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At first, 250 milligrams (mg) two times a day.

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Prior to the initiation of divalproex sodium delayed-release tablets therapy, evaluation for UCD should be considered in the following patients: 1) those with a history of unexplained encephalopathy or coma, encephalopathy associated with a protein load, pregnancy-related or postpartum encephalopathy, unexplained mental retardation, or history of elevated plasma ammonia or glutamine; 2) those with cyclical vomiting and lethargy, episodic extreme irritability, ataxia, low BUN, or protein avoidance; 3) those with a family history of UCD or a family history of unexplained infant deaths (particularly males); 4) those with other signs or symptoms of UCD.

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Depakote is the brand name for the medication divalproex sodium (or valproate semisodium).

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Pancreatitis; Divalproex sodium capsules (sprinkle) should ordinarily be discontinued (5.

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Patients, their caregivers, and families should be counseled that AEDs, including divalproex sodium extended-release tablets, may increase the risk of suicidal thoughts and behavior and should be advised of the need to be alert for the emergence or worsening of symptoms of depression, any unusual changes in mood or behavior, or the emergence of suicidal thoughts, behavior, or thoughts about self-harm.

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When divalproex sodium extended-release tablets are given in doses 8% to 20% higher than the total daily dose of divalproex sodium delayed-release tablets, the two formulations are bioequivalent.

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Figure 2 presents the proportion of patients (X axis) whose percentage reduction from baseline in complex partial seizure rates was at least as great as that indicated on the Y axis in the adjunctive therapy study.

After the burst of activity the blood flow to the in the area affected is decreased for two to six hours.

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Doctors have studied large numbers of people to find out how well Depakote ER and the other medicines that contain valproate control seizures.

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