Tag Archives: h1n1

Quelle Surprise: The WHO has Advisors with Industry Ties

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Sheeple:  please stop believing the bulls#!t about flu bugs, viruses and other contagion that are ‘going around’.

This story reveals that we’re likely at the tip of the iceberg when it comes to conflict in the pharmaceutical, media and medical communities.  Even though these people are responsible for … being responsible … they declared a pandemic with H1N1 and will likely declare many more.

Our health is not their priority.  Their bottom line is what matters most.

The next wave is already launched and people are already panicking.

Don’t worry.  If you fall for it, the only thing you’ve already caught is stupidity.

WHO list reveals flu advisors with industry ties

(AFP) – Aug 11, 2010

GENEVA — Five of the 15 experts that advised the World Health Organisation about swine flu pandemic alerts had received support from the drugs industry, including for flu vaccine research, the WHO revealed on Wednesday.

The agency released for the first time a list of the 15 members of the Emergency Committee headed by Australian tropical diseases professor John Mackenzie, who was the only member publicly named during the outbreak.

They came from Africa, Asia, Europe, Latin and North America, the list posted on the WHO’s website showed.

Most were scientific researchers and epidemiologists, along with a Senegalese diplomat, public health officials from Thailand and Chile as well as two specialists on international air travel and health. The list can be seen at http://www.who.int/ihr/emerg_comm_members_2009/en/index.html.

Critics had raised concerns about potential conflicts of interest that might have helped the drugs industry influence decisions on huge orders for special vaccines against A(H1N1) flu.

The WHO has repeatedly denied those claims, underlining that it had vetted members and maintained secrecy over their identities to protect them from undue pressure while the outbreak of swine flu was underway.

Six people declared interests to the UN health agency, including five researchers who disclosed past or current support from pharmaceutical firms, according to the WHO list.

Nancy Cox, from the US Centers for Disease Control, disclosed financial support from a drugs industry group, the International Federation of Pharmaceutical Manufacturers and Associations (IFPMA) for flu vaccine research and work on viruses in her unit.

US professor Arnold Monto declared current and past consultancies on pandemic or seasonal influenza research for GSK, Novartis, Roche, Baxter and Sanofi Pasteur.

He also declared a grant from Sanofi for a clinical trial in 2007-2008 related to influenza vaccines.

John Wood’s research unit at Britain’s National Institute for Biological Standards and Control (NIBSC), had undertaken research for Sanofi Pasteur, CSL, IFPMA, Novartis and Powdermed on influenza vaccine.

Professor Maria Zambon’s laboratory at the UK Health Protection Agency Centre for Infection received funding from several vaccine makers, including Sanofi, Novartis, CSL, Baxter and GSK.

British professor Neil Ferguson, an advisor to the committee, had acted as a consultant for Roche and GSK Biologicals until 2007, according to the list.

The WHO said those interests “do not give rise to a conflict of interest such that the experts concerned should be partially or totally excluded from participation in the Emergency Committee.”

The panel provided expert advice to the WHO Director General Margaret Chan about the new swine flu virus, allowing her to raise the alert when it was first uncovered in Mexico and the United States in April 2009.

It was also instrumental in the declaration of a pandemic with global spread of the disease in June 2009, triggering a chain of public health precautions including development and production of an influenza vaccine.

However, swine flu turned out to be less severe than feared.

As the virus petered out in North America and Europe in late 2009, governments sought to offload costly and huge stocks of unused vaccines and some European parliamentarians claimed the scare was unjustified.

Chan announced on Tuesday that the A(H1N1) influenza pandemic was officially over after more than 18,500 people died.

The WHO estimated that about 300 million people had been vaccinated worldwide.

WHO Knew? EU Parliament to Investigate “Swine Flu Swindle”

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WHO Knew?

Research Credit:  Global Research.

The European Union Parliament will open an investigation into the influence of pharmaceutical companies on decision makers, particularly the World Health Organization (WHO).

Full translation from this source:

The Council of Europe member states will launch an inquiry in January 2010 on the influence of the pharmaceutical companies on the global swine flu campaign, focusing especially on extent of the pharma‘s industry’s influence on WHO. The Health Committee of the EU Parliament has unanimously passed a resolution calling for the inquiry. The step is a long-overdue move to public transparency of a “Golden Triangle” of drug corruption between WHO, the pharma industry and academic scientists that has permanently damaged the lives of millions and even caused death.


