Archive for the ‘H1N1/Swine Flu’ Category

Obama bought shares in Baxter. Baxter is a subsidiary company of Bayer AG. Bayer AG is Hitler’s “IG Farben group”

In 2005, Barack Obama bought more than $50,000 worth of stock in a biotech concern that was starting to develop a drug to treat avian flu, whose major investors included some of his biggest political donors.What are Obama’s investments in biotech companies apparently developing the “bird” and “swine” flu vaccine?

George W. Bush announced the International Partnership on Avian and Pandemic Influenza at the United Nations General Assembly on September 14, 2005, placing the US under UN and WHO law in the event of a pandemic “emergency”. Mr. Obama’s sale of his shares in the two companies ended what appears to have been a brief foray into highly speculative investing that stood out amid an otherwise conservative portfolio of mutual funds and cash accounts, a review of his Senate disclosure statements shows. He earned $2,000 on the biotech company, “AVI BioPharma”, and lost $15,000 on the satellite communications concern, Skyterra, according to Mr. Burton of the Obama campaign. Earlier that year, in April, 2005, Barack Obama introduced the “first comprehensive bill” to deal with the bird flu threat, the Avian act. According to reports, Obama made significant investments in biotech companies involved in the development of bird and swine flu. By MIKE McINTIRE Published: March 7, 2007
Baxter International Inc. and Subsidiaries
BAXTER INTERNATIONAL INC
Form: 11-K
Filing Date: 6/29/2009 AVI BIOPHARMA INC
Display Filing Info For Baxter SubsidiariesDisplay Filing Info or Google “Baxter International Inc. and Subsidiaries Incentive Investment Plan under “Display Filing Info”
Medimmune Awarded Contract for Influenza Virus Vaccine

Posted on: Sunday, 7 August 2005,

MedImmune Vaccines Inc., (*Flumist) Gaithersburg, Md., is being awarded a maximum $8,118,000 firm fixed price, indefinite quantity (base year only) contract for Influenza Virus Vaccine (Nasal Spray for Army, Navy, Air Force, and Marine Corps)
Can the nasal spray flu vaccine give you the flu?

Unlike the flu shot, the nasal spray flu vaccine does contain live viruses CDC 9/07/09
George Bush suspends Davis-Bacon Bill in Katrina affected areas By Ivan Osorio on 9.13.05 On September 8, 2005. President Bush, suspended the Davis-Bacon Act, the federal “prevailing wage” law, in the areas affected by Hurricane Katrina.
Jefferson Parish President Aaron Broussard appeared on Meet the Press Sunday he described FEMA’s criminal activities.”We had Wal-Mart deliver three trucks of water, trailer trucks of water. FEMA turned them back. They said we didn’t need them. This was a week ago. FEMA–we had 1,000 gallons of diesel fuel on a Coast Guard vessel docked in my parish. The Coast Guard said, “Come get the fuel right away.” When we got there with our trucks, they got a word. “FEMA says don’t give you the fuel.” Yesterday–yesterday–FEMA comes in and cuts all of our emergency communication lines. They cut them without notice. Our sheriff, Harry Lee, goes back in, he reconnects the line. He posts armed guards on our line and says, “No one is getting near these lines.” Why would FEMA, an organization supposedly tasked with helping in a time of crisis, deliberately cut police communication lines? This is a blatant example of sabotage and a sick push to make the disaster worse.by BywaterBlues, 9/7/05
Dyan French, New Orleans Activist Leader, who stayed in New Orleans during the hurricane and its aftermath, gives evidence to the congressional committee. She claimed the city’s levees were purposely bombed. By Eunice Moscoso, Washington
December 8, 2005
Hal Turner, who the ADL lists as a white supremist, who wrote an article September. 9, 2005 that “burn marks and explosive residue was found on the levee debris”. Divers inspecting the ruptured walls found burn marks on the debris. A source who spoke on condition of anonymity said, “We found traces of boron-enhanced fluoronitramino explosives as well as PBXN-111 embedded in the debris. This would indicate at least two separate types of explosive devises”. In 1927 the levees there were exploded using 39 tons of dynamite for ten consecutive days. James Pierce Butler Jr., President of Canal Bank with ties to Chase Bank in New York and President of the elite Boston Club, manipulated state and federal governments into dynamiting the levee outside of New Orleans – flooding out thousands of people, to relieve pressure on the city. (“Rising Tide: The Great Mississippi Flood of 1927 and How It Changed America”. John Barry)
The Federal Emergency Management Agency said it plans to stop paying for hotel and motel rooms for Katrina and Rita evacuees beginning Dec. 1, including 19,000 hurricane evacuees still in Houston hotels. By ARMANDO VILLAFRANCA Nov. 16, 2005
More than 5,000 hurricane victims came to Los Angeles County in the storm’s wake and were put up in local hotels. Evacuees who didn’t get an extension had to leave their hotels Tuesday, when there were 238 rooms in Los Angeles County paid for by the Federal Emergency Management Agency. By the end of Tuesday, 82 people had left. Some, got an extension until Monday and others until March 1. February 09, 2006|Stephen Clark
30 Days’ Notice at the FEMA Trailer . Eviction letters go out to about 3,000 Katrina victims, who are told they’re ineligible. The Nation May 20, 2006|Richard Fausset
President Bush marked the first anniversary of Hurricane Katrina by acknowledging the government’s failures in responding to the disaster, vowing that the federal government would “learn the lessons of Katrina,” and “stay as long as it takes, to help our brothers and sisters build a new Gulf Coast where every citizen feels part of the great promise of America Dateline: August 26, 2006

