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Valex CR 300
Presentation: Each controlled-release tablet contains Sodium Valproate BP equivalent to Valproic Acid 300 mg.
Indications: Valex CR (Sodium Valproate Controlled-Release) is indicated for the treatment of:
The controlled-release formulation is intended for once-daily or twice-daily dosing to help maintain more stable blood levels.
Dosage and Administration: Dosage should be individualized and determined by a healthcare professional. Valex CR tablets should be swallowed whole and not crushed or chewed. They can be taken with or without food. When converting from immediate-release valproate to Valex CR, the total daily dose may remain the same but the dosing schedule may change (e.g., twice daily to once daily).
Side Effects: Common adverse reactions may include nausea, vomiting, indigestion, diarrhea, abdominal cramps, transient hair loss, weight gain, tremor, and drowsiness. Less common but potentially serious side effects include hepatotoxicity, pancreatitis, and hyperammonemia.
Precautions: Valex CR is contraindicated in patients with known hypersensitivity to valproate, hepatic disease or significant hepatic dysfunction, and known urea cycle disorders. Caution should be exercised in patients with a history of hepatic dysfunction, pancreatitis, or bleeding disorders. Women of childbearing potential should use effective contraception due to the risk of teratogenicity. Regular monitoring of liver function and platelet count may be necessary.
Storage: Store below 25°C, protected from light and moisture. Keep out of reach of children.
Note: This information is a general overview. Sodium Valproate is a prescription medication and should be used under the strict guidance of a healthcare professional. Always consult your doctor for specific prescribing information and management.
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