Showing posts with label swine flu. Show all posts
Showing posts with label swine flu. Show all posts

Tuesday, November 24, 2009

No flu shot mandate for doctors

Dcotors no being mandated to take H1N1 vaccine.  A good move, but not sure I agree with the reliance on hand sanitizer.  Soap and Water washing frequently is vital.

AMA meeting: No flu shot mandate for doctors; hand sanitizer pushed


The AMA will study if there's any benefit from requiring all health professionals to receive influenza vaccine.

By KEVIN B. O'REILLY AND DAMON ADAMS, amednews staff. Posted Nov. 23, 2009.
Houston -- The AMA House of Delegates rejected a proposal to mandate vaccinations for health care professionals but approved other policy to prevent the spread of seasonal flu and influenza A(H1N1).
A resolution by the Infectious Diseases Society of America said the AMA should back universal seasonal and H1N1 flu immunizations unless health professionals have medical contraindications or religious objections. In October, New York state announced that it was requiring all health professionals to get the H1N1 immunization, but the mandate was suspended later that month due to vaccine shortages.

"It is our ethical duty to do no harm and prevent transmission of disease to patients," said Michael L. Butera, MD, an alternate delegate who spoke on behalf of IDSA. "Despite educational efforts, we have 40% to 70% immunization rates that are woefully inadequate." Mandates may be "the only way to achieve" the goal of universal vaccination, he said.

But delegates balked at the idea of a vaccination mandate, saying that requirements should be a last resort and can be counterproductive if implemented poorly. The house directed the AMA to study the ethical and scientific intricacies of the issue further.

Delegates said hand sanitizer dispensers should be available in well-trafficked areas and urged large gathering places to develop plans in line with Centers for Disease Control and Prevention recommendations.

Physicians briefed on H1N1

During a session at the Interim Meeting, two CDC officials briefed delegates on the latest epidemiological data on H1N1 and how best to manage the disease. They addressed hospitalization rates, vaccine availability, dosing and vaccine testing.
Most cases of H1N1 have not required hospital care. But the highest hospitalization rates have been for children through age 4, said Anthony E. Fiore, MD, MPH, a medical epidemiologist in the CDC Influenza Division. Among hospitalized adults, 70% have an underlying medical condition. If a patient appears to have the virus, treatment should be started as soon as possible. "We encourage people not to delay treatment awaiting laboratory confirmation."

Physicians and other health care professionals need to take precautions to make sure they don't get sick, said Michael Bell, MD, associate director for infection control at the CDC Division of Healthcare Quality Promotion. Most exposure risk in hospitals is from sick workers, not patients. He cited an example of a resident at an Ohio hospital who infected 166 people with the virus.
To prevent the spread of H1N1 in physician practices, sick workers should stay home, and ill patients should be kept away from noninfected patients. Dr. Bell recommended vaccination for doctors and their staffs, saying it doesn't make sense to put patients at risk by skipping shots.

Health care personnel who develop a fever and respiratory symptoms should be excluded from work for at least 24 hours after the fever subsides, the CDC said. Workers who develop acute respiratory symptoms without fever should be allowed to work unless assigned to areas with severely immunocompromised patients. In those cases, workers should be reassigned temporarily or excluded from work for seven days from the onset of symptoms.

Meanwhile, CDC officials on Nov. 12 said about 22 million Americans had been sickened by H1N1 and about 4,000 had died, including 540 children. About 42 million doses of vaccine have been created.
"The amount coming out will increase rapidly in the next few weeks," Dr. Fiore said.

In a Nov. 10 letter to doctors, Food and Drug Administration Commissioner Margaret A. Hamburg, MD, said no serious adverse events attributed to the vaccine had emerged in clinical trials on more than 3,600 patients. She encouraged physicians to report any vaccine-related problems to the Vaccine Adverse Event Reporting System.

Colette R. Willins, MD, a family physician in Westlake, Ohio, and a delegate for the American Academy of Family Physicians, was among the physicians at the AMA Interim Meeting who voiced frustration about not receiving H1N1 vaccines yet.

"They keep telling us to watch for it," she said. "I can't even get my staff vaccinated."

The print version of this content appeared in the Nov 30, 2009 issue of American Medical News.

Tuesday, September 29, 2009

Beware TAMIFLU

UPDATE: September 2009
Following on reports of dosing and packaging problems with children's Tamiflu, we now learn that water treatment is unable to keep your water free from another drug that may have harmful side effects.

It certainly appears that makers of Tamiflu failed to include water quality considerations as they promote their product, with problematic issues.
Tamiflu Detected in Sewage Discharge and River Water in Japan

Another Comment on Swine Flu Vax Of 2009 - Unlicensed And Untested
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Originally posted October 2005 -

For several years I have posted information on the risks of flu vaccines and medical treatment related to flu. This year (2006-present) we seem to have a high alert to drive citizens to the jab by fear more so that in the past. I would encourage you to take the following information under serious consideration.

FLU VACCINE HAS RISKS.

You can find more on leaflady.org about immunity, colds, flu, prevention and help. If you need further information send your request here: http://www.leaflady.org/feedback.htm


Human-To-Human H5N1 Transmission During Tamiflu Prophylaxis

By Dr. Henry L. Niman, PhD
Recombinomics.com

"An H5N1 influenza virus, A/Hanoi/30408/2005, was isolated on 27 February 2005 from a 14-year-old Vietnamese girl (patient 1) who had received a prophylactic dose (75mg once a day) of oseltamivir from 24 to 27 February and was given a therapeutic dose (75mg twice daily) for 7 days starting on 28 February. No virus was isolated from specimens after the administration of increased doses of oseltamivir. The patient recovered and was discharged from hospital on 14 March 2005.

The timing of infection in these two patients, together with the lack of known interaction of the girl with poultry, raises the possibility that the virus could have been transmitted from brother to sister."

The above comments from a pre-released Nature paper raise serious questions about the prophalactic use of Tamiflu and human-to-human (H2H) of H5N1. The sister, Nguyen Thi Ngoan, of the index case, Nguyen Si Tuan, was taking the FDA approved prophylactic dose of Tamiflu, 1 pill per day. However, even while on Tamiflu, she developed H5N1 bird flu symptoms. Genetic analysis of the virus suggested that she was infected by her brother, even though she was taking Tamiflu.

The above paper focuses on resistance markers in isolated clones from the sister. However, the brother and sister were part of a large case cluster of H5N1 infections. The grandfather of the two patients also tested positive for H5N1 antibodies. Although H5N1 was not isolated, it is not clear if the grandfather was taking Tamiflu when his grandson was in the hospital.

Similarly, the index case's nurse developed avian influenza. He maintained that he had no exposure to poultry, yet developed laboratory confirmed H5N1. It is not clear if the nurse was taking Tamiflu at the time of his infection.

There was a second nurse who developed bird flu symptoms. She tested negative for H5N1 by PCR. Results from serum tests were not disclosed.

The effectiveness of Tamiflu against H5N1 was also raised in in vivo mice experiments. Mice were given the equivalent of 20 pills of Tamiflu per day. This high level was justified by observations on species specific differences in metabolism. However, even after correcting for species differences, the mice were treated with an equivalent of two pills per day. However, the dose was based on treatment, even though the mice were give the drug four hours before infection. However, even with these favorable conditions, 50% of the mice died if treated for 5 days. If treated for 8 days, the percentage dead fell to 20%..These mice studies raised dosing questions for oseltamivir against H5N1. Use at the FDA approved level, priced less than ideal results.

Similarly, the cluster of human cases described above raises dosing question. The H5N1 appeared to be susceptible to a doubled dose of Tamiflu and the isolated H5n1 was sensitive to Relenza. However, nations are stockpiling Tamiflu, and the above results suggest that the FDA approved dose for prophylaxis may be inadequate.

Similarly, Tamiflu resistance is another concern. The number of H5N1 cases in Vietnam is still relatively small. It is unclear how many people in Vietnam are on Tamiflu. The identification of a Tamiflu resistant variant in the small number of people being treated is cause for concern. Similarly, prophylactic treatment in health care workers and family members may not have been sufficiently high to prevent H5N1 infections.

