Nexrica Capsule 75mg (Pregabalin)

Adult dose

This medication is taken orally twice a day independent of food. 1. Neuropathic pain - Peripheral neuropathic pain: Starting dose of 150 mg per day, can increase to 300 mg per day after 3 to 7 days, and if necessary, can increase to a maximum of 600 mg at 7-day intervals. - Central neuropathic pain: Starting dose of 150 mg per day, can increase to 300 mg per day after one week.

Child dose

The safety and efficacy data for children under 12 years of age and adolescents aged 12 to 17 years is insufficient, and administration is not recommended.

This medication may increase the risk of suicidal thoughts or behaviors, so it is important to closely monitor for changes in mood, abnormal behavior, or symptoms of depression while taking it. Patients with allergies to any of the ingredients or specific genetic disorders, such as lactose intolerance, should not use this medication. Diabetic patients should be cautious as weight gain may require adjustments in the dosage of blood sugar control medications. If adverse reactions such as angioedema occur, stop taking the medication immediately and monitor for swelling around the face or mouth. Elderly patients should be especially cautious in the early stages of use due to the risk of falls from dizziness or drowsiness. Temporary blurred vision or changes in vision may occur, and any abnormal symptoms should be consulted with a doctor. Sudden discontinuation of this medication may lead to withdrawal symptoms such as insomnia, headaches, or anxiety, so dosage should be gradually reduced according to a doctor's instructions. There is a risk of drug abuse, so caution is needed for those with a history of mental illness or drug abuse. Patients with compromised kidney function may require dosage adjustments. Patients with heart disease should be cautious of the potential for congestive heart failure. Co-administration with opioid analgesics poses a risk of central nervous system depression, so special care should be taken when using them together. This medication may cause dizziness and drowsiness, so driving or operating dangerous machinery should be avoided until the effects are confirmed after taking the medication. In early pregnancy, there is a risk of fetal malformations, so women who are pregnant or planning to become pregnant should consult a doctor before use and should use effective contraception. While breastfeeding, this medication may pass into breast milk, so it is necessary to discuss with a doctor whether to stop breastfeeding or discontinue the medication. Overdose may manifest symptoms such as confusion, drowsiness, and depression, and may require treatments such as hemodialysis if necessary. Keep out of reach of children, and it is safer not to transfer to another container. If serious adverse symptoms such as skin rash, fever, or breathing difficulties occur during use, stop taking the medication immediately and inform healthcare professionals.

Serious side effects

Hives, severe swelling (angioedema), chest tightness, difficulty breathing, cold sweat, pallor, severe rash accompanied by high fever, blisters, skin peeling, pain in mucous membranes of mouth/eyes, shortness of breath or difficulty breathing, asthma attacks, respiratory abnormalities accompanied by cough and fever, jaundice (yellowing of skin or eyes), profound lethargy, sudden and severe headaches, thunderclap headaches, seizures, confusion, visual disturbances, paralysis.

Mild side effects

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

This medication may be sensitive to air or moisture, so it is important to store it in a tightly sealed container. Additionally, to maintain its effectiveness, it should be stored at a cool temperature between 15 to 30 degrees Celsius.

Appearance

A hard capsule with a reddish-brown top and white bottom, containing white powder that is white or light yellow in color.

Package unit

30 capsules/bottle