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Trials. 2010; 11: 37.
Published online Apr 13, 2010. doi:  10.1186/1745-6215-11-37
PMCID: PMC2867979

Reporting bias in medical research - a narrative review

Abstract

Reporting bias represents a major problem in the assessment of health care interventions. Several prominent cases have been described in the literature, for example, in the reporting of trials of antidepressants, Class I anti-arrhythmic drugs, and selective COX-2 inhibitors. The aim of this narrative review is to gain an overview of reporting bias in the medical literature, focussing on publication bias and selective outcome reporting. We explore whether these types of bias have been shown in areas beyond the well-known cases noted above, in order to gain an impression of how widespread the problem is. For this purpose, we screened relevant articles on reporting bias that had previously been obtained by the German Institute for Quality and Efficiency in Health Care in the context of its health technology assessment reports and other research work, together with the reference lists of these articles.

We identified reporting bias in 40 indications comprising around 50 different pharmacological, surgical (e.g. vacuum-assisted closure therapy), diagnostic (e.g. ultrasound), and preventive (e.g. cancer vaccines) interventions. Regarding pharmacological interventions, cases of reporting bias were, for example, identified in the treatment of the following conditions: depression, bipolar disorder, schizophrenia, anxiety disorder, attention-deficit hyperactivity disorder, Alzheimer's disease, pain, migraine, cardiovascular disease, gastric ulcers, irritable bowel syndrome, urinary incontinence, atopic dermatitis, diabetes mellitus type 2, hypercholesterolaemia, thyroid disorders, menopausal symptoms, various types of cancer (e.g. ovarian cancer and melanoma), various types of infections (e.g. HIV, influenza and Hepatitis B), and acute trauma. Many cases involved the withholding of study data by manufacturers and regulatory agencies or the active attempt by manufacturers to suppress publication. The ascertained effects of reporting bias included the overestimation of efficacy and the underestimation of safety risks of interventions.

In conclusion, reporting bias is a widespread phenomenon in the medical literature. Mandatory prospective registration of trials and public access to study data via results databases need to be introduced on a worldwide scale. This will allow for an independent review of research data, help fulfil ethical obligations towards patients, and ensure a basis for fully-informed decision making in the health care system.

Background

The reporting of research findings may depend on the nature and direction of results, which is referred to as "reporting bias" [1,2]. For example, studies in which interventions are shown to be ineffective are sometimes not published, meaning that only a subset of the relevant evidence on a topic may be available [1,2]. Various types of reporting bias exist (Table (Table1),1), including publication bias and outcome reporting bias, which concern bias from missing outcome data on 2 levels: the study level, i.e. "non-publication due to lack of submission or rejection of study reports", and the outcome level, i.e. "the selective non-reporting of outcomes within published studies" [3].

Table 1
Definitions of some types of reporting bias1

Reporting bias on a study level

Results of clinical research are largely underreported or reported with delay. Various analyses of research protocols submitted to institutional review boards and research ethics committees in Europe, the United States, and Australia found that on average, only about half of the protocols had been published, with higher publication rates in Anglo-Saxon countries [4-10].

Similar analyses have been performed of trials submitted to regulatory authorities: a cohort study of trials supporting new drugs approved by the Food and Drug Administration (FDA) identified over 900 trials of 90 new drugs in FDA reviews; only 43% of the trials were published [11]. Wide variations in publication rates have been shown for specific indications [12-16]. The selective submission of clinical trials with positive outcomes to regulatory authorities has also been described [17]. Even if trials are published, the time lapse until publication may be substantial [8,18,19].

There is no simple classification of a clinical trial into "published" or "unpublished", as varying degrees of publication exist. These range from full-text publications in peer-reviewed journals that are easily identifiable through a search in bibliographic databases, to study information entered in trial registries, so-called grey literature (e.g. abstracts and working papers), and data on file in drug companies and regulatory agencies, which may or may not be provided to health technology assessment (HTA) agencies or other researchers after being requested. If such data are transmitted, they may then be fully published or not (e.g. the German Institute for Quality and Efficiency in Health Care [Institut für Qualität und Wirtschaftlichkeit im Gesundheitswesen, IQWiG] publishes all data used in its assessment reports [20], whereas the UK National Institute for Clinical Excellence [NICE] may accept "commercial in confidence" data [21]).

Even if studies are presented at meetings, this does not necessarily mean subsequent full publication: an analysis of nearly 30,000 meeting abstracts from various disciplines found a publication rate of 63% for randomized or controlled clinical trials [22].

Reporting bias on an outcome level

Selective reporting within a study may involve (a) selective reporting of analyses or (b) selective reporting of outcomes. This may include, for example, the reporting of (a) per-protocol (PP) versus intention-to-treat (ITT) analyses or adjusted versus unadjusted analyses, and (b) outcomes from different time points or statistically significant versus non-significant outcomes [3,23].

Various reviews have found extensive selective reporting in study publications [3,14,24-28]. For example, comparisons of publications with study protocols have shown that primary outcomes had been newly introduced, omitted, or changed in about 40% to 60% of cases [3,24]. Selective reporting particularly concerns the underreporting of adverse events [12,29-32]. For example, an analysis of 192 randomized drug trials in various indications showed that only 46% of publications stated the frequency of specific reasons for treatment discontinuation due to toxicity [29]. Outcomes are not only selectively reported, but negative results are reported in a positive manner and conclusions are often not supported by results data [16,26,33-35]. For instance, a comparison of study characteristics reported in FDA reviews of New Drug Applications (NDAs) with those reported in publications found that 9 of 99 conclusions had been changed in the publications, all in favour of the new drug [26].

Factors associated with reporting bias

Characteristics of published studies

The fact that studies with positive or favourable results are more likely to be published than those with negative or unfavourable results was already addressed in the 1950s [36], and has since been widely confirmed [3,6-8,14,37-40]. Studies with positive or favourable results have been associated with various other factors such as faster publication [8,18,19,37], publication in higher impact factor journals [7,41], a greater number of publications [7] (including covert duplicate publications [42]), more frequent citation [43-45], and more likely publication in English [46].

Several other factors have been linked to successful publication, for example, methodological quality [47], study type [47], sample size [5,7,48], multicentre status [5,6,41], and non-commercial funding [5,6,49,50]. However, for some factors, these associations are inconsistent [6,37].

Submission and rejection of studies

One of the main reasons for the non-publication of negative studies seems to be the non-submission of manuscripts by investigators, not the rejection of manuscripts by medical journals. A follow-up of studies approved by US institutional review boards showed that only 6 of 124 unpublished studies had actually been rejected for publication [6]. A prospective cohort study of 745 manuscripts submitted to JAMA showed no statistically significant difference in publication rates between studies with positive and those with negative results [51], which has been confirmed by further analyses of other journals [47,52]. Author surveys have shown that the most common reasons for not submitting papers were negative results and a lack of interest, time, or other resources [39-41,53].

The role of the pharmaceutical industry

An association has been shown between industry sponsorship or industry affiliation of authors and positive research outcomes and conclusions, both in publications of primary studies and in systematic reviews [49,54-63]. For example, in a systematic review of the scope and impact of financial conflicts of interest in biomedical research, an aggregation of the results of 8 analyses of the relation between industry sponsorship and outcomes showed a statistically significant association between industry sponsorship and pro-industry conclusions [55]. A comparison of the methodological quality and conclusions in Cochrane reviews with those in industry-supported meta-analyses found that the latter were less transparent, less critical of methodological limitations of the included trials, and drew more favourable conclusions [57]. In addition, publication constraints and active attempts to prevent publication have been identified in industry-sponsored research [55,64-68]. Other aspects of industry involvement, such as design bias, are beyond the scope of this paper.

Rationale, aim and procedure

IQWiG produces HTA reports of drug and non-drug interventions for the decision-making body of the statutory health care funds, the Federal Joint Committee. The process of report production includes requesting information on published and unpublished studies from manufacturers; unfortunately, compliance by manufacturers is inconsistent, as recently shown in the attempted concealment of studies on antidepressants [69]. Reporting bias in antidepressant research has been shown before [16,70]; other well-known cases include Class I anti-arrhythmic drugs [71,72] and selective COX-2 inhibitors [73,74].

The aim of this narrative review was to gain an overview of reporting bias in the medical literature, focussing on publication bias and selective outcome reporting. We wished to explore whether this type of bias has been shown in areas beyond the well-known cases noted above, in order to obtain an impression of how widespread this problem is. The review was based on the screening of full-text publications on reporting bias that had either been obtained by the Institute in the context of its HTA reports and other research work or were identified by the screening of the reference lists of the on-site publications. The retrieved examples were organized according to indications and interventions. We also discuss the effects of reporting bias, as well as the measures that have been implemented to solve this problem.

The term "reporting bias" traditionally refers to the reporting of clinical trials and other types of studies; if one extends this term beyond experimental settings, for example, to the withholding of information on any beneficial medical innovation, then an early example of reporting bias was noted by Rosenberg in his article "Secrecy in medical research", which describes the invention of the obstetrical forceps. This device was developed by the Chamberlen brothers in Europe in the 17th century; however, it was kept secret for commercial reasons for 3 generations and as a result, many women and neonates died during childbirth [75]. In the context of our paper, we also considered this extended definition of reporting bias.

Findings

We identified reporting bias in 40 indications comprising around 50 different interventions. Examples were found in various sources, e.g. journal articles of published versus unpublished data, reviews of reporting bias, editorials, letters to the editor, newspaper reports, expert and government reports, books, and online sources. The following text summarizes the information presented in these examples. More details and references to the background literature are included in Additional file 1: Table S2.

Mental and behavioural disorders

Reporting bias is common in psychiatric research (see below). This also includes industry-sponsorship bias [76-82].

Depression

Turner et al compared FDA reviews of antidepressant trials including over 12,000 patients with the matching publications and found that 37 out of 38 trials viewed as positive by the FDA were published [16]. Of the 36 trials having negative or questionable results according to the FDA, 22 were unpublished and 11 of the 14 published studies conveyed a positive outcome. According to the publications, 94% of the trials had positive results, which was in contrast to the proportion reported by the FDA (51%). The overall increase in effect size in the published trials was 32%. In a meta-analysis of data from antidepressant trials submitted to the FDA, Kirsch et al requested data on 6 antidepressants from the FDA under the Freedom of Information Act. However, the FDA did not disclose relevant data from 9 of 47 trials, all of which failed to show a statistically significant benefit over placebo. Data from 4 of these trials were available on the GlaxoSmithKline (GSK) website. In total, the missing data represented 38% of patients in sertraline trials and 23% of patients in citalopram trials. The analysis of trials investigating the 4 remaining antidepressants showed that drug-placebo differences in antidepressant efficacy were relatively small, even for severely depressed patients [83].

Selective serotonin reuptake inhibitors (SSRIs)

One of the biggest controversies surrounding unpublished data was the withholding of efficacy and safety data from SSRI trials. In a lawsuit launched by the Attorney General of the State of New York it was alleged that GSK had published positive information about the paediatric use of paroxetine in major depressive disorder (MDD), but had concealed negative safety and efficacy data [84]. The company had conducted at least 5 trials on the off-label use of paroxetine in children and adolescents but published only one, which showed mixed results for efficacy. The results of the other trials, which did not demonstrate efficacy and suggested a possible increased risk of suicidality, were suppressed [84]. As part of a legal settlement, GSK agreed to establish an online clinical trials registry containing results summaries for all GSK-sponsored studies conducted after a set date [85,86].

Whittington et al performed a systematic review of published versus unpublished data on SSRIs in childhood depression. While published data indicated a favourable risk-benefit profile for some SSRIs, the inclusion of unpublished data indicated a potentially unfavourable risk-benefit profile for all SSRIs investigated except fluoxetine [70].

Newer antidepressants

IQWiG published the preliminary results of an HTA report on reboxetine, a selective norepinephrine reuptake inhibitor, and other antidepressants. At least 4600 patients had participated in 16 reboxetine trials, but the majority of data were unpublished. Despite a request for information the manufacturer Pfizer refused to provide these data. Only data on about 1600 patients were analysable and IQWiG concluded that due to the risk of publication bias, no statement on the benefit or harm of reboxetine could be made [69,87]. The preliminary HTA report mentioned above also included an assessment of mirtazapine, a noradrenergic and specific serotonergic antidepressant. Four potentially relevant trials were identified in addition to 27 trials included in the assessment, but the manufacturer Essex Pharma did not provide the study reports. Regarding the other trials, the manufacturer did not send the complete study reports, so the full analyses were not available. IQWiG concluded that the results of the assessment of mirtazapine may have been biased by unpublished data [69,87]. After the behaviour of Pfizer and Essex Pharma had been widely publicized, the companies provided the majority of study reports for the final HTA report. The preliminary report's conclusion on the effects of mirtazapine was not affected by the additional data. For reboxetine, the analysis of the published and unpublished data changed the conclusion from "no statement possible" to "no benefit proven" [88].

