Neuropain Capsule 150 mg (Pregabalin)

Adult dose

This medication is administered orally divided into two doses per day regardless of meals. 1. Neuropathic pain - Peripheral neuropathic pain: Starting dose of 150 mg per day, increasing to 300 mg per day within 3 to 7 days, may be increased to a maximum of 600 mg per day if necessary. - Central neuropathic pain: Starting dose of 150 mg per day, increasing to 300 mg per day after one week, followed by an additional increase to 600 mg per day after another week.

Child dose

For children under 12 years and adolescents aged 12 to 17, safety and efficacy data are insufficient, so administration is not recommended.

This medication may increase the risk of suicidal thoughts or behaviors, so if mood changes or symptoms of depression appear during treatment, it is essential to consult a doctor immediately. Patients with allergies to any components of this medication or specific genetic lactose metabolism disorders should not take it. Diabetic patients should be cautious as weight gain may require adjustments to blood glucose control medications. If symptoms of severe allergic reactions such as angioedema occur, discontinue the medication immediately and consult medical personnel. Elderly individuals should be careful during the initial doses due to the risk of dizziness or drowsiness leading to falls. Visual disturbances such as blurred vision may occur, and if symptoms persist, consultation with a physician is recommended. Withdrawal symptoms such as insomnia, headache, and anxiety may emerge after discontinuation, so abrupt cessation should be avoided. Patients with a history of drug abuse may have a higher risk of misuse of this medication, so caution is advised during use. Patients with impaired renal function may require dose adjustments. Patients with severely compromised cardiac function should use this medication cautiously. When taking with other drugs that have central nervous system depressant effects, there is an increased risk of drowsiness or respiratory depression, so caution is required. During early pregnancy, it may affect the fetus, so it should generally not be used, except in special circumstances, and women of childbearing age should use effective contraception. Lactating women should consider discontinuing breastfeeding or the medication, as this medication can be transmitted through breast milk. This medication may cause dizziness and drowsiness, so it is advisable to avoid driving or operating hazardous machinery after taking it. Serious skin reactions may occur rarely, so if any unusual symptoms such as rash or swelling appear, inform medical personnel immediately. In the case of overdose, symptoms such as confusion, drowsiness, and seizures may occur, so the prescribed dosage must be followed. Blood dialysis may be necessary if required. Special precautions are necessary for children and the elderly, and children should be kept out of reach of this medication.

Serious side effects

Hives, severe swelling (including angioedema), chest tightness, difficulty breathing, cold sweat, paleness, severe rash with high fever, blisters, peeling skin, pain in oral/ocular mucous membranes, shortness of breath or difficulty breathing, asthma attacks, respiratory abnormalities accompanied by cough and fever, yellowing of skin or eyes (jaundice), profound lethargy, sudden and very severe headache, thunderclap headache, seizures, disorientation, visual disturbances, coma

Mild side effects

• Dizziness
• drowsiness
• confusion
• impaired sense of direction
• irritability
• depression
• euphoria
• decreased libido
• insomnia
• depersonalization

This medication can be sensitive to air and moisture, so it must be stored in a tightly closed container. It is advisable to maintain the storage temperature between 15 to 30 degrees Celsius. Proper storage helps preserve the medication's effectiveness over time.

Appearance

A white or pale yellow powder contained in white hard capsules with white upper and lower parts.

Package unit

30 capsules/bottle, 200 capsules/bottle