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Differences in Adverse Effect Reporting in Placebo Groups in SSRI and Tricyclic Antidepressant Trials: A Systematic Review and Meta-Analysis
Abstract
Background Biases in adverse effect reporting in randomized controlled trials (RCTs) [e.g. due to investigator expectations or assessment quality] can be quantified by studying the rates of adverse events reported in the placebo arms of such trials.Objective We compared the rates of adverse effects reported in the placebo arms of tricyclic antidepressant (TCA) trials and placebo arms of selective serotonin reuptake inhibitor (SSRI) trials.Methods We conducted a literature search for RCTs across PUBMED, Scopus and the Cochrane Central Register of Controlled Trials (CENTRAL). Only studies allowing adverse effect analysis were included. Publication year ranged from 1981 to 2007.Results Our systematic review and meta-analysis included 143 placebocontrolled RCTs and data from 12,742 patients. Only 21% of studies used structured and systematic adverse effect ascertainment strategies. The way in which trials recorded adverse events influenced the rate of adverse effects substantially. Systematic assessment led to higher rates than less systematic assessment. Far more adverse effects were reported in TCA-placebo groups compared with SSRI-placebo groups, e.g. dry mouth (odds ratio [OR] = 3.5; 95% CI 2.9, 4.2); drowsiness (OR = 2.7; 95%CI 2.2, 3.4); constipation (OR= 2.7; 95%CI 2.1, 3.6); sexual problems (OR =2.3; 95%CI 1.5, 3.5). Regression analyses controlling for various influencing factors confirmed the results.Conclusion Adverse effect profiles reported in clinical trials are strongly influenced by expectations from investigators and patients. This difference cannot be attributed to ascertainment methods. Adverse effect patterns of the drug group are closely related to adverse effects of the placebo group. These results question the validity of the assumption that adverse effects in placebo groups reflect the 'drug-unspecific effects'.
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In the citing paper
“significantly more profound adverse effects were reported in TCA-placebo groups compared with SSRI-placebo groups.”
From Addressing the Side Effects of Contemporary Antidepressant Drugs: A Comprehensive Review (2018) · cites this paper as [106]
In the citing paper
“adverse effect profiles between SSRIs and TCAs are prone to systematic expectation influences.”
From Addressing the Side Effects of Contemporary Antidepressant Drugs: A Comprehensive Review (2018) · cites this paper as [106]
In the citing paper
“dry mouth (odds ratio [OR] = 3.5; 95% CI: 2.9–4.2), drowsiness (OR = 2.7; 95% CI: 2.2–3.4), constipation (OR= 2.7; 95% CI: 2.1–3.6), sexual problems (OR =2.3; 95% CI 1.5–3.5) were more frequent in the placebo group with the TCAs study than the placebo group or the SSRIs study.”
From Addressing the Side Effects of Contemporary Antidepressant Drugs: A Comprehensive Review (2018) · cites this paper as [106]
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Meißner, C., Warren, C. V., Fadai, T., Müller, A., Zapf, A., Lezius, S., Ozga, A.-K., Falkenberg, I., Kircher, T., & Nestoriuc, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26598848
Self-citationMüller, A., Konigorski, S., Meißner, C., Fadai, T., Warren, C. V., Falkenberg, I., Kircher, T., & Nestoriuc, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26626822
Self-citationMeißner, C., Warren, C. V., Fadai, T., Müller, A., Zapf, A., Lezius, S., Ozga, A.-K., Falkenberg, I., Kircher, T., & Nestoriuc, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26598851
Self-citationMüller, A., Konigorski, S., Meißner, C., Fadai, T., Warren, C. V., Falkenberg, I., Kircher, T., & Nestoriuc, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26626819
Self-citationSelf-reported antidepressant side effects in psychiatric patients with depressive disorders
von Knorring, J., Baryshnikov, I., Jylhä, P., Talaslahti, T., & Isometsä, E. (2026) · Nordic Journal of Psychiatry · doi:10.1080/08039488.2026.2686197
Does Adding Nocebo Avoidance Strategies Increase the Strength of Nocebo Education?
Spotts, E. K., & Geers, A. L. (2026) · European Journal of Health Psychology · doi:10.1027/2512-8442/a000207
Metadata
- Authors
- Rief, W., Nestoriuc, Y., von Lilienfeld-Toal, A., Dogan, I., Schreiber, F., Hofmann, S. G., Barsky, A. J., & Avorn, J.
- Affiliations
- Philipps University of Marburg (DE)
- Boston University (US)
- Brigham and Women's Hospital (US)
- Corresponding author
- Rief, Winfried
- Venue
- Drug Safety
- Published
- 2009-11
- Volume
- 32
- Issue
- 11
- Pages
- 1041-1056
- ISSN
- 0114-5916 (ISSN-L)
- OpenAlex
- W59643826
- Semantic Scholar
- 50b250c59bddc89685a35b4cffa7ab9cf1b7a1e4
- Cited by
- 202
- References
- 192
- Citations by year
- 2026: 3 · 2025: 6 · 2024: 11 · 2023: 6 · 2022: 15 · 2021: 14 · 2020: 12 · 2019: 18 · 2018: 16 · 2017: 11 · 2016: 17 · 2015: 15 · 2014: 16 · 2013: 11 · 2012: 16
- FWCI
- 12.82
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Drug Safety (publishedVersion)
- PubMed (publishedVersion)
- Radboud Repository (Radboud University) (submittedVersion)
- Topics
- Social Sciences › Decision Sciences › Statistics, Probability and Uncertainty › Meta-analysis and systematic reviews
- Health Sciences › Nursing › Issues, ethics and legal aspects › Pharmaceutical industry and healthcare
- Physical Sciences › Mathematics › Statistics and Probability › Statistical Methods in Clinical Trials
- Keywords
- placebo group, selective serotonin reuptake inhibitors, tricyclic antidepressants, investigator bias, xerostomia, sleepiness, constipation, sexual dysfunction, antidepressant trials
- MeSH terms
- Antidepressive Agents, Tricyclic, Humans, Regression Analysis, Research Personnel, Bias, Randomized Controlled Trials as Topic, Selective Serotonin Reuptake Inhibitors, Antidepressive Agents, Second-Generation, Research Subjects
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