Hundreds of thousands of our Louisiana neighbors fled to Texas for dry land and a chance at a better life. Nearly 60% are unemployed. This population is accustomed to working. Before the hurricane, only 6% of evacuees were out of work. Long-term housing is a major concern for Katrina evacuees. Nearly 135,000 evacuees, including 55,000 children, live in homes that receive FEMA housing subsidies that are set to expire within the next few months. *Don Baylor, Jr. is a Policy Analyst at the Center for Public Policy Priorities in Austin

National Security and Homeland Security Presidential Directive NSPD-51/ HSPD-20 “Martial Law bill”
Office of the Press Secretary

May 9, 2007 Implementation Actions

(4) Continuity requirements shall be incorporated into daily operations of all executive departments and agencies. As a result of the asymmetric threat environment, adequate warning of potential emergencies that could pose a significant risk to the homeland might not be available, and therefore all continuity planning shall be based on the assumption that no such warning will be received.

Emphasis will be placed upon geographic dispersion of leadership, staff, and infrastructure in order to increase survivability and maintain uninterrupted Government Functions. Risk management principles shall be applied to ensure that appropriate operational readiness decisions are based on the probability of an attack or other incident and its consequences. …(22) Revocation. Presidential Decision Directive 67 of October 21, 1998 (”Enduring Constitutional Government and Continuity of Government Operations”), including all Annexes thereto, is hereby revoked.
PDD-NSC-67 Enduring Constitutional Government and Continuity of Government Operations

Late last month, the Pentagon tapped five major defense contractors to provide wide-ranging support in global counter-narcotics operations. The contract, worth up to $15 billion over the next five years, illustrates the extent to which the Defense Department is relying on contractors to perform critical missions while combat forces are stretched thin by operations in Iraq and Afghanistan.

