Evidence map›Paper›PMID 34449705›Full record

ReviewNeurology international2021

Selective Serotonin Reuptake Inhibitors and Adverse Effects: A Narrative Review.

Amber N Edinoff, Haseeb A Akuly, Tony A Hanna, Carolina O Ochoa, Shelby J Patti, Yahya A Ghaffar, Alan D Kaye, Omar Viswanath, Ivan Urits, Andrea G Boyer and 2 more

Abstract readReview
In one paragraph

Review in Neurology international, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 220 papers, 15 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
220citing papers in PubMed, 15 pooled it
–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

220 citing papers in PubMed, 15 syntheses or guidelines pooled it.

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  10. The epidemiology and phenomenology of non-antipsychotic-induced dystonia: a hybrid systematic-narrative review.European psychiatry : the journal of the Association of European Psychiatrists · 2025
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  19. The efficacy of adjunctiveThe British journal of psychiatry : the journal of mental science · 2025
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160 more citing papers are in PubMed but not listed here.

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

12 authors.

Amber N EdinoffDepartment of Psychiatry and Behavioral Medicine, Louisiana State University Health Science Center Shreveport, Shreveport, LA 71103, USA.
Haseeb A AkulyDepartment of Psychiatry and Behavioral Medicine, Louisiana State University Health Science Center Shreveport, Shreveport, LA 71103, USA.ORCID 0000-0003-2805-0811
Tony A HannaDepartment of Psychiatry and Behavioral Medicine, Louisiana State University Health Science Center Shreveport, Shreveport, LA 71103, USA.
Carolina O OchoaSchool of Medicine, Louisiana State University Health Shreveport, Shreveport, LA 71103, USA.
Shelby J PattiSchool of Medicine, Louisiana State University Health Shreveport, Shreveport, LA 71103, USA.
Yahya A GhaffarSchool of Medicine, Louisiana State University Health Shreveport, Shreveport, LA 71103, USA.
Alan D KayeDepartment of Anesthesiology, Louisiana State University Health Shreveport, Shreveport, LA 71103, USA.
Omar ViswanathCollege of Medicine-Phoenix, University of Arizona, Phoenix, AZ 85004, USA.
Ivan UritsDepartment of Anesthesiology, Louisiana State University Health Shreveport, Shreveport, LA 71103, USA.ORCID 0000-0002-3652-6085
Andrea G BoyerDepartment of Psychiatry and Behavioral Sciences, Medical University of South Carolina, Charleston, SC 29464, USA.
Elyse M CornettDepartment of Anesthesiology, Louisiana State University Health Shreveport, Shreveport, LA 71103, USA.ORCID 0000-0001-7961-3931
Adam M KayeDepartment of Pharmacy Practice, Thomas J. Long School of Pharmacy and Health Sciences, University of the Pacific, Stockton, CA 95211, USA.ORCID 0000-0002-7224-3322

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Depression is the most prevalent psychiatric disorder in the world, affecting 4.4% of the global population. Despite an array of treatment modalities, depressive disorders remain difficult to manage due to many factors. Beginning with the introduction of fluoxetine to the United States in 1988, selective serotonin reuptake inhibitors (SSRIs) quickly became a mainstay of treatment for a variety of psychiatric disorders. The primary mechanism of action of SSRIs is to inhibit presynaptic reuptake of serotonin at the serotonin transporter, subsequently increasing serotonin at the postsynaptic membrane in the serotonergic synapse. The six major SSRIs that are marketed in the USA today, fluoxetine, citalopram, escitalopram, paroxetine, sertraline, and fluvoxamine, are a group of structurally unrelated molecules that share a similar mechanism of action. While their primary mechanism of action is similar, each SSRI has unique pharmacokinetics, pharmacodynamics, and side effect profile. One of the more controversial adverse effects of SSRIs is the black box warning for increased risk of suicidality in children and young adults aged 18-24. There is a lack of understanding of the complexities and interactions between SSRIs in the developing brain of a young person with depression. Adults, who do not have certain risk factors, which could be confounding factors, do not seem to carry this increased risk of suicidality. Ultimately, when prescribing SSRIs to any patient, a risk-benefit analysis must factor in the potential treatment effects, adverse effects, and dangers of the illness to be treated. The aim of this review is to educate clinicians on potential adverse effects of SSRIs.

Indexed as

adverse effectsselective serotonin reuptake inhibitorssuicidality

Identifiers

PMID34449705
PMCPMC8395812

What OpenQuestion holds

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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 OpenQuestion graph.