The parliament motion was introduced by Dr. Wolfgang Wodarg, former SPD Member of the German Bundestag and now chairman of the Health Committee of PACE (Parliamentary Assembly of the Council  of Europe). Wodarg is a medical doctor and epidemiologist, a specialist in lung disease and environmental medicine, who considers the current “pandemic” Swine Flu campaign of the WHO to be “one of the greatest medicine scandals of the Century.”[1]

The text of the resolution just passed by a sufficient number in the Council of Europe Parliament says among other things, “In order to promote their patented drugs and vaccines against flu, pharmaceutical companies influenced scientists and official agencies, responsible for public health standards to alarm governments worldwide and make them squander tight health resources for inefficient vaccine strategies and needlessly expose millions of healthy people to the risk of an unknown amount of side-effects of insufficiently tested vaccines. The “bird-flu”-campaign (2005/06) combined with the “swine-flu”-campaign seem to have caused a great deal of damage not only to some vaccinated patients and to public health-budgets, but to the credibility and accountability of important international health-agencies.”[2]

The Parliamentary inquiry will look into the issue of „falsified pandemic“ that was declared by WHO in June 2009 on the advice of its group of academic experts, SAGE, many of whose members have been documented to have intense financial ties to the same pharmaceutical giants such as GlaxoSmithKline, Roche, Novartis, who benefit from the production of drugs and untested H1N1 vaccines. They will investigate the influence of the pharma industry in creation of a worldwide campaign against the so-called H5N1 “Avian Flu”  and H1N1 Swine Flu. The inquiry will be given “urgent” priority in the general assembly of the parliament.

In his official statement to the Committee, Wodarg criticized the influence of the pharma industry on scientists and officials of WHO, stating that it has led to the situation where “unnecessarily millions of healthy people are exposed to the risk of poorly tested vaccines,” and that, for a flu strain that is “vastly less harmful” than all previous flu epidemics.

Wodarg says the role of the WHO and its the pandemic emergency declaration in June needs to be the special focus of the European Parliamentary inquiry. For the first time, the WHO criteria for a pandemic was changed in April 2009 as the first Mexico cases were reported, to make not the actual risk of a disease but the number of cases of the disease basis to declare “Pandemic.” By classifying the swine flu as pandemic, nations were compelled to implement pandemic plans and also the purchase swine flu vaccines. Because WHO is not subject to any parliamentary control, Wodarg argues it is necessary for governments to insist on accountability. The inquiry will also to look at the role of the two critical agencies in Germany issuing guidelines on the pandemic, the Paul-Ehrlich and the Robert-Koch Institute.

Can H1N1 Vaccine Be Trusted Based on This News?

Original story link:  http://thebulletin.us/articles/2009/10/25/top_stories/doc4ae4b76d07e16766677720.txt

Merck’s Gardasil product was smeared in this article, but another product called Cervarix, developed by Glaxo-Smith Kline, was also brought into the story to demonstrate the lack of confidence in their products concerning cervical cancer.

When these kind of accusations and call for more research are made, what does it say about the H1N1 vaccination that millions of Canadians stood in line for?

Copy of the original story:

Dr. Diane Harper, lead researcher in the development of two human papilloma virus vaccines, Gardasil and Cervarix, said the controversial drugs will do little to reduce cervical cancer rates and, even though they’re being recommended for girls as young as nine, there have been no efficacy trials in children under the age of 15.

Dr. Harper, director of the Gynecologic Cancer Prevention Research Group at the University of Missouri, made these remarks during an address at the 4th International Public Conference on Vaccination which took place in Reston, Virginia on Oct. 2-4. Although her talk was intended to promote the vaccine, participants said they came away convinced the vaccine should not be received.

“I came away from the talk with the perception that the risk of adverse side effects is so much greater than the risk of cervical cancer, I couldn’t help but question why we need the vaccine at all,” said Joan Robinson, Assistant Editor at the Population Research Institute.