Awardees include Raytheon Technical Services Co., Lockheed Martin Co., Northrop Grumman Corp., Arinc Inc., and Blackwater USA. 09/12/07 By Katherine McIntire Peters
Senate approves $1 Billion dollar gang bill San Bernardino County Sun 09/22/2007
Senate and Bush Agree On Terms of Spying Bill and Telecom Immunity :Telecom Companies Receive Immunity By Jonathan Weisman and Ellen Nakashima Washington Post Staff Writers Thursday, October 18, 2007
Homeland Security Presidential Directive
HOMELAND SECURITY PRESIDENTIAL DIRECTIVE/HSPD-21 Office of the Press Secretary 10/18/07
(2) In this directive:
(a) The term “biosurveillance” means the process of active data-gathering with appropriate analysis
and interpretation of biosphere data that might relate to disease activity and threats to human or
animal health – whether infectious, toxic, metabolic, or otherwise, and regardless of intentional or
natural origin – in order to achieve early warning of health threats, early detection of health events, and
overall situational awareness of disease activity;
(b) The term “catastrophic health event” means any natural or manmade incident, including terrorism,
that results in a number of ill or injured persons sufficient to overwhelm the capabilities of immediate
local and regional emergency response and health care systems;
At the end of May, the doors closed at Renaissance Village, the FEMA trailer park outside of Baton Rouge that had been home to hundreds of families, its end hastened by an official acknowledgment of unhealthy levels of formaldehyde in the trailers. Those who were left at the park at the end, most of whom were among the neediest of the evacuees, began moving out on their own.
In light of ‘the early promise” (made by George Bush,” to help our brothers and sisters build a new Gulf Coast”) that the recovery from the hurricane would provide the chance to address New Orleans’s social ills, the farewell to the trailer park might have been an opportunity for a fresh start, with families fortified by more than three years of government support and charity programs. But when the park closed earlier than expected, government planners said “they” were left “unprepared”.
By SHAILA DEWAN
Published: August 4, 2008 “Out of Fema Park, Clinging to a Fraying Lifeline
Last month, CNN revealed that the Federal Emergency Management Agency had stored $85 million worth of household items in warehouses for two years. Instead of giving the supplies to victims of the 2005 hurricane, FEMA declared them surplus and gave them all away to federal agencies and 16 states in February.
The state of Louisiana — the most hard-hit by the storm — had not asked for any of the supplies, prompting outrage in the community after the original CNN report.
By Abbie Boudreau and Scott Zamost
CNN Special Investigations Unit Tue July 8, 2008
video: http://www.youtube.com/watch?v=_0j8bFa05ZA

Baxter flu vaccines contaminated with H5N1 – otherwise known as the human form of avian flu, one of the most deadly biological weapons on earth with a 60% kill rate – were received by labs in the Czech Republic, Germany, and Slovenia. On Friday, the company’s director of global bioscience communications confirmed what scientists have suspected. “It was live,” Christopher Bona said in an email. The contaminated product, which Baxter calls “experimental virus material,” was made at the Orth-Donau research facility. Baxter makes its flu vaccine — including a human H5N1 vaccine for which a licence is expected shortly — at a facility in the Czech Republic. People familiar with biosecurity rules are dismayed by evidence that human H3N2 and avian H5N1 viruses somehow co-mingled in the Orth-Donau facility. That is a dangerous practice that should not be allowed to happen, a number of experts insisted. While H5N1 doesn’t easily infect people, H3N2 viruses do. If someone exposed to a mixture of the two had been simultaneously infected with both strains, he or she could have served as an incubator for a hybrid virus able to transmit easily to and among people. That mixing process, called reassortment, is one of two ways pandemic viruses are created.
“Was this just a criminal negligence or it was an attempt to provoke pandemia using vaccination against flu to spread the disease – as happened with the anti-B hepatitis vaccination with vaccines containing the HIV virus in US? – and then cash for the vaccines against H5N1 which Baxter develops? How could on Earth a virus as H5N1 come to the ordinary flu vaccines? Don’t they follow even basic precautions in the american pharma companies?” states the translation. The fact that Baxter mixed the deadly H5N1 virus with a mix of H3N2 seasonal flu viruses is the smoking gun. The H5N1 virus on its own has killed hundreds of people, but it is less airborne and more restricted in the ease with which it can spread. However, when combined with seasonal flu viruses, which as everyone knows are super-airborne and easily spread, the effect is a potent, super-airbone, super deadly biological weapon. This is not the first time that vaccine companies have been caught distributing vaccines contaminated with deadly viruses.

