Reporting Bias in Drug Trials Submitted to the Food and Drug Administration: Review of Publication and Presentation

Kristin Rising; Peter Bacchetti; Lisa Bero

doi:10.1371/journal.pmed.0050217

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Peer-reviewed

Research Article

Reporting Bias in Drug Trials Submitted to the Food and Drug Administration: Review of Publication and Presentation

Kristin Rising,

¤ Current address: Department of Internal Medicine, Boston Medical Center, Boston, Massachusetts, United States of America

Affiliation School of Medicine, University of California San Francisco, San Francisco, California, United States of America
⨯
Peter Bacchetti,

Affiliation Department of Epidemiology and Biostatistics, University of California San Francisco, San Francisco, California, United States of America
⨯
Lisa Bero

*To whom correspondence should be addressed. E-mail: berol@pharmacy.ucsf.edu

Affiliation Clinical Pharmacy and Health Policy, University of California San Francisco, San Francisco, California, United States of America
⨯

Reporting Bias in Drug Trials Submitted to the Food and Drug Administration: Review of Publication and Presentation

Kristin Rising,
Peter Bacchetti,
Lisa Bero

Published: November 25, 2008
https://doi.org/10.1371/journal.pmed.0050217

About the Authors

Kristin Rising

¤ Current address: Department of Internal Medicine, Boston Medical Center, Boston, Massachusetts, United States of America

Affiliation School of Medicine, University of California San Francisco, San Francisco, California, United States of America

Peter Bacchetti

Affiliation Department of Epidemiology and Biostatistics, University of California San Francisco, San Francisco, California, United States of America

Lisa Bero

*To whom correspondence should be addressed. E-mail: berol@pharmacy.ucsf.edu

Affiliation Clinical Pharmacy and Health Policy, University of California San Francisco, San Francisco, California, United States of America

Competing Interests

The authors have declared that no competing interests exist.

Author Contributions

KR contributed to the design, acquisition of data, analysis and interpretation of data, drafting of the manuscript, critical revision of the manuscript, and obtaining fellowship funding. PB contributed to the analysis and interpretation of data, critical revision of manuscript, and statistical analysis. LB contributed to the conception and design, acquisition of data, analysis and interpretation of data, drafting of manuscript, critical revision of manuscript, administrative support, and supervision.

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Drug research and development
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Publication ethics
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Clinical trials
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