2003
DOI: 10.1046/j.0306-5251.2001.01508.x-i1
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Concomitant overdosing of other drugs in patients with paracetamol poisoning

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Cited by 6 publications
(11 citation statements)
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“…During the 8 d of active treatment with fluoxetine, mean norfluoxetine concentrations rose from 25 to 80 ng/mL. During the 14 to 31 d after sessation oftreatment they went from 55 to 45 ng/mL (226). Further discussion on the effect of long half-life of SSRI metabolites can be found in the relevant chapter in this monograph.…”
Section: Lnteractions With Serotonin Selective Reuptake Lnhibitorsmentioning
confidence: 96%
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“…During the 8 d of active treatment with fluoxetine, mean norfluoxetine concentrations rose from 25 to 80 ng/mL. During the 14 to 31 d after sessation oftreatment they went from 55 to 45 ng/mL (226). Further discussion on the effect of long half-life of SSRI metabolites can be found in the relevant chapter in this monograph.…”
Section: Lnteractions With Serotonin Selective Reuptake Lnhibitorsmentioning
confidence: 96%
“…Pharmacokinetically significant drug interactions have, however, been identified (Table 23). Fluoxetine was found to inhibit the elimination of alprazolam (225,226) and diazepam (227), but was reported as without effect on clonazepam (226) and triazolam (228).…”
Section: Lnteractions With Serotonin Selective Reuptake Lnhibitorsmentioning
confidence: 97%
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“…In studies on the pharmacodynamic responses no effect was found for midazolam [274,278] or temazepam [281]. Interestingly, Kroboth et al [281] found minimal stimulation to the benzodiazepine effect in woman taking oral contraceptives along with alprazolam, triazolam, and lorazepam. The finding for lorazepam was contrary to the pharmacokinetic response.…”
Section: Interactions With Oral Contraceptivesmentioning
confidence: 99%
“…Metabolism of acetaminophen occurs primarily by phase II conjugation of the aromatic hydroxyl group with glucuronic acid (~60%) and sulfuric acid (~30%) and a much smaller fraction (~5%) is oxidized by CYP2E1 into the reactive metabolite N-acetyl-p-benzoquinone imine (NAPQI) [280]. Normally, the NAPQI metabolite is either reduced back to acetaminophen or inactivated by conjugation with glutathione, a scavenger of free radicals, and then excreted in urine after further phase II metabolism to produce cysteine and mercapturic acid [281]. A schematic diagram of the metabolism of acetaminophen in the body is shown in Fig.…”
Section: Drug Interactions Involving Cyp2e1mentioning
confidence: 99%