Nexrica Capsule 50 mg (Pregabalin)

Adult dose

This medication should be taken orally in two divided doses per day, regardless of meals. 1. Neuropathic pain 1) Peripheral neuropathic pain: An initial dose of 150 mg per day may be administered, which can be increased to 300 mg daily after 3 to 7 days. Subsequently, the daily dose can be increased to a maximum of 600 mg at intervals of 7 days. 2) Central neuropathic pain: An initial dose of 150 mg per day is administered, and after one week, can be increased to 300 mg per day.

Child dose

The safety and efficacy data for children under 12 years of age and adolescents aged 12-17 years is insufficient, therefore use in this population is not recommended.

This medication may increase the risk of suicidal thoughts or behaviors, so if mood changes or symptoms of depression occur during treatment, you should inform your doctor immediately. This medication should not be used by patients with an allergy to its components or those with a genetic intolerance to lactose. Diabetic patients may need to adjust their blood sugar control medications due to weight gain following the use of this drug. If symptoms of angioedema occur, the medication should be stopped immediately, and elderly patients should be cautious of injuries due to dizziness or drowsiness. This medication may cause blurred vision or changes in eyesight, so consult a doctor if symptoms occur. If the medication is suddenly discontinued, withdrawal symptoms such as insomnia, headache, and anxiety may occur, so it should be tapered off gradually as instructed by a physician. Patients with a history of substance abuse should use this medication carefully due to the potential for misuse or dependence. Patients with impaired kidney function should adjust their dosage of this medication, and those with heart disease should also exercise caution. When used in conjunction with other drugs that have central nervous system depressant effects, there is a risk of respiratory depression, so be cautious when combining medications. During early pregnancy, it may affect the fetus, so it is advisable for pregnant women not to use it, and women of childbearing age should use effective contraception. Breastfeeding women should either discontinue breastfeeding or consult a physician since this medication may be passed into breast milk. Before driving or operating dangerous machinery, confirm whether this medication causes dizziness or drowsiness, and avoid such activities if symptoms are present. In cases of overdose, symptoms like confusion, drowsiness, and depression may occur, so immediate medical attention should be sought for appropriate treatment. Keep out of reach of children and be careful not to transfer the medication to another container.

Serious side effects

Hives, severe swelling (including angioedema, facial swelling), chest tightness, difficulty breathing, cold sweat, paleness, severe rash with high fever, blisters, skin peeling, pain in oral/eye mucosa, Stevens-Johnson syndrome, toxic epidermal necrolysis, pulmonary edema, liver abnormalities (jaundice), sudden and severe headache, thunderclap headache, seizures, confusion of consciousness, vision changes, paralysis, significantly reduced urine output, elevated blood pressure.

Mild side effects

• Dizziness
• drowsiness
• confusion
• loss of directional sense
• irritability
• depression
• euphoria
• decreased libido
• insomnia
• depersonalization

This medication should be stored in a tightly sealed container to prevent air or moisture from entering. Additionally, it is advisable to keep it at room temperature between 15°C and 30°C, avoiding direct sunlight.

Appearance

A hard capsule with an upper dark blue and a lower white part filled with white powder.

Package unit

30 capsules/bottle