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http://www.judicialwatch.org/news/2010/sep/judicial-watch-uncovers-fda-records-detailing-16-new-deaths-tied-gardasil Washington, DC -- September 28, 2010 Judicial Watch, the public interest group that investigates and prosecutes government corruption, announced today that it has received new documents from the U.S. Food and Drug Administration (FDA) under the provisions of the Freedom of Information Act (FOIA), detailing reports of adverse reactions to the vaccination for human papillomavirus (HPV), Gardasil. The adverse reactions include 16 new deaths (including four suicides) between May 2009 and September 2010. The FDA also produced 789 “serious” reports, with 213 cases resulting in permanent disability and 25 resulting in a diagnosis of Guillain Barre Syndrome. Adverse report excerpts include: A nineteen year old girl with no medical history except occasional cases bronchitis received Gardasil and in 53 days, had “Headache, Nausea, dizziness, chilling, tiredness, shortness of breath, complained of chest plain, severe cramps.” She experienced an Acute Cardiac Arrhythmia. Attempts to resuscitate her resulted in a sternal fracture, but were unsuccessful and the patient died. — V. 356938 A thirteen year old girl was vaccinated on July 17th, 2009. Ten days later, she developed a fever and was treated. However, “the patient did not recover and was admitted to the hospital on [August 8th]…She developed dyspnoea and went into a coma…she expired [that day] at around 9:00 pm. The cause of death was determined as ‘death due to viral fever.’ … This event occurred after 23 days of receiving first dose of Gardasil. — V. 380081 Thirteen days after vaccination, a ten year old girl developed “progressive loss of strength in lower and upper extremities almost totally…Nerve conduction studies [showed Guillain Barre Syndrome].” Case was “considered to be immediately life-threatening.” — V. 339375 One mother of a 13-year old girl who died 37 days after receiving the vaccination noted in a report: “I first declined getting her the vaccination but her doctor ensured me that it was safe…” After her daughter complained of a severe headache, no feeling in her foot and a tingling feeling in her leg, a doctor’s appointment was set for October 23, 2009. “My daughter never made it to Oct[ober] 23rd, which is also her birthday,” the mother noted. “She passed on Oct[ober] 17th, I found her cold unresponsive in her room at 7am....” “To say Gardasil has a suspect safety record is a big understatement. These reports are troubling and show that the FDA and other public health authorities may be asleep at the switch,” said Judicial Watch President Tom Fitton. “In the meantime, the public relations push for Gardasil by Merck and politicians on Capitol Hill continues. No one should require this vaccine for young children.”

GARDASIL is the vaccine promoted as protection against various types of cervical cancer supposedly caused by the HPV virus, and obviously is intended for other purposes. Even with the number of deaths and injury from the vaccine the ads ran non-stop on TV while state and federal governments tried to find ever newer and more invasive ways of making mandatory vaccination a reality. They got their wish; Obamacare calls for mandatory vaccination and proof of updates to vaccinations in order to get any healthcare.

Neither, Gardasil® nor any of the individual active ingredients have been previously approved for commercial marketing or use under the Food, Drug, and Cosmetic Act, the Public Health Service Act, or the Virus-Serum-Toxin Act, according to their application for patent.

Gardasil! It isn’t just for the girls!

In 2010 Merck was still waiting for the blessings of FDA to make mandatory their Gardasil vaccine for boys. As recently as November 2010, FDA was thinking of changing the terminology for male Gardasil from “Mandatory” to “Recommended”; after all, we’re dealing with the family jewels here and these are far more important than a few dead ovaries. But approval did come after the male version of Gardasil was tested on 602 young men from the ages of 9 to 26. (I can’t help but wonder how many of these young men knew they were being tested with this deadly vaccine).

Please note in this next article that Gardasil has been expanded to include far more than cervical cancer and includes the observation that “HPV is THOUGHT to be the cause”…not, is the cause or, we know it’s the cause, or we can prove conclusively, or there is substantial evidence,…they just think it could be. This is a broad and vague claim and totally without any conclusive supporting evidence.

Med Page Today:

WASHINGTON — An FDA advisory panel has expressed its support for expanding the indication on the quadrivalent human papillomavirus recombinant vaccine Gardasil to prevent anal intraepithelial neoplasia and anal cancer in males and females ages 9 through 26.

Gardasil was approved in 2006 to prevent genital warts and cervical, vulvar, and vaginal cancer in females ages 9 to 26; the vaccine’s indication was expanded in 2009 to include prevention of genital warts in males of that age range.

FDA’s Vaccines and Related Biological Products Advisory Committee agreed that the three-dose vaccine should also be used to prevent anal intraepithelial neoplasia and anal cancer caused by HPV strains 6, 11, 16, and 18. HPV is thought to be the cause of 90% of anal cancers.”

