Share this on:
 E-mail
21
VIEWS
0
COMMENTS
 
SHARES
About this iReport
  • Not vetted for CNN

  • Click to view NRajamannan's profile
    Posted October 17, 2013 by
    NRajamannan
    Location
    Chicago, Illinois
    Assignment
    Assignment
    This iReport is part of an assignment:
    Shutdown over: What next?

    More from NRajamannan

    In 2013:THE UNSUSPECTING PATIENTS WITH NO FDA PROTECTION DURING CLINICAL TESTING OF DEVICES

     

    There are human experiments that are currently being run at top hospitals across the country without informed consent while patients are under general anesthesia. Patients are not given the opportunity to provide informed consent for the testing of newly developed heart devices.

     

    A recently published expose, The Myxo File Part I -XII, published on Amazon.com and Kindle Direct Publishing provide the documents from the FDA, communications with the White House and Congress to try and get help for the patients. So far, the requests for an investigation, over 5 years still no response. President Barak Obama, inquired into the situation twice but the FDA is not reporting to the White House, the over 4,000 adverse events and over 645 deaths from these heart devices.

     

    Communications and letters from the White House are in the Myxo File Part II.

     

    The Company reported to the SEC that a new device was being invented for myxomatous mitral valve disease. The company provided a similar disclosure to the US patent office regarding the 40 new claims for a new invention. However, the FDA was not informed of the clinical trial until 2 years after the initial prototypes were manufactured and the disclosure was from a patient.

     


    The Honorable Senator John McCain. First Lady Obama, and Senator Richard Lugar are the only Government Individuals who wrote on behalf of the patients in Illinois and Indiana to the FDA.

     

    Patients are suffering while under general anesthesia. The Myxo File Part I –XII, demonstrates the heart attack, cardiac arrest and repeat surgery in patients who never agreed to be guinea pigs.

     


    These experiments would benefit the company and the inventor in royalties and profits, but the facts regarding the adverse events were left out of the final scientific publication. The laws that protect human subjects date back to World War II after the Nuremberg Trials, and are currently protected under the Common Rule. HHS, FDA, NIH, are responsible for the protection of these human lives in the United States and no response from these US Federal agencies to help the victims of illegal surgical human experiments.

     

    Human beings have the right to know if they receive an experimental device while under general anesthesia.

     

    Nalini Rajamannan, Christian Newswire December 2012

     

    http://www.ushmm.org/wlc/en/article.php?
    ModuleId=10005168

     


    "NAZI MEDICAL EXPERIMENTS

     


    Result of a medical experiment on a prisoner. Buchenwald concentration camp, Germany, date uncertain.
    — US Holocaust Memorial Museum

     

    During World War II, a number of German physicians conducted painful and often deadly experiments on thousands of concentration camp prisoners without their consent.

     

    Unethical medical experimentation carried out during the Third Reich may be divided into three categories...."

     

    "The second category of experimentation aimed at developing and testing pharmaceuticals and treatment methods for injuries and illnesses which German military and occupation personnel encountered in the field. At the German concentration camps of Sachsenhausen, Dachau, Natzweiler, Buchenwald, and Neuengamme, scientists tested immunization compounds and sera for the prevention and treatment of contagious diseases, including malaria, typhus, tuberculosis, typhoid fever, yellow fever, and infectious hepatitis. The Ravensbrueck camp was the site of bone-grafting experiments and experiments to test the efficacy of newly developed sulfa (sulfanilamide) drugs. At Natzweiler and Sachsenhausen, prisoners were subjected to phosgene and mustard gas in order to test possible antidotes.?"

     

    See CNN Ireport Confirming the Data of the Official Launch of the Device on the US market January 2007

     

    http://ireport.cnn.com/docs/DOC-1049059

     

    The device was tested from March 2007 through December 2006 during the validation stage of Testing the device as per the Design Controls fas per FDA regulations for the evoluation of a device in the Design Master Record or “justification to file"

     

    http://www.theindianalawyer.com/dtci-justification-to-file-on-medical-device-review/PARAMS/article/26508
    DTCI: 'Justification to file' on medical device review
    John P. Twohy , From DTCIJune 8, 2011

     

    See CNN Ireport for Lack of Informed Consent:
    http://ireport.cnn.com/docs/DOC-1049058
    Wall Street Journal, Mundy and Favole 2009

     

    See CNN Ireport for Clinical Study:
    http://ireport.cnn.com/docs/DOC-1049058

     

    See CNN Ireports for Adverse Events and Deaths:
    Over 4,000 Adverse events and over 645 deaths:
    http://ireport.cnn.com/docs/DOC-1047294
    http://ireport.cnn.com/docs/DOC-1049511

     

    See CNN Ireport for the Falsified Data and Heart Attack Missing from the FDA Compliance Review:

     

    http://ireport.cnn.com/docs/DOC-1049629

     

    Northwestern University Response to the Investigation:

     

    See CNN ireport:
    http://ireport.cnn.com/docs/DOC-1046932

     

    The Response required by HHS as posted on the Northwestern University Website and the Invitation to the President of the University to protect the Innocents as delivered in the Myxo file Part IV:

     

    http://www.research.northwestern.edu/ori/reporting-concerns/index.html

    What do you think of this story?

    Select one of the options below. Your feedback will help tell CNN producers what to do with this iReport. If you'd like, you can explain your choice in the comments below.
    Be and editor! Choose an option below:
      Awesome! Put this on TV! Almost! Needs work. This submission violates iReport's community guidelines.

    Comments

    Log in to comment

    iReport welcomes a lively discussion, so comments on iReports are not pre-screened before they post. See the iReport community guidelines for details about content that is not welcome on iReport.

    Add your Story Add your Story