Davis's Drug Guide
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phenytoin

Pharmacokinetics

Absorption: Absorbed slowly from the GI tract. Bioavailability differs among products; the Dilantin and Phenytek preparations are considered to be "extended" products. Other products are considered to be prompt release.

Distribution: Distributes into CSF and other body tissues and fluids. Enters breast milk; crosses the placenta, achieving similar maternal/fetal levels. Preferentially distributes into fatty tissue.

Protein Binding: Adults 90–95%; ↓ protein binding in neonates (up to 20% free fraction available), infants (up to 15% free), and patients with hyperbilirubinemia, hypoalbuminemia, severe renal dysfunction or uremia.

Metabolism and Excretion: Mostly metabolized by the liver; minimal amounts excreted in the urine.

Half-life: 22 hr (range 7–42 hr).

TIME/ACTION PROFILE (anticonvulsant effect)

ROUTEONSETPEAKDURATION
PO2–24 hr (1 wk)*1.5–3 hr6–12 hr
PO-ER2–24 hr (1 wk)4–12 hr12–36 hr
IV0.5–1 hr (1 wk)rapid12–24 hr

*( ) = time required for onset of action without a loading dose

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