Thus, the proper dose of Tamiflu and the frequency of resistance in Vietnam remains unclear. Similarly, the impact of wider use of Tamiflu in Indonesia is another area of concern.

webmaster@recombinomics.com ©2005 Recombinomics. All rights reserved.
Wednesday, November 29, 2006
Tamiflu dangers reported
OTTAWA (Reuters) - Canada has asked Swiss drug maker Roche AG to warn consumers of possible health risks linked to its influenza drug Tamiflu, the health department said on Wednesday.

Ottawa took the step after receiving international reports of side-effects such as hallucinations and abnormal behavior, including self-harm. The reports include cases involving children and teenagers, primarily in Japan.

"Health Canada has requested that the manufacturer ... update the Canadian prescribing information for Tamiflu to include this new information," the department said in a statement.

According to Health Canada, there have been 84 reports as of November 11 of Canadian patients having adverse effects when using Tamiflu. Ten of those cases involved fatalities...


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Friday, September 11, 2009

Swine Flu and Tamiflu: A comment

According to a recent study conducted by the Indian health ministry on the first 82 deaths due to swine flu in India, patients admitted to hospital died on average 3 days after commencing treatment with Tamiflu.

Thursday, September 10, 2009

Dual Standard at FDA

Remember SARS?

I do, and back in 2002(2003 and 2004) there was a similar campaign by the FDA to ban any information about natural products useful for respiratory illnesses including the mass marketing of SARS.

Sound familiar? Seems like another mass marketing campaign is underway on the latest version of a created respiratory illness. The same ploy seems to be apparent according to Marc Ullman's article below about Alli and competing products from the natural products industry.

This has been a repetitive behavior for decades now, includes the tryptophan / Prozac war and a few other events.

I happened to have been attacked by the FDA when the SARS controversy was raging. In typical government style due process was absent and the charge of the light brigade was in full force.

How I learned about it was from an article in the Seattle PI where reference was made to the product I offered for flu at that time (and still offer) that may be helpful. The PI staff writer quoted me yet never made any effort to contact me and speak with me directly. I tracked him down and eventually after getting to the top gun managed to get a retraction in the on-line version of the PI.

Not being alone in the number of products attacked by Mark McClellan's goons I created a web page listing the products attacked along with information about them. Most of the data on this page, except for using Echinacea, works well for the current "swine flu" issue. (Echinacea and some other natural products cause too much of a stimulation of your immune system for this created virus compound.)

The other action I took was to contact McClellan, a Harvard grad, and provide him with the clinical data about the product on my web site. This product was studied thoroughly in clinical research at Dana Farber, the well known cancer institute, a part of Harvard. The product was also proven effective.

The only data that FDA allowed to be in the news was about experimental product under development at Roche, and not proven to be effective.

The mind set is that nothing can be used or considered effective against anything unless it comes from Big PhARMA. This of course is one major reason why the mainstream "health"industry is on its self-created collision course.

Now you see another instant replay over liver damaging Alli and a weight loss/diet supplement.

Another word to the wise from Natural Health News...
GSK vs. The Supplement Industry: Who Wins? Written by: Marc Ullman 8/26/2009

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FDA receives “32 reports of liver injury including 27 requiring hospitalization” in users of GlaxoSmithKline’s Alli OTC weight loss drug. FDA receives 23 reports of liver injury including one death in users of the dietary supplement Hydroxycut. Guess which one is still on the market.

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On May 1, 2009 FDA issued an urgent alert warning consumers “to immediately stop using Hydroxycut products by Iovate Health Sciences Inc., of Oakville, Ontario.” According to the Agency’s press release, it had received 23 reports of serious health problems, including one death, that appeared to be associated with the use of the dietary supplement. At the same time, Iovate issued a “voluntary recall” of 64 different Hydroxycut products, covering, according to some news reports over 9 million product units.

On June 6 and June 18, 2009 FDA updated its list of drug products it was monitoring for “potential signals of serious risks” indicating that the Agency was reviewing the status of GSK’s Alli (orlistat) OTC weight loss drug and was “continuing to evaluate this issue to determine the need for any regulatory action” Alli was, however, allowed to remain on the market. On August 24, 2009 FDA issued an “Early Communication about Ongoing Safety Review of Weight Loss Drug Orlistat” stating that the “Review includes both prescription drug Xenical and OTC drug Alli”. The “communication” stated that “FDA received 32 reports of serious liver injury in patients taking orlistat. Of those cases, 27 reported hospitalization and six resulted in liver failure. Thirty of the adverse events occurred outside the United States. The most commonly reported adverse events included yellowing of the skin or whites of the eyes (jaundice), weakness, and stomach pain.” Despite this, the Agency advised that “consumers taking Xenical should continue to take it as prescribed, and those using over-the-counter Alli should continue to use the product as directed.”

Just in case you’re still wondering who wins as between the supplement industry and GSK, consider the following:

● In April 2004 FDA banned the sale of ephedra containing dietary supplements based upon the Agency’s conclusion that such products constituted an unreasonable risk to public health. As part of the basis for its action FDA cited a 2003 Rand Corporation study that concluded, in part, “Over the short term (four to six months), ephedrine, ephedrine plus caffeine, and supplements containing ephedra or ephedra plus caffeine promoted modest increases in weight loss, about 2 pounds per month more than the weight loss of persons taking the placebo.” This level of weight loss was found to offer no benefit to public health.

● On February 7, 2007 FDA approved the sale of Alli as an OTC weight loss remedy. The Agency took this action despite reports of severe side effects including “incontinence” (uncontrollable diarrhea) and “oily spotting” (anal leakage). Among the factors cited by FDA in support of its decision was evidence that Alli users lost 5-10 pounds over 6 months, about a 50% increase compared with diet and exercise alone. Unless FDA uses some kind of “new math” that I have yet to hear of, this amounts to slightly less than the 2 pounds a month it found insignificant for ephedra.

9 million units of recalled Hydroxycut and one ban of ephedra later, it seems that as between the supplement industry and GSK there is little doubt who wins at FDA.

Thursday, August 27, 2009

Saturday, August 22, 2009

Scientist Issues Swine Flu Vaccine Warning

Does virus vaccine increase the risk of cancer?

The swine flu vaccine has been hit by new cancer fears after a German health expert gave a shock warning about its safety.

Lung specialist Wolfgang Wodarg has said that there are many risks associated with the vaccine for the H1N1 virus.

He has grave reservations about the firm Novartis who are developing the vaccine and testing it in Germany. The vaccination is injected “with a very hot needle”, Wodarg said.

The nutrient solution for the vaccine consists of cancerous cells from animals and "we do not know if there could be an allergic reaction".

But more importantly, some people fear that the risk of cancer could be increased by injecting the cells.

The vaccine - as Johannes Löwer, president of the Paul Ehrlich Institute, has pointed out - can also cause worse side effects than the actual swine flu virus.

Wodrag also described people’s fear of the pandemic as an "orchestration": “It is great business for the pharmaceutical industry,” he told the ‘Neuen Presse’.

Swine flu is not very different from normal flu. “On the contrary if you look at the number of cases it is nothing compared to a normal flu outbreak,” he added.

The chairman of the health committee in the European Council has urged for a careful and calm reaction to the virus.

Up until now, the producers of the vaccine did not know how many orders they would have by the autumn, but the German Government is now a guaranteed customer.

Even the pharmaceutical companies are trying to exploit the fear of the swine flu pandemic

http://www.bild.de/BILD/news/bild-english/world-news/2009/08/07/swine-flu-health-expert-warning/does-virus-vaccine-increase-risk-of-cancer.html#%23

21.08.2009 - 12:33 UHR

9/18/2009 - Another similar opinion

Sunday, August 16, 2009

Vaccine Side Effects Known, Facts Hidden

This is one more piece in the puzzle that you should take into consideration when considering your options with this untested and unproven vaccine.
Swine flu jab link to killer nerve disease: Leaked letter reveals concern of neurologists over 25 deaths in America

A warning that the new swine flu jab is linked to a deadly nerve disease has been sent by the Government to senior neurologists in a confidential letter.

The letter from the Health Protection Agency, the official body that oversees public health, has been leaked to The Mail on Sunday, leading to demands to know why the information has not been given to the public before the vaccination of millions of people, including children, begins.

It tells the neurologists that they must be alert for an increase in a brain disorder called Guillain-Barre Syndrome (GBS), which could be triggered by the vaccine.GBS attacks the lining of the nerves, causing paralysis and inability to breathe, and can be fatal.