In 2006 it was revealed that Bayer Corporation had discovered that their injection drug, which was used by hemophiliacs, was contaminated with the HIV virus. Internal documents prove that after they positively knew that the drug was contaminated, they took it off the U.S. market only to dump it on the European, Asian and Latin American markets, knowingly exposing thousands, most of them children, to the live HIV virus. Government officials in France went to prison for allowing the drug to be distributed. The documents show that the FDA colluded with Bayer to cover-up the scandal and allowed the deadly drug to be distributed globally. No Bayer executives ever faced arrest or prosecution in the United States. 02/27/2009 By Helen Branswell, THE CANADIAN PRESS
secret facility developed by Blackwater under pseudonyms:

“Xe”
“Raven Development”
“Southwest Law Enforcement” in Otay Mesa.

The City of San Diego “refused” to issue occupancy permits when City Planners learned of the true extent of the 66,000 square foot facility, but Blackwater took the city to federal court, where Judge Marilyn Huff, a George H. W. Bush appointee, ruled in favor of Blackwater, thereby forcing the city to accept the warfare training facility without discretionary review. Thursday, March 12, 2009 (reposted Oct 17, 2009 Activist San Diego & East County Magazine)
Presidential candidate and former congresswoman, Cynthia McKinney, has claimed that 5,000 looters were killed in the aftermath of Hurricane Katrina. McKinney claimed to have spoken to a mother who said that her son had confided in her that he was involved with the executions of several looters who were subsequently dumped in the swamp. She also claimed that officials at the Red Cross had corroborated her story.

Previous reports have said that far more people were slain by Blackwater and other authorities then previously reported. Allegedly, Blackwater mercenaries employed their same controversial tactics that have gotten them into trouble in Iraq, in New Orleans against looters Casey Gane-McCalla October 2, 2008
Welfare vanishes as poverty soars. Eighteen states actually cut their welfare rolls in the midst of the crisis. Michigan, one of two states with official unemployment of more than 9 percent, cut its welfare rolls by 13 percent. Of the 12 states where unemployment grew most rapidly, eight of them either cut the rolls or kept them the same.Of the 10 states with the highest child poverty rates, eight kept caseloads level or further reduced the rolls. Five states had double-digit reductions in the welfare rolls, including Texas, which ended assistance to 15 percent of recipients.
These cuts, primarily aimed at women, come at a time when joblessness among women without a high school degree and aged 20 to 24 rose to 23.9 percent—from 17.9 percent a year ago. Celia Hagert of the Center for Public Policy in Austin, Texas, told the Times, “We’re really just pushing families off the program.”
Rhode Island closed the cases of 2,200 children because their families had been on the rolls longer than the 60-month lifetime limit. “Welfare vanishes as poverty soars” By Fred Goldstein Published Feb 4, 2009
The Associated Press Cairo, Egypt, June 4. President Barack Obama won the 2009 Nobel Peace Prize today for “his extraordinary efforts to strengthen international diplomacy and cooperation between peoples, ” the Norwegian Nobel Committee said, citing his outreach to the Muslim world and attempts to curb nuclear proliferation. October 09, 2009 By The Associated Press
Pandemic Is Declared: On June 11, 2009, the World Health Organization (WHO) raised the worldwide pandemic alert level to Phase 6 in response to the ongoing global spread of the novel influenza A (H1N1) virus. A Phase 6 designation indicates that a global pandemic is underway.
On July 13, a World Health Organization (WHO) Global Alert headlined, “WHO recommendations on pandemic (H1N1) 2009 vaccinations” suggest that “universally mandated” ones are coming. WHO “recommendations” are binding on all 194 member countries in case a pandemic emergency is declared under the 2005 International Health Regulations Act and April 2009 WHO pandemic plan.” Stephen Lendman
Baxter International Inc. has completed testing and evaluation of the A/H1N1 influenza virus and is now in full-scale production of a commercial A/H1N1 vaccine using its Vero cell culture technology. Baxter received an A/H1N1 strain from the US Centers for Disease Control and Prevention [a World Health Organization (WHO) Collaborating Center] in early May and is diligently working to deliver a pandemic vaccine for use as early as July.
June 17, 2009 …Wednesday, June 17, 2009
House Panel Approves Obama’s Sweeping Health Bill – The measure is designed to extend health insurance to millions who now lack it, at the same time it strives to slow the growth in medical costs nationwide — Obama’s twin goals. Jul 31, 2009
Judge: Swine flu is reason to suspend constitutional rights: A Superior Court judge ruled Tuesday that there is legal justification to keep the Central Men’s Jail under medical quarantine – at least for a couple of days – to control a swine flu outbreak.

