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)
| ROUTE | ONSET | PEAK | DURATION |
|---|
| PO | 2–24 hr (1 wk)* | 1.5–3 hr | 6–12 hr |
| PO-ER | 2–24 hr (1 wk) | 4–12 hr | 12–36 hr |
| IV | 0.5–1 hr (1 wk) | rapid | 12–24 hr |
*( ) = time required for onset of action without a loading dose
phenytoin has been found in Davis's Drug Guide
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