WebDec 24, 2015 · Citalopram is metabolized mainly in the liver via N-demethylation to its main metabolite, demethylcitalopram by CYP2C19 and CYP3A4 7. Other metabolites include … WebJan 23, 2008 · Citalopram is a weak in vitro inhibitor of CYP-2D6, and it has weak or no effects on CYP-1A2, CYP-2C19, and CYP-3A4. 51 Drug Interactions: With respect to pharmacokinetic drug interactions, …
Smoking and antidepressants pharmacokinetics: a systematic review
Webcitalopram clomipramine diazepam imipramine: lansoprazole phenytoin omeprazole R-warfarin: CYP2D6: amiodarone chloroquine cimetidine clomipramine diphenhydramine fluoxetine fluphenazine haloperidol paroxetine perphenazine propafenone propoxyphene quinacrine quinidine ritonavir sertaline terbinafine thioridazine: None: amitriptyline … WebSep 15, 2024 · Citalopram (Monograph) Brand name: CeleXA Drug class: Selective Serotonin-reuptake Inhibitors - Serotonin-reuptake Inhibitors - SSRIs VA class: CN609 Chemical name: 1- [3- (Dimethylamino)-propyl]-1- (p-fluorophenyl)-5-phthalancarbonitrile Molecular formula: C 20 H 21 FN 2 O CAS number: 59729-33-8 Medically reviewed by … phonak c shells
Citalopram and Escitalopram Pathway, Pharmacokinetics
WebMetabolism Citalopram is metabolized to demethylcitalopram (DCT), didemethylcitalopram (DDCT), citalopram-N-oxide, and a deaminated propionic acid derivative. In humans, unchanged citalopram is the predominant compound in plasma. At steady state, the concentrations of citalopram's metabolites, DCT and DDCT, in plasma … Webas citalopram and DCT was about 10% and 5%, respectively. The systemic clearance of citalopram was 330 mL/min, with approximately 20% of that due to renal clearance. Citalopram is metabolized to demethylcitalopram (DCT), didemethylcitalopram (DDCT), citalopram-N-oxide, and a deaminated propionic acid derivative. In humans, unchanged WebJul 13, 2024 · Antidepressants used in therapeutic dosing ranges are associated with causing several adverse drug reactions including hepatotoxicity. Paroxetine, fluoxetine, fluvoxamine, citalopram, mirtazapine and venlafaxine are associated with reversible liver injury upon discontinuation of the agent. how do you get toca life world