Bielpregabalin Capsule 75 mg (Pregabalin)

Adult dose

This medication should be taken in divided doses twice daily, regardless of meals. 1. Neuropathic pain 1) Peripheral neuropathic pain: Starting dose of 150 mg once daily; the dose may be increased to 300 mg once daily after 3 to 7 days, and to a maximum of 600 mg once daily at 7-day intervals if necessary. 2) Central neuropathic pain: Starting dose of 150 mg once daily; after 1 week, the dose may be increased up to 300 mg once daily.

Child dose

Administration is not recommended for children under 12 years of age and adolescents aged 12-17, as safety and efficacy data are insufficient.

This medication may increase the risk of suicidal thoughts or behaviors, so it is essential to consult a physician immediately if mood or behavior changes occur during treatment. Patients with hypersensitivity to this medication or with certain genetic conditions like lactose intolerance should not take this drug. Diabetes patients should be careful as weight gain may require dosage adjustments of their blood glucose control medications. If allergic reactions such as angioedema occur, discontinue use immediately and inform healthcare personnel. Elderly patients may experience dizziness or drowsiness when taking this medication and should be cautious of falling risks until accustomed to its effects. Visual disturbances or changes in vision may occur; if these symptoms arise, consult a physician. Sudden discontinuation of this medication can lead to withdrawal symptoms such as insomnia, headaches, nausea, and anxiety, so dosage should be adjusted according to physician’s instructions. There is a risk of drug misuse, so patients with a history of substance abuse should be particularly cautious and monitored for unusual behaviors. Patients with impaired kidney function may require dosage adjustments, and patients with heart failure need careful observation when taking this medication. Using this medication in combination with opioid analgesics may increase the risk of central nervous system depression, so caution should be exercised. This medication can cause respiratory depression, thus requiring consideration of dosage adjustments in patients with respiratory or kidney diseases and in the elderly. In early pregnancy, there may be a risk of fetal malformations; therefore, women who are pregnant or planning to become pregnant should consult a physician and use effective contraception. During breastfeeding, this medication may be excreted in breast milk and could affect the baby, so careful consideration of breastfeeding and medication use is necessary. When engaging in potentially hazardous activities such as driving or operating machines, be cautious as dizziness or drowsiness may occur. Severe skin reactions can rarely occur; if skin rashes, redness, or blisters develop, discontinue use immediately and inform a physician. In case of overdose, symptoms may include confusion, drowsiness, and depression, and emergency treatment such as dialysis may be necessary.

Serious side effects

Hives, extreme swelling, chest tightness, difficulty breathing, cold sweat, paleness, severe rash with fever, blisters, skin peeling, pain in mucous membranes of mouth/eyes, shortness of breath, asthma attack, respiratory issues accompanied by cough and fever, yellowing of skin or eyes, extreme lethargy, sudden and severe headache, thunderclap headache, seizures, confusion of consciousness, visual disturbances, paralysis, significantly reduced urine output

Mild side effects

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

This medication should be stored in a tightly sealed container to protect against air or moisture. Ideal storage temperature is between 15 and 30 degrees Celsius.

Appearance

Brownish-red hard capsule with a white or light yellow powder inside.

Package unit

30 capsules/bottle, 100 capsules/bottle