Dr. Harper began her remarks by explaining that 70 percent of all HPV infections resolve themselves without treatment within a year. Within two years, the number climbs to 90 percent. Of the remaining 10 percent of HPV infections, only half will develop into cervical cancer, which leaves little need for the vaccine.

She went on to surprise the audience by stating that the incidence of cervical cancer in the U.S. is already so low that “even if we get the vaccine and continue PAP screening, we will not lower the rate of cervical cancer in the US.”

There will be no decrease in cervical cancer until at least 70 percent of the population is vaccinated, and even then, the decrease will be minimal.

Apparently, conventional treatment and preventative measures are already cutting the cervical cancer rate by four percent a year. At this rate, in 60 years, there will be a 91.4 percent decline just with current treatment. Even if 70 percent of women get the shot and required boosters over the same time period, which is highly unlikely, Harper says Gardasil still could not claim to do as much as traditional care is already doing.

Dr. Harper, who also serves as a consultant to the World Health Organization, further undercut the case for mass vaccination by saying that “four out of five women with cervical cancer are in developing countries.”

Ms. Robinson said she could not help but wonder, “If this is the case, then why vaccinate at all? But from the murmurs of the doctors in the audience, it was apparent that the same thought was occurring to them.”

However, at this point, Dr. Harper dropped an even bigger bombshell on the audience when she announced that, “There have been no efficacy trials in girls under 15 years.”

Merck, the manufacturer of Gardasil, studied only a small group of girls under 16 who had been vaccinated, but did not follow them long enough to conclude sufficient presence of effective HPV antibodies.

This is not the first time Dr. Harper revealed the fact that Merck never tested Gardasil for safety in young girls. During a 2007 interview with KPC News.com, she said giving the vaccine to girls as young as 11 years-old “is a great big public health experiment.”

At the time, which was at the height of Merck’s controversial drive to have the vaccine mandated in schools, Dr. Harper remained steadfastly opposed to the idea and said she had been trying for months to convince major television and print media about her concerns, “but no one will print it.”

“It is silly to mandate vaccination of 11 to 12 year old girls,” she said at the time. “There also is not enough evidence gathered on side effects to know that safety is not an issue.”

When asked why she was speaking out, she said: “I want to be able to sleep with myself when I go to bed at night.”

Since the drug’s introduction in 2006, the public has been learning many of these facts the hard way. To date, 15,037 girls have officially reported adverse side effects from Gardasil to the Vaccine Adverse Event Reporting System (VAERS). These adverse reactions include Guilliane Barre, lupus, seizures, paralysis, blood clots, brain inflammation and many others. The CDC acknowledges that there have been 44 reported deaths.

Dr. Harper also participated in the research on Glaxo-Smith-Kline’s version of the drug, Cervarix, currently in use in the UK but not yet approved here. Since the government began administering the vaccine to school-aged girls last year, more than 2,000 patients reported some kind of adverse reaction including nausea, dizziness, blurred vision, convulsions, seizures and hyperventilation. Several reported multiple reactions, with 4,602 suspected side-effects recorded in total. The most tragic case involved a 14 year-old girl who dropped dead in the corridor of her school an hour after receiving the vaccination.

The outspoken researcher also weighed in last month on a report published in the Journal of the American Medical Association that raised questions about the safety of the vaccine, saying bluntly: “The rate of serious adverse events is greater than the incidence rate of cervical cancer.”

Ms. Robinson said she respects Dr. Harper’s candor. “I think she’s a scientist, a researcher, and she’s genuine enough a scientist to be open about the risks. I respect that in her.”

However, she failed to make the case for Gardasil. “For me, it was hard to resist the conclusion that Gardasil does almost nothing for the health of American women.”

HOT: GSK Pulls Vaccine Due to Potential for Life-Threatening Allergies

Gee.  It’s a good thing we waived the right to sue GSK on their untested vaccine.

Here’s a hot story about the brew for Canada that people are in a big hurry to have pumped into their arms:
http://www.google.com/hostednews/ap/article/ALeqM5hv_UnE27MKQefLNmQxLUqQF557NQD9C5TKJG0

Sorry folks.  Have you thought of taking Vitamin D capsules instead?

What a massive cluster f**k this whole thing has become.

Monkeys playing with their own feces could have managed this situation better.