The letter, sent to about 600 neurologists on July 29, is the first sign that there is concern at the highest levels that the vaccine itself could cause serious complications.

It refers to the use of a similar swine flu vaccine in the United States in 1976 when:

More people died from the vaccination than from swine flu.

500 cases of GBS were detected.
The vaccine may have increased the risk of contracting GBS by eight times.
The vaccine was withdrawn after just ten weeks when the link with GBS became clear.
The US Government was forced to pay out millions of dollars to those affected.
Read complete article...

Saturday, August 15, 2009

Nature Cures: More Herbs for Flu

The tradition of Ayurveda offers us yet another natural, herbal approach to stave off flu and "swine" flu.
Indian herb: Tulsi (basil) can help keep swine flu away: Ayurvedic experts

Lucknow, May 27: Wonder herb Tulsi can not only keep the dreaded swine flu at bay but also help in fast recovery of an afflicted person, Ayurvedic practitioners claim.

"The anti-flu property of Tulsi has been discovered by medical experts across the world quite recently. Tulsi improves the body's overall defence mechanism including its ability to fight viral diseases. It was successfully used in combating Japanese Encephalitis and the same theory applies to swine flu," Dr U K Tiwari, a herbal medicine practitioner says.

Apart from acting as a preventive medicine in case of swine flu, Tulsi can help the patient recover faster.

"Even when a person has already contracted swine flu, Tulsi can help in speeding up the recovery process and also help in strengthening the immune system of the body," he claims.

Dr Bhupesh Patel, a lecturer at Gujarat Ayurved University, Jamnagar is also of the view that Tulsi can play an important role in controlling swine flu.

"Tulsi can control swine flu and it should be taken in fresh form. Juice or paste of at least 20-25 medium sized leaves should be consumed twice a day on an empty stomach."

This increases the resistance of the body and, thereby, reduces the chances of inviting swine flu," believes Patel.

Polio Vaccine Backfires in Nigeria; It Can Be Cured

In Canada, in the 40s, 50s, 60s, when polio was a major public health concern, MDs were curing it with iodine. This surely is a very inexpensive way to address this crisis currently if one could get the information to the right place.

People in the US who did receive live vaccine, just as the one currently creating the problem in Africa, have died or now, years later, live with post-polio syndrome or other severe diseases known to be related to the vaccine.

This information is important to in regard to the current flu situation. Surely it is safer than an untested vaccine when the government provides a risk free status to the manufacturers.

Vitamin C Treatment of Polio

Looks like instant replay...
Polio surge in Nigeria after vaccine virus mutates
LONDON (AP) — Polio, a dreaded paralyzing disease stamped out in the industrialized world, is spreading in Nigeria despite efforts to stamp it out. And health officials say in some cases, it's caused by the vaccine used to fight it.

In July, the World Health Organization issued a warning that this vaccine-spread virus might extend beyond Africa. So far, 124 Nigerian children have been paralyzed this year — about twice those afflicted in 2008.

The polio problem is just the latest challenge to global health authorities trying to convince wary citizens that vaccines can save them from dreaded disease. For years, myths have abounded about vaccines — that they were the Western world's plan to sterilize Africans or give them AIDS. The sad polio reality fuels misguided fears and underscores the challenges authorities face using a flawed vaccine. complete article
More information about the benefits of iodine...

Read comment by Dr. Patricia Doyle

Friday, August 7, 2009

Flu and Mixed Messages

UPDATE: August 14 - Czech Republic takes Baxter to task for not guaranteeing swine flu vaccine safety.
Prague – The U.S. pharmaceutical firm Baxter which manufactures a vaccine against the swine flu in its Czech branch will not ensure the vaccine for the Czech Republic in the case of a pandemic, Baxter media representative Jana Cechova told CTK today. The Czech Republic has relied on the factory in Bohumil, Central Bohemia. In its original pandemic plan, the Czech Republic reckoned with vaccines for 60 percent of the population, while the updated plan involves vaccines for 25 percent and the Tamiflu and Relenza antivirotics for the same number.

“No contract for the delivery of the vaccines A(H1N1) between Baxter and the Czech Republic has been concluded,” Cechova said.

The websit tn.cz writes that the Czech Health Ministry has explained its stopping the talks with Baxter by the firm’s inability to guarantee that the vaccine is safe and who will bear the risks for possible side-effects.

“It is a pity, but, unfortunately, at the moment when we accepted the bids, Baxter was unable to confirm that it will deliver a registered vaccine,” Health Minister Dana Juraskova said.

Over 60 Czechs have caught the swine flu, but no fatality has been registered.”

http://www.ceskenoviny.cz/domov/zpravy/pri-pandemii-nebude-mit-cr-vakciny-od-baxtera/391208?id=391210

UPDATE: CDC lumps all pneumonia deaths in the same category as flu. WSJ reported that CDC inflates statistics 1500% when covering this topic.
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While its full steam ahead on the swine flu and vaccine manufacturing insanity a recent article exposes a critical issue supporting the views opposing the pandemic propaganda, the need for a vaccine, and its news you need to hear.

Just consider these components from of Mike Stobbe's AP Article "Ouch! Early flu shot season comes with 3 jabs"

Ouch! is the operative word here, and please let me know if this isn't confusing:

> Experts suggest you get that first shot as early as this month (August)

> Scientists believe the swine flu vaccine will be most effective if given in two doses, about three weeks apart, although testing is still under way to check that.

> Scientists are just beginning to test the safety and effectiveness of the new swine flu vaccine, work that is expected to take months.

> "I think it's safe to say we expect some confusion," said Kristine Sheedy, a CDC communications specialist.

Well, my suggestion is that you skip the Flu Folly and read more here, here, here, here, and here before you readily give up your body to experimentation.

Retired Vax Scientist Would Never Vaccinate His Kids

Tuesday, August 4, 2009

Herbal Medicine for H1N1

It is terribly unfortunate that here in the US, the Big Pharma controlled FDA, along with FTC, HHS and our paid-for-protecting-corporate-America officials and the mainstream media and medical conclaves do not want any non-drug information disseminated here.

See natural options here and here

And please also refer to the unique garlic product in the right column, ALLI-C.

See the entire photo album


Workers prepare herbal medicines at Traditional Chinese Medicine Hospital in Beijing
Chinese pharmacy workers prepare traditional Chinese medicine (TCM) packets of various herbs at the Beijing Traditional Chinese Medicine Hospital in Beijing on July 23, 2009. In order to bring TCM into full play in the prevention and treatment of Type A influenza H1N1, or swine flu, the Beijing Administration of TCM has set up a special service path for people to obtain herbal packets that doctors claim will help prevent H1N1 infection. (UPI Photo/Stephen Shaver)

Monday, August 3, 2009

2005 "Swine" Flu

Emerging Infectious Diseses, Volume 14, Number 9–September 2008
Dispatch
Human Case of Swine Influenza A (H1N1) Triple Reassortant Virus Infection, Wisconsin
Alexandra P. Newman,1 Erik Reisdorf, Jeanne Beinemann, Timothy M. Uyeki, Amanda Balish, Bo Shu, Stephen Lindstrom, Jenna Achenbach, Catherine Smith, and Jeffrey P. Davis
Author affiliations: Centers for Disease Control and Prevention, Atlanta, Georgia, USA (A.P. Newman, T.M. Uyeki, A. Balish, B. Shu, S. Lindstrom, J. Achenbach, C. Smith); Wisconsin Division of Public Health, Madison, Wisconsin, USA (A.P. Newman, J.P. Davis); Wisconsin State Laboratory of Hygiene, Madison (E. Reisdorf); and Sheboygan County Health and Human Services, Sheboygan, Wisconsin, USA (J. Beinemann)

Abstract
Zoonotic infections with swine influenza A viruses are reported sporadically. Triple reassortant swine influenza viruses have been isolated from pigs in the United States since 1998. We report a human case of upper respiratory illness associated with swine influenza A (H1N1) triple reassortant virus infection that occurred during 2005 following exposure to freshly killed pigs.

http://www.cdc.gov/eid/content/14/9/1470.htm
Suggested citation for this article
Newman AP, Reisdorf E, Beinemann J, Uyeki TM, Balish A, Shu B, et al. Human case of swine influenza A (H1N1) triple reassortant virus infection, Wisconsin. Emerg Infect Dis [serial on the Internet]. 2008 Sep [date cited]. Available from http://www.cdc.gov/EID/content/14/9/1470.htm

DOI: 10.3201/eid1409.080305
1Current affiliation: New York State Department of Health, Albany, New York, USA.