Bipolar disorder

Lamotrigine

A review by Nassir Ghaemi et al of data on lamotrigine in bipolar disorder provided on the GSK website showed that data from negative trials were available on the website but that the studies had not been published in detail or publications emphasized positive secondary outcomes instead of negative primary ones. Outside of the primary area of efficacy (prophylaxis of mood episodes), the drug showed very limited efficacy in indications such as acute bipolar depression, for which clinicians were supporting its use [35].

Gabapentin

Gabapentin, a GABA analogue, was approved by the FDA in 1993 for a certain type of epilepsy, and in 2002 for postherpetic neuralgia. As of February 1996, 83% of gabapentin use was for epilepsy, and 17% for off-label indications (see the expert report by Abramson [89]). As the result of a comprehensive marketing campaign by Pfizer, the number of patients in the US taking gabapentin rose from about 430,000 to nearly 6 million between 1996 and 2001; this increase was solely due to off-label use for indications, including bipolar disorder. As of September 2001, 93.5% of gabapentin use was for off-label indications [89]. In a further expert report, Dickersin noted "extensive evidence of reporting bias" [34], which she further analysed in a recent publication with Vedula et al [90]. Concerning the trials of gabapentin for bipolar disorders, 2 of the 3 trials (all published) were negative for the primary outcome. However, these publications showed "extensive spin and misrepresentation of data" [34].

Schizophrenia

Quetiapine

The Washington Post reported that a trial on quetiapine, an atypical antipsychotic, was "silenced" in 1997, the same year it was approved by the FDA to treat schizophrenia. The study ("Study 15") was not published. Patients taking quetiapine had shown high rates of treatment discontinuations and had experienced significant weight increases. However, data presented by the manufacturer AstraZeneca in 1999 at European and US meetings actually indicated that the drug helped psychotic patients lose weight [91].

Panic disorder

Paroxetine

Turner described an example of reporting bias in the treatment of panic disorder: according to a review article, 3 "well designed studies" had apparently shown that the controlled-release formulation of paroxetine had been effective in patients with this condition. However, according to the corresponding FDA statistical review, only one study was strongly positive, the second study was non-significant regarding the primary outcome (and marginally significant for a secondary outcome), and the third study was clearly negative [92].

Further examples of reporting bias in research on mental and behavioural disorders are included in Additional file 1: Table S2.

Disorders of the nervous system

Alzheimer's disease

Rofecoxib

Internal company analyses and information provided by the manufacturer Merck & Co to the FDA on rofecoxib, a selective COX-2 inhibitor, were released during litigation procedures. The documents referred to trials investigating the effects of rofecoxib on the occurrence or progression of Alzheimer's disease. Psaty and Kronmal performed a review of these documents and 2 trial publications and showed that, although presenting mortality data, the publications had not included analyses or statistical tests of these data and both had concluded that regarding safety, rofecoxib was "well tolerated". In contrast, in April 2001, Merck's internal ITT analyses of pooled data from these 2 trials showed a significant increase in total mortality. However, this information was neither disclosed to the FDA nor published in a timely fashion [74]. Rofecoxib was taken off the market by Merck in 2004 [93], among allegations that the company had been aware of the safety risks since 2000 [73].

Acute pain

Valdecoxib

In their article "An untold story?", Lenzer and Brownlee reported the case of valdecoxib, another selective COX-2 inhibitor withdrawn from the market due to cardiovascular concerns [94,95]. In 2001, the manufacturer Pfizer had applied for approval in 4 indications, including acute pain. The application for acute pain was rejected and some of the information about the corresponding trials removed from the FDA website for confidentiality reasons. Further examples of reporting bias in research on pain are presented in Additional file 1: Table S2.

Migraine

Gabapentin

According to the expert report by Dickersin, all 3 trials on gabapentin for migraine showed negative results for the primary outcome. Substantial reporting bias was present. One trial was fully published (seemingly with a redefined primary outcome showing positive results in a subgroup of patients), one was unpublished, and preliminary (positive) results were presented for the third trial [34].

Disorders of the circulatory system

Coronary heart disease (bleeding prophylaxis during bypass surgery)

Aprotinin

In his article on observational studies on drug safety, Hiatt reported the case of aprotinin, an antifibrinolytic drug formerly marketed to reduce bleeding during heart bypass graft surgery. In 2006, data from 2 published observational studies indicated serious concerns about the drug's safety [96]. The FDA subsequently convened an expert meeting in which the safety data presented by the manufacturer Bayer did not reveal any increased risk of fatal or nonfatal cardiovascular events. However, it turned out that Bayer had not presented additional observational data, which, according to an FDA review, indicated that aprotinin may be associated with an increased risk of death and other serious adverse events. In November 2007 Bayer suspended the worldwide marketing of aprotinin, after requests and advice from various drug regulating authorities [97].

Prevention of arrhythmia

Class I anti-arrhythmic drugs

In a clinical trial conducted in 1980, 9 out of 49 patients with suspected acute myocardial infarction treated with a class Ic anti-arrhythmic drug (lorcainide) died, versus only one patient in the placebo group; the investigators interpreted this finding as an "effect of chance" [71]. The development of lorcainide was discontinued for commercial reasons, and the results of the trial were not published until 1993. The investigators then stated that if the trial had been published earlier, it "might have provided an early warning of trouble ahead" [71]. Instead, during the 1980s, class I drugs were widely used, even though concerns as to their lack of effect were published as early as 1983 [98,99]. Further reviews and trials confirmed this suspicion, as well as an increase in mortality [100-102]. In his book "Deadly Medicine", Moore described the consequences as "America's worst drug disaster", which had "produced a death toll larger than the United States' combat losses in wars such as Korea and Vietnam" [72]. Further examples of reporting bias in research on disorders of the circulatory system are presented in Additional file 1: Table S2.

Disorders of the digestive system

Irritable bowel syndrome

Alosetron

Barbehenn et al compared a published trial on alosetron, a 5-HT3 antagonist, in women with irritable bowel syndrome with data obtained from the FDA [103]. She noted that according to the graphics in the publication, which presented relative differences in pain and discomfort scores, the drug seemed effective. However, when plotting the absolute data from the FDA review, the data points were almost superimposable. After discussions with the FDA about potential serious side effects, the drug was withdrawn from the market by the manufacturer in 2000, but reapproved with restrictions in 2002 [104]. A further example of reporting bias in research on disorders of the digestive system is presented in Additional file 1: Table S2.

Disorders of the genitourinary system/Perinatal medicine

Urinary incontinence

Duloxetine

Lenzer and Brownlee also reported cases of suicide in a trial investigating the selective serotonin and noradrenalin reuptake inhibitor duloxetine for a new indication, urinary incontinence in women. However, the FDA refused to release data on these cases, citing trade secrecy laws. These laws "permit companies to withhold all information, even deaths, about drugs that do not win approval for a new indication, even when the drug is already on the market for other indications" [94]. Two examples of reporting bias in perinatal research are presented in Additional file 1: Table S2.

Disorders of the musculoskeletal system

Osteoarthritis

Rofecoxib

In 2000, a trial comparing upper gastrointestinal toxicity of rofecoxib, a selective COX-2 inhibitor, and naproxen in over 8000 patients with rheumatoid arthritis reported that rofecoxib was associated with significantly fewer clinically important upper gastrointestinal events. The significantly lower myocardial infarction rate in the naproxen group was attributed to a cardioprotective effect of naproxen (VIGOR trial, [105]). Concerns about the risk of selective COX-2-inhibitor-related cardiovascular events were raised as early as 2001 [106], and in 2002, an analysis including previously unpublished data from FDA reports of the VIGOR trial showed a statistically significant increase of serious cardiovascular thrombotic events in patients using rofecoxib [107].

Celecoxib

In their article on access to pharmaceutical data at the FDA, Lurie and Zieve presented the example of the selective COX-2 inhibitor celecoxib: in a journal publication of a trial investigating the gastrointestinal toxicity with celecoxib versus other pain medications, the study authors concluded that the drug was associated with a lower incidence of gastrointestinal ulcers after 6 months of therapy [108,109]. However, they failed to disclose that at the time of publication they had already received data for the full study period (12 months), which showed no advantage over the comparator drugs for the above outcome [109].

Disorders of the skin

Atopic dermatitis

Evening primrose oil

In his editorial "Evening primrose oil for atopic dermatitis - Time to say goodnight", Williams reported that he and his colleague, who had performed an individual patient meta-analysis of evening primrose oil for atopic dermatitis commissioned by the UK Department of Health, were not given permission to publish their report, which included 10 previously unpublished studies. After submission of the report to the Department of Health, Searle, the company then responsible for product marketing, required the authors and referees to sign a written statement that the contents of the report had not been leaked. Other research had not shown convincing evidence of a benefit, and in 2002 the UK Medicines Control Agency withdrew marketing authorisation [66].

Endocrine and metabolic disorders

Diabetes mellitus type 2

Rosiglitazone

The US cardiologist Steven Nissen commented on safety issues surrounding rosiglitazone, a thiazolidinedione used to treat type 2 diabetes. After the drug's approval, the FDA was informed in August 2005 by the manufacturer GSK that it had performed a meta-analysis of 42 randomized clinical trials of rosiglitazone, which suggested a 31% increase in the risk of ischaemic cardiovascular complications. GSK posted this finding on its website. However, neither GSK nor the FDA disseminated their findings in a broad way to the scientific community and the public [110]. The safety concerns were supported by a controversially discussed meta-analysis performed by Nissen and Wolski, who found that treatment with rosiglitazone was associated with a significantly increased risk of myocardial infarction and an increase in the risk of death from cardiovascular causes that had borderline significance [111]. More examples of reporting bias in diabetes research are presented in Additional file 1: Table S2.

Hypercholesterolaemia

Ezetimibe and simvastatin

In his article "Controversies surround heart drug study" Mitka described a trial that compared the 2 anticholesterol drugs ezetimibe and simvastatin versus simvastatin alone in patients with heterozygous familial hypercholesterolaemia [112]. No statistically significant difference between treatment groups was found for the primary outcome (mean change in the carotid intima-media thickness) after 2 years [113]. The trial, which was sponsored by Merck & Co. and Schering-Plough, was concluded in April 2006. A delay of almost 2 years in the reporting of results followed amidst allegations that the manufacturers had attempted to change the study endpoints prior to the publication of results [112]. A further case of reporting bias in research on ezetimibe is included in Additional file 1: Table S2.

Cerivastatin

Psaty et al conducted a review of the published literature on the statin cerivastatin and also analysed internal company documents that became available during litigation procedures [114]. In the published literature, cerivastatin was associated with a substantially higher risk of rhabdomyolysis than other statins; this particularly referred to cerivastatin-gemfibrozil combination therapy. Cerivastatin was launched in the US in 1998 by Bayer, and within 3 to 4 months, internal documents indicated there had been multiple cases of cerivastatin-gemfibrozil interactions. However, it took more than 18 months until a contraindication about the concomitant use of the 2 drugs was added to the package insert. The unpublished data available in 1999 also suggested an association between high-dose cerivastatin monotherapy and rhabdomyolysis. In 1999/2000, the company analysed FDA adverse event reporting system data, which suggested that compared with atorvastatin, cerivastatin monotherapy substantially increased the risk of rhabdomyolysis. However, these findings were not disseminated or published. Cerivastatin was removed from the market in August 2001 [114]. In the same month, the German Ministry of Health accused Bayer of withholding vital information from its federal drug agency [115].

Thyroid disorders

Levothyroxine

The Wall Street Journal reported the suppression of the results of a trial comparing the bioavailability of generic and brand-name levothyroxine products in the treatment of hypothyroidism; the investigators had concluded that the products were bioequivalent and in most cases interchangeable [116,117]. The trial was completed in 1990; over the next 7 years, the manufacturer of the brand-name product Synthroid, Boots pharmaceuticals, successfully delayed publication [65]. The manuscript was finally published in 1997.

Menopausal symptoms

Tibolone

A study investigating tibolone, a synthetic steroid, in breast-cancer patients with climacteric complaints was terminated prematurely after it was shown that this drug significantly increased the risk of cancer recurrence [118]. According to the German TV programme Frontal 21, the manufacturer (Schering-Plough, formerly NV Organon) informed regulatory authorities and ethics committees, as well as study centres and participants. However, the study results were not published until 1.5 years later [119].

Neoplasms

Oncology is another area in which reporting bias is common [40,50,54,120-127]. A review of over 2000 oncology trials registered in ClinicalTrials.gov showed that less than 20% were available in PubMed, with substantial differences between trials sponsored by clinical trial networks and those sponsored by industry regarding both publication rates (59% vs. 6%) and the proportion of trials with positive results (50% vs. 75%) [50].

