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2. Fluvoxamine is a potent inhibitor of the metabolism of caffeine in vitro. Rasmussen BB; Nielsen TL; Brøsen K Pharmacol Toxicol; 1998 Dec; 83(6):240-5. PubMed ID: 9868741 [TBL] [Abstract][Full Text] [Related]
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9. Theophylline has no advantages over caffeine as a putative model drug for assessing CYPIA2 activity in humans. Rasmussen BB; Brøsen K Br J Clin Pharmacol; 1997 Mar; 43(3):253-8. PubMed ID: 9088579 [TBL] [Abstract][Full Text] [Related]
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18. Disposition of fluvoxamine in humans is determined by the polymorphic CYP2D6 and also by the CYP1A2 activity. Carrillo JA; Dahl ML; Svensson JO; Alm C; Rodríguez I; Bertilsson L Clin Pharmacol Ther; 1996 Aug; 60(2):183-90. PubMed ID: 8823236 [TBL] [Abstract][Full Text] [Related]
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