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British Journal of Clinical Pharmacology logoLink to British Journal of Clinical Pharmacology
. 1978 Apr;5(4):313–318.

Pharmacokinetics of valproic acid after oral and intravenous administration

E Perucca, G Gatti, G M Frigo, A Crema
PMCID: PMC1429296

Abstract

1 The kinetics of sodium valproate (di-n-propyl-acetate, Depakine®) have been studied in six healthy volunteers after administration of single oral and intravenous doses (800 mg).

2 Kinetic parameters were similar for both routes of administration. In all subjects absorption was rapid and complete. Half-lives ranged from 11-15 h. Apparent volumes of distribution were relatively low (0.147 ± 0.004 l/kg) and showed little variation amongst individuals.

3 The factors responsible for the poor correlation between dosage and serum levels during chronic treatment and therapeutic implications are discussed.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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