Ovarian cancer

Combination chemotherapy

In one of the earliest publications measuring the effects of reporting bias, Simes compared published oncology trials and trials identified in cancer registries that investigated the survival impact of initial alkylating agent (AA) therapy versus combination chemotherapy (CC) in advanced ovarian cancer. A meta-analysis of the published trials showed a significant survival advantage for CC; however, no such advantage was shown in the meta-analysis of registered trials [121].

Multiple myeloma

Combination chemotherapy

The above study also investigated the survival impact of AA/prednisone versus CC in multiple myeloma. The meta-analysis of published trials demonstrated a significant survival advantage for CC. A survival benefit was also shown in the registered trials; however, the estimated magnitude of the benefit was reduced [121]. A further example of reporting bias in cancer research is presented in Additional file 1: Table S2.

Disorders of the blood

Thalassaemia major

Iron-chelation agents

In his editorial "Thyroid storm", Rennie, among other things, discussed events surrounding a US researcher who had been involved in a trial investigating the effects of an oral iron-chelation agent in patients with thalassaemia major. She had initially published an optimistic article on the effects of this agent. However, further research showed a lack of effectiveness and a potential safety risk. She had signed a confidentiality agreement but, because of her concerns, decided to break confidentiality and report her results at a meeting; the manufacturer unsuccessfully attempted to block her presentation [128].

Bacterial, fungal, and viral infections

Influenza

Oseltamivir

The BMJ and Channel 4 News reported on the difficulties in obtaining data for an updated Cochrane review on neuraminidase inhibitors in influenza [129]. A previous analysis of oseltamivir, which was used in the prior Cochrane review [130], was based on 10 industry-sponsored trials of which only 2 had been published in peer-reviewed journals [131]. The manufacturer Roche initially declined to provide the necessary data to reproduce the analysis and then only provided a selection of files [129]. The Cochrane authors (Jefferson et al) subsequently concluded that "Evidence on the effects of oseltamivir in complications from lower respiratory tract infections, reported in our 2006 Cochrane review, may be unreliable" [132]. Roche has since agreed to provide public access to study summaries and password-protected access to the full study reports [129].

HIV/AIDS

Anti-HIV agents

Ioannidis et al identified several examples of publication bias in trials investigating medications against HIV. At least 13 trials of 6 antiviral agents including at least 3779 patients had remained unpublished for more than 3 years from the time of their meeting presentation or completion. At least 9 of these trials had negative preliminary or final results. For example, 2 large negative isoprinosine trials were unpublished, whilst a positive trial had been published in a high impact journal [33]. Further examples of reporting bias in research on infections are presented in Additional file 1: Table S2.

Acute trauma

Acute spinal cord injury

High-dose steroids

Lenzer and Brownlee described the concerns of neurosurgeons regarding the use of high-dose steroids in patients with acute spinal cord injury. They noted that one neurosurgeon believed that several thousand patients had died as a result of this intervention; 2 surveys showed that many other neurosurgeons shared his concerns. The single available study, which had been funded by the NIH, was potentially flawed and several researchers had unsuccessfully lobbied for the release of the underlying data [94].

Shock

Human albumin infusion

In the UK Health Committee's 2004-2005 report on the influence of the pharmaceutical industry, Chalmers mentioned a systematic review of human albumin solution, which is used in the treatment of shock, e.g. in patients with burns. The results showed no evidence that albumin was helpful and suggested that this intervention may actually be harmful. Although the UK Medicines Control Agency subsequently slightly modified the labelling, it kept confidential the evidence upon which the drug had been re-licensed in 1993 [133,134].

Vaccinations

HIV-1 vaccine

McCarthy reported the case of an HIV-1 vaccine study that was terminated early when no difference in efficacy between the vaccine and placebo was found. After the lead investigators refused to include a post-hoc analysis arguing that it had not been part of the study protocol and that invalid statistical methods had been used, the manufacturer, Immune Response, filed an (unsuccessful) claim seeking to prevent publication. After publication, the manufacturer filed a claim against the study's lead investigators and their universities asking for US $7-10 million in damages [135].

Cancer vaccines

Rosenberg provided various examples of how researchers and companies withheld information on cancer vaccines for competitive reasons; for example, researchers were asked to keep information confidential that might have prevented cancer patients from receiving ineffective or even harmful doses of a new agent [75].

Other indications

Nocturnal leg cramps

Quinine

Man-Song-Hing et al performed a meta-analysis including unpublished individual patient data (IPD) obtained from the FDA on trials investigating quinine for the treatment of nocturnal leg cramps. They showed that the pooling only of published studies overestimated efficacy by more than 100% [136]. Further examples of reporting bias in other indications are presented in Additional file 1: Table S2.

Further research areas

Reporting bias has also been shown in other research areas, such as genetics [137,138], effects of passive smoking [139,140] and nicotine [141,142], and effects of air pollution [143].

Discussion

The numerous examples identified show that reporting bias concerns not only previously highlighted therapies such as antidepressants, pain medication, or cancer drugs, but affects a wide range of indications and interventions. Many cases involved the withholding of study data by manufacturers and regulatory agencies or the active attempt to suppress publication by manufacturers, which either resulted in substantial delays in publication (time-lag bias) or no publication at all.

Limitations of the review

The review does not provide a complete overview of reporting bias in clinical research. Although our efforts to identify relevant literature went beyond the usual efforts applied in narrative reviews, the review is non-systematic and we emphasized this feature in the title. A substantial amount of relevant literature was available in-house and further relevant literature was obtained by screening reference lists. We dispensed with our initial plan to conduct a systematic review to identify cases of reporting bias, as we noticed that many cases were not identifiable by screening titles and abstracts of citations from bibliographic databases, but were "hidden" in the discussion sections of journal articles or mentioned in other sources such as newspapers, books, government reports or websites. As a search of bibliographic databases and the Internet using keywords related to reporting bias produces thousands of potentially relevant hits, we would therefore have had to obtain and read an excessive amount of full texts in order to ensure that we had not missed any examples. This was not feasible due to resource limitations. However, within the framework of a previous publication [144] we had conducted a literature search in PubMed, and some of the citations retrieved formed the basis of our literature pool for the current review. In spite of this non-systematic approach, we were able to identify dozens of cases of reporting bias in numerous indications.

Another potential limitation of the review is the validity of the sources describing cases of reporting bias. Although the majority of examples were identified in peer-reviewed journals, several cases were based on information from other sources such as newspaper articles and websites. However, we also regard these sources to be valuable as they provide a broader overview of reporting bias beyond well-known examples and also offer a starting point for more systematic research on the additional examples identified.

Effects of reporting bias

Published evidence tends to overestimate efficacy and underestimate safety risks. The extent of misestimation is often unknown. The few identified comparisons that quantified overestimates of treatment effects in fully published versus unpublished or not fully published data showed wide variations in their results. Comparisons of pooled published versus pooled published and unpublished FDA data showed a greater treatment effect of 11% to 69% for individual antidepressants, 32% for the class of antidepressants [16], and over 100% for an agent to treat nocturnal leg cramps [136]. In addition, published studies have shown a 9% to 15% greater treatment effect than grey literature studies [145,146]. Thus, the conclusions of systematic reviews and meta-analyses based on published evidence alone may be misleading [5,7,38]. This is a serious concern as these documents are being used increasingly to support decision making in the health care system. Reporting bias may consequently result in inappropriate health care decisions by policy makers and clinicians, which harm patients, waste resources, and misguide future research [4,5,34].

Trial registration and public access to study data

There is an ethical obligation to publish research findings [120,147-150]. For example, patients who participate in clinical trials do so in the belief that they are contributing to medical progress, and this will only be the case if these trials are published. Deliberate non- or selective reporting represents unethical behaviour and scientific misconduct [34,147]. Public access to study data may also help identify safety problems at an earlier stage, which in the past have in some cases not always been detected by regulatory authorities [151-153]. Two concepts can help solve the issue of reporting bias: firstly, the mandatory and prospective registration of clinical trials, and secondly, the mandatory publication of full study results in results databases after study completion.

Non-industry initiatives

One of the first searchable computerized international registries of clinical trials was introduced in the United States in 1967; since then, several national and international trial registries have been created [154], such as the US government's trial registry and results database ClinicalTrials.gov (see Tse et al for an update on this registry [155,156]). The various controversies surrounding reporting bias, particularly the non-reporting of safety data, accelerated the movement both for trial registration and the establishment of results databases. Numerous researchers, organizations, regulatory and governmental authorities started various initiatives to achieve these goals [148,157-165].

In 2004, the International Committee of Medical Journal Editors (ICMJE) announced that it would make registration of clinical trials in a public registry a condition of consideration for publication [158]; this statement has since been updated [166,167].

In 2006, the WHO established the International Clinical Trials Registry Platform (ICTRP) in an initiative to bring national trial registries together in a global network providing a single point of access to registered trials [157]. However, to date no consensus has been found between the parties involved concerning which characteristics must be made publicly available at registration [168].

Section 801 of the US FDA Amendments Act 2007 (FDAAA, [169]) requires the registration at inception of all clinical trials involving a drug, biological product, or device regulated by the FDA. Trials must be registered on ClinicalTrials.gov and a defined set of results must be posted in the same registry within 12 months of study completion. Exceptions are phase I drug trials and early feasibility device trials. Non-compliance is sanctioned with monetary fines [163,170].

In 2004, the European Agency for the Evaluation of Medicinal Products (now European Medicines Agency) launched the European clinical trials database EudraCT (eudract.emea.europa.eu) to provide national authorities with a common set of information on clinical trials conducted in the EU. The database was initially supposed to be available only to the responsible authorities of the member states, as well as to the European Commission and the European Medicines Agency [171]. In 2006, the regulation on medicinal products for paediatric use was published, which required that information about European paediatric clinical trials of investigational medicinal products was to be made publicly available on EudraCT [172,173], and in February 2009, the European Commission published a guideline including the list of data fields to be made public [174]. On the same date, a similar list was published for all trials [175]. However, the legal obligation to publish information on trials in adults is not fully clear, and it is also unclear when all relevant information from EudraCT will be made publicly accessible.

With the introduction of the above-mentioned legislation, regulatory agencies are on the one hand helping to solve the problem of reporting bias, but on the other hand, they are also part of the problem: several of the examples identified refer to the non-publication or active withholding of study data by regulatory agencies [83,94,109,133]. This is partly due to existing confidentiality regulations such as Exemption 4 of the US Freedom of Information Act [176]. To solve the problems resulting from this situation, current legislation has to be changed to allow for the publication of comprehensive information on study methods and results by regulatory agencies. In his essay "A taxpayer-funded clinical trials registry and results database", Turner called for increased access to the FDA information sources, which would at least enable the assessment of drugs marketed in the USA [92]. Although the FDA posts selected reviews of NDAs on its website after the approval process following the Electronic Freedom of Information Act [177], the availability of these reviews is limited [92]. Moreover, according to the FDAAA, the results of older trials of approved drugs or of drugs that were never approved need not be disclosed [170], which is why a retrospective registry and results database is needed [178].

Industry initiatives

In 2002, the US Pharmaceutical Research and Manufacturers Association (PhRMA) member companies committed themselves to the registration of all hypothesis-testing clinical trials at initiation and to the timely disclosure of summary results, regardless of outcome [179,180]. PhRMA also launched the clinical study results database ClinicalStudyResults.org in 2004. In 2005, a similar commitment was made by several pharmaceutical industry associations [181], which has since been updated [182]. Following the legal settlement in the paroxetine case, GSK established a trial registry on its website moc.retsigerydutslacinilc-ksg and other large companies have followed. In 2008, the German Association of Research-Based Pharmaceutical Companies (VFA) published a position paper on the issue of publication bias and claimed that, because of the voluntary self-commitment of the pharmaceutical industry and the introduction of legislation for the reporting of study data, publication bias had become a "historical" topic [183]. However, even after the update of the position paper in January 2009 [184], in Germany alone further attempts by drug companies to withhold study data have occurred [69], which shows that voluntary self-commitment is insufficient.

Conclusions

Reporting bias is widespread in the medical literature and has harmed patients in the past. Mandatory prospective registration of trials and public access to study data via results databases need to be introduced on a worldwide level. This would help fulfil ethical obligations towards patients by enabling proactive publication and independent reviews of clinical trial data, and ensure a basis for fully informed decision making in the health care system. Otherwise, clinical decision making based on the "best evidence" will remain an illusion.

Competing interests

Non-financial competing interests: All authors are employees of the German Institute for Quality and Efficiency in Health Care. In order to produce unbiased HTA reports, the Institute depends on access to all of the relevant data on the topic under investigation. We therefore support the mandatory worldwide establishment of trial registries and study results databases.

