Using Booking Data to Model Drug User Arrest Rates: A Preliminary to Estimating the Prevalence of Chronic Drug Use

Hepatobiliary disposition of valproic ac

Hepatobiliary disposition of valproic acid and valproate glucuronide: Use of a pharmacokinetic model to examine the rate-limiting steps and potential sites of drug interactions

✍ C L Booth; G M Pollack; K L Brouwer 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 271 KB

with phenobarbital-associated impairment of canalicu-Previous work in this laboratory has suggested that lar egress of some organic anions. This work further supthe nonlinear disposition of valproic acid (VPA) in the ports the utility of pharmacokinetic modeling in: (1) derat may be due to nonlinear