Alliance for Human Research Protection

AHRP Honors Exemplary Professionals

Fred Baughman, MD

Fred A. Baughman, Jr.

Carl Elliott, MD

Carl Elliott, MD

Curt D. Furberg, MD

Curt D. Furberg, MD

David Graham, MD

David Graham, MD

Diane Harper, MD

Diane Harper, MD

Bernadine Healy, MD

Bernadine Healy, MD

Anthony Morris, MD

Anthony Morris, MD

Loren Mosher, MD

Loren Mosher, MD

Florence Nightingale

Florence Nightingale

Nancy Olivieri, MD

Nancy Olivieri, MD

Maurice Pappworth, MD

Maurice Pappworth

John Pesando, MD

John Pesando, MD

Jacob Puliyel, MD

Jacob Puliyel, MD

John Thompson, MD

John Thompson, MD

Dr. Andrew Wakefield

Dr. Andrew Wakefield

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- Unsafe Vaccines
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dubious ethics

An Ethically Dubious Blood Experiment: RECESS

January 21, 2010 |

AHRP is concerned about the ethics and safety of human subjects in a blood storage experiment ( RECESS) sponsored
by the National Heart Lung and Blood Institute.

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Categorized Vulnerable Groups | Tagged FDA, Informed Consent, Trauma Patients, Clinical Practice, New England Journal of Medicine, dubious ethics, experiment increases risk, death

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Board Member: David Egilman, MD

1. Expert witness David Egilman wins billions—and makes enemies—as he fights companies over public health, Science Magazine 2019

2. Court Records Show How a Medical Device ‘Seeding Trial’ Disguised Marketing as Science Health News Review,2018

3. J&J seeks retraction of paper critical of Pinnacle hip study

4. Grave fraudulence in medical device research: a narrative review of the PIN seeding study for the Pinnacle hip system, Accountability in Research 2018; Joan E. Steffen, B.A., Ella A. Fassler, B.S., Kevin J. Reardon, M.A., & David S. Egilman, M.D., M.P.H.

5. Artificial Hip Maker Demands Retraction Of A Paper Calling Its Research ‘Grave Fraudulence’ STAT News 2018

6. Corporate Corruption of Science—Another Asbestos Example, American Journal of Industrial Medicine

7. Sudden Shift at a Public Health Journal Leaves Scientists Feeling Censored ProPublica

8. ‘YOU WANT A DESCRIPTION OF HELL?’ OXYCONTIN’S 12-HOUR PROBLEM, Los Angeles Times, 2016 Excerpt: For a brief moment three years ago, it seemed the problems with 12-hour dosing might get wider attention. The FDA had called for public input on how to make painkiller labels safer. Dr. David Egilman, a Brown University professor of family medicine who had served as a plaintiff’s expert in unsuccessful suits against Purdue, saw it as an opportunity to alert agency officials to problems with OxyContin’s 12-hour claim.

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It is clearer and clearer to me that life is not held sacred in this country; it is cheap.

— Sen. Mike Gravel

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