Authors' contributions

NM and BW had the idea for the manuscript. NM, HK, YBS, and JK screened reference lists. JK and YBS reviewed titles and abstracts of potentially relevant citations identified in the screening process. NM extracted relevant examples from the full-text publications. BW and TK checked the extracted examples. NM drafted the first version of the manuscript. The remaining authors contributed important intellectual content to the final version. All authors approved the final version.

Supplementary Material

Additional file 1:

Table S2: Examples of reporting bias in the medical literature. Extracts from 50 publications presenting examples of reporting bias.

Acknowledgements

The authors thank Dirk Eyding, Daniel Fleer, Elke Hausner, Regine Potthast, Andrea Steinzen, and Siw Waffenschmidt for helping to screen reference lists and Verena Wekemann for formatting citations.

Funding source

This work was supported by the German Institute for Quality and Efficiency in Health Care. All authors are employees of the Institute.

References

  • Green S, Higgins S, editors. Glossary. Cochrane Handbook for Systematic Reviews of Interventions 4.2.5. http://www.cochrane.org/resources/handbook/ Last update May 2005 [accessed 22 Feb 2010]
  • Sterne J, Egger M, Moher D. In: Cochrane handbook for systematic reviews of interventions. Higgins JPT, Green S, editor. Chichester: Wiley; 2008. Addressing reporting biases; pp. 297–334. full_text.
  • Dwan K, Altman DG, Arnaiz JA, Bloom J, Chan AW, Cronin E, Decullier E, Easterbrook PJ, Von Elm E, Gamble C, Ghersi D, Ioannidis JP, Simes J, Williamson PR. Systematic review of the empirical evidence of study publication bias and outcome reporting bias. PLoS ONE. 2008;3:e3081. doi: 10.1371/journal.pone.0003081. [PMC free article] [PubMed] [Cross Ref]
  • Blumle A, Antes G, Schumacher M, Just H, Von Elm E. Clinical research projects at a German medical faculty: follow-up from ethical approval to publication and citation by others. J Med Ethics. 2008;34:e20. doi: 10.1136/jme.2008.024521. [PubMed] [Cross Ref]
  • Von Elm E, Rollin A, Blumle A, Huwiler K, Witschi M, Egger M. Publication and non-publication of clinical trials: longitudinal study of applications submitted to a research ethics committee. Swiss Med Wkly. 2008;138:197–203. [PubMed]
  • Dickersin K, Min YI, Meinert CL. Factors influencing publication of research results: follow-up of applications submitted to two institutional review boards. JAMA. 1992;267:374–378. doi: 10.1001/jama.267.3.374. [PubMed] [Cross Ref]
  • Easterbrook PJ, Berlin JA, Gopalan R, Matthews DR. Publication bias in clinical research. Lancet. 1991;337:867–872. doi: 10.1016/0140-6736(91)90201-Y. [PubMed] [Cross Ref]
  • Stern JM, Simes RJ. Publication bias: evidence of delayed publication in a cohort study of clinical research projects. BMJ. 1997;315:640–645. [PMC free article] [PubMed]
  • Pich J, Carne X, Arnaiz JA, Gomez B, Trilla A, Rodes J. Role of a research ethics committee in follow-up and publication of results. Lancet. 2003;361:1015–1016. doi: 10.1016/S0140-6736(03)12799-7. [PubMed] [Cross Ref]
  • Decullier E, Lheritier V, Chapuis F. Fate of biomedical research protocols and publication bias in France: retrospective cohort study. BMJ. 2005;331:19–24. doi: 10.1136/bmj.38488.385995.8F. [PMC free article] [PubMed] [Cross Ref]
  • Lee K, Bacchetti P, Sim I. Publication of clinical trials supporting successful new drug applications: a literature analysis. PLoS Med. 2008;5:e191. doi: 10.1371/journal.pmed.0050191. [PMC free article] [PubMed] [Cross Ref]
  • Hemminki E. Study of information submitted by drug companies to licensing authorities. Br Med J. 1980;280:833–836. doi: 10.1136/bmj.280.6217.833. [PMC free article] [PubMed] [Cross Ref]
  • MacLean CH, Morton SC, Ofman JJ, Roth EA, Shekelle PG. How useful are unpublished data from the Food and Drug Administration in meta-analysis? J Clin Epidemiol. 2003;56:44–51. doi: 10.1016/S0895-4356(02)00520-6. [PubMed] [Cross Ref]
  • Melander H, Ahlqvist-Rastad J, Meijer G, Beermann B. Evidence b(i)ased medicine: selective reporting from studies sponsored by pharmaceutical industry; review of studies in new drug applications. BMJ. 2003;326:1171–1173. doi: 10.1136/bmj.326.7400.1171. [PMC free article] [PubMed] [Cross Ref]
  • Benjamin DK Jr, Smith PB, Murphy MD, Roberts R, Mathis L, Avant D, Califf RM, Li JS. Peer-reviewed publication of clinical trials completed for pediatric exclusivity. JAMA. 2006;296:1266–1273. doi: 10.1001/jama.296.10.1266. [PMC free article] [PubMed] [Cross Ref]
  • Turner EH, Matthews AM, Linardatos E, Tell RA, Rosenthal R. Selective publication of antidepressant trials and its influence on apparent efficacy. N Engl J Med. 2008;358:252–260. doi: 10.1056/NEJMsa065779. [PubMed] [Cross Ref]
  • Bardy AH. Bias in reporting clinical trials. Br J Clin Pharmacol. 1998;46:147–150. doi: 10.1046/j.1365-2125.1998.00759.x. [PMC free article] [PubMed] [Cross Ref]
  • Ioannidis JP. Effect of the statistical significance of results on the time to completion and publication of randomized efficacy trials. JAMA. 1998;279:281–286. doi: 10.1001/jama.279.4.281. [PubMed] [Cross Ref]
  • Hopewell S, Clarke M, Stewart L, Tierney J. Time to publication for results of clinical trials. Cochrane Database Syst Rev. 2007. p. MR000011. [PubMed]
  • Institute for Quality and Efficiency in Health Care. General methods: version 3.0. http://www.iqwig.de/download/IQWiG_General_methods_V-3-0.pdf Last update 27 May 2008 [accessed 22 Feb 2010]
  • National Institute for Health and Clinical Excellence. Guide to the methods of technology appraisal. London. 2008.
  • Scherer RW, Langenberg P, Von Elm E. Full publication of results initially presented in abstracts. Cochrane Database Syst Rev. 2007. p. MR000005. [PubMed]
  • Altman D. Outcome reporting bias in meta-analyses. http://www.chalmersresearch.com/bmg/docs/t2p1.pdf Last update 2007 [accessed 24 Feb 2010]
  • Chan AW, Hrobjartsson A, Haahr MT, Gotzsche PC, Altman DG. Empirical evidence for selective reporting of outcomes in randomized trials: comparison of protocols to published articles. JAMA. 2004;291:2457–2465. doi: 10.1001/jama.291.20.2457. [PubMed] [Cross Ref]
  • Chan AW, Altman DG. Identifying outcome reporting bias in randomised trials on PubMed: review of publications and survey of authors. BMJ. 2005;330:753. doi: 10.1136/bmj.38356.424606.8F. [PMC free article] [PubMed] [Cross Ref]
  • Rising K, Bacchetti P, Bero L. Reporting bias in drug trials submitted to the Food and Drug Administration: review of publication and presentation. PLoS Med. 2008;5:e217. doi: 10.1371/journal.pmed.0050217. [PMC free article] [PubMed] [Cross Ref]
  • Chan AW, Krleza-Jeric K, Schmid I, Altman DG. Outcome reporting bias in randomized trials funded by the Canadian Institutes of Health Research. CMAJ. 2004;171:735–740. [PMC free article] [PubMed]
  • Al-Marzouki S, Roberts I, Evans S, Marshall T. Selective reporting in clinical trials: analysis of trial protocols accepted by The Lancet. Lancet. 2008;372:201. doi: 10.1016/S0140-6736(08)61060-0. [PubMed] [Cross Ref]
  • Ioannidis JP, Lau J. Completeness of safety reporting in randomized trials: an evaluation of 7 medical areas. JAMA. 2001;285:437–443. doi: 10.1001/jama.285.4.437. [PubMed] [Cross Ref]
  • Hazell L, Shakir SA. Under-reporting of adverse drug reactions: a systematic review. Drug Saf. 2006;29:385–396. doi: 10.2165/00002018-200629050-00003. [PubMed] [Cross Ref]
  • Bonhoeffer J, Zumbrunn B, Heininger U. Reporting of vaccine safety data in publications: systematic review. Pharmacoepidemiol Drug Saf. 2005;14:101–106. doi: 10.1002/pds.979. [PubMed] [Cross Ref]
  • Loke YK, Derry S. Reporting of adverse drug reactions in randomised controlled trials: a systematic survey. BMC Clin Pharmacol. 2001;1:3. doi: 10.1186/1472-6904-1-3. [PMC free article] [PubMed] [Cross Ref]
  • Ioannidis JP, Cappelleri JC, Sacks HS, Lau J. The relationship between study design, results, and reporting of randomized clinical trials of HIV infection. Control Clin Trials. 1997;18:431–444. doi: 10.1016/S0197-2456(97)00097-4. [PubMed] [Cross Ref]
  • Dickersin K. Reporting and other biases in studies of Neurontin for migraine, psychiatric/bipolar disorders, nociceptive pain, and neuropathic pain. http://dida.library.ucsf.edu/pdf/oxx18r10 Last update 10 Aug 2008 [accessed 26 Feb 2010]
  • Nassir Ghaemi S, Shirzadi AA, Filkowski M. Publication bias and the pharmaceutical industry: the case of lamotrigine in bipolar disorder. Medscape J Med. 2008;10:211. [PMC free article] [PubMed]
  • Sterling T. Publication decisions and their possible effects on inferences drawn from tests of significances. J Am Stat Assoc. 1959;54:30–34. doi: 10.2307/2282137. [Cross Ref]
  • Hopewell S, Loudon K, Clarke MJ, Oxman AD, Dickersin K. Publication bias in clinical trials due to statistical significance or direction of trial results. Cochrane Database Syst Rev. 2009. p. MR000006. [PubMed]
  • Song F, Eastwood AJ, Gilbody S, Duley L, Sutton AJ. Publication and related biases. Health Technol Assess. 2000;4:1–115. [PubMed]
  • Dickersin K, Chan S, Chalmers TC, Sacks HS, Smith H Jr. Publication bias and clinical trials. Control Clin Trials. 1987;8:343–353. doi: 10.1016/0197-2456(87)90155-3. [PubMed] [Cross Ref]
  • Krzyzanowska MK, Pintilie M, Tannock IF. Factors associated with failure to publish large randomized trials presented at an oncology meeting. JAMA. 2003;290:495–501. doi: 10.1001/jama.290.4.495. [PubMed] [Cross Ref]
  • Timmer A, Hilsden RJ, Cole J, Hailey D, Sutherland LR. Publication bias in gastroenterological research: a retrospective cohort study based on abstracts submitted to a scientific meeting. BMC Med Res Methodol. 2002;2:7. doi: 10.1186/1471-2288-2-7. [PMC free article] [PubMed] [Cross Ref]
  • Tramer MR, Reynolds DJ, Moore RA, McQuay HJ. Impact of covert duplicate publication on meta-analysis: a case study. BMJ. 1997;315:635–640. [PMC free article] [PubMed]
  • Gotzsche PC. Reference bias in reports of drug trials. Br Med J (Clin Res Ed) 1987;295:654–656. doi: 10.1136/bmj.295.6599.654. [PMC free article] [PubMed] [Cross Ref]
  • Kjaergard LL, Gluud C. Citation bias of hepato-biliary randomized clinical trials. J Clin Epidemiol. 2002;55:407–410. doi: 10.1016/S0895-4356(01)00513-3. [PubMed] [Cross Ref]
  • Ravnskov U. Quotation bias in reviews of the diet-heart idea. J Clin Epidemiol. 1995;48:713–719. doi: 10.1016/0895-4356(94)00222-C. [PubMed] [Cross Ref]
  • Egger M, Zellweger-Zahner T, Schneider M, Junker C, Lengeler C, Antes G. Language bias in randomised controlled trials published in English and German. Lancet. 1997;350:326–329. doi: 10.1016/S0140-6736(97)02419-7. [PubMed] [Cross Ref]
