Valex Injection 500 mg/5 ml is an intravenous formulation of Sodium Valproate, designed for the management of epilepsy and seizure disorders when oral administration is not feasible. This injectable preparation provides rapid and effective control of seizures, making it suitable for acute episodes, status epilepticus, or patients unable to take oral medication.
Valex Injection works by enhancing gamma-aminobutyric acid (GABA) levels in the brain, stabilizing neuronal activity, and reducing the frequency and intensity of seizures. It is also indicated for bipolar disorder management, prophylaxis of migraine, and febrile convulsions. The solution is formulated for intravenous slow injection or infusion, ensuring safe and effective systemic delivery.
রেজিস্টার্ড চিকিৎসকের পরামর্শ অনুযায়ী ঔষধ সেবন করুন
Primary Anti-Epileptic Drugs
Valex Injection 500 mg/5 ml is indicated for:
Acute management of epilepsy and seizure disorders
Status epilepticus or prolonged convulsive episodes
Bipolar disorder for rapid stabilization of mood
Prophylaxis of migraine
Febrile convulsions in pediatric patients
Post-traumatic epilepsy prevention
Sodium Valproate, the active ingredient in Valex Injection, exerts its antiepileptic effect by increasing GABA concentrations in the central nervous system, enhancing inhibitory neurotransmission, and stabilizing neuronal firing.
Mechanism of Action:
Increases brain GABA levels
Reduces abnormal electrical activity in neurons
Provides broad-spectrum seizure control across partial, generalized, myoclonic, atonic, and absence seizures
Pharmacokinetics:
Rapid systemic absorption via intravenous route
Metabolized in the liver, partially excreted in urine
Half-life: approximately 9–16 hours in adults
Adults:
Initial dose: 400–800 mg IV over 3–5 minutes, depending on body weight
Maximum daily dose: 2.5 g
Can be administered as slow intravenous injection or continuous infusion
Children:
Initial dose: 20–30 mg/kg/day IV
Maximum: 40 mg/kg/day
Dosing can be adjusted according to clinical response and plasma drug levels
Administration Guidelines:
Administer slowly to avoid cardiovascular adverse effects
Use compatible diluents such as 0.9% Sodium Chloride or 5% Dextrose
Monitor for sedation, hypotension, and other potential adverse effects during infusion
Known hypersensitivity to Sodium Valproate or related compounds
Severe liver dysfunction or hepatic disease
Pregnancy (particularly in the first trimester) unless benefits outweigh risks
Common adverse effects include:
Gastrointestinal: nausea, vomiting
CNS: sedation, tremor, dizziness
Rare but serious: hepatotoxicity, pancreatitis, hyperammonemia
Dermatologic: rash, alopecia
Frequent monitoring of liver function tests, plasma levels, and coagulation parameters is recommended during therapy.
Adjust dose in renal impairment
Avoid abrupt discontinuation to prevent seizure recurrence
Use with caution in patients on multiple antiepileptic drugs
Monitor for CNS depression or sedation during IV administration
Pregnancy: Crosses the placenta; associated with neural tube defects (anencephaly, spina bifida)
Lactation: Excreted in breast milk; caution advised
Store below 30°C, away from light
Keep out of reach of children
Do not freeze
Valex Injection increases GABAergic activity in the brain, stabilizing neuronal excitability and providing broad-spectrum seizure control, suitable for both acute and chronic management of epilepsy.
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