Lacomax Oral Solution 50 mg/5 ml contains Lacosamide, an antiepileptic medication indicated for the management of partial-onset seizures in adults and pediatric patients aged 4 years and older. It is used either as monotherapy or as adjunctive therapy in patients who require additional seizure control. Lacosamide helps to stabilize hyperexcitable neuronal membranes and inhibit repetitive neuronal firing, reducing the frequency and severity of seizures. Its oral solution formulation allows accurate dosing for pediatric patients and individuals who have difficulty swallowing tablets.
রেজিস্টার্ড চিকিৎসকের পরামর্শ অনুযায়ী ঔষধ সেবন করুন
Antiepileptic Drug (AED)
Lacomax Oral Solution is indicated for:
Partial-onset seizures in adults and children aged 4 years and above
Adjunctive therapy in patients whose seizures are not adequately controlled with other antiepileptic medications
Suitable for patients who require flexible dosing, especially children and elderly patients
By targeting sodium channels in the brain, Lacosamide reduces abnormal electrical activity, helping to control seizure events and improve patient quality of life.
Lacosamide selectively enhances slow inactivation of voltage-gated sodium channels, stabilizing hyperexcitable neuronal membranes without affecting normal neuronal activity. Unlike some other sodium channel blockers, Lacosamide does not alter fast inactivation or normal neuronal conduction, which minimizes effects on normal brain function.
Absorption: Rapid and nearly complete oral absorption
Metabolism: Partially metabolized in the liver via CYP2C19 and non-CYP pathways
Excretion: Primarily excreted in urine, mostly as unchanged drug
Half-life: Approximately 13 hours, allowing for twice-daily dosing in most patients
Lacosamide demonstrates linear pharmacokinetics, with minimal drug-drug interactions compared to other antiepileptic drugs.
Adults:
Initial dose: 50 mg twice daily
Titration: Increase by 50 mg twice daily at one-week intervals as tolerated
Maintenance dose: 100–200 mg twice daily (maximum 400 mg/day)
Pediatric Patients (4–16 years):
Initial dose: 1 mg/kg twice daily
Titration: Increase weekly by 1 mg/kg twice daily
Maintenance dose: 3–6 mg/kg twice daily (maximum 200 mg/day)
Administration Instructions:
The oral solution can be taken with or without food
Use the provided measuring device to ensure accurate dosing
Do not mix with other liquids unless recommended by a healthcare provider
Hypersensitivity to Lacosamide or any component of the formulation
Patients with known PR interval prolongation or severe cardiac conduction disorders without close monitoring
Common side effects include:
Dizziness, headache, and nausea
Fatigue and somnolence
Diplopia (double vision) or blurred vision
Rarely, cardiac conduction abnormalities such as PR interval prolongation
Most adverse effects are mild to moderate and often resolve with continued treatment.
Use caution in patients with heart disease, especially those with conduction abnormalities
May cause dizziness or ataxia; avoid driving or operating machinery until response is known
Gradual titration is recommended to minimize adverse effects
Monitor renal and hepatic function in patients with impairment
Lacosamide has a low potential for interactions but may interact with other antiepileptics or drugs affecting cardiac conduction
Concomitant use with digoxin or calcium channel blockers requires monitoring
Pregnancy: Use only if clearly needed; limited data suggest low teratogenic risk
Breastfeeding: Lacosamide is excreted in breast milk; caution is advised
Store in a cool, dry place below 30°C, protected from light and moisture
Keep out of reach of children
Use the reconstituted solution within the period recommended on the label
Lacosamide acts by enhancing slow inactivation of voltage-gated sodium channels, stabilizing hyperexcitable neurons and preventing repetitive firing. This targeted mechanism reduces abnormal neuronal excitability while preserving normal neuronal signaling, effectively controlling partial-onset seizures.
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