  • Lee KP, Boyd EA, Holroyd-Leduc JM, Bacchetti P, Bero LA. Predictors of publication: characteristics of submitted manuscripts associated with acceptance at major biomedical journals. Med J Aust. 2006;184:621–626. [PubMed]
  • Callaham ML, Wears RL, Weber EJ, Barton C, Young G. Positive-outcome bias and other limitations in the outcome of research abstracts submitted to a scientific meeting. JAMA. 1998;280:254–257. doi: 10.1001/jama.280.3.254. [PubMed] [Cross Ref]
  • Lexchin J, Bero LA, Djulbegovic B, Clark O. Pharmaceutical industry sponsorship and research outcome and quality: systematic review. BMJ. 2003;326:1167–1170. doi: 10.1136/bmj.326.7400.1167. [PMC free article] [PubMed] [Cross Ref]
  • Ramsey S, Scoggins J. Commentary: practicing on the tip of an information iceberg? Evidence of underpublication of registered clinical trials in oncology. Oncologist. 2008;13:925–929. doi: 10.1634/theoncologist.2008-0133. [PMC free article] [PubMed] [Cross Ref]
  • Olson CM, Rennie D, Cook D, Dickersin K, Flanagin A, Hogan JW, Zhu Q, Reiling J, Pace B. Publication bias in editorial decision making. JAMA. 2002;287:2825–2828. doi: 10.1001/jama.287.21.2825. [PubMed] [Cross Ref]
  • Okike K, Kocher MS, Mehlman CT, Heckman JD, Bhandari M. Publication bias in orthopaedic research: an analysis of scientific factors associated with publication in the Journal of Bone and Joint Surgery (American Volume) J Bone Joint Surg Am. 2008;90:595–601. doi: 10.2106/JBJS.G.00279. [PubMed] [Cross Ref]
  • Dickersin K, Min YI. NIH clinical trials and publication bias. Online J Curr Clin Trials. 1993. Doc No 50:[4967 words; 4953 paragraphs]. [PubMed]
  • Hartmann M, Knoth H, Schulz D, Knoth S. Industry-sponsored economic studies in oncology vs studies sponsored by nonprofit organisations. Br J Cancer. 2003;89:1405–1408. doi: 10.1038/sj.bjc.6601308. [PMC free article] [PubMed] [Cross Ref]
  • Bekelman JE, Li Y, Gross CP. Scope and impact of financial conflicts of interest in biomedical research: a systematic review. JAMA. 2003;289:454–465. doi: 10.1001/jama.289.4.454. [PubMed] [Cross Ref]
  • Sismondo S. Pharmaceutical company funding and its consequences: a qualitative systematic review. Contemp Clin Trials. 2008;29:109–113. doi: 10.1016/j.cct.2007.08.001. [PubMed] [Cross Ref]
  • Jorgensen AW, Hilden J, Gotzsche PC. Cochrane reviews compared with industry supported meta-analyses and other meta-analyses of the same drugs: systematic review. BMJ. 2006;333:782. doi: 10.1136/bmj.38973.444699.0B. [PMC free article] [PubMed] [Cross Ref]
  • Liss H. Publication bias in the pulmonary/allergy literature: effect of pharmaceutical company sponsorship. Isr Med Assoc J. 2006;8:451–454. [PubMed]
  • Ridker PM, Torres J. Reported outcomes in major cardiovascular clinical trials funded by for-profit and not-for-profit organizations: 2000-2005. JAMA. 2006;295:2270–2274. doi: 10.1001/jama.295.19.2270. [PubMed] [Cross Ref]
  • Als-Nielsen B, Chen W, Gluud C, Kjaergard LL. Association of funding and conclusions in randomized drug trials: a reflection of treatment effect or adverse events? JAMA. 2003;290:921–928. doi: 10.1001/jama.290.7.921. [PubMed] [Cross Ref]
  • Perlis CS, Harwood M, Perlis RH. Extent and impact of industry sponsorship conflicts of interest in dermatology research. J Am Acad Dermatol. 2005;52:967–971. doi: 10.1016/j.jaad.2005.01.020. [PubMed] [Cross Ref]
  • Bhandari M, Busse JW, Jackowski D, Montori VM, Schünemann H, Sprague S, Mears D, Schemitsch EH, Heels-Ansdell D, Devereaux PJ. Association between industry funding and statistically significant pro-industry findings in medical and surgical randomized trials. CMAJ. 2004;170:477–480. [PMC free article] [PubMed]
  • Kjaergard LL, Als-Nielsen B. Association between competing interests and authors' conclusions: epidemiological study of randomised clinical trials published in the BMJ. BMJ. 2002;325:249. doi: 10.1136/bmj.325.7358.249. [PMC free article] [PubMed] [Cross Ref]
  • Lauritsen K, Havelund T, Laursen LS, Rask-Madsen J. Withholding unfavourable results in drug company sponsored clinical trials. Lancet. 1987;1:1091. doi: 10.1016/S0140-6736(87)90515-0. [PubMed] [Cross Ref]
  • Wise J. Research suppressed for seven years by drug company. BMJ. 1997;314:1145. [PMC free article] [PubMed]
  • Williams HC. Evening primrose oil for atopic dermatitis. BMJ. 2003;327:1358–1359. doi: 10.1136/bmj.327.7428.1358. [PMC free article] [PubMed] [Cross Ref]
  • Henry DA, Kerridge IH, Hill SR, McNeill PM, Doran E, Newby DA, Henderson KM, Maguire J, Stokes BJ, Macdonald GJ, Day RO. Medical specialists and pharmaceutical industry-sponsored research: a survey of the Australian experience. Med J Aust. 2005;182:557–560. [PubMed]
  • Gotzsche PC, Hrobjartsson A, Johansen HK, Haahr MT, Altman DG, Chan AW. Constraints on publication rights in industry-initiated clinical trials. JAMA. 2006;295:1645–1646. doi: 10.1001/jama.295.14.1645. [PubMed] [Cross Ref]
  • Stafford N. German agency refuses to rule on drug's benefits until Pfizer discloses all trial results. BMJ. 2009;338:b2521. doi: 10.1136/bmj.b2521. [PubMed] [Cross Ref]
  • Whittington CJ, Kendall T, Fonagy P, Cottrell D, Cotgrove A, Boddington E. Selective serotonin reuptake inhibitors in childhood depression: systematic review of published versus unpublished data. Lancet. 2004;363:1341–1345. doi: 10.1016/S0140-6736(04)16043-1. [PubMed] [Cross Ref]
  • Cowley AJ, Skene A, Stainer K, Hampton JR. The effect of lorcainide on arrhythmias and survival in patients with acute myocardial infarction: an example of publication bias. Int J Cardiol. 1993;40:161–166. doi: 10.1016/0167-5273(93)90279-P. [PubMed] [Cross Ref]
  • Moore TJ. Deadly medicine: why tens of thousands of heart patients died in America's worst drug disaster. New York: Simon & Schuster; 1995.
  • Mathews A, Martinez B. E-mails suggest Merck knew Vioxx's dangers at early stage. Wall Street Journal. 2004. p. A1.
  • Psaty BM, Kronmal RA. Reporting mortality findings in trials of rofecoxib for Alzheimer disease or cognitive impairment: a case study based on documents from rofecoxib litigation. JAMA. 2008;299:1813–1817. doi: 10.1001/jama.299.15.1813. [PubMed] [Cross Ref]
  • Rosenberg SA. Secrecy in medical research. N Engl J Med. 1996;334:392–394. doi: 10.1056/NEJM199602083340610. [PubMed] [Cross Ref]
  • Baker CB, Johnsrud MT, Crismon ML, Rosenheck RA, Woods SW. Quantitative analysis of sponsorship bias in economic studies of antidepressants. Br J Psychiatry. 2003;183:498–506. doi: 10.1192/bjp.183.6.498. [PubMed] [Cross Ref]
  • Moncrieff J. Clozapine v. conventional antipsychotic drugs for treatment-resistant schizophrenia: a re-examination. Br J Psychiatry. 2003;183:161–166. doi: 10.1192/bjp.183.2.161. [PubMed] [Cross Ref]
  • Montgomery JH, Byerly M, Carmody T, Li B, Miller DR, Varghese F, Holland R. An analysis of the effect of funding source in randomized clinical trials of second generation antipsychotics for the treatment of schizophrenia. Control Clin Trials. 2004;25:598–612. doi: 10.1016/j.cct.2004.09.002. [PubMed] [Cross Ref]
  • Procyshyn RM, Chau A, Fortin P, Jenkins W. Prevalence and outcomes of pharmaceutical industry-sponsored clinical trials involving clozapine, risperidone, or olanzapine. Can J Psychiatry. 2004;49:601–606. [PubMed]
  • Perlis RH, Perlis CS, Wu Y, Hwang C, Joseph M, Nierenberg AA. Industry sponsorship and financial conflict of interest in the reporting of clinical trials in psychiatry. Am J Psychiatry. 2005;162:1957–1960. doi: 10.1176/appi.ajp.162.10.1957. [PubMed] [Cross Ref]
  • Heres S, Davis J, Maino K, Jetzinger E, Kissling W, Leucht S. Why olanzapine beats risperidone, risperidone beats quetiapine, and quetiapine beats olanzapine: an exploratory analysis of head-to-head comparison studies of second-generation antipsychotics. Am J Psychiatry. 2006;163:185–194. doi: 10.1176/appi.ajp.163.2.185. [PubMed] [Cross Ref]
  • Kelly RE Jr, Cohen LJ, Semple RJ, Bialer P, Lau A, Bodenheimer A, Neustadter E. Relationship between drug company funding and outcomes of clinical psychiatric research. Psychol Med. 2006;36:1647–1656. doi: 10.1017/S0033291706008567. [PubMed] [Cross Ref]
  • Kirsch I, Deacon BJ, Huedo-Medina TB, Scoboria A, Moore TJ, Johnson BT. Initial severity and antidepressant benefits: a meta-analysis of data submitted to the Food and Drug Administration. PLoS Med. 2008;5:e45. doi: 10.1371/journal.pmed.0050045. [PMC free article] [PubMed] [Cross Ref]
  • Office of the Attorney General. Major pharmaceutical firm concealed drug information. http://www.oag.state.ny.us/media_center/2004/jun/jun2b_04.html Last update 02 Jun 2004 [accessed 24 Feb 2010]
  • Office of the Attorney General. Settlement sets new standard for release of drug information. http://www.oag.state.ny.us/media_center/2004/aug/aug26a_04.html Last update 26 Aug 2004 [accessed 26 Feb 2010]
  • Gibson L. GlaxoSmithKline to publish clinical trials after US lawsuit. BMJ. 2004;328:1513. doi: 10.1136/bmj.328.7455.1513-a. [PMC free article] [PubMed] [Cross Ref]
  • Institute for Quality and Efficiency in Health Care. Bupropion, mirtazapine and reboxetine in the treatment of depression: executive summary of preliminary report; commission no A05-20C. http://www.iqwig.de/download/A05-20C_Executive_summary_Bupropion_mirtazapine_and_reboxetine_in_the_treatment_of_depression.pdf Last update 29 May 2009 [accessed 26 Feb 2010] [PubMed]
  • Institute for Quality and Efficiency in Health Care. Antidepressants: benefit of reboxetine not proven. http://www.iqwig.de/antidepressants-benefit-of-reboxetine-not-proven.981.en.html Last update 24 Nov 2009 [accessed 26 Feb 2010]
  • Abramson J. Expert report. http://dida.library.ucsf.edu/pdf/oxx18v10 Last update 11 Aug 2008 [accessed 26 Feb 2010]
  • Vedula SS, Bero L, Scherer RW, Dickersin K. Outcome reporting in industry-sponsored trials of gabapentin for off-label use. N Engl J Med. 2009;361:1963–1971. doi: 10.1056/NEJMsa0906126. [PubMed] [Cross Ref]
  • Vedantam S. A silenced drug study creates an uproar. Washington Post. 2009. p. A01.
  • Turner EH. A taxpayer-funded clinical trials registry and results database. PLoS Med. 2004;1:e60. doi: 10.1371/journal.pmed.0010060. [PMC free article] [PubMed] [Cross Ref]
  • Singh D. Merck withdraws arthritis drug worldwide. BMJ. 2004;329:816. doi: 10.1136/bmj.329.7470.816-a. [PMC free article] [PubMed] [Cross Ref]
  • Lenzer J, Brownlee S. An untold story? BMJ. 2008;336:532–534. doi: 10.1136/bmj.39504.662685.0F. [PMC free article] [PubMed] [Cross Ref]
  • Waknine Y. Bextra withdrawn from market. Medscape Today [Online] 2005. http://www.medscape.com/viewarticle/502642