Find more articles by entering 'Tamiflu' or 'Flu' in the search window.
Wednesday, November 29, 2006
Tamiflu dangers reported
OTTAWA (Reuters) - Canada has asked Swiss drug maker Roche AG to warn consumers of possible health risks linked to its influenza drug Tamiflu, the health department said on Wednesday.

Ottawa took the step after receiving international reports of side-effects such as hallucinations and abnormal behavior, including self-harm. The reports include cases involving children and teenagers, primarily in Japan.

"Health Canada has requested that the manufacturer ... update the Canadian prescribing information for Tamiflu to include this new information," the department said in a statement.

According to Health Canada, there have been 84 reports as of November 11 of Canadian patients having adverse effects when using Tamiflu. Ten of those cases involved fatalities...


Tamiflu not effective
Relenza, Tamiflu
Tamiflu

Saturday, August 1, 2009

Flu Vaccine Man-Made

August 1, 2009
New Evidence: That The ‘Swine Flu’ Pandemic Is Man-Made
Filed under: World — Tags: flu, Pandemic, swine flu — Satinder SINGH @ 7:36 am

Murder suspects are either convicted or acquitted at trial based on the prosecution’s presentation of EVIDENCE which usually hinges on MOTIVE, OPPORTUNITY, and TIME-LINES combined with physical documents. To gather such hard evidence, detectives and/or federal agents often spend months following leads and interviewing witnesses. In the trial phase, re-creating the sequence of events is essential. I submit this paper will provide more than enough hard evidence to at least result in a series of criminal indictments of charges of MASS MURDER, and CONSPIRACY TO COMMIT WORLD GENOCIDE against Novartis Pharmaceutical principals and agents and others.

PRIMARY MOTIVE

The Primary Motive behind this alleged criminal activity is also the primary cause of most murders in the world today, and that motivation is simply: BIG MONEY. Billions of Dollars of windfall profits from government contracts worldwide, as a matter of fact.
I will provide evidence that will show that Novartis Pharmaceuticals of Basel, Switzerland has conspired with corrupt “scientists” at the U.S. Army Institute of Pathology Ft. Detrick, Maryland, to create a “novel” strain of weaponized “influenza” virus by means of “reverse engineering” the deadly 1918 killer strain which strain was maliciously and surreptitiously released upon the world in March and April of 2009 for the primary purpose of creating a panic-stricken world-wide demand for Novartis vaccine material.

The evidence will also clearly show that the Novartis vaccine material is in reality designed to facilitate the further mutation of the pandemic into more lethal waves of increasingly virulent and deadly disease, rather than to curtail and limit the existing outbreak. The evidence will show that Novartis is willingly being used, (and extremely well-paid) to facilitate the edicts of the global elite’s Club of Rome; which edicts clearly call for a massive and sudden depopulation of certain segments of the earth’s human population.

PRIMARY EVIDENCE

To realize such windfall profits on an engineered, global flu pandemic, detailed covert planning must take place of course.
Patents protecting the proprietary flu vaccine must be applied for and secured before the pandemic virus is released in order to minimize the competition and maximize the profit potentials. In a biological attack of this nature, timing is extremely critical.
Indeed, the evidence is clear Novartis applied for just such a patent on Nov. 4, 2005, and the U.S. Patent Office accepted this application and granted US 20090047353A1 for a “Split Influenza Vaccine with Adjuvants” on February 19, 2009. (See bottom of page).

With this patent now secured, the conspirators were now free to create the demand for their “novel” split influenza vaccine by releasing a “novel” split-influenza (combining multiple viruses) pandemic virus from a weapons lab test-tube into unsuspecting human hosts. http://www.washingtonpost.com/wp-dyn/content/article/2009/06/17/AR2009061703271.html

The so-called “Swine Flu” grabbing headlines today is actually a recombinant, or “split-influenza” virus consisting of A-strain Bird-Flu (H5N1), Swine Flu (H1N1) and multiple strains of human flu (H3N2). Likewise, the 1918 Killer Flu that killed untold millions of people was a recombinant or “split-influenza” virus composed of Bird flu, Swine Flu, and multiple strains of human flu.

CRIMINAL TIMELINE

The criminal timeline begins in 1997, when Dr. Jeffrey Taubenberger assembled a team of geneticists and microbiologists to analyze the genome structure, and then to REPRODUCE (i.e. reverse engineer) what is arguably one of the most deadly viral structures the world has ever been cursed with the 1918 killer flu virus. According to numerous published stories and reports, Taubenberger and his team utilized super-computers to map the complex RNA and DNA structures of the killer virus, then utilized human plasmids to successfully re-create the 1918 killer. Taubenberger completed his work in early 2005, then immediately left the employ of the U.S. Army at Ft. Detrick to take a much more lucrative position with the National Institutes of Health. His new focus was to create a VACCINE against the very same 1918 killer flu that he and his team had, just months earlier, successfully “reverse engineered” and created.

This researcher is very confident that a focused criminal investigation would likely reveal prima facia evidence that Taubenberger was in reality working for Novartis while employed with the N.I.H. and was quite likely the primary author of Novartis’ Nov. 6, 2005 “provisional” patent application. On page 2, paragraph 32 of the patent publication we read, quote: “The influenza virus [that the 'invention vaccine' is designed to protect against] may be a reassortant strain, and may have been obtained by reverse genetics techniques. Reverse genetics techniques allow influenza viruses with desired genome segments to be prepared in vitro using plasmids.” The remnant of the paragraph then goes into very specific detail as to the actual mechanics of how the pandemic virus was actually created by Taubenberger’s Ft. Detrick team. At the very least, the author of the patent application had to have studied Taubenberger’s various published reports on his work at Detrick, for the wording and science is virtually verbatim.

Furthermore, this paragraph is even more damning by the words “may have been obtained”. Who “obtained” this virus and for what reason was it “obtained”? Keep in mind the CDC and HHS would have Americans believe that the pandemic viral outbreak is totally a “natural” occurrence if so then how could Novartis have such an incredible advance knowledge to the point of developing a vaccine with such absolutely PERFECT TIMING???

WHO EXACTLY IS “NOVARTIS”??

Novartis International AG is simply the world’s largest, multi-national pharmaceutical company with over $53 Billion USD revenue generated in 2008. It’s headquarters is located in Basel, Switzerland, home of the vaunted “Swiss Guards” who provide all security measures for the Vatican and the Club of Rome. The company logo symbolizes the “eternal flame” of the Illuminati “enlightened ones”. Dig into Novartis International AG’s long history, and one finds that it began as a component of the infamous I.G. Farben combine, which in turn was primarily responsible for the rise of Adolph Hitler and the German/Austrian Third Reich.

Dig a bit deeper and you find that Novartis also wholly owns a company called Sandoz which was the inventor of LSD and other strong hallucinogenic “truth” drugs, and was the supplier of LSD to the CIA allowing them to scale new heights with their covert “MK ULTRA” mind control experiments. Documents released to U.S. Congressional investigators in 1977 show that Sandoz Labs had arranged for certain Nazi scientists to gain new identities in Allen Dulles’ CIA at the conclusion of WWII. This was accomplished under a secret extraction program called “Operation Paper Clip”.

The address listed on the Novartis Patent applications is a P.O. Box in Emeryville, California. Up until the summer of 2005, this Emeryville California address belonged to Chiron Inc. the world’s second-largest INFLUENZA VACCINE MANUFACTURER. Chiron was doing very well, with reported sales of $357 million in fiscal 2002. Chiron’s sales nearly doubled, peaking at a whopping $678 million in 2003 and it was mostly due to the marketing and sale of FLU VACCINE CONTRACTS to the federal government. Novartis, which owned much of Chiron’s stock, was very pleased, until disaster struck in 2004 — the entire year’s stock of flu vaccine was found to be contaminated and was condemned.

Stock values plummeted on the news. With the stock at a historic low, Novartis quickly purchased the remainder of Chiron’s stock and began immediately to work on the massive “novel pandemic flu” vaccine that they somehow knew would soon have worldwide demand especially if they controlled the exclusive patent they could effectively “corner the pandemic flu vaccine market”!!

