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Vera Sharav, a medical activist, is the founder of the Alliance for Human Research Protection, and an activist against some practices of the biomedical industry, particularly in matters of patient consent and children. Sharav was born in Romania and survived the Holocaust as a child; her father did not survive. Her mother emigrated. Notability is a fun tool for taking and organizing notes. Students can draw and type notes, or record audio notes. There are features to capture sound and images from the classroom, as well as add media like photos. Notes can be shared via email or through services like Google Drive and Dropbox.

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Vera Sharav, a medical activist, is the founder of the Alliance for Human Research Protection,[1][2] and an activist against some practices of the biomedical industry, particularly in matters of patient consent and children.

Biography[edit]

Sharav was born in Romania and survived the Holocaust as a child; her father did not survive. Her mother emigrated to the United States while she was cared for by relatives; she rejoined her mother, in New York City, when she was 8. She attended City College of New York and studied art history, and after marriage and two children she went back to school, to the Pratt Institute, where in 1971 she received her master's in library science.[3]

Sharav became an activist against aspects of biomedical research after her teenage son died of a fatal reaction to clozapine, which he had been prescribed for schizo-affective disorder. In her 'vitriolic blog' she criticizes the industry which, she claims, is profit-driven, lies to its consumers, and misleads people into participating in trials it pretends are medical treatment. Of particular interest to her are the 'waivers of informed consent' issued by the Food and Drug Administration, which allow unconscious or incapacitated subjects to be tested.[3]

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How to hide caller id on iphone. Her criticism of clinical studies where patient consent is questionable led her to campaign against Northfield Laboratories, manufacturers of the blood substitute PolyHeme; she filed complaints and started an email campaign which led the media and then the US Senate to investigate the matter. Sharav claimed the product was toxic, and that the people and communities on which it was tested had not been properly informed of the risks.[3]

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Methods and assessment[edit]

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Sharav's methods are praised by some and criticized by others. Marcia Angell, former editor of The New England Journal of Medicine, senior lecturer at the Harvard Medical School, and industry critic praised her: 'I see her as someone the research establishment badly needs'. Arthur Caplan, professor of medical ethics at the University of Pennsylvania, sees her as a 'dangerous gadfly' who is not always well-versed in the science of some of the treatments she criticizes: 'It's crazy to say you won't do the research if you can't get good informed consent when the alternative could be death'. He agrees, though, that she is justified in trying to stop trials that involve children if the purpose is extending market rights.[3]

Other experiments that drew Sharav's ire involved the testing of HIV drugs on toddlers in the foster care system of New York City, and she 'helped scuttle government research that would have paid low-income Florida families $970 to test their children’s exposure to household pesticides'.[4]

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References[edit]

  1. ^Ault, Alicia (3 April 2004). 'Children need more protection in clinical trials, says IOM'. The Lancet. 363 (9415): 1119. doi:10.1016/S0140-6736(04)15934-5. ISSN0140-6736. PMID15068011. S2CID12012969.
  2. ^'Test of anthrax vaccine in children gets tentative OK'. Reuters. 19 March 2013. Retrieved 7 July 2020.
  3. ^ abcdSchmidt, Charlie (1 September 2008). 'Profile: Vera Sharav'. Nature Biotechnology. 26 (9): 965. doi:10.1038/nbt0908-965. ISSN1546-1696. PMID18779796. S2CID37650615.
  4. ^'Patients' rights advocate battles against medical establishment'. STAT. 18 August 2016. Retrieved 7 July 2020.


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