  • Hiatt WR. Observational studies of drug safety--aprotinin and the absence of transparency. N Engl J Med. 2006;355:2171–2173. doi: 10.1056/NEJMp068252. [PubMed] [Cross Ref]
  • Tuffs A. Bayer withdraws heart surgery drug. BMJ. 2007;335:1015. doi: 10.1136/bmj.39395.644826.DB. [PMC free article] [PubMed] [Cross Ref]
  • Furberg CD. Effect of antiarrhythmic drugs on mortality after myocardial infarction. Am J Cardiol. 1983;52:32C–36C. doi: 10.1016/0002-9149(83)90629-X. [PubMed] [Cross Ref]
  • Antes G. Tödliche Medizin. Unpublizierte Studien - harmlos? [Fatal medicine. Unpublished studies - harmless?] MMW Fortschr Med. 2006;148:8. [PubMed]
  • Hine LK, Laird N, Hewitt P, Chalmers TC. Meta-analytic evidence against prophylactic use of lidocaine in acute myocardial infarction. Arch Intern Med. 1989;149:2694–2698. doi: 10.1001/archinte.149.12.2694. [PubMed] [Cross Ref]
  • MacMahon S, Collins R, Peto R, Koster RW, Yusuf S. Effects of prophylactic lidocaine in suspected acute myocardial infarction: an overview of results from the randomized, controlled trials. JAMA. 1988;260:1910–1916. doi: 10.1001/jama.260.13.1910. [PubMed] [Cross Ref]
  • Preliminary report: effect of encainide and flecainide on mortality in a randomized trial of arrhythmia suppression after myocardial infarction. The Cardiac Arrhythmia Suppression Trial (CAST) Investigators. N Engl J Med. 1989;321:406–412. [PubMed]
  • Barbehenn E, Lurie P, Wolfe SM. Alosetron for irritable bowel syndrome. Lancet. 2000;356:2009–2010. doi: 10.1016/S0140-6736(05)72978-0. [PubMed] [Cross Ref]
  • Moynihan R. Alosetron: a case study in regulatory capture, or a victory for patients' rights? BMJ. 2002;325:592–595. doi: 10.1136/bmj.325.7364.592. [PMC free article] [PubMed] [Cross Ref]
  • Bombardier C, Laine L, Reicin A, Shapiro D, Burgos-Vargas R, Davis B, Day R, Ferraz MB, Hawkey CJ, Hochberg MC, Kvien TK, Schnitzer TJ. VIGOR Study Group. Comparison of upper gastrointestinal toxicity of rofecoxib and naproxen in patients with rheumatoid arthritis. N Engl J Med. 2000;343:1520–1528. doi: 10.1056/NEJM200011233432103. [PubMed] [Cross Ref]
  • Mukherjee D, Nissen SE, Topol EJ. Risk of cardiovascular events associated with selective COX-2 inhibitors. JAMA. 2001;286:954–959. doi: 10.1001/jama.286.8.954. [PubMed] [Cross Ref]
  • McCormack JP, Rangno R. Digging for data from the COX-2 trials. CMAJ. 2002;166:1649–1650. [PMC free article] [PubMed]
  • Silverstein FE, Faich G, Goldstein JL, Simon LS, Pincus T, Whelton A, Makuch R, Eisen G, Agrawal NM, Stenson WF, Burr AM. Gastrointestinal toxicity with celecoxib vs nonsteroidal anti-inflammatory drugs for osteoarthritis and rheumatoid arthritis: the CLASS study: a randomized controlled trial. JAMA. 2000;284:1247–1255. doi: 10.1001/jama.284.10.1247. [PubMed] [Cross Ref]
  • Lurie P, Zieve A. Sometimes the silence can be like the thunder: access to pharmaceutical data at the FDA. Law Contemp Probl. 2008;69:85–97.
  • Nissen S, Califf R. A conversation about rosiglitazone. Medscape Diabetes & Endocrinology [Online] 2007. http://www.medscape.com/viewarticle/561666
  • Nissen SE, Wolski K. Effect of rosiglitazone on the risk of myocardial infarction and death from cardiovascular causes. N Engl J Med. 2007;356:2457–2471. doi: 10.1056/NEJMoa072761. [PubMed] [Cross Ref]
  • Mitka M. Controversies surround heart drug study: questions about Vytorin and trial sponsors' conduct. JAMA. 2008;299:885–887. doi: 10.1001/jama.299.8.885. [PubMed] [Cross Ref]
  • Kastelein JJ, Akdim F, Stroes ES, Zwinderman AH, Bots ML, Stalenhoef AF, Visseren FL, Sijbrands EJ, Trip MD, Stein EA, Duivenvoorden R, Veltri EP, Marais AD, de Groot E. ENHANCE Investigators. Simvastatin with or without ezetimibe in familial hypercholesterolemia. N Engl J Med. 2008;358:1431–1443. doi: 10.1056/NEJMoa0800742. [PubMed] [Cross Ref]
  • Psaty BM, Furberg CD, Ray WA, Weiss NS. Potential for conflict of interest in the evaluation of suspected adverse drug reactions: use of cerivastatin and risk of rhabdomyolysis. JAMA. 2004;292:2622–2631. doi: 10.1001/jama.292.21.2622. [PubMed] [Cross Ref]
  • Tuffs A. Bayer faces potential fine over cholesterol lowering drug. BMJ. 2001;323:415. doi: 10.1136/bmj.323.7310.415. [PMC free article] [PubMed] [Cross Ref]
  • King RT Jr. Bitter pill: how a drug firm paid for university study, then undermined it. Wall Street Journal. 1996;1:A13.
  • Dong BJ, Hauck WW, Gambertoglio JG, Gee L, White JR, Bubp JL, Greenspan FS. Bioequivalence of generic and brand-name levothyroxine products in the treatment of hypothyroidism. JAMA. 1997;277:1205–1213. doi: 10.1001/jama.277.15.1205. [PubMed] [Cross Ref]
  • Kenemans P, Bundred NJ, Foidart JM, Kubista E, von Schoultz B, Sismondi P, Vassilopoulou-Sellin R, Yip CH, Egberts J, Mol-Arts M, Mulder R, van Os S, Beckmann MW. LIBERATE Study Group. Safety and efficacy of tibolone in breast-cancer patients with vasomotor symptoms: a double-blind, randomised, non-inferiority trial. Lancet Oncol. 2009;10:135–146. doi: 10.1016/S1470-2045(08)70341-3. [PubMed] [Cross Ref]
  • Lippegaus O, Prokscha S, Thimme C. Verharmloste Gefahren. Krebs durch Hormonbehandlung [Trivialised dangers. Cancer caused by hormone therapy] http://frontal21.zdf.de/ZDFde/inhalt/11/0,1872,7593675,00.html Last update 2009 [accessed 26 Feb 2010]
  • Doroshow JH. Commentary: publishing cancer clinical trial results: a scientific and ethical imperative. Oncologist. 2008;13:930–932. doi: 10.1634/theoncologist.2008-0168. [PubMed] [Cross Ref]
  • Simes RJ. Publication bias: the case for an international registry of clinical trials. J Clin Oncol. 1986;4:1529–1541. [PubMed]
  • Takeda A, Loveman E, Harris P, Hartwell D, Welch K. Time to full publication of studies of anti-cancer medicines for breast cancer and the potential for publication bias: a short systematic review. Health Technol Assess. 2008;12:iii–x. 1-46. [PubMed]
  • Peppercorn J, Blood E, Winer E, Partridge A. Association between pharmaceutical involvement and outcomes in breast cancer clinical trials. Cancer. 2007;109:1239–1246. doi: 10.1002/cncr.22528. [PubMed] [Cross Ref]
  • Kyzas PA, Loizou KT, Ioannidis JP. Selective reporting biases in cancer prognostic factor studies. J Natl Cancer Inst. 2005;97:1043–1055. [PubMed]
  • Begg CB, Pocock SJ, Freedman L, Zelen M. State of the art in comparative cancer clinical trials. Cancer. 1987;60:2811–2815. doi: 10.1002/1097-0142(19871201)60:11<2811::AID-CNCR2820601136>3.0.CO;2-P. [PubMed] [Cross Ref]
  • Kyzas PA, Denaxa-Kyza D, Ioannidis JP. Almost all articles on cancer prognostic markers report statistically significant results. Eur J Cancer. 2007;43:2559–2579. [PubMed]
  • Manheimer E, Anderson D. Survey of public information about ongoing clinical trials funded by industry: evaluation of completeness and accessibility. BMJ. 2002;325:528–531. doi: 10.1136/bmj.325.7363.528. [PMC free article] [PubMed] [Cross Ref]
  • Rennie D. Thyroid storm. JAMA. 1997;277:1238–1243. doi: 10.1001/jama.277.15.1238. [PubMed] [Cross Ref]
  • Godlee F, Clarke M. Why don't we have all the evidence on oseltamivir? BMJ. 2009;339:b5351. doi: 10.1136/bmj.b5351. [PubMed] [Cross Ref]
  • Jefferson TO, Demicheli V, Di Pietrantonj C, Jones M, Rivetti D. Neuraminidase inhibitors for preventing and treating influenza in healthy adults. Cochrane Database Syst Rev. 2006;3:CD001265. [PubMed]
  • Kaiser L, Wat C, Mills T, Mahoney P, Ward P, Hayden F. Impact of oseltamivir treatment on influenza-related lower respiratory tract complications and hospitalizations. Arch Intern Med. 2003;163:1667–1672. doi: 10.1001/archinte.163.14.1667. [PubMed] [Cross Ref]
  • Jefferson T, Jones M, Doshi P, Del Mar C. Neuraminidase inhibitors for preventing and treating influenza in healthy adults: systematic review and meta-analysis. BMJ. 2009;339:b5106. doi: 10.1136/bmj.b5106. [PMC free article] [PubMed] [Cross Ref]
  • The influence of the pharmaceutical industry; formal minutes, oral and written evidence. Vol. 2. London: Stationery Office; 2005. [House of Commons, Health Committee (Series Editor): Report of session 2004-05; vol 4]
  • Cochrane Injuries Group Albumin Reviewers. Human albumin administration in critically ill patients: systematic review of randomised controlled trials. BMJ. 1998;317:235–240. [PMC free article] [PubMed]
  • McCarthy M. Company sought to block paper's publication. Lancet. 2000;356:1659. doi: 10.1016/S0140-6736(00)03166-4. [Cross Ref]
  • Man-Son-Hing M, Wells G, Lau A. Quinine for nocturnal leg cramps: a meta-analysis including unpublished data. J Gen Intern Med. 1998;13:600–606. doi: 10.1046/j.1525-1497.1998.00182.x. [PMC free article] [PubMed] [Cross Ref]
  • Marshall E. Is data-hoarding slowing the assault on pathogens? Science. 1997;275:777–780. doi: 10.1126/science.275.5301.777. [PubMed] [Cross Ref]
  • Campbell EG, Clarridge BR, Gokhale M, Birenbaum L, Hilgartner S, Holtzman NA, Blumenthal D. Data withholding in academic genetics: evidence from a national survey. JAMA. 2002;287:473–480. doi: 10.1001/jama.287.4.473. [PubMed] [Cross Ref]
  • Misakian AL, Bero LA. Publication bias and research on passive smoking: comparison of published and unpublished studies. JAMA. 1998;280:250–253. doi: 10.1001/jama.280.3.250. [PubMed] [Cross Ref]
  • Barnes DE, Bero LA. Why review articles on the health effects of passive smoking reach different conclusions. JAMA. 1998;279:1566–1570. doi: 10.1001/jama.279.19.1566. [PubMed] [Cross Ref]
  • Hilts PJ. Philip Morris blocked paper showing addiction, panel finds. New York Times. 1994. p. A7.
  • Hilts PJ. Scientists say Philip Morris withheld nicotine findings. New York Times. 1994. pp. A1–A7.
  • Anderson HR, Atkinson RW, Peacock JL, Sweeting MJ, Marston L. Ambient particulate matter and health effects: publication bias in studies of short-term associations. Epidemiology. 2005;16:155–163. doi: 10.1097/01.ede.0000152528.22746.0f. [PubMed] [Cross Ref]
  • Peinemann F, McGauran N, Sauerland S, Lange S. Negative pressure wound therapy: potential publication bias caused by lack of access to unpublished study results data. BMC Med Res Methodol. 2008;8:4. doi: 10.1186/1471-2288-8-4. [PMC free article] [PubMed] [Cross Ref]
  • McAuley L, Pham B, Tugwell P, Moher D. Does the inclusion of grey literature influence estimates of intervention effectiveness reported in meta-analyses? Lancet. 2000;356:1228–1231. doi: 10.1016/S0140-6736(00)02786-0. [PubMed] [Cross Ref]
  • Hopewell S, McDonald S, Clarke M, Egger M. Grey literature in meta-analyses of randomized trials of health care interventions. Cochrane Database Syst Rev. 2007. p. MR000010. [PubMed]
  • Chalmers I. Underreporting research is scientific misconduct. JAMA. 1990;263:1405–1408. doi: 10.1001/jama.263.10.1405. [PubMed] [Cross Ref]
