Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Marianne Dragheim"'
Publikováno v:
Journal of Psychiatric Research. 101:72-79
This study aimed to evaluate if efficacy and tolerability of switching to vortioxetine is independent of previous SSRI or SNRI treatment in patients who had been inadequately treated for their current major depressive episode. Patients from a double-
Publikováno v:
European Neuropsychopharmacology. 26:979-993
The efficacy and safety of vortioxetine, an antidepressant approved for the treatment of adults with major depressive disorder (MDD), was studied in 11 randomized, double-blind, placebo-controlled trials of 6/8 weeks׳ treatment duration. An aggregat
Publikováno v:
The International Journal of Neuropsychopharmacology
Digital.CSIC. Repositorio Institucional del CSIC
instname
INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Digital.CSIC. Repositorio Institucional del CSIC
instname
INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
The efficacy, safety, and tolerability of Lu AA21004 vs. placebo using venlafaxine XR as active reference in patients with DSM-IV-TR major depressive disorder (MDD) were evaluated. Lu AA21004 is a novel antidepressant that is a 5-HT3 and 5-HT7 recept
Autor:
Marianne Dragheim, Atul R. Mahableshwarkar, Yinzhong Chen, Anita H. Clayton, William Palo, Paula L. Jacobsen
Publikováno v:
CNS spectrums. 21(5)
ObjectiveAntidepressants are frequently associated with treatment-emergent sexual dysfunction (TESD). Vortioxetine, which was approved for patients with major depressive disorder (MDD), has a receptor profile that suggests limited impact on sexual fu
Publikováno v:
European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology. 22(7)
The efficacy, safety, and tolerability of Lu AA21004 versus placebo, using duloxetine as active reference, in patients with DSM-IV-TR diagnosed major depressive disorder (MDD) were evaluated in this 8-week, multi-site study. Patients (n=766) had a ba
Publikováno v:
European Neuropsychopharmacology. 22:S255-S256
Publikováno v:
European Neuropsychopharmacology. 21:S396-S397
Publikováno v:
European Neuropsychopharmacology. 24:S466
Publikováno v:
European Neuropsychopharmacology. 19:S426-S427
Publikováno v:
European Neuropsychopharmacology. 21:S390