Gabapentin Capsule 150 milligrams (Pregabalin)

Adult dose

This drug is administered orally in two divided doses per day, regardless of meals. 1. Neuropathic Pain - Peripheral Neuropathic Pain: Initial dose of 150 mg per day, with the possibility of increasing to 300 mg per day within 3 to 7 days. If necessary, it can be further increased to a maximum of 600 mg per day at intervals of 7 days. - Central Neuropathic Pain: Initial dose of 150 mg per day, with an increase to 300 mg per day after one week.

Child dose

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

This medicine may increase the risk of suicidal thoughts or behaviors, so if mood changes or abnormal behaviors occur during treatment, it is essential to inform a healthcare professional. Individuals allergic to any ingredients in this medicine or those with certain genetic disorders should not take it. Diabetic patients should be cautious as they may need to adjust the dosage of blood sugar control medications due to weight gain. If severe allergic reactions such as angioedema occur, the medication should be discontinued immediately. Elderly individuals may be at increased risk of falls due to dizziness or drowsiness, so they should be especially careful in the early stages of treatment. If vision changes such as blurriness occur, patients should consult a doctor. Sudden discontinuation of this drug may lead to withdrawal symptoms such as insomnia, headache, and anxiety, so it should be tapered off gradually under medical supervision. Patients with a history of substance abuse need to be particularly cautious as they have a higher possibility of misuse with this medication. Patients with impaired kidney function may require dose adjustments. Patients with severe heart disease should consult a doctor before taking this drug. Caution is needed when this drug is combined with opioid analgesics as it may intensify central nervous system depression symptoms. Patients with respiratory disease, kidney disease, and the elderly may be at higher risk for severe respiratory depression, and dosage adjustments may be necessary. There is a risk of fetal abnormalities in early pregnancy, so this medication should not be taken during pregnancy, and women of childbearing age should use effective contraception. While breastfeeding, consider discontinuing either the drug or breastfeeding as this drug may pass into breast milk. Before engaging in hazardous activities such as driving or operating machinery, verify whether dizziness or drowsiness occurs due to this medication. In cases of overdose, symptoms such as confusion, drowsiness, depression, and seizures may occur, so immediate medical attention is required. This medicine should be kept out of reach of children and should not be transferred to other containers.

Serious side effects

Hives, severe swelling, chest tightness, difficulty breathing, cold sweat, pallor, severe rash with fever, blisters, skin peeling, pain in mucous membranes of the mouth/eyes, shortness of breath or difficulty breathing, asthma attacks, respiratory problems with cough and fever, jaundice, extreme lethargy, sudden and severe headaches, thunderclap headache, seizures, confusion, visual disturbances, paralysis, and markedly reduced urine output

Mild side effects

• Dizziness
• drowsiness
• confusion
• disturbances in perception
• irritability
• depression
• euphoric feelings
• decreased libido
• insomnia
• depersonalization

This medicine should be stored in a tightly sealed container to prevent exposure to air or moisture. It is best to maintain a storage temperature between 15 and 30 degrees Celsius. This will help maintain the drug's effectiveness for a longer period.

Appearance

A hard capsule containing white or light yellow powder with a white opaque top and bottom.

Package unit

30 capsules/bottle, 100 capsules/bottle