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Depakote

Valproate semisodium (INN) or divalproex sodium (USAN) consists of a compound of sodium valproate and valproic acid in a 1:1 molar relationship in an enteric coated form. It is used in UK and US for the treatment of the manic episodes of bipolar disorder, and in the US for the treatment of epilepsy and migraine headaches. Its chemical name is sodium hydrogen bis(2-propylpentanoate). The extended release formulation allows for a single daily dose. more...

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Formulations

US

  • Tablets – Depakote® and Depakote ER® by Abbott Laboratories.

UK

  • Tablets – Depakote® by Sanofi-Aventis.

Canada

  • Tablets – Epival® by Abbott Laboratories. Generic formulations include Novo-Divalproex

Read more at Wikipedia.org


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Depakote formula dilemma
From Nurse Practitioner, 8/1/02 by Cohen, Hedy

Safe Prescribing

Manufacturers of Depakote (delayed-- release tablets), a drug usually prescribed for seizures, have marketed Depakote ER, an extended-release tablet formulation of divalproex sodium intended for migraine sufferers. Serious complications may occur if Depakote ER is confused with Depakote delayed-- release tablets, a formulation that is released over an 8- to 12-hour period and can be taken more than once daily. When Depakote ER is given more than once a day, potential adverse effects include hypotension, sedation, heart block, or deep coma.

The authors of Safe Prescribing are the following staff from the Institute for Safe Medication Practices II$MP): Hedy Cohen, RN, BSN, vice-president nursing; Judy Smetzer, RN, BSN, director, risk management; and Michael Cohen, RPh, MS, FASHP, president ISMP, a nonprofit organization, derives its reports from the USP Medication Errors Reporting Program. To report medication errors, call the USP at 1-800-23-ERROR (233-7767). To contact ISMP, call 215-947-7797 or e-mail ismpinfo@ismp.org.

Copyright Springhouse Corporation Aug 2002
Provided by ProQuest Information and Learning Company. All rights Reserved

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