Presta Capsule 75 mg (Pregabalin)

Adult dose

This medication is taken orally, divided into two doses per day, regardless of food. 1. Neuropathic Pain - Peripheral Neuropathic Pain: Starting dose of 150 mg per day, can be increased to 300 mg per day after 3 to 7 days, and later increased to a maximum of 600 mg per day at 7-day intervals. - Central Neuropathic Pain: Starting dose of 150 mg per day, increased to 300 mg one week later.

Child dose

Use is not recommended for pediatric patients under 12 years of age and adolescents aged 12 to 17 due to insufficient safety and efficacy data.

This medication may increase the risk of suicidal thoughts or behaviors, so careful monitoring for abnormal changes in mood or behavior is necessary during treatment. Avoid administration if there is hypersensitivity to this medication or if specific genetic conditions such as lactose intolerance are present. Diabetic patients may need to adjust the dosage of blood sugar control medications due to weight gain. If symptoms of angioedema occur, discontinuation of the medication should be immediate, and caution is necessary for the elderly due to the risk of injury from dizziness or drowsiness. Blurred vision or changes in eyesight may occur, and these symptoms may improve upon discontinuation of the medication. Withdrawal symptoms such as insomnia, headache, and anxiety may occur upon discontinuation, so consultation with medical staff is necessary. Patients with a history of substance abuse should be cautious due to the risk of misuse, and monitoring for signs of misuse or dependence is required. Patients with decreased kidney function may require dose adjustments. Patients with heart disease should use this medication carefully due to the risk of heart failure during treatment. Co-administration with opioid analgesics may increase the risk of central nervous system depression, so caution is warranted. During early pregnancy, there may be a risk of fetal malformations; therefore, use during pregnancy should be avoided, and women of childbearing age should employ effective contraceptive methods. During lactation, this medication can be transmitted to breast milk and may affect infants, so consideration should be given to discontinuing breastfeeding or the medication. Caution is needed when driving or operating machinery due to the risk of accidents caused by dizziness and drowsiness. Severe skin reactions may occur, so immediate discontinuation is necessary if any skin abnormal symptoms arise. In cases of overdose, symptoms such as confusion, drowsiness, and seizures may occur, and treatment such as hemodialysis may be necessary. This medication should be kept out of reach of children, and transferring it to other containers may reduce its quality, so caution is needed.

Serious side effects

• Hives
• severe swelling (edema)
• angioedema
• facial swelling
• flushing
• chest tightness
• difficulty breathing
• respiratory distress
• respiratory suppression
• severe allergic reactions

Mild side effects

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

This medication should be stored in a tightly closed container to protect it from air and humidity, preferably at room temperature between 15 and 30 degrees Celsius. Storing it this way helps maintain the medication's efficacy and ensures safe use.

Appearance

Hard capsules with a reddish-brown upper part and a white lower part containing white or pale yellow powder.

Package unit

100 capsules/bottle, 30 capsules/bottle