OTHER CRIMINAL ACTIVITIES

I would submit that killing tens of thousands of innocent humans via the systemic creation of a “pandemic” in order to make billions of dollars is vile enough, but there is also evidence that there is an even more heinous hidden agenda at work here, and it is spelled GENOCIDE.

It is no mystery that Adolph Hitler advocated the elevation of a Nordic “Master Race” that would rule the world in a “New Order of the Ages” called the “Third Reich”. Sadly, not all of the EUGENIC/GENOCIDAL National Socialists were executed at Nuremburg.
In reality, the elite financiers that actually dictated the agenda to Hitler, merely went underground, willing to bide their time until their godless agenda to liquidate BILLIONS of people could be successfully implemented.

The evidence that the Novartis-controlled “Pandemic Vaccine” may well be a tool of mass genocide, is actually quite overwhelming.
At this point, some readers may scoff and ask: “Why would any company want to kill off their customers?” The answer is that these “customers” control large blocks of assets and equity. As Kissinger’s “NSSM-200″ report outlines, the “spoils” of genocide include controlling large tracts of land and mineral assets. This is secondary, of course, to their warped dream of creating a Utopian World Order with only 500 million “worthy” humans allowed to share in it.

WHAT’S THE EVIDENCE?

While George H.W. Bush was busy saving the world from the evil dictator Saddam Hussein in 1991, pursuant to his U.N. speech to create a “new world order” an agenda for an “Initiative for Eco-92 Earth Charter” elitist meeting happened to fall into honest, Christian hands. This agenda basically reiterated the genocide outlined in Henry Kissinger’s infamous NSSM-200 report of 1974, and called for “the immediate reduction of world population.” The entire report can be downloaded at:

My extensive research shows that by 1992, the massive death rate of AIDS had simply not materialized to the Elite’s satisfaction, and a more efficient mass killer had to be engineered in order to fulfill the edicts cut into the “Georgia Guidestones”.

Evidence shows that like the 2009 “Novel” Flu Virus the HIV virus was also engineered and manufactured in the labs of Ft. Detrick.

In 1969, during a House Appropriations Committee hearing, the Defense Department’s Biological Warfare (BW) division at Ft. Detrick requested funds to develop, through complex gene-splicing (i.e. genetic engineering) a “novel” new disease that would both be resistant to, and break down a victim’s immune system. The Congressional Record reads:

“Within the next 5 to 10 years it would probably be possible to make a new infective micro-organism which could differ in certain important respects from any known disease-causing organisms. Most important of these is that it might be refractory to the immunological and therapeutic processes upon which we depend to maintain our relative freedom from infectious diseases.”

The funds for this “Dr. Strangelove” project were somehow approved. AIDS “magically” appeared within the requested time frame, and of course, just happens to exhibit the exact characteristics specified by the Ft. Detrick scientists.

Three years later, in 1972, the fledgling World Health Organization (WHO) published a very similar proposal to the one submitted to the U.S. House Appropriations Committee in 1969. The WHO proposed that: “An attempt should be made to ascertain whether viruses can in fact exert selective effects on immune function, e.g., by …affecting T cell function as opposed to B cell function. The possibility should also be looked into that the immune response to the virus itself may be impaired if the infecting virus damages more or less selectively the immune cells responding to the viral antigens.” (Bulletin of the W.H.O., vol. 47, p 257- 274.) This is a “textbook” clinical description of the function of the HIV/AIDS virus.

The W.H.O. shortly thereafter begins a massive “smallpox vaccination” program in Africa in 1975. Within two years, millions of smallpox vaccines are provided by Novartis et. al, under U.N.I.C.E.F. funding. A decade later, it is determined by independent journalists in the U.K. that the incidence of AIDS infections’ MAPPED AND GRAPHED EPICENTERS in Africa coincided exactly with the locations of the W.H.O. smallpox vaccination program centers in the mid-1970’s (Source, The London Times, May 11, 1987). Some 14,000 Haitians then on UN ‘humanitarian missions’ to Central Africa were also vaccinated in this campaign, and soon contracted HIV. Personnel actually conducting the vaccinations of the Haitians maintain they had been completely unaware that the vaccine was anything other than a routine shot.

In 1987, Dr. Hilleman, head of all vaccine production of Merck Pharmaceuticals stunned the world with his public admissions that the mass vaccination campaigns of the 1950s and ’60s likely caused thousands of cancer deaths each year. This was due to the presence of a cancer-causing virus that contaminated the first polio vaccine, according to Dr. Hilleman. Known as SV40, the virus originated from dead monkeys whose kidney cells were used to culture the first Salk vaccines. Doctors estimate that the virus was injected into tens of millions during the vaccination campaigns, including several million in Canada, before being detected and screened out in 1963. Those born between 1941 and 1961 are thought to be most at risk of having been infected with SV40, and are estimated to have a 300% greater chance of developing cancer. According to Hilleman MERCK KNEW THE VACCINES WERE INFECTED WITH SV40, but distributed them anyway. See http://www.youtube.com/watch?v=edikv0zbAlU

Furthermore, research doctors in New Orleans reported in 1963 that a percentage of the Salk polio vaccines were found to have attenuated, (live) viruses, which actually CAUSED tens of thousands of polio cases during the 1950’s.

Following the successful liberation of Kuwait in Operation Desert Storm, hundreds of thousands of victorious American troops are suddenly stricken with a wide variety of auto-immune disorders that doctors named the Gulf War Syndrome, (GWS). After a decade of medical investigation, the culprit is finally determined to be an ingredient in the anthrax vaccinations mandatorily given to the troops. This offending “adjuvant” is a synthetic material known as squalene aka, oil-in-water adjuvant. Writer and Gulf War correspondent Gary Matsumoto documents this entire, tragic saga in his seminal book, “Vaccine-A”. See www.vaccine-a.com.

Understanding these historical facts is very important for this reason: Those that ignore history are doomed to repeat it. This is doubly true when it comes to blindly accepting a “novel” mass vaccination for a weaponized, “reverse engineered” virus.

The historical record is very clear attenuated, live viruses in vaccines SPREAD the disease very effectively. When combined with SQUALENE ADJUVANT ­ the virus becomes many times more potent and lethal. When given to CHILDREN IN SCHOOLS, millions of “typhoid Matts and Marys” will be spreading the disease exponentially.

Chillingly, the Novartis patent for the “novel pandemic flu” declares that “African green monkey kidney cells” will be used for the “viral growth substrate” ­ i.e. the carrier medium.
(Page 3, paragraph 0037) We also see that “oil-in-water” squalene-based adjuvants will also be included (page 8 0098) but most incredible of all, because this is a “recombinant” and “novel” split vaccine, it is deemed necessary to include fragments of attenuated viruses (i.e. live pathogens) in the vaccine medium.

On July 13, 2009, the W.H.O. sanctioned this lunacy by declaring: “In view of the anticipated limited vaccine availability at global level and the potential need to protect against “drifted” strains of virus, it is recommended that promoting production and use of vaccines such as those that are formulated with oil-in-water adjuvants and live attenuated influenza vaccines is important.”

In conclusion and summation, it should be evident that the “2009 Swine Flu” could just as easily be called the “Bird Flu” because it is as much H5N1 (bird flu) as H1N1 (pig flu.) Novartis knew this in 2005 when it received hundreds of millions of dollars from Mike Leavitt’s HHS to develop and patent the “bird flu” vaccine. I publicly charge that Novartis had advance knowledge of this “combination” because they had been in consultation with Jeffrey Taubenberger for years.

It is further evident that Novartis’ patent provides for “influenza vaccine kits” to be provided to other pharmaceutical manufacturers as well. These “kits” are the basic raw ingredients needed for the other companies to build their own vaccines under their own label.

In 2005, this “jobbing” of separate ingredients by multiple companies would never have been allowed because of the legal liability issues involved. However, in 2009, all liabilities for death and disability from faulty or contaminated vaccines have been stripped away. Any wrongful death or disability lawsuits against Novartis or any other company will today be summarily dismissed.
Novartis today has carte blanche blanket immunity for their actions and any large pharmaceutical company who so desires, can join them at the feeding troughs just by paying millions for their “kits”.

