SynthesisBritish journal of clinical pharmacology2008
Is there evidence for biased reporting of published adverse effects data in pharmaceutical industry-funded studies?
Synthesis in British journal of clinical pharmacology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 9 of them syntheses that pooled 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.
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.
Who cites it
29 citing papers in PubMed, 9 syntheses or guidelines pooled it, 69 citations in OpenAlex.
- Polyunsaturated fatty acids (PUFA) for attention deficit hyperactivity disorder (ADHD) in children and adolescents.The Cochrane database of systematic reviews · 2023Pooled it
- Industry sponsorship and research outcome: systematic review with meta-analysis.Intensive care medicine · 2018Pooled it
- Industry sponsorship and research outcome.The Cochrane database of systematic reviews · 2017Pooled it
- Reporting of Adverse Events in Published and Unpublished Studies of Health Care Interventions: A Systematic Review.PLoS medicine · 2016Pooled it
- Janus kinase-1 and Janus kinase-2 inhibitors for treating myelofibrosis.The Cochrane database of systematic reviews · 2015Pooled it
- Quality of reporting in systematic reviews of adverse events: systematic review.BMJ (Clinical research ed.) · 2014Pooled it
- Safety of off-label erythropoiesis stimulating agents in critically ill patients: a meta-analysis.Intensive care medicine · 2013Pooled it
- Polyunsaturated fatty acids (PUFA) for attention deficit hyperactivity disorder (ADHD) in children and adolescents.The Cochrane database of systematic reviews · 2012Pooled it
- The financing of drug trials by pharmaceutical companies and its consequences. Part 1: a qualitative, systematic review of the literature on possible influences on the findings, protocols, and quality of drug trials.Deutsches Arzteblatt international · 2010Pooled it
- Quantifying new threats to health and biomedical literature integrity from rapidly scaled publications and problematic research.Journal of clinical epidemiology · 2026Article
- Reply: Fetal safety of dydrogesterone: clarifying the role of pharmacovigilance.Human reproduction open · 2025Article
- Review
- A Scoping Review on Use of Drugs Targeting the JAK/STAT Pathway in Psoriasis.Frontiers in medicine · 2022Article
- Article
- Assessment of Adverse Events in Protocols, Clinical Study Reports, and Published Papers of Trials of Orlistat: A Document Analysis.PLoS medicine · 2016Article
- Comments on manuscript--Zheng, J., Huynh, T., Gasparon, M., Ng, J. and Noller, B., 2013. Human health risk assessment of lead from mining activities at semi-arid locations in the context of total lead exposure. Environmental Science and Pollution Research, 20, 8404-8416.Environmental science and pollution research international · 2015Article
- Quality assessment of observational studies in a drug-safety systematic review, comparison of two tools: the Newcastle-Ottawa Scale and the RTI item bank.Clinical epidemiology · 2014Article
- The Drug Facts Box: Improving the communication of prescription drug information.Proceedings of the National Academy of Sciences of the United States of America · 2013Article
- Physician and stakeholder perceptions of conflict of interest policies in oncology.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2013Article
- SPIRIT 2013 explanation and elaboration: guidance for protocols of clinical trials.BMJ (Clinical research ed.) · 2013 · on this mapArticle
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors at 1 institution in 1 country.
Funding
Abstract
aimTo investigate whether adverse effects data for the sponsor's product are presented more favourably in pharmaceutical industry-funded studies than in non-industry-funded studies.
methodsWe conducted a systematic review of methodological evaluations that had assessed the relationship between industry funding and the reported risk of adverse effects. Searches were undertaken in 10 databases and supplemented with other sources of information such as handsearching, citation searching, checking conference proceedings and discussion with experts. Two reviewers independently screened the records and carried out data extraction for potentially relevant papers. We included studies that compared the results and interpretation of the adverse effects data according to funding source (e.g. adverse effects data in pharmaceutical industry research vs. data from nonprofit organizations, or from one manufacturer vs. another). Methodological evaluations were excluded if categories of funding source were not explicitly specified by the researchers, and if we were uncertain that industry-funded studies were present in the evaluation.
resultsThe search strategy yielded 4,069 hits, of which six methodological evaluations met our inclusion criteria. One survey of 370 trials covering a wide range of topics found that trials with industry sponsors had more complete reporting of adverse effects compared with non-industry-funded trials, whereas another survey of 504 inhaled corticosteroid studies showed no apparent difference after confounding factors were adjusted for. In contrast, we found evidence from post hoc subgroup analyses involving two products where the likelihood of harm was of a lower magnitude in manufacturer-funded studies compared with nonmanufacturer-funded studies. There is also evidence from four methodological evaluations that authors with industry funding were more likely than authors without pharmaceutical funding to interpret and conclude that a drug was safe, even among studies that did find a statistically significant increase in adverse effects for the sponsored product.
conclusionsOur review indicates that industry funding may not be a major threat to bias in the reporting of the raw adverse effects data. However, we are concerned about potential bias in the interpretation and conclusions of industry-funded authors and studies.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.