Depakote ER tablets contain divalproex sodium in a once-a-day extended-release formulation equivalent to and mg of valproic acid. In a placebo-controlled clinical trial of acute mania or mixed type, patients were dosed to a clinical response with a trough plasma concentration between 85 and mcg/mL. Depakote adalah merek dagang atau merek paten dari obat sodium (natrium) divalproat. Obat ini dikenal sebagai obat antikejang atau epilepsi.
These considerations may make selection of therapy. Differently in combination with other depakote 250 ml, ALDACTONE is higher for patients who cannot. 8 Rosemary Considerations for Diuretic Drugs. Nursing Looping; Nursing Diagnoses; Implementation with Rationale; Evaluation. 9 Utilization.
Formulations: Depakene is available in the following formulations: mg/5 ml liquid suspension; mg capsule. Depakote is available in the following formulations: mg sprinkles; mg tablets; mg delayed-release tablet. Depakote initial dose: mg PO BID for 1 week Low serum albumin levels may cause an increase in unbound drug (while total concentration may appear normal); Epilepsy: mcg/mL total valproate; Mania: mcg/mL total Depakote or Depakote Sprinkles: If daily dose > mg, give as divided dose.
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