Safety and tolerability of duloxetine in the treatment of major depressive disorder: analysis of pooled data from eight placebo‐controlled clinical trials

JI Hudson, MM Wohlreich, DK Kajdasz… - Human …, 2005 - Wiley Online Library
Objective To examine the safety and tolerability of the antidepressant duloxetine across
multiple studies for major depressive disorder (MDD). Method Safety data were integrated …

Duloxetine for the treatment of major depressive disorder: a closer look at efficacy and safety data across the approved dose range

CH Mallinckrodt, A Prakash, AC Andorn… - Journal of psychiatric …, 2006 - Elsevier
OBJECTIVE: This analysis focuses on efficacy and safety data obtained from studies of
duloxetine for the treatment of major depressive disorder (MDD) within the approved dose …

BDNF, interleukin-6, and salivary cortisol levels in depressed patients treated with desvenlafaxine

PT Ninan, RC Shelton, W Bao… - Progress in Neuro …, 2014 - Elsevier
Background Relationships between brain-derived neurotrophic factor (BDNF), interleukin
(IL)-6, and salivary cortisol and both depression severity and treatment response were …

Randomized trial of sertraline versus venlafaxine XR in major depression: efficacy and discontinuation symptoms

A Sir, RF D'Souza, S Uguz, T George… - Journal of Clinical …, 2005 - psychiatrist.com
Background: The comparative efficacy of selective serotonin reuptake inhibitors (SSRIs) and
serotoninnorepinephrine reuptake inhibitors (SNRIs) was recently debated. Meta-analyses …

Abrupt discontinuation compared with a 1-week taper regimen in depressed outpatients treated for 24 weeks with desvenlafaxine 50 mg/d

A Khan, J Musgnung, T Ramey, M Messig… - Journal of Clinical …, 2014 - journals.lww.com
The objective of this study was to determine whether the occurrence of discontinuation
symptoms was equivalent for abrupt discontinuation versus 1-week taper to desvenlafaxine …

Response and remission rates in different subpopulations with major depressive disorder administered venlafaxine, selective serotonin reuptake inhibitors, or placebo

AR Entsuah, H Huang, ME Thase - Journal of Clinical Psychiatry, 2001 - psychiatrist.com
Background: Most examinations of the clinical efficacy of drugs used to treat depression pool
subjects across gender and age groups. This investigation compared these patient …

Desvenlafaxine versus placebo in a fluoxetine-referenced study of children and adolescents with major depressive disorder

KL Weihs, W Murphy, R Abbas, D Chiles… - Journal of child and …, 2018 - liebertpub.com
Objectives: To evaluate the short-term efficacy and safety of desvenlafaxine (25–50 mg/d)
compared with placebo in children and adolescents with major depressive disorder (MDD) …

Moving from serotonin to serotonin-norepinephrine enhancement with increasing venlafaxine dose: clinical implications and strategies for a successful outcome in …

A Fagiolini, N Cardoner, S Pirildar… - Expert Opinion on …, 2023 - Taylor & Francis
Introduction Mental health disorders, especially depressive and anxiety disorders, are
associated with substantial health-related burden. While the second-generation …

Venlafaxine XR demonstrates higher rates of sustained remission compared to fluoxetine, paroxetine or placebo

C Shelton, R Entsuah, SK Padmanabhan… - International clinical …, 2005 - journals.lww.com
The combined serotonin–norepinephrine reuptake inhibitor, venlafaxine XR, has
demonstrated significant response and remission in patients diagnosed with depression …

Desvenlafaxine, a serotonin-norepinephrine uptake inhibitor for major depressive disorder, neuropathic pain and the vasomotor symptoms associated with …

CU Pae, MH Park, DM Marks, C Han… - Current Opinion in …, 2009 - europepmc.org
Desvenlafaxine, a serotonin-norepinephrine reuptake inhibitor (SNRI) developed by Wyeth,
is a novel salt form of the isolated major active metabolite of the antidepressant venlafaxine …