  • World Medical Association. Declaration of Helsinki: ethical principles for medical research involving human subjects. http://www.wma.net/en/30publications/10policies/b3/index.html Last update Oct 2008 [accessed 26 Feb 2010] [PubMed]
  • Pearn J. Publication: an ethical imperative. BMJ. 1995;310:1313–1315. [PMC free article] [PubMed]
  • Trials of war criminals before the Nuremberg Military Tribunals under Control Council Law no10. Vol. 2. Washington, D.C.: US Government Printing Office; 1949. The Nuremberg code; pp. 181–182.
  • Healy D. Did regulators fail over selective serotonin reuptake inhibitors? BMJ. 2006;333:92–95. doi: 10.1136/bmj.333.7558.92. [PMC free article] [PubMed] [Cross Ref]
  • Topol EJ. Failing the public health: rofecoxib, Merck, and the FDA. N Engl J Med. 2004;351:1707–1709. doi: 10.1056/NEJMp048286. [PubMed] [Cross Ref]
  • Rennie D. When evidence isn't: trials, drug companies and the FDA. J Law Policy. 2007;15:991–1012.
  • Dickersin K, Rennie D. Registering clinical trials. JAMA. 2003;290:516–523. doi: 10.1001/jama.290.4.516. [PubMed] [Cross Ref]
  • Tse T, Williams RJ, Zarin DA. Update on Registration of Clinical Trials in ClinicalTrials.gov. Chest. 2009;136:304–305. doi: 10.1378/chest.09-1219. [PMC free article] [PubMed] [Cross Ref]
  • Tse T, Williams RJ, Zarin DA. Reporting "basic results" in ClinicalTrials.gov. Chest. 2009;136:295–303. doi: 10.1378/chest.08-3022. [PMC free article] [PubMed] [Cross Ref]
  • WHO clinical trials initiative to protect the public. Bull World Health Organ. 2006;84:10–11. [PMC free article] [PubMed]
  • De Angelis C, Drazen JM, Frizelle FA, Haug C, Hoey J, Horton R, Kotzin S, Laine C, Marusic A, Overbeke AJ, Schroeder TV, Sox HC, Weyden MB Van Der. International Committee of Medical Journal Editors. Clinical trial registration: a statement from the International Committee of Medical Journal Editors. N Engl J Med. 2004;351:1250–1251. doi: 10.1056/NEJMe048225. [PubMed] [Cross Ref]
  • Deutsches Cochrane Zentrum, Deutsches Netzwerk Evidenzbasierte Medizin. Stellungnahme [Comment] http://www.ebm-netzwerk.de/netzwerkarbeit/images/stellungnahme_anhoerung_probandenschutz.pdf Last update 22 Sep 2004 [accessed 26 Feb 2010]
  • Krleza-Jeric K. International dialogue on the Public Reporting Of Clinical Trial Outcome and Results: PROCTOR meeting. Croat Med J. 2008;49:267–268. doi: 10.3325/cmj.2008.2.267. [PMC free article] [PubMed] [Cross Ref]
  • Krleza-Jeric K, Chan AW, Dickersin K, Sim I, Grimshaw J, Gluud C. Principles for international registration of protocol information and results from human trials of health related interventions: Ottawa statement (part 1) BMJ. 2005;330:956–958. doi: 10.1136/bmj.330.7497.956. [PMC free article] [PubMed] [Cross Ref]
  • European Research Council. ERC Scientific Council guidelines on open access. http://erc.europa.eu/pdf/ScC_Guidelines_Open_Access_revised_Dec07_FINAL.pdf Last update 17 Dec 2007 [accessed 25 Feb 2010]
  • Groves T. Mandatory disclosure of trial results for drugs and devices. BMJ. 2008;336:170. doi: 10.1136/bmj.39469.465139.80. [PMC free article] [PubMed] [Cross Ref]
  • Steinbrook R. Public access to NIH-funded research. N Engl J Med. 2005;352:1739–1741. doi: 10.1056/NEJMp058088. [PubMed] [Cross Ref]
  • Dickersin K. Report from the Panel on the Case for Registers of Clinical Trials at the Eighth Annual Meeting of the Society for Clinical Trials. Control Clin Trials. 1988;9:76–81. [PubMed]
  • De Angelis CD, Drazen JM, Frizelle FA, Haug C, Hoey J, Horton R, Kotzin S, Laine C. Is this clinical trial fully registered? A statement from the International Committee of Medical Journal Editors. N Engl J Med. 2005;352:2436–2438. doi: 10.1056/NEJMe058127. [PubMed] [Cross Ref]
  • Laine C, Horton R, DeAngelis CD, Drazen JM, Frizelle FA, Godlee F, Haug C, Hebert PC, Kotzin S, Marusic A, Sahni P, Schroeder TV, Sox HC, Weyden MB Van der, Verheugt FW. Clinical trial registration--looking back and moving ahead. N Engl J Med. 2007;356:2734–2736. doi: 10.1056/NEJMe078110. [PubMed] [Cross Ref]
  • Krleza-Jeric K. Clinical trial registration: the differing views of industry, the WHO, and the Ottawa Group. PLoS Med. 2005;2:e378. doi: 10.1371/journal.pmed.0020378. [PMC free article] [PubMed] [Cross Ref]
  • Food and Drug Administration. FDA Amendments Act (FDAAA) of 2007, public law no. 110-85 §801. http://frwebgate.access.gpo.gov/cgi-bin/getdoc.cgi?dbname=110_cong_public_laws&docid=f:publ085.110.pdf Last update 2007 [accessed 26 Feb 2010]
  • Wood AJJ. Progress and deficiencies in the registration of clinical trials. N Engl J Med. 2009;360:824–830. doi: 10.1056/NEJMsr0806582. [PubMed] [Cross Ref]
  • European Medicines Agency. EMEA launches EudraCT database. http://www.emea.europa.eu/pdfs/general/direct/pr/1258904en.pdf Last update 06 May 2004 [accessed 25 Feb 2010]
  • Smyth RL. Making information about clinical trials publicly available. BMJ. 2009;338:b2473. doi: 10.1136/bmj.b2473. [PubMed] [Cross Ref]
  • Regulation (EC) No 1901/2006 of the European Parliament and of the Council of 12 December 2006 on medicinal products for paediatric use and amending regulation (EEC) no 1768/92, directive 2001/20/EC, directive 2001/83/EC and regulation (EC) No 726/2004. Official J Eur Commun. 2006;49:L378/1–L378/19.
  • European Commission. List of fields to be made public from EudraCT for paediatric clinical trials in accordance with article 41 of regulation (EC) no 1901/2006 and its implementing guideline 2009/C28/01. http://ec.europa.eu/enterprise/pharmaceuticals/eudralex/vol-10/2009_02_04_guidelines_paed.pdf Last update 26 Mar 2009 [accessed 26 Feb 2010]
  • European Commission. List of fields contained in the 'EudraCT' clinical trials database to be made public, in accordance with Article 57(2) of Regulation (EC) No 726/2004 and its implementing guideline 2008/c168/021. http://ec.europa.eu/enterprise/pharmaceuticals/eudralex/vol-10/2009_02_04_guideline.pdf Last update 04 Feb 2009 [accessed 25 Feb 2010]
  • Committee on Government Reform. A citizen's guide on using the Freedom of Information Act and the Privacy Act of 1974 to request government records. http://www.fas.org/sgp/foia/citizen.pdf Last update 20 Sep 2005 [accessed 26 Feb 2010]
  • Food and Drug Administration. Executive summary of the Food and Drug Administration's consumer roundtable on consumer protection priorities. http://www.fda.gov/ohrms/dockets/dockets/00n_1665/cr00001.pdf Last update 2000 [accessed 26 Feb 2010]
  • Turner EH. Closing a loophole in the FDA Amendments Act. Science. 2008;322:44–46. doi: 10.1126/science.322.5898.44c. [PubMed] [Cross Ref]
  • Pharmaceutical Research and Manufacturers of America. PhRMA clinical trial registry proposal. http://www.phrma.org/node/446 Last update 2010 [accessed 26 Feb 2010]
  • Principles on the conduct of clinical trials and communication of clinical trial results. Washington DC: Pharmaceutical Research and Manufacturers of America; 2002.
  • International Federation of Pharmaceutical Manufacturers & Associations. Joint position on the disclosure of clinical trial information via clinical trial registries and databases. http://www.phrma.org/files/attachments/2005-01-06.1113.PDF Last update 2005 [accessed 24 Feb 2010]
  • International Federation of Pharmaceutical Manufacturers & Associations. Joint position on the disclosure of clinical trial information via clinical trial registries and databases. http://www.ifpma.org/pdf/Revised_Joint_Industry_Position_26Nov08.pdf Last update Nov 2008 [accessed 11 Mar 2010]
  • Verband Forschender Arzneimittelhersteller. VFA-Positionspapier zum Thema "publication bias" [VFA position paper on the subject of "publication bias"] Berlin: VFA; 2008.
  • Verband Forschender Arzneimittelhersteller. VFA-Positionspapier zum Thema "publication bias" [VFA position paper on the subject of "publication bias"] http://www.vfa.de/download/SAVE/de/presse/positionen/pos-publication-bias.html/pos-publication-bias.pdf Last update Jan 2009 [accessed 26 Feb 2010]
  • Mathew SJ, Charney DS. Publication bias and the efficacy of antidepressants. Am J Psychiatry. 2009;166:140–145. doi: 10.1176/appi.ajp.2008.08071102. [PubMed] [Cross Ref]
  • Abbott A. British panel bans use of antidepressant to treat children. Nature. 2003;423:792. [PubMed]
  • Mitka M. FDA alert on antidepressants for youth. JAMA. 2003;290:2534. doi: 10.1001/jama.290.19.2534. [PubMed] [Cross Ref]
  • Garland EJ. Facing the evidence: antidepressant treatment in children and adolescents. CMAJ. 2004;170:489–491. [PMC free article] [PubMed]
  • Herxheimer A, Mintzes B. Antidepressants and adverse effects in young patients: uncovering the evidence. CMAJ. 2004;170:487–489. [PMC free article] [PubMed]
  • Dyer O. GlaxoSmithKline faces US lawsuit over concealment of trial results. BMJ. 2004;328:1395. doi: 10.1136/bmj.328.7453.1395. [PMC free article] [PubMed] [Cross Ref]
  • Jureidini JN, McHenry LB, Mansfield PR. Clinical trials and drug promotion: selective reporting of study 329. Int J Risk Safety Med. 2008. pp. 73–81.
  • Institute for Quality and Efficiency in Health Care. Preliminary report on antidepressants published. http://www.iqwig.de/index.867.en.html Last update 10 Jun 2009 [accessed 26 Feb 2010]
  • Steinman MA, Bero LA, Chren MM, Landefeld CS. Narrative review: the promotion of gabapentin: an analysis of internal industry documents. Ann Intern Med. 2006;145:284–293. [PubMed]
  • Steinman MA, Harper GM, Chren MM, Landefeld CS, Bero LA. Characteristics and impact of drug detailing for gabapentin. PLoS Med. 2007;4:e134. doi: 10.1371/journal.pmed.0040134. [PMC free article] [PubMed] [Cross Ref]
  • Landefeld CS, Steinman MA. The Neurontin legacy: marketing through misinformation and manipulation. N Engl J Med. 2009;360:103–106. doi: 10.1056/NEJMp0808659. [PubMed] [Cross Ref]
  • Mack A. Examination of the evidence for off-label use of gabapentin. J Manag Care Pharm. 2003;9:559–568. [PubMed]
  • Petersen M. Memos cast shadow on drug's promotion. New York Times. 2002. p. C2.
  • U.S. Department of Justice. Warner-Lambert to pay $430 million to resolve criminal & civil health care liability relating to off-label promotion. http://www.usdoj.gov/opa/pr/2004/May/04_civ_322.htm Last update 13 May 2004 [accessed 13 Mar 2010]
  • Feeley J, Cronin Fisk M. AstraZeneca Seroquel studies 'buried,' papers show (update 3) http://www.bloomberg.com/apps/news?pid=20601087&sid=aS_.NqzMArG8# Last update 27 Feb 2009 [accessed 19 Mar 2010]
  • Milford P. AstraZeneca may link Seroquel, diabetes, doctor says (update 1) http://www.bloomberg.com/apps/news?pid=newsarchive&sid=ayzJsK2HlF6s Last update 11 Mar 2009 [accessed 19 Mar 2010]
