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Tuesday 2 September 2014
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Even FDA Stops Merck’s Gardasil Expansion

FDA Rejects Merck’s Attempt to Expand Deadly Gardasil to Older Women

Contributing writer, Anthony Gucciardi

The Food and Drug Administration, a very pro-vaccine government organization, has stopped Merck’s attempts to increase the approved age range for death-linked HPV vaccine Gardasil to 45. It appears that even the FDA is concerned about the effects of the Gardasil immunization, which has been tied to over 49 deaths along with countless negative reactions that have led to hospitalizations and crippled health.

The FDA stated that clinical data presented by Merck, the creator of the vaccine, failed to show that Gardasil effectively prevented infections in women 27 to 45 years old. This is particularly shocking due to the fact that pharmaceutical companies oftentimes illegally alter the numeric turnouts of studies regarding the effectiveness and safety of their drugs and immunizations. What this means is that in the event Merck smeared the results, they were still unconvincing enough to pass by the FDA, an agency that allows for genetically modified foods to be consumed by United States despite the warnings of health experts and major studies worldwide.

The rejection will also lead to changes on the Gardasil label. The label will now state that the product ”has not been demonstrated to prevent HPV-related cervical intraepithelial neoplasia 2/3 or worse in women older than 26 years of age,” says Merck.

Gardasil is dangerous and ineffective at all ages

Gardasil, of course, is highly ineffective and unsafe at any age. One recently compelling piece of evidence against the Gardasil vaccine is the finding of rDNA inside the vaccine vials. SANE Vax, a vaccine research organization, tested vials of Gardasil to get a better understanding as to why the vaccine has resulted in so many deaths and adverse health reactions. What they found was that more than a dozen of the Gardasil vaccine vials studied were contaminted with the rDNA of the human Papillomavirus  Virus (HPV).

This rDNA is not naturally occurring, and has serious implications. It is the result of genetically modified HPV virus, meaning a heavily altered form of HPV is actually added to the vaccine during its manufacturing process.

In addition, the vials were not only found within the United States. Vials were also collected from Australia, New Zealand, Spain, Poland and France.

Dr. Lee, the pathologist who ran the tests, explained:

Natural HPV DNA does not remain in the bloodstream for very long. However, the HPV DNA in Gardasil is not ‘natural’ DNA. It is a recombinant HPV DNA (rDNA) — genetically engineered — to be inserted into yeast cells for VLP (virus-like-particle) protein production. rDNA is known to behave differently from natural DNA. It may enter a human cell, especially in an inflammatory lesion caused by the effects of the aluminum adjuvant, via poorly understood mechanisms. Once a segment of recombinant DNA is inserted into a human cell, the consequences are hard to predict.

Children are being injected with genetically modified forms of the very virus that Gardasil seeks to “treat” with unknown consequence. With possible mutation of affected cells, the HPV rDNA may cause irrevocable damage to young bodies worldwide, in addition to the deaths and other side effects it has already been linked to.

Stay away from this vaccine.

Source:

http://www.activistpost.com/2011/10/fda-rejects-mercks-attempt-to-expand.html

 

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2 thoughts on “Even FDA Stops Merck’s Gardasil Expansion

  1. Laevern

    Gardasil other HPV Vaccines / skipped Regulations
    How did other vaccines go on the market fast tracked illegally
    Gardasil is Fast Tracked illegally

    EPA environmental protection agency makes the Regulations

    CDC and FDA follow?

    Mercks account on all web searches never a word of the EPA
    DID They skip the EPA

    In Pesticides EPA governs with regulations

    testing of pesticides before the product goes legal
    Round-up weed killer non-selective

    That testing of pesticides when finished went to the EPA
    Then the EPA created an MSDS of the product and
    sends

    it to whom makes the product legal CDC FDA

    I dont know who

    but I let by Commercial pesticide license expire and thats how
    FIFRA this act creates agencies to follow what they stand for with authority regulations
    EPA gets the paperwork of required Regulated testings that takes 20 yeaRS OR SO

    Then of to FDA to finish the legal process
    They knew how to do their job??
    CDC has nothing to do with pesticides
    CDC is probably (quality control-a paper work trail)

    gardasil skipped the EPA?
    and FDA -CDC did not notice??????????????????????????????????????????????///They must have dissappeared and someones doing their job

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