe allergic reaction, such as angioedema, occur, the medication should be discontinued immediately. Elderly patients should be cautious as this drug may cause dizziness or drowsiness, increasing the risk of falls, and may result in loss of consciousness or confusion. Some patients may experience blurred vision or visual changes, and if symptoms are severe, they should consult a doctor. If this medication is suddenly discontinued, withdrawal symptoms such as insomnia, headache, and anxiety may occur; therefore, it should be tapered off gradually under medical supervision. Patients with a history of substance abuse may be at a higher risk for misuse or dependence on this drug, so they should discuss this with their healthcare provider before starting treatment. Patients with impaired kidney function need dosage adjustments, and those with heart failure should use it cautiously. Co-administration with opioids may increase central nervous system depressant effects, leading to serious side effects such as respiratory depression; caution should be exercised. This drug may pose a risk of fetal malformations during early pregnancy, so it is advisable for pregnant women to avoid it, and women of childbearing age should use effective contraceptive methods. While breastfeeding, this drug may pass into breast milk and affect the infant, so it is important to consult with a healthcare provider regarding breastfeeding. Dizziness or drowsiness may occur, so caution is advised when driving or operating hazardous machinery. In case of overdose, symptoms such as confusion, drowsiness, depression, and seizures may occur, and treatment such as dialysis may be necessary. This drug should be kept out of reach of children and should not be transferred to another container. If a severe rash or allergic reaction occurs, discontinue use immediately and inform a healthcare provider.

Serious side effects

Hives, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, pallor, severe rash with high fever, blisters, peeling skin, pain in oral or ocular mucosa, shortness of breath or difficulty breathing, asthma attacks, respiratory abnormalities accompanied by cough and fever, jaundice (yellowing of skin or eyes), extreme lethargy, sudden and severe headache, thunderclap headache, seizures, altered consciousness, visual disturbances, paralysis, urination

Mild side effects

• Dizziness
• drowsiness
• increased appetite
• loss of appetite
• hypoglycemia
• confusion
• disorientation
• irritability
• depression
• euphoria

This drug is sensitive to air and moisture, so it should be stored in a tightly sealed container. It is best to maintain storage temperatures between 15 to 30 degrees Celsius.

Appearance

A hard capsule with white upper part and white lower part containing a powder that is white or pale yellow.

Package unit

30 capsules/bottle, 100 capsules/bottle