  • Whalen J. AstraZeneca chalks up Seroquel dismissal in State Court. Wall Street Journal Health Blog [Online] 2009. http://blogs.wsj.com/health/2009/06/10/astrazeneca-chalks-up-seroquel-dismissal-in-state-court
  • Kapczinski F, Lima MS, Souza JS, Schmitt R. Antidepressants for generalized anxiety disorder. Cochrane Database Syst Rev. 2003. p. CD003592. [PubMed]
  • Bang LM, Keating GM. Paroxetine controlled release. CNS Drugs. 2004;18:355–364. doi: 10.2165/00023210-200418060-00003. [PubMed] [Cross Ref]
  • Lenzer J. NIH secrets: study break. http://www.ahrp.org/cms/index2.php?option=com_content&do_pdf=1&id=398 Last update 19.10.2006 [accessed 13 Mar 2010]
  • Ray WA, Stein CM, Daugherty JR, Hall K, Arbogast PG, Griffin MR. COX-2 selective non-steroidal anti-inflammatory drugs and risk of serious coronary heart disease. Lancet. 2002;360:1071–1073. doi: 10.1016/S0140-6736(02)11131-7. [PubMed] [Cross Ref]
  • Juni P, Nartey L, Reichenbach S, Sterchi R, Dieppe PA, Egger M. Risk of cardiovascular events and rofecoxib: cumulative meta-analysis. Lancet. 2004;364:2021–2029. doi: 10.1016/S0140-6736(04)17514-4. [PubMed] [Cross Ref]
  • Curfman GD, Morrissey S, Drazen JM. Expression of concern: Bombardier et al., "Comparison of upper gastrointestinal toxicity of rofecoxib and naproxen in patients with rheumatoid arthritis," N Engl J Med 2000;343:1520-8. N Engl J Med. 2005;353:2813–2814. doi: 10.1056/NEJMe058314. [PubMed] [Cross Ref]
  • Waxman HA. The lessons of Vioxx: drug safety and sales. N Engl J Med. 2005;352:2576–2578. doi: 10.1056/NEJMp058136. [PubMed] [Cross Ref]
  • Waxman HA. The Marketing of Vioxx to Physicians (Memorandum to Democratic members of the Government Reform Committee) 2005.
  • Krumholz HM, Ross JS, Presler AH, Egilman DS. What have we learnt from Vioxx? BMJ. 2007;334:120–123. doi: 10.1136/bmj.39024.487720.68. [PMC free article] [PubMed] [Cross Ref]
  • Charatan F. Merck to pay $58 m in settlement over rofecoxib advertising. BMJ. 2008;336:1208–1209. doi: 10.1136/bmj.39591.705231.DB. [PMC free article] [PubMed] [Cross Ref]
  • DeAngelis CD, Fontanarosa PB. Impugning the integrity of medical science: the adverse effects of industry influence. JAMA. 2008;299:1833–1835. doi: 10.1001/jama.299.15.1833. [PubMed] [Cross Ref]
  • Hill KP, Ross JS, Egilman DS, Krumholz HM. The ADVANTAGE seeding trial: a review of internal documents. Ann Intern Med. 2008;149:251–258. [PubMed]
  • Ross JS, Hill KP, Egilman DS, Krumholz HM. Guest authorship and ghostwriting in publications related to rofecoxib: a case study of industry documents from rofecoxib litigation. JAMA. 2008;299:1800–1812. doi: 10.1001/jama.299.15.1800. [PubMed] [Cross Ref]
  • Moynihan R. Merck defends Vioxx in court, as publisher apologises for fake journal. BMJ. 2009;338:b1914. doi: 10.1136/bmj.b1914. [PubMed] [Cross Ref]
  • West RR, Jones DA. Publication bias in statistical overview of trials: example of psychological rehabilitation following myocardial infarction [Abstract] Proceedings of the 2nd International Conference on the Scientific Basis of Health Services and 5th Annual Cochrane Colloquium; 1997 Oct 8-12; Amsterdam. Amsterdam. 1999. p. 17.
  • Mangano DT, Tudor IC, Dietzel C. The risk associated with aprotinin in cardiac surgery. N Engl J Med. 2006;354:353–365. doi: 10.1056/NEJMoa051379. [PubMed] [Cross Ref]
  • Karkouti K, Beattie WS, Dattilo KM, McCluskey SA, Ghannam M, Hamdy A, Wijeysundera DN, Fedorko L, Yau TM. A propensity score case-control comparison of aprotinin and tranexamic acid in high-transfusion-risk cardiac surgery. Transfusion (Paris) 2006;46:327–338. [PubMed]
  • Hauser RG, Maron BJ. Lessons from the failure and recall of an implantable cardioverter-defibrillator. Circulation. 2005;112:2040–2042. doi: 10.1161/CIRCULATIONAHA.105.580381. [PubMed] [Cross Ref]
  • Kesselheim AS, Mello MM. Confidentiality laws and secrecy in medical research: improving public access to data on drug safety. Health Aff (Millwood) 2007;26:483–491. doi: 10.1377/hlthaff.26.2.483. [PubMed] [Cross Ref]
  • Sackner-Bernstein JD, Kowalski M, Fox M, Aaronson K. Short-term risk of death after treatment with nesiritide for decompensated heart failure: a pooled analysis of randomized controlled trials. JAMA. 2005;293:1900–1905. doi: 10.1001/jama.293.15.1900. [PubMed] [Cross Ref]
  • Camilleri M, Northcutt AR, Kong S, Dukes GE, McSorley D, Mangel AW. Efficacy and safety of alosetron in women with irritable bowel syndrome: a randomised, placebo-controlled trial. Lancet. 2000;355:1035–1040. doi: 10.1016/S0140-6736(00)02033-X. [PubMed] [Cross Ref]
  • Horton R. Lotronex and the FDA: a fatal erosion of integrity. Lancet. 2001;357:1544–1545. doi: 10.1016/S0140-6736(00)04776-0. [PubMed] [Cross Ref]
  • Lenzer J. FDA warns that antidepressants may increase suicidality in adults. BMJ. 2005;331:70. doi: 10.1136/bmj.331.7508.70-b. [PMC free article] [PubMed] [Cross Ref]
  • Lenzer J. Drug secrets: what the FDA isn't telling. Slate Magazine. 2005. http://www.slate.com/id/2126918
  • Saunders MC, Dick JS, Brown IM, McPherson K, Chalmers I. The effects of hospital admission for bed rest on the duration of twin pregnancy: a randomised trial. Lancet. 1985;2:793–795. doi: 10.1016/S0140-6736(85)90792-5. [PubMed] [Cross Ref]
  • Nissen SE. The DREAM trial. Lancet. 2006;368:2049. doi: 10.1016/S0140-6736(06)69825-5. [PubMed] [Cross Ref]
  • Drazen JM, Morrissey S, Curfman GD. Rosiglitazone: continued uncertainty about safety. N Engl J Med. 2007;357:63–64. doi: 10.1056/NEJMe078118. [PubMed] [Cross Ref]
  • Home PD, Pocock SJ, Beck-Nielsen H, Gomis R, Hanefeld M, Jones NP, Komajda M, McMurray JJ. Rosiglitazone evaluated for cardiovascular outcomes: an interim analysis. N Engl J Med. 2007;357:28–38. doi: 10.1056/NEJMoa073394. [PubMed] [Cross Ref]
  • Nathan DM. Rosiglitazone and cardiotoxicity: weighing the evidence. N Engl J Med. 2007;357:64–66. doi: 10.1056/NEJMe078117. [PubMed] [Cross Ref]
  • Psaty BM, Furberg CD. The record on rosiglitazone and the risk of myocardial infarction. N Engl J Med. 2007;357:67–69. doi: 10.1056/NEJMe078116. [PubMed] [Cross Ref]
  • Psaty BM, Furberg CD. Rosiglitazone and cardiovascular risk. N Engl J Med. 2007;356:2522–2524. doi: 10.1056/NEJMe078099. [PubMed] [Cross Ref]
  • Rosen CJ. The rosiglitazone story: lessons from an FDA Advisory Committee meeting. N Engl J Med. 2007;357:844–846. doi: 10.1056/NEJMp078167. [PubMed] [Cross Ref]
  • Singh S, Loke YK, Furberg CD. Long-term risk of cardiovascular events with rosiglitazone: a meta-analysis. JAMA. 2007;298:1189–1195. doi: 10.1001/jama.298.10.1189. [PubMed] [Cross Ref]
  • Shuster JJ, Schatz DA. The rosiglitazone meta-analysis: lessons for the future. Diabetes Care. 2008;31:e10. doi: 10.2337/dc07-2147. [PubMed] [Cross Ref]
  • Friedrich JO, Beyene J, Adhikari NK. Rosiglitazone: can meta-analysis accurately estimate excess cardiovascular risk given the available data? Re-analysis of randomized trials using various methodologic approaches. BMC Res Notes. 2009;2:5. doi: 10.1186/1756-0500-2-5. [PMC free article] [PubMed] [Cross Ref]
  • Home PD, Pocock SJ, Beck-Nielsen H, Curtis PS, Gomis R, Hanefeld M, Jones NP, Komajda M, McMurray JJ. Rosiglitazone evaluated for cardiovascular outcomes in oral agent combination therapy for type 2 diabetes (RECORD): a multicentre, randomised, open-label trial. Lancet. 2009;373:2125–2135. doi: 10.1016/S0140-6736(09)60953-3. [PubMed] [Cross Ref]
  • Merck/Schering-Plough Pharmaceuticals. Merck/Schering-Plough Pharmaceuticals provides results of the ENHANCE trial. http://www.msppharma.com/msppharma/documents/press_release/ENHANCE_news_release_1-14-08.pdf Last update 14 Jan 2008 [accessed 13 Mar 2010]
  • Greenland P, Lloyd-Jones D. Critical lessons from the ENHANCE trial. JAMA. 2008;299:953–955. doi: 10.1001/jama.299.8.953. [PubMed] [Cross Ref]
  • Lenzer J. Unreported cholesterol drug data released by company. BMJ. 2008;336:180–181. doi: 10.1136/bmj.39468.610775.DB. [PMC free article] [PubMed] [Cross Ref]
  • Berenson A. Data about Zetia risks was not fully revealed. New York Times. 2007.
  • Furberg CD, Pitt B. Withdrawal of cerivastatin from the world market. Curr Control Trials Cardiovasc Med. 2001;2:205–207. doi: 10.1186/CVM-2-5-205. [PMC free article] [PubMed] [Cross Ref]
  • Wooltorton E. Bayer pulls cerivastatin (Baycol) from market. CMAJ. 2001;165:632. [PMC free article] [PubMed]
  • Marwick C. Bayer is forced to release documents over withdrawal of cerivastatin. BMJ. 2003;326:518. doi: 10.1136/bmj.326.7388.518/a. [PMC free article] [PubMed] [Cross Ref]
  • Piorkowski JD Jr. Bayer's response to "potential for conflict of interest in the evaluation of suspected adverse drug reactions: use of cerivastatin and risk of rhabdomyolysis". JAMA. 2004;292:2655–2657. doi: 10.1001/jama.292.21.2655. [PubMed] [Cross Ref]
  • Zinberg DS. A cautionary tale. Science. 1996;273:411. doi: 10.1126/science.273.5274.411. [PubMed] [Cross Ref]
  • Begg CB, Berlin JA. Publication bias and dissemination of clinical research. J Natl Cancer Inst. 1989;81:107–115. doi: 10.1093/jnci/81.2.107. [PubMed] [Cross Ref]
  • Nathan DG, Weatherall DJ. Academia and industry: lessons from the unfortunate events in Toronto. Lancet. 1999;353:771–772. doi: 10.1016/S0140-6736(99)00072-0. [PubMed] [Cross Ref]
  • Harris G. Approval of antibiotic worried safety officials. New York Times. 2006.
  • Ross DB. The FDA and the case of Ketek. N Engl J Med. 2007;356:1601–1604. doi: 10.1056/NEJMp078032. [PubMed] [Cross Ref]
  • Johansen HK, Gotzsche PC. Problems in the design and reporting of trials of antifungal agents encountered during meta-analysis. JAMA. 1999;282:1752–1759. doi: 10.1001/jama.282.18.1752. [PubMed] [Cross Ref]
  • McKenzie R, Fried MW, Sallie R, Conjeevaram H, Di Bisceglie AM, Park Y, Savarese B, Kleiner D, Tsokos M, Luciano C. Hepatic failure and lactic acidosis due to fialuridine (FIAU), an investigational nucleoside analogue for chronic hepatitis B. N Engl J Med. 1995;333:1099–1105. doi: 10.1056/NEJM199510263331702. [PubMed] [Cross Ref]
  • Blumsohn A. Authorship, ghostscience, access to data and control of the pharmaceutical scientific literature: who stands behind the word? Prof Ethics Rep. 2006;19:1–4.
  • Bracken MB, Shepard MJ, Holford TR, Leo-Summers L, Aldrich EF, Fazl M, Fehlings M, Herr DL, Hitchon PW, Marshall LF, Nockels RP, Pascale V, Perot PL Jr, Piepmeier J, Sonntag VK, Wagner F, Wilberger JE, Winn HR, Young W. Administration of methylprednisolone for 24 or 48 hours or tirilazad mesylate for 48 hours in the treatment of acute spinal cord injury: results of the Third National Acute Spinal Cord Injury Randomized Controlled Trial. JAMA. 1997;277:1597–1604. doi: 10.1001/jama.277.20.1597. [PubMed] [Cross Ref]

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