Lyrica Capsule 150mg (Pregabalin)

Adult dose

This medication is taken orally regardless of meals, with the total daily dose divided into two doses. For neuropathic pain (peripheral and central): The starting dose is 150 mg per day, which can be increased to 300 mg per day within 3 to 7 days based on patient response and tolerability. For central neuropathic pain, increase to 300 mg per day after 1 week, and thereafter up to 600 mg may be administered at intervals of 7 days. Epilepsy

This medication may increase the risk of suicidal thoughts or behaviors, so you should inform your healthcare provider immediately if you experience depression or mood changes while taking it. Patients with allergies to any of the ingredients in this medication or those with a genetic lactose intolerance should not take this medication. Diabetic patients should be cautious as weight gain caused by this medication may affect blood sugar control. If allergic reactions such as angioedema occur, usage should be discontinued immediately, and elderly patients should be careful to avoid falls due to dizziness or drowsiness. This medication can cause visual disturbances such as blurred vision, and you should consult your healthcare provider if symptoms appear. Suddenly stopping this medication may lead to withdrawal symptoms such as insomnia, headache, and anxiety, so you should adjust the dosage according to your healthcare provider's instructions. Patients with a history of substance abuse are at greater risk of misuse and dependency on this medication and should exercise special caution when taking it. Patients with impaired kidney function may require dose adjustments, and those with heart disease should also use this medication with caution. Taking this medication with opioids may increase central nervous system depressant effects, posing a risk of respiratory difficulties. Pregnant women should avoid this medication in early pregnancy due to the risk of fetal malformations, and women of childbearing age should use effective contraception. During breastfeeding, this medication may be passed into breast milk and affect infants, so you should discuss whether to breastfeed with your healthcare provider. Before driving or operating machinery, verify whether you experience dizziness or drowsiness after taking this medication; avoid these activities if symptoms are present. In case of overdose, symptoms such as confusion, drowsiness, and depression may occur, so avoid overdose and seek medical attention immediately if abnormalities are noted. Keep this medication out of the reach of children, and it is safer not to transfer it to other containers.

Serious side effects

Hives, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, pallor, severe rash with high fever, blisters, skin peeling, pain in oral/ocular mucosa, shortness of breath or difficulty breathing, asthma attack, respiratory issues accompanied by cough and fever, yellowing of skin or eyes (jaundice), extreme lethargy, sudden and severe headaches, thunderclap headache, seizures, consciousness disturbances, visual disturbances, paralysis, urination

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 protect it from air and moisture. It is recommended to store it at a temperature between 15°C and 30°C, avoiding extremes.

Appearance

White or light yellow powder contained in a white hard capsule with a white upper and lower part

Package unit

30 capsules/bottle, 60 capsules/bottle