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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, 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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There have been accusations of widespread corruption in connection with the promotion of this vaccine. It has not been shown to prevent one single case of cervical cancer. It has been shown to cause far more adverse effects than other vaccines.
It has been shown to cause deaths. Long term side effects are unknown. It increases the risk of brain damage. It causes seizures. It causes outbreak of genital and facial warts. It probably increases the risk of blood clots. It possibly increases risk of miscarriage or babies born with anomalies.
Seven out of ten get a new illness after taking the vaccine. Read that sentence again.
If it is taken when HPV is already present it increases the risk of cancer by over 44%.
It increases the risk of positive PAP smears. It is not tested to see if it causes cancer. It may also cause cancer through replacement (new virus strains which replace the ones removed may be more cancer causing). It may cause cancer due to the presence of recombinant (gene manipulated) DNA. Other consequences due to the presence of this DNA are unknown and may be horrific.
Thank you FDA for seeing the Dangers involved with this product. Now, lets stop it totally. Must more females die or have unforgivable side effects. If it takes more attorneys to create lawsuits, then so be it.
Dr. Jim
What is your stand on surgery & radiation treatment for prostate cancer?
Finally the FDA wakes up!?!
If men carry the HPV, why don’t we just screen and test men, find the carriers, and TREAT them? Why are women always the guinea pigs? Maybe if men took birth control, that lowered THEIR hormones, we’d have a few less wars and rapes… have a nice day! ; )
I like your comments, Meg! In case you haven’t visited http://www.truthaboutgardasil.org, please do!
Please….if the FDA woke up it wouldn’t even be on the market!!!
Let’s not do the hand clap dance and make it sound as if they are looking out for our best interest…Yikes!!!
I am so happy citizens are speaking out in such large numbers regarding FDA corruption. The pressure is on them. However, I am not convinced they are suddenly beginning to work in behalf of the people at all. We need to see sweeping action in so many different areas.
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