How Much Do Patients Need to Know About a Potentially Risky Treatment?

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By Ellen Gabler, Steve Eder and Allie Pitchon from NYT Health https://ift.tt/wvAVLag
via IFTTT Hospitals, Blood, Biotechnology and Bioengineering, Ethics and Official Misconduct, Surgery and Surgeons, Regulation and Deregulation of Industry, Medicine and Health, Research An unapproved product made from umbilical cord blood was used at a prominent New York hospital. After an F.D.A. warning came an internal complaint: Patients should have been told.

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