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In 2008 Merck planned the expansion of Gardasil injections targeting young boys and says the most important new opportunity for the vaccine will be for its use in males. (Merck claims: The vaccine could help prevent males from contracting Human Papilloma virus and spreading it to females through sexual contact.) Merck was on track to seek approval for use in males by the end of 2008 and of course now they have approval. And how many of the deaths and other injuries to young boys and men will go under-reported while MERCK profits?

Gardasil was never tested for cancer causing agents or proof of cancer prevention. It still has not been tested or proven to prevent cervical cancer or any of the other afflictions it claims to prevent. They just “think” it might.

In the interim, Merck’s sales of Gardasil have plummeted beginning back in 2007. Merck claims the reason was that women and girls forgot to go back for the second and third shots.

“We have put in place substantial reminder programs that allow them to improve the ability to remember to go back to the second and third dose. So, we’re doing it by mail, we’re doing it by e-mail, we’re doing it by text messages, and a variety of different technologies to be able to make sure [that] they get to their second, and third doses.”

Only they didn’t come back. Many who received the first shots suffered from partial paralysis, seizures, fevers, muscle spasms and a host of other symptoms. Although every effort was made by Merck and the CDC to squash or minimalize any adverse event reporting, the stories leaked out and the news wasn’t good. The CDC as of 2010 had posted these responses to Gardasil among hundreds of adverse events:

Examples:

“Pt had unwitnessed seizure on 5/21/09. H/O probable seizure activity in the past 6 wks. After seizure, pt has had complaint of headache, dizziness, weakness, balance difficulty. 7/6/09 MR received for DOS 5/21-24/2009 with D/C DX: Seizure. Headache. Pt presented to ER after episode of unresponsiveness with limb flexion, staring, and fall. Disoriented with slurred speech, inappropriate affect, weakness, tiredness and severe H/A after. Recent episodes of involuntary fluttering of R hand. Started on Depakote.

(Depakote is a psychotropic drug used for bi-polar disorder)

Body aches, fatigue, blisters inside mouth, swollen glands, sores on lips and gums, swollen lips were also reported in many cases.”

The VAER report (Vaccine Adverse Event Report) is populated with reports of seizures, fainting, involuntary flailing of limbs, rashes, fevers, paralysis, vomiting, muscle contractions, ringing in the ears, blurred vision, and many other symptoms which appeared immediately after the first injection of Gardasil. It will be years before we know the long term and most likely devastating effects of this killer vaccine.

Gardasil contains extremely high levels of aluminum and polysorbate 80, a known cause of sterility in lab tests on mice, and also known to cause sterility in humans. High levels of other neurotoxic chemicals and the presence of thimerisol, a derivitive of mercury is said to be present although MERCK continues to deny that allegation.

Thanks to the Vaccine Liability Fund, funded in whole by US taxpayers, MERCK will never be held responsible or liable for the deaths and injuries they have caused and instead will simply add up the billions in profits while taxpayers foot the bill for the damages.

Cynthia Janek wrote an article in 2006 for the New American called “FDA and HPV….when did they know?….(follow up). Janek’s research revealed:

“ …the FDA knew back in 2003 that a HPV is not the actual cause of cervical cancer. The actual cause is a ‘persistent HPV infection that may act as a tumor promoter in cancer induction.’”

“What we have here is proof that there is scientific evidence that has been published in the past 15 years that states that HPV infection does not bear a direct relationship to the forming of cervical cancer. It also tells us that HPV, if allowed to will be taken care of by our own body’s natural processes. . .“most infections are short-lived and not associated with cervical cancer.” With this being said, why do we need Gardasil when our own body is more than capable of eradicating HPV?

What we need is a government policy to assist women with the cost of getting follow-up tests when persistent HPV infection is present. This would make more sense and our government would save so much money on these types of programs instead of $360 each for the Gardasil vaccination.” MERCK applied to the FDA for approval of the vaccine to be used on older women.”

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As MERCK can produce not one independent test trial that proves the link between HPV and cervical cancer, and has even less evidence that Gardasil in fact will prevent any form of cervical cancer, one might think the FDA would have no hesitation in denying access to the market for this lethal vaccine. Oh! We could only dream! The FDA, noted for its funding by the same companies who seek their approval, was dragging its feet, but gave its approval of the extended vaccine in 2010.

As the FDA states with regards to many pharmaceuticals, death is an acceptable side affect. Acceptable to whom? MERCK? Now that the male version of the vaccine is on the market, I believe all males at MERCK and followed by everyone at the FDA should receive the initial doses. We should vaccinate all their children too…….we don’t need successive generations of genocidal monsters.

http://www.renewamerica.com/columns/janak/071220