If this isn’t the pinnacle of criminality, then I don’t know what is.

Novartis, if this “novel split vaccine” is so wonderful and safe, why do you require such blanket protection from litigation?
http://www.daily.pk/7780/new-evidence-that-the-‘swine-flu’-pandemic-is-man-made/

Tuesday, July 14, 2009

The Tenth in the FLU Series

UPDATE: 28 July - Startling New Evidence That The 'Swine Flu' Pandemic Is Man-Made

UPDATE: 18 July - Now that the propaganda is in full swing to turn your child's school into a vaccination clinic perhaps you'd like to wonder why HHS is acting to protect the vaccine manufacturer's from lawsuits in case things go wrong.

Just this move alone, following on an almost $2 Billion vaccine purchase of something unproven and by the time it gets to market won't be effective because of viral mutation, gives you a big window for questioning this move and contacting your member of congress to ask just why their constituents are being used as lab rats without informed consent and without protection for their health.
Legal immunity set for swine flu vaccine makers
------------------------------
UPDATE: 15 July - Last evening's news reports on the need you'll have to not be able to rely on just one dose of the rush-to-market and untested "swine flu" vaccine. You'll purportedly require up to three shots in addition to the "regular" flu shot which is announced to be pushed on you in September, ahead of the usual fall "flu" propaganda schedule, usually scheduled in October/November.

Please do your research now in order to protect your health and that of your loved ones, especially the children.

Please see new information added at the end of this article, and thank you.
------------------------------
Here at Natural Health News we've been posting on this topic for some time and there are nine other posts on the site, staring from last fall. Some of the posts contain links to our main URL (leaflady.org) where you'll find much more information.

Look at the recent marketing campaign (propaganda by any other name should smell so sweet) from HHS to get an idea how the plan is to co-opt undiscerning citizens into this insanity - http://www.hhs.gov/

Sebelius has said nothing about the swine flu vaccine, the fact it is made in chicken eggs and how this is a risk to people with chicken and chicken egg allergy (I am one but of course I know how to avoid this and am not the only allergy prone person).

We also know that Tamiflu is useless yet HHS is already spending billions on what may be a useless vaccine and a useless product.
from Newsmax.com
Vaccine May Be More Dangerous Than Swine FluTuesday, July 7, 2009
By: Dr. Russell Blaylock

An outbreak of swine flu occurred in Mexico this spring that eventually affected 4,910 Mexican citizens and resulted in 85 deaths. By the time it spread to the United States, the virus caused only mild cases of flu-like illness.

Thanks to air travel and the failure of public health officials to control travel from Mexico, the virus spread worldwide. Despite predictions of massive numbers of deaths and the arrival of doomsday, the virus has remained a relatively mild disease, something we know happens each year with flu epidemics.

Worldwide, there have only been 311 deaths out of 70,893 cases of swine flu. In the United States, 27,717 cases have resulted in 127 deaths. Every death is a tragedy, but such a low death rate should not be the basis of a draconian government policy.

It is helpful to recall that the Centers for Disease Control with the collusion of the media, constantly tell us that 36,000 people die from the flu each year, a figure that has been shown to be a lie. In this case, we are talking about 300 plus deaths for the entire world.

This virus continues to be an enigma for virologists. In the April 30, 2009 issue of Nature, a virologist was quoted as saying,“Where the hell it got all these genes from we don’t know.” Extensive analysis of the virus found that it contained the original 1918 H1N1 flu virus, the avian flu virus (bird flu), and two new H3N2 virus genes from Eurasia. Debate continues over the possibility that swine flu is a genetically engineered virus.

Naturally, vaccine manufacturers have been in a competitive battle to produce the first vaccine. The main contenders have been Baxter Pharmaceuticals and Novartis Pharmaceuticals, the latter of which recently acquired the scandal-ridden Chiron vaccine company. Both of these companies have had agreements with the World Health Organization to produce a pandemic vaccine.

The Baxter vaccine, called Celvapan, has had fast track approval. It uses a new vero cell technology, which utilizes cultured cells from the African green monkey. This same animal tissue transmits a number of vaccine-contaminating viruses, including the HIV virus.

The Baxter company has been associated with two deadly scandals. The first event occurred in 2006 when hemophiliac components were contaminated with HIV virus and injected in tens of thousands of people, including thousands of children. Baxter continued to release the HIV contaminated vaccine even after the contamination was known.

The second event occurred recently when it was discovered that Baxter had released a seasonal flu vaccine containing the bird flu virus, which would have produced a real world pandemic, to 18 countries. Fortunately, astute lab workers in the Czech Republic discovered the deadly combination and blew the whistle before a worldwide disaster was unleashed.

Despite these two deadly events, WHO maintains an agreement with Baxter Pharmaceuticals to produce the world’s pandemic vaccine.

Novartis, the second contender, also has an agreement with WHO for a pandemic vaccine. Novartis appears to have won the contract, since their vaccine is near completion. What is terrifying is that these pandemic vaccines contain ingredients, called immune adjuvants that a number of studies have shown cause devastating autoimmune disorders, including rheumatoid arthritis, multiple sclerosis and lupus.

Animal studies using this adjuvant have found them to be deadly. A study using 14 guinea pigs found that when they were injected with the special adjuvant, only one animal survived. A repeat of the study found the same deadly outcome.

So, what is this deadly ingredient? It is called squalene, a type of oil. The Chiron company, maker of the deadly anthrax vaccine, makes an adjuvant called MF-59 which contains two main ingredients of concern—squalene and gp120. A number of studies have shown that squalene can trigger all of the above-mentioned autoimmune diseases when injected.

The MF-59 adjuvant has been used in several vaccines. These vaccines, including tetanus and diphtheria, are the same vaccines frequently associated with adverse reactions.

I reviewed a number of studies on this adjuvant and found something quite interesting. Several studies done on human test subjects found MF-59 to be a very safe immune adjuvant. But when I checked to see who did these studies, I found—to no surprise—that they were done by the Novartis Pharmaceutical Company and Chiron Pharmaceutical Company, which have merged. They were all published in “prestigious” medical journals. Also, to no surprise, a great number of studies done by independent laboratories and research institutions all found a strong link between MF-59 and autoimmune diseases.

Squalene in vaccines has been strongly linked to the Gulf War Syndrome. On August 1991, Anthony Principi, Secretary of Veterans Affairs admitted that soldiers vaccinated with the anthrax vaccine from 1990 to 1991 had an increased risk of 200 percent in developing the deadly disease amyotrophic lateral sclerosis (ALS), also called Lou Gehrig’s disease. The soldiers also suffered from a number of debilitating and life-shortening diseases, such as polyarteritis nodosa, multiple sclerosis (MS), lupus, transverse myelitis (a neurological disorder caused by inflammation of the spinal cord), endocarditis (inflammation of the heart’s inner lining), optic neuritis with blindness and glomerulonephritis (a type of kidney disease).

Because squalene, the main ingredient in MF-59, can induce hyperimmune responses and induce autoimmunity, a real danger exists for prolonged activation of the brain’s immune cells, the microglia. This type of prolonged activation has been strongly associated with such diseases as multiple sclerosis, Alzheimer’s disease, Parkinson’s disease, ALS and possibly vaccine-related encephalitis. It has been shown that activation of the systemic immune system, as occurs with vaccination, rapidly activates the brain’s microglia at the same time, and this brain inflammation can persist for long periods.

So, how would the gp120 get into the brain? Studies of other immune adjuvants using careful tracer techniques have shown that they routinely enter the brain following vaccination. What most people do not know, even the doctors who recommend the vaccines, is that most such studies by pharmaceutical companies observe the patients for only one to two weeks following vaccination—these types of reactions may take months or even years to manifest.

It is obvious that the vaccine manufacturers stand to make billions of dollars in profits from this WHO/government-promoted pandemic. Novartis, the maker of the new pandemic vaccine, recently announced that they would not give free vaccines to impoverished nations—everybody pays.

One must keep in mind that once the vaccine is injected, there is little you can do to protect yourself—at least by conventional medicine. It will mean a lifetime of crippling illness and early death.

There are much safer ways to protect oneself from this flu virus, such as higher doses of vitamin D3, selective immune enhancement using supplements, and a good diet.
© 2009 Newsmax. All rights reserved.

