Pregabalin Capsule 75mg (Pregabalin)

Adult dose

This medication is taken orally in divided doses twice a day without regard to meals. 1. Neuropathic Pain 1) Peripheral Neuropathic Pain: Starting dose of 150 mg once daily, can be increased to 300 mg once daily within 3 to 7 days, and may be further increased to a maximum of 600 mg once daily at 7-day intervals as needed. 2) Central Neuropathic Pain: Starting dose of 150 mg once daily, may be increased to 300 mg once daily after one week.

Child dose

The use of this medication is not recommended for children under 12 years of age and adolescents aged 12 to 17 years due to insufficient safety and efficacy data.

This medication may increase the risk of suicidal thoughts or behavior, so it is important to closely monitor any abnormal changes in mood or behavior during treatment. Patients with hypersensitivity to this medication or genetic conditions such as lactose intolerance should not use it. Diabetic patients may need to adjust their blood sugar control medications due to potential weight gain. If serious allergic reactions such as angioedema occur, the use of this medication should be stopped immediately. Elderly patients may have an increased risk of falls due to dizziness or drowsiness and should be monitored closely. Visual disturbances or changes in vision may occur, and if symptoms are severe, discontinuation of the medication should be considered. Withdrawal symptoms such as insomnia, headaches, and anxiety may occur when discontinuing the medication, so consultation with a healthcare provider is recommended. Patients with a history of substance abuse may be at higher risk for misuse of this medication, so it should be used cautiously. Dose adjustments may be necessary for patients with impaired renal function. Patients with cardiovascular conditions should use this medication with caution. Caution is advised when taking this medication together with opioid analgesics due to increased risk of central nervous system depression. Patients with compromised respiratory function or elderly individuals are at risk of severe respiratory depression and may need dose adjustments. Pregnant women are advised not to use this medication during early pregnancy due to potential risks of fetal malformation, and women of childbearing age should use effective contraception. Breastfeeding women should consider discontinuing breastfeeding or stopping the medication, as it can be transmitted through breast milk. It is safest to avoid hazardous activities such as driving or operating machinery until dizziness or drowsiness subside after taking this medication. Severe skin reactions may occur; report any skin abnormality immediately to a healthcare provider. In case of overdose, symptoms such as drowsiness, confusion, and depression may manifest, and treatment such as blood dialysis may be required.

Serious side effects

• Hives
• severe swelling (edema)
• feeling of chest tightness
• difficulty breathing
• angioedema
• cold sweat
• paleness
• severe allergic reactions
• severe rash with high fever
• blisters

Mild side effects

• Dizziness
• drowsiness
• confusion
• disorientation
• irritability
• depression
• euphoric feelings
• decreased libido
• insomnia
• depersonalization

This medication should be stored in a tightly sealed container to protect it from air and moisture, preferably in a cool place between 15 to 30 degrees Celsius.

Appearance

Hard capsule with reddish-brown upper and white lower part containing white powder that appears white or light yellow.

Package unit

30 capsules/bottle, 60 capsules/bottle