Here’s another article about what’s actually in some of the vaccines.

Here are some notes from the article, which comment on an information leaflet distributed by GSK:

  • Trial results for the H5N1 vaccine (the earlier cousin to the H1N1 vaccine):  the product leaflet mentions a study in which the company injected the vaccine into pregnant rats. It found “an increased incidence of fetal malformations” and “delayed neurobehavioural maturation”
  • The leaflet also mentions a study on ferrets. The animals were given adjuvanted and nonadjuvanted H5N1 vaccines and then exposed to the flu. The ferrets that got the adjuvanted vaccine were protected by the vaccine. But those that got the nonadjuvanted vaccine all died.  [This is a massive concern for pregnant women being advised to get the nonadjuvanted version of the H1N1 vaccine].
  • The leaflet also says four of 253 people studied experienced “severe adverse reactions”. Three of the four were deemed to be unrelated to the vaccine, but one case of hypersensitivity (which can mean anything from an allergic reaction to autoimmune disease) was determined “to be related to vaccination”.  That one serious reaction might not sound like a lot, but it actually translates into a rate of 395 cases per 100,000 people. That’s more than 50 times the rate of hospitalization due to H1N1 itself: 7.3 per 100,000 Canadians.
  • Soldiers who received the vaccine had almost 7.5 times the rate of heart inflammation of nonvaccinated personnel, according to a study by U.S. military medical researchers in 2004 in the American Journal of Epidemiology.
  • One of the best examples involves a controversial ingredient present in the H1N1 vaccine: thimerosal. Thimerosal is a form of mercury used in some vaccines as a preservative. Drug makers agreed to phase it out of most vaccines after the U.S. Food and Drug Administration found in 1999 that mercury levels in children who had gotten multiple shots often exceeded safety levels set by the Environmental Protection Agency (EPA). Nonetheless, thimerosal still remains in many flu vaccines.
  • Controversy has raged for years about whether or not thimerosal is behind soaring childhood autism rates. While that debate continues, a 2008 study in the U.K. journal Toxicological and Environmental Chemistry found that boys who were given a vaccine containing thimerosal were nine times more likely to have developmental problems than unvaccinated boys.
  • Simple math tells us an average Canadian pregnant woman—weighing 80 kilograms at term—gets about 56 percent more than the daily safe level of mercury when given a dose of the nonadjuvanted vaccine. By the EPA’s stricter standards, that same dose is actually triple its daily safe level.
  • What’s more, Shaw notes, those daily safety levels were set for consumption of mercury in food, not for injection directly into the body. Injecting a neurotoxin like mercury has much more impact than eating it, he said.
  • Squalene is another controversial component of the swine-flu vaccine.  Debate has raged for years about whether or not squalene is responsible for Gulf War syndrome.
  • Another component of the H1N1 vaccine adjuvant:  polysorbate 80.  Studies have found it can cause severe allergic reactions and hypersensitivity.

My advice folks:  run, don’t walk, away from the clinics.

Research Credit on both stories:  www.cryptogon.com

Don’t Shoot Me: Boy Suffers From Rare Disease After H1N1 Shot

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This story from MSNBC captures the essence of why I’m OK with letting other people get their shot at my expense.

As I read about how a young boy lost most of his muscle control after getting the H1N1 vaccination, this quote struck me:

Since the start of the H1N1 vaccine campaign, the CDC has repeatedly warned that certain conditions, such as miscarriage, heart attack and even GBS occur regardless of immunization, and officials have urged the public not to blame the vaccine for the illnesses, but to report promptly any suspected side effects.

And of the reported 4,000 plus people that have died from H1N1 (without any indication of time period), some of those people actually had H1N1.

Meanwhile, in Canada, I read a report that the original estimated cost per vaccination was $16.  Very reasonable, I suppose.

However, now that the media has done a sufficient job of whipping the public into a frenzy, that price has nearly doubled to $30.

When the Conservative government promised Canada that all Canadians would have access to the vaccine, did they not think to book the original price in a contract?  What kind of business people are these folks?

And what picture does that paint of the supplier?  Should this 100% increase in price (with no limit in place) be considered extortion?

It’s a good thing Canadians have bottomless pockets.

Category: Canada, media, The Corporation | Tags: ,

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