Here is an eleventh opinion - Mandatory Swine Flu Vaccination Alert
and here is a related story

Monday, June 15, 2009

Listen to Dr. Niman on Swine Flu

77 June UPDATE:
06/17/2009 Ben Fulford
新型インフルエンザのワクチンは大量虐殺のための生物兵器のようだ
オーストリアに住んでいる科学ジャーナリストによると、新型インフルエンザのワクチンは大量虐殺のための生物兵器であると言う。日本の厚生労働省や医師会は既に医師達にそのワクチンやタミフルを大量に配る指令を出している。これを支持している人物は後に全人類の敵として指名手配されるだろう。とにかく日本人には絶対にワクチンを拒んでもらいたい。もし下記の英語の記事をボランティアで日本語に訳せる方がいたら是非お願いします。なるべく多くの人達にこれを理解してもらわないと沢山の人々が殺されてしまう。

Virus mix-up by lab could have resulted in pandemic

Baxter has been caught red handed nearly triggering pandemic, they are also moving ahead, together with allied pharma companies, with supplying the "vaccine" for pandemics

the criminal charges I filed against Baxter and WHO with the Austrian police (in German) but with an English translation partially

The swine flu vaccine is designed to weaponize the H1N1 virus

A journalist in Austria has forwarded proof that the anti-swine flu vaccine they are trying to mandatorily make everyone take is actually designed to weaponize the H1N1 virus and kill billions of people. We issue a warning to all Medical associations and WHO staff: if you try to proceed with this plan you will be labeled as enemies of humanity and there will be a bounty placed on each of you.

Virus mix-up by lab could have resulted in pandemic

Baxter has been caught red handed nearly triggering pandemic, they are also moving ahead, together with allied pharma companies, with supplying the "vaccine" for pandemics

the criminal charges I filed against Baxter and WHO with the Austrian police (in German) but with an English translation partially.

16 June UPDATE: Some additional resources re H1N1 and how swine flu vaccines can be harmful to your health.

ORIGINAL POST DATE 5/1/09: LISTEN FREE

Dr. Henry L. Niman Explains The Scientific Reality Of The Swine Flu Outbreak.
... Essential Information

wxpi

Read more on FLU, from a different perspective.

Monday, May 25, 2009

H1N1 Fast-track Vaccine to be Tested by Navy

UPDATE:11 June, 09
So Now it's a Pandemic?
------------
Another "lab rats r us" scenario on its way to be tested on perhaps unwilling people as a "direct order" to participate in human trials.
SAN DIEGO, May 21, 2009 (GlobeNewswire via COMTEX) -- Vical Incorporated /quotes/comstock/15*!vicl/quotes/nls/vicl (VICL 2.13, -0.12, -5.33%) announced today that in the two weeks since launching its program to develop a vaccine against H1N1 influenza (swine flu), the company has completed development of a prototype H1 vaccine, produced an initial supply of research-grade material, and initiated immunogenicity testing in animals. Assuming a successful outcome of this testing and a commitment for program-specific external funding, the company is ready to advance directly to large-scale cGMP manufacturing of vaccine for human clinical trials to be conducted by the U.S. Navy. Read more...


UPDATE on swine flu from Dr. Niman

Thursday, April 30, 2009

Homeopathy Effective for FLU

"Ohio reported that 24,000 cases of flu treated allopathically had a mortality rate of 28.2% while 26,000 cases of flu treated homeopathically had a mortality rate of 1.05%."

Here's a good resource for more infomation.

Read more about homeopathy and FLU

Wednesday, April 29, 2009

Dr. Levy on Vitamin C

Viral Poppycock - "For a population of seven million people, Hong Kong has stockpiled 20 million treatment courses of Tamiflu, a medicine to which the new swine flu virus has not yet developed resistance but it’s a toss up which is more dangerous, the swine flu or Tamiflu. Dr. Russell Blaylock writes, “I was in the military during the first swine flu scare in 1976. At the time it became policy that all soldiers would be vaccinated for swine flu. As a medical officer I refused and almost faced a court martial, but the military didn't want the bad publicity. Despite the assurance by all the experts in virology, including Dr. Sabin, the epidemic never materialized. What did materialize were 500 cases of Gullian-Barre paralysis, including 25 deaths-not due to the swine flu itself, but as a direct result of the vaccine.”Courtesy Mark Sircus

Originally posted: Saturday, October 28, 2006

VITAMIN C AGAINST THE FLU (and bird flu) SAFELY AND EFFECTIVELY©

Dr. Thomas Levy is one of the world’s experts in effects of vitamin C on viruses. Here’s what he says “Regarding the bird flu, I have not found any virus for which vitamin C does not exert a virucidal effect, as long as enough vitamin C reaches the virus, such as in any acute infection. I don't know about Tamiflu, but the vitamin C is virtually devoid of negative side effects.”

Although there no studies yet published specifically treating Asian bird flu with vitamin C, immune expert Dr Robert Cathcart, who has treated thousands of cases of life threatening infectious diseases with high dose vitamin C says “Treatment of the bird flu with massive doses of ascorbate would be the same as any other flu except that the severity of the disease indicates that it may take unusually massive doses of ascorbic acid orally or even intravenous sodium ascorbate. I have not seen any flu yet that was not cured or markedly ameliorated by massive doses of vitamin C.”

Antiviral drugs, such as Tamiflu, work by inhibiting something called neuraminidase, produced by viruses and essential for their ability to replicate. So too does vitamin C but this is only one of more than ten ways that vitamin C knocks out viruses, both by inhibiting the virus itself, and by strengthening the body’s own immune response, for example by improving the number of function of immune cells (eg macrophages, lymphocytes and neutrophils), upping interferon and nitric oxide and making more antibodies which target viruses. Vitamin C also has direct antiviral effects and has been shown to inhibit viral replication in laboratory studies, such as HIV-infected immune cells. In the case of HIV viral infection was inhibited by 99% within four days, according to research published by the National Academy of Sciences. (It is really a tragedy that this research hasn’t been followed up with a large scale human trials, but the sad truth is that, even though vitamin C has been shown to outperform AZT in lab studies , there’s no money in it. So it appears that there is sufficient biological plausibility for its role against the flu, but since we don't have the controlled human trials, it’s not proven. It’s a tragedy that these studies aren’t done for life-threatening diseases such as HIV and bird flu, but the sad truth is there’s no money in it because vitamin C is cheap to make and not patentable – unlike drugs such as Tamiflu. Vitamin C, in high doses, has been well proven to be non-toxic in both adults and children over many years. The same cannot be said for this new generation of antiviral drugs.

However, we do know that vitamin C reduces the severitiy of colds and flu. Over 20 controlled trials using at least 1 gram a day against the common cold have been published, showing that the duration is typically decreased by about 25% and symptoms are much less severe. You are going to need much more than this if you contract any kind of flu. One recent human trial found that students who took hourly doses of 1,000 mg of vitamin C for the first 6 hours and then 3 times daily had a decrease in symptoms of 85% compared to students in the control group. In the case of bird flu that might well be the difference between life and death.

It’s highly likely that vitamin C would be effective against bird flu if you can get the dose high enough. Dr Mark Levine, who works for the National Institutes of Health in the US, has shown that you can get plasma levels up to 200mcmol/l with 3 grams of vitamin C six times a day, at which point vitamin C becomes profoundly anti-viral. However, with intravenous infusion of 100g a day concentration goes up to 15,000mcmol/l. No virus has yet been shown to survive at that level.

The ideal amount of vitamin C for any flu is up to ‘bowel tolerance’. Start with 1 gram an hour. If you get diarrhoea halve this dose. If you don’t, double it. There are some forms of vitamin C, notably sodium ascorbate with riboperine, and lipospheric vitamin C that allow even more to be absorbed without reaching bowel tolerance. They are marginally better than straight ascorbic acid. Some people find ascorbic acid too acidic, in which case an ascorbate, such as sodium ascorbate, can be taken. It might be useful to have a supply at hand if an epidemic does break out. There is no harm in having 100 grams a day short-term, stopping once all symptoms are gone. If even this didn’t stop the flu I’d find a doctor who could administer intravenous sodium ascorbate. The trick with any infection is not to get it in the first place by keeping your immune system strong. I take 1 gram of vitamin C twice a day. If Asian flu breaks out I’m doubling that to 4 grams – one every 6 or so hours, and taking 1 gram an hour if I get any symptoms.

