TDS Pregabalin Capsule 75 mg

Adult dose

This medication should be taken orally in two divided doses per day, with or without food. 1. Neuropathic Pain - Peripheral neuropathic pain: Initial dose may be 150 mg per day; after 3-7 days, it may be increased to 300 mg per day, and if necessary, it can be further increased to a maximum of 600 mg daily at 7-day intervals. - Central neuropathic pain: Initial dose may be 150 mg per day; after one week, it can be increased to 300 mg daily.

Child dose

Use is not recommended for children under 12 years of age and adolescents between 12-17 years due to insufficient safety and efficacy data.

This medication may increase the risk of suicidal thoughts or behaviors, so any changes in mood or behavior should be carefully monitored during treatment. Do not use if you are allergic to any ingredients in this medication, and patients with certain genetic conditions like lactose intolerance should also avoid it. Diabetic patients may need to adjust the dosage of their blood sugar-lowering medications due to weight gain after using this medication. If symptoms of angioedema such as swelling of the face or neck occur, discontinue use immediately. Elderly patients should be cautious as this medication may increase the risk of dizziness or drowsiness, leading to a higher risk of falls. This medication may temporarily blur vision or cause changes in vision; consult a doctor if these symptoms occur. Abruptly stopping this medication may result in withdrawal symptoms such as insomnia, headache, or anxiety; it should be tapered according to a doctor's instructions. Because of the risk of drug abuse, patients with a history of mental health issues should be particularly cautious, and any signs of abuse should be reported to healthcare personnel immediately. Patients with heart disease or congestive heart failure should use this medication cautiously. Using this medication in conjunction with opioid analgesics may enhance CNS depressant effects, leading to risks such as difficulty breathing. Pregnant women should avoid this medication during early pregnancy due to the risk of fetal malformations, and women of childbearing potential should use effective contraception. Breastfeeding women should consult a doctor before taking this medication, as it may transfer to breast milk and affect the baby. It is advisable to avoid activities requiring concentration, such as driving or operating dangerous machinery, until dizziness or drowsiness has subsided after taking this medication. In cases of overdose, symptoms such as confusion, drowsiness, or depression may occur, and treatment such as dialysis may be necessary if required. This medication should be stored out of reach of children and should not be transferred to other containers.

Serious side effects

Hives, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, pallor, severe rash with fever, blisters, skin peeling, pain in oral/ocular mucosa, shortness of breath or difficulty breathing, asthma attacks, respiratory abnormalities accompanied by cough + fever, yellowing of skin or eyes (jaundice), overall severe lethargy, sudden and severe headache, thunderclap headache, seizures, confusion of consciousness, vision abnormalities, paralysis, urine

Mild side effects

• Dizziness
• drowsiness
• confusion
• loss of direction sense
• irritability
• depression
• elation
• decreased libido
• insomnia
• depersonalization

This medication should be stored in a tightly closed container to avoid exposure to air or moisture. Additionally, it is best to keep it in a location that avoids extreme temperatures, maintaining a room temperature between 15 to 30 degrees Celsius.

Appearance

A hard capsule with a reddish-brown upper part and a white lower part containing white powder that is white or light yellow in color.

Package unit

30 capsules/bottle, 60 capsules/bottle, 100 capsules/bottle