Valproic acid and depakote 60 mg

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This medicinal product is subject to additional monitoring. This will allow quick identification of new safety information.

Depakote mg Tablets - Summary of Product Characteristics (SmPC) - (eMC)

Healthcare professionals valproic acid and asked to valproic acid and depakote 60 mg any suspected adverse reactions. It is also known as divalproex sodium USAN. Treatment of manic episode in bipolar disorder when lithium is contraindicated or not tolerated.

The continuation of treatment after manic episode could be considered in patients who have responded to Depakote for acute mania. The tablets should be swallowed whole with a drink of water, and not crushed or chewed.

The daily dosage should be established according to age and body weight. The wide variation in individual sensitivity to Depakote should also be considered. The daily dosage should be established and controlled individually by the treating physician.

Here initial valproic acid and depakote 60 mg daily dose is mg.

Prolonged-release formulations can be valproic acid and once or twice daily. The dose should be increased as rapidly as possible to achieve the lowest therapeutic dose which produces the desired valproic acid and depakote 60 mg effect. The daily dose should be adapted to the clinical response to establish the lowest effective dose for the individual patient.

The mean daily dose usually ranges between — mg valproate. Continuation of treatment of manic episodes in bipolar disorder should be adapted individually using the link effective dose.

Although the pharmacokinetics of Depakote are modified in the elderly, they have limited clinical significance and dosage should be determined click the basis of clinical response. The safety and valproic acid and depakote 60 mg of Depakote for and depakote treatment of manic episodes in depakote disorder have not been evaluated in patients aged less valproic acid 18 years.

It may be necessary to decrease dosage. Dosage should be adjusted according to clinical monitoring since monitoring of plasma concentrations may valproic acid and depakote 60 mg misleading see section 5.

Salicylates should not be used concomitantly with Depakote since they depakote visit web page same metabolic pathway see sections 4.

Liver dysfunction, including hepatic failure resulting in fatalities, has occurred in patients whose valproic acid and included valproic acid see sections 4. In addition in conjunction with Depakote, concomitant use in children under 3 years can increase the risk of liver toxicity see section 4.

Valproate must be initiated and supervised by a specialist experienced in the depakote of bipolar disorder.

Depakote 500mg Tablets

Valproate should not be used in female children or women of childbearing potential unless other treatments are ineffective or not tolerated see sections 4.

Valproate is prescribed and dispensed according to the Valproate Pregnancy Prevention Programme see depakote 4. The benefits depakote valproic acid and depakote 60 mg should be carefully reconsidered at regular treatment reviews see section 4. Valproate should preferably be prescribed as monotherapy and at the lowest effective dose, if possible as a prolonged release formulation. The daily dose should be divided valproic acid at least two single doses see section and depakote.

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