Aaron Kesselheim

Aaron Seth Kesselheim is an American physician, attorney, and medical researcher who serves as a professor of Medicine and member of the Center for Bioethics at Harvard Medical School. He is also a member of the Division of Pharmacoepidemiology and Pharmacoeconomics in the Department of Medicine at Brigham and Women’s Hospital, where he created and leads the Program On Regulation, Therapeutics, And Law (PORTAL). In 2020, he was inducted into the National Academy of Medicine. Provided by Wikipedia
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  1. 1
    Rising health care costs and life-cycle management in the pharmaceutical market.
    by Aaron S Kesselheim
    Published 2013-01-01
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  2. 2
    Same song, different audience: pharmaceutical promotion targeting non-physician health care providers.
    by James S Yeh, Aaron S Kesselheim
    Published 2013-11-01
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  3. 3
    The Case for Reforming Drug Naming: Should Brand Name Trademark Protections Expire upon Generic Entry?
    by Ameet Sarpatwari, Aaron S Kesselheim
    Published 2016-02-01
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  4. 4
    The next forum for unraveling FDA off-label marketing rules: State and federal legislatures.
    by Michael S Sinha, Aaron S Kesselheim
    Published 2018-05-01
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  5. 5
    An Uninformative Truth: The Logic of Amarin's Off-Label Promotion.
    by Spencer Phillips Hey, Aaron S Kesselheim
    Published 2016-03-01
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  6. 6
    Clinicians' contributions to the development of coronary artery stents: a qualitative study of transformative device innovation.
    by Aaron S Kesselheim, Shuai Xu, Jerry Avorn
    Published 2014-01-01
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  7. 7
    Prescribing systemic steroids for acute respiratory tract infections in United States outpatient settings: A nationwide population-based cohort study.
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  8. 8
    Medical students' exposure to and attitudes about the pharmaceutical industry: a systematic review.
    by Kirsten E Austad, Jerry Avorn, Aaron S Kesselheim
    Published 2011-05-01
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  9. 9
    Evaluating the evidence behind the surrogate measures included in the FDA's table of surrogate endpoints as supporting approval of cancer drugs
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  10. 10
    How does medical device regulation perform in the United States and the European union? A systematic review.
    by Daniel B Kramer, Shuai Xu, Aaron S Kesselheim
    Published 2012-01-01
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    Article
  11. 11
    Biomarker-Defined Subsets of Common Diseases: Policy and Economic Implications of Orphan Drug Act Coverage.
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  12. 12
    Continual learning in medical devices: FDA's action plan and beyond
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  13. 13
    Strategies and practices in off-label marketing of pharmaceuticals: a retrospective analysis of whistleblower complaints.
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  14. 14
    Repurposing existing drugs for new uses: a cohort study of the frequency of FDA-granted new indication exclusivities since 1997
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  15. 15
    Paying physicians to prescribe generic drugs and follow-on biologics in the United States.
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  16. 16
    Conflict of interest reporting by authors involved in promotion of off-label drug use: an analysis of journal disclosures.
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  17. 17
    Postmarket surveillance of medical devices: a comparison of strategies in the US, EU, Japan, and China.
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  18. 18
    A correlation analysis to assess event-free survival as a trial-level surrogate for overall survival in early breast cancer
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  19. 19
    Competition and price among brand-name drugs in the same class: A systematic review of the evidence.
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  20. 20
    Did FDA Decisionmaking Affect Anti-Psychotic Drug Prescribing in Children?: A Time-Trend Analysis.
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