Patrick Holford interviews Dr. Thomas Levy –

Despite hundreds of published studies, the true power of vitamin C as an infection fighter is vastly under-appreciated. Dr Thomas Levy, a doctor from Colorado, has painstakingly reviewed all of the research in his book Vitamin C, Infectious Diseases, and Toxins: Curing the Incurable. Here, he tells me of the true proven power of vitamin C.

PH For which infectious diseases has vitamin C been proven to both cure and prevent, if given in sufficient amounts?

TL In the medical literature, more than enough evidence and data has been published to conclude that vitamin C, administered properly, has cured and can continue to cure acute viral hepatitis, measles, mumps, viral encephalitis, chickenpox and herpes infections, viral pneumonia, influenza, diphtheria, tetanus, streptococcal infections, pseudomonas infections and staphylococcal infections. Prevention against the contraction of these infections and other infections involves the daily dosing of lower amounts of vitamin C than the amounts needed to cure a given infection. This prevention can almost always be overwhelmed, however, when a large enough acute exposure of an infectious agent is encountered.

PH Let's take a look at mumps, for example, which is very much in the news as more parents choose not to have their children given the MMR vaccination. What would you recommend?

TL This is a subject of great controversy. In general, I am opposed to vaccinations, since it is clear to me that the proper use of vitamin C can easily cope with the many different agents for which vaccination is offered. However, having a good specific, antibody-armed immune system is desirable as well. Therefore, when the vaccine is preservative-free (particularly from methylmercury in the form of thimerosol), the child is old enough to have a reasonably mature immune system (2 years or older), and the child is not acutely ill and has not recently been ill, then immunisation may be of benefit. However, before the vaccination, I would give the child a gram of vitamin C a day per year of life (2 grams or more) for at least a week before the vaccination and continuing for at least a week after the vaccination. This has the effect of protecting against any acute toxic insults associated with the vaccination, while maximizing the vitamin C-augmented antibody response to the vaccine.

PH How strong is the scientific evidence to support what you are saying and why is this evidence not being acted on?

TL The scientific evidence is very strong. I can only speculate as to why it seems to be ignored, but the entire medical system worldwide is based on doctors regarding very specific and limited sources of information as being the only reliable sources of medical information. Insurance companies generally only cover mainstream treatments. A great deal of money is spent, directly and indirectly, to convince doctors and the public that anything not learned directly in medical school or later provided through very specific channels is simply not to be trusted, much less even properly evaluated.

PH If a person, or child, contracts any of these diseases, how does one know how much vitamin C to take?

TL As Dr Klenner repeatedly described in his many papers, vitamin C must continue to be administered in appropriately high doses until a positive clinical response is seen, and then lower doses can be given. In other words, Dr Klenner would use whatever dose necessary to see a positive clinical response. This meant anything from 35 to 65 grams for a first dose, given intravenously. In terms of oral supplementation, take as much as you can tolerate, starting with 2 or 3 grams every three to four hours.

PH Is there any danger in taking these kinds of amounts?

TL Unless you are a patient with advanced renal failure, the answer appears to be no. In fact, very large studies have clearly defined that vitamin C not only does not cause kidney stones in patients with normal kidney function, it will often help to dissolve stones that were already present before the vitamin C administration began.

PH Your book is immensely thorough and well researched. How are we going to get this vital, life-saving and inexpensive treatment taken seriously? How many more people have to suffer and die unnecessarily?

TL I wish I knew. I wrote the book from both a medical and a legal perspective. I wanted physicians who are brave enough to do what is best for their patients to have as much scientific backing as possible for the vitamin C-based therapies that they choose, especially if they end up having to defend what they are doing in a court of law.

PH What types of vitamin C should be taken?

TL Vitamin C comes as mineral ascorbates, ascorbic acid, sodium ascorbate, and in a liposome-encapsulated form. If administered intravenously, the sodium ascorbate form is always desirable for an acute illness. When not available, the liposome-coated form, called lipospheric vitamin C, appears to have a very high bioavailability with virtually no bowel tolerance dose [ie diarrhoea inducing], which typically impedes the very high oral dosing of vitamin C.

Tuesday, April 28, 2009

SWINE FLU PRECAUTIONS

UPDATE: 10 August - Since this article was posted in April we have added numerous articles regarding this issue so please that the time to look for these new and important posts: Search for Flu, Swine Flu, Vitamin C, Dr. Levy, FluMist, Tamiflu, Relenza, Flu Shot or related titles.
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Suggestion from orthomolecular expert Dr Phil Bate -
SWINE FLU PRECAUTIONS AND POSSIBLE AID TO RECOVERY

Besides washing your hands and wearing a mask (which isn't much good).

Vitamin C is a viricide, but it has to be taken often and in amounts to kill the virus. That means that it has to be taken at least every four hours if you are possibly exposed, and in at least 2000 mg to saturate the bloodstream.

Of course, avoid places with lots of people during this period. If you are going out during the day, take 2000 mg of C before any exposure. During exposure and immediately exposure, take C every two hours, and at the end of possible exposure.

If you get any flu symptoms, start taking 2000 mg every two hours until you get diarrhea, and then back off to just below this amount for that time until the diarrhea stops. (Start with 2 every 3-4 hours, etc)

Masks get moist and this creates a breeding ground for bacteria.

Both vitamin C and vitamin A are good to have on hand. Vitamin A in the proper high dose range for short periods will protect you from pneumonia that often accompanies flu.

Otherwise, take all precautions and avoid using Tamiflu and Relenza

http://naturalhealthnews.blogspot.com/2007/11/warning-tamiflu-and-relenza-hazards.html

http://naturalhealthnews.blogspot.com/2005/10/beware-tamiflu.html

http://naturalhealthnews.blogspot.com/2009/04/flu-news.html

Meanwhile the FDA and CDC are pushing Tamiflu and Relenza as reported in Medscape News.
FDA Okays Emergency Use of Antiviral Drugs, Diagnostic Test for Swine Flu
by Robert Lowes

April 28, 2009 — State and local public health agencies will have more leeway to treat swine influenza with antiviral medications under an emergency order issued yesterday by the US Food and Drug Administration. The order also will authorize and widen the use of a diagnostic test that, unlike others in use, can precisely identify the new strain of swine flu.

To date, the Centers for Disease Control and Prevention (CDC) have confirmed 64 cases of swine flu in the United States. Worldwide, confirmed cases have emerged in Canada, New Zealand, Scotland, Israel, Spain, and Mexico, which appears to be epicenter, since travel to Mexico figures into many infections elsewhere. In addition, Mexico is the only country where the influenza has resulted in death; authorities there say 152 deaths were likely caused by the virus. In the 6 other countries, infected patients generally have experienced only mild symptoms.

The FDA's Emergency Use Authorization (EUA) relaxes current restrictions on 2 antiviral medications — zanamivir (Relenza) and oseltamivir (Tamiflu) — that the CDC recommends for preventing and treating swine influenza A (H1N1). Oseltamivir currently is approved for patients aged 1 year and older. Under the EAU, healthcare providers can administer oseltamivir to patients younger than 1 year and provide alternate dosing to patients aged 1 year and older.

The EAU did not alter the age parameters for zanamivir, approved to treat acute, uncomplicated cases of influenza in adults and children older than 7 years who have been symptomatic for fewer than 2 days, as well as prevent influenza in adults and children aged 5 years and older.

However, the FDA order allows both drugs to be distributed by a wider range of healthcare workers, including volunteers, in accordance with state and local law. In addition, both medications can be distributed without complying with the usual label requirements.

The FDA order follows a decision by the Department of Health and Human Services on Sunday to distribute one fourth of its stockpile of oseltamivir and zanamivir to state governments.

The EUA also authorizes the use of a diagnostic test called a reverse-transcriptase polymerase chain reaction (RT-PCR) swine influenza panel to test for the virus and allows the CDC to distribute it to public health agencies. Two other available tests — rapid influenza antigen and immunofluroscence — can detect the new swine influenza virus, but they only identify probable cases because they cannot distinguish between seasonal influenza A and swine influenza, which is a subtype of A. In contrast, RT-PCR can conclusively confirm a case of swine influenza.

Journalist Robert Lowes is a freelance writer for Medscape.
Medscape Medical News © 2009 Medscape, LLC

 
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