Evidence map›Paper›PMID 42410139›Full record

ReviewClinical drug investigation2026

Desvenlafaxine as a Potential First-Line Treatment for Major Depressive Disorder: A Comprehensive Review and Consensus-Based Clinical Perspective on Efficacy, Safety and Patient Selection Profiles.

Claudia Carmassi, Christoph U Correll, Javier de Diego-Adeliño, Antonio Vian-Lains, Ciro Oliveira, Alex Schneider-Pérez, Vikas Mohan Sharma

Abstract readReview
In one paragraph

Review in Clinical drug investigation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Claudia CarmassiDepartment of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
Christoph U CorrellDepartment of Child and Adolescent Psychiatry, Universitätsmedizin Charité Berlin, Berlin, Germany.
Javier de Diego-AdeliñoPsychiatry Department, Hospital de la Santa Creu i Sant Pau, Carrer de Sant Quintí, 89, 08041, Barcelona, Spain. fdiego@santpau.cat.
Antonio Vian-LainsHighfield Healthcare, Dublin, Ireland.
Ciro OliveiraPsychiatric Clinic, Hospital Júlio de Matos (ULS São José), Avenida do Brasil, n.º 53, 1700-063, Lisbon, Portugal. cirooliveira@ulssjose.min-saude.pt.ORCID http://orcid.org/0009-0006-0889-4100
Alex Schneider-PérezGlobal Medical Affairs Department, Neuraxpharm, Barcelona, Catalonia, Spain.
Vikas Mohan SharmaGlobal Medical Affairs Department, Neuraxpharm, Barcelona, Catalonia, Spain.

Funding

Neuraxpharm Funding of the writing of the manuscript
6 · The paper itself

Abstract

Major depressive disorder is a leading cause of disability worldwide, with significant challenges in treatment response, adherence and functional recovery. Despite the availability of numerous antidepressants, a substantial proportion of patients fail to achieve remission with initial therapy, underscoring the need for effective first-line treatment options. Desvenlafaxine, a serotonin-noradrenaline reuptake inhibitor, has demonstrated efficacy and safety in major depressive disorder, while its pharmacokinetic properties result in minimal drug-drug interactions. This narrative review evaluates clinical evidence supporting the use of desvenlafaxine as a first-line treatment and examines patient subgroups that may benefit most from this antidepressant. A comprehensive literature review was conducted to evaluate the evidence on desvenlafaxine in the treatment of major depressive disorder. This was supplemented by clinical insights discussed during a virtual advisory board meeting held on 16 December, 2024, attended by the authors-psychiatrists from Italy, Germany, Spain, Ireland and Portugal-together with representatives from Neuraxpharm, who market desvenlafaxine. The available evidence suggests that desvenlafaxine offers early symptom relief, sustained efficacy across diverse major depressive disorder symptom clusters, and benefits for patients with anhedonia, fatigue, cognitive dysfunction and functional impairment. Its tolerability and safety profile, including a lower risk of weight gain and drug-drug interactions, contributes to its ease of use and improved adherence. Based on the authors' clinical consensus, desvenlafaxine may be particularly suitable for working-age adults, perimenopausal and menopausal women, those with general medical comorbidities or polypharmacy concerns, and individuals requiring an antidepressant with a broad mechanism of action. In addition, its predictable pharmacokinetics make it a practical choice in primary care settings. While most current guidelines typically recommend selective serotonin reuptake inhibitors as first-line treatment, the favourable tolerability profile and efficacy of desvenlafaxine across diverse symptom clusters may support its consideration as a first-line option in select patient populations.

Indexed as

Antidepressive AgentsDesvenlafaxine SuccinateMajor Depressive DisorderSerotonin and Noradrenaline Reuptake InhibitorsConsensusHumansPatient SelectionTreatment OutcomeAntidepressive AgentsDesvenlafaxine SuccinateSerotonin and Noradrenaline Reuptake Inhibitors

Identifiers

PMID42410139
PMCPMC13486089

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.