Pharmacokinetics and bioavailability comparison of generic and branded citalopram 20 mg tablets: an open-label, randomized-sequence, two-period crossover study …

T Jiang, Z Rong, Y Xu, B Chen, Y Xie, C Chen… - Clinical drug …, 2013 - Springer
Background Citalopram is a selective serotonin reuptake inhibitor (SSRI) mainly prescribed
to treat major depression. Objective The aim of this study was to compare the …

Effects of CYP2C19 genetic polymorphism on the steady-state concentration of citalopram in patients with major depressive disorder

MS Zastrozhin, VY Skryabin, AE Petukhov… - The …, 2021 - nature.com
Citalopram is commonly prescribed to patients suffering from major depressive disorder.
Some of them do not respond adequately to therapy with citalopram, while many of them …

Estimation of CYP 2 D 6* 10 genotypes on citalopram disposition in C hinese subjects by population pharmacokinetic assay

B Chen, Y Xu, T Jiang, R Feng, J Sun… - Journal of clinical …, 2013 - Wiley Online Library
What is known and objective There is great interindividual variability in citalopram (CIT)
pharmacokinetics. We attempted to establish a population pharmacokinetic (PPK) model of …

Evaluation of the influence of sex and CYP2C19 and CYP2D6 polymorphisms in the disposition of citalopram

S Fudio, AM Borobia, E Piñana, E Ramírez… - European journal of …, 2010 - Elsevier
We investigate the impact of sex and genotype on citalopram disposition in 35 healthy
volunteers who received an oral dose of 20mg citalopram within a single-dose …

[HTML][HTML] Effect of CYP2C19 Pharmacogenetic Testing on Predicting Citalopram and Escitalopram Tolerability and Efficacy: A Retrospective, Longitudinal Cohort Study

M Mahajna, R Abu Fanne, M Berkovitch, E Tannous… - Biomedicines, 2023 - mdpi.com
Background—Various antidepressant agents are metabolized by the CYP2C19 enzyme,
including Citalopram and Escitalopram. Variation in CYP2C19 expression might give rise to …

Pharmacokinetic comparison of oral solution and tablet formulations of citalopram: a single-dose, randomized, crossover study

MM Gutierrez, W Abramowitz - Clinical therapeutics, 2000 - Elsevier
Background: Citalopram tablets fulfill most dosing needs in the treatment of depression, but
some patients may have difficulty swallowing tablets and thus may be less likely to comply …

Phenotype-genotype relationship and clinical effects of citalopram in Chinese patients

OQP Yin, YK Wing, Y Cheung, ZJ Wang… - Journal of clinical …, 2006 - journals.lww.com
Although the relationship of CYP2C19 polymorphism to citalopram disposition has been
studied in healthy subject, this relationship in combination with dynamic effects (clinical …

Pharmacokinetics of citalopram in relation to genetic polymorphism of CYP2C19

BN Yu, GL Chen, N He, DS Ouyang, XP Chen… - Drug metabolism and …, 2003 - ASPET
The study was designed to define the contribution of cytochrome P450 2C19 (CYP2C19)
and cytochrome P450 3A4 (CYP3A4) to citalopram N-demethylation and to evaluate the …

[PDF][PDF] Bioavailability of Two Oral Tablet Formulations of citalopram 20 mg: Single-Dose, Open-Label, Randomized, Two-Period Crossover Comparison in Healthy …

JA Palma-Aguirre, LG Mireya, CST de Jesus… - J Bioequiv …, 2010 - researchgate.net
Background: Fluconazole is a triazole antifungal agent labeled for use in the treatment of
oropharyngeal and esophageal candidiasis and cryptococcal meningitis, marketed in …

Simultaneous determination of citalopram and its metabolite in human plasma by LC–MS/MS applied to pharmacokinetic study

T Jiang, Z Rong, L Peng, B Chen, Y Xie, C Chen… - … of Chromatography B, 2010 - Elsevier
A simple sensitive and robust method for simultaneous determination of citalopram and
desmethylcitalopram was developed using liquid chromatography tandem mass …