Davis's Drug Guide

gabapentin

Pharmacokinetics

Absorption: Well absorbed after oral administration by active transport. At larger doses, transport becomes saturated and absorption decreases (bioavailability ranges from 60% for a 300-mg dose to 35% for a 1600-mg dose)

Distribution: Crosses blood-brain barrier; enters breast milk

Metabolism and Excretion: Eliminated mostly by renal excretion of unchanged drug

Half-life: 5–7 hr (normal renal function); up to 132 hr in anuria

TIME/ACTION PROFILE (blood levels)

ROUTEONSETPEAKDURATION
POrapid2–4 hr8 hr



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