Judge Thomas Goethals said the “significant medical public health event” in the men’s jail is good cause to temporarily suspend constitutional guarantees to speedy trials, preliminary hearings and arraignments for some criminal case defendants OC Registers 07 August 2009

U.S. President Barack Obama has signed a proclamation declaring 2009 H1N1 swine flu a national emergency; *making experimental vaccination “mandatory”. Reuters Oct 24, 2009
FBI Kills Islamic Cleric, Arrests Followers, for Being Muslims at the Wrong Time in America”. Imam Luqman was a representative of the Detroit Muslim community to the ‘National Ummah’ and the general assembly (Shura) of the Muslim Alliance in North America (MANA) – by Stephen Lendman Monday, November 02, 2009
Obama details Afghan war plan, troop increases
Dec . 1, 2009 Associated Press
More Africans in US Prisons than in all of Africa’s Prisons combined*
In fact it’s worse than even that since the United States of America has only 4% of the world’s “Black” population yet it contains over half of the Earth’s “Black” Prisoners.
Peace be upon you

references:
Nasal vaccine for swine flu: I was in this Naval Experiment before Swine Flu in 2005

Mounting Debilities and Deaths from H1N1 Vaccine

Posted by admin On December - 5 - 2009

A Review of Four Approved Swine Flu Vaccines’ Ingredients

Posted by admin On November - 18 - 2009

Review of Four Approved Swine Flu Vaccines’ Ingredients
Posted by: Dr. Mercola
November 05 2009 | 100,717 views

vaccine ingredientsBy Dr. Mercola

I’ve said it before, but I’ll say it again: I’m not anti-vaccines, but rather pro vaccine-safety. That means, I strongly believe that we should only inject substances into our bodies, and especially into the bodies of infants and the unborn, that have been rigorously studied and proven safe both short-term and long-term.

As it stands now, we’ve spent decades injecting materials into the bodies of young and old alike, without sufficient amounts of safety testing of the ingredients, and our society is showing the signs of this neglect.

Neurological dysfunction and disorders such as autism and Alzheimer’s have been growing steadily and show no signs of slowing down.

Mercury, in the form of thimerosal, is included in the majority of all flu vaccines as a preservative in multi-dose vials. Thimerosal-free single-dose vials are typically reserved for infants under the age of three, and pregnant women only.

I recently published a long list of studies confirming the health dangers of thimerosal — proof that those who claim “thimerosal has never been shown to cause any damage” are not telling you the truth. There’s plenty of evidence to the contrary, and if you missed that article, I recommend you review it now.

But thimerosal is not the only questionable and potentially dangerous ingredient in flu vaccines.

Adjuvants Explained

In order for a vaccine to be considered effective, your immune response to the vaccine should be to produce antibodies to the live or dead viruses in the vaccine (the antigen). An adjuvant is a substance added to a vaccine to improve your immune response to the antigen. The word comes from the Latin adjuvare, which means “to help.”

By adding adjuvants the vaccine can contain less viral antigens, which reduces production costs.

Unfortunately, many of these adjuvants are highly toxic.

There are several types of adjuvants. Some of the most commonly used ones include:

* Aluminium hydroxide
* Aluminium phosphate
* Calcium phosphate

Other adjuvants include oil-based emulsions such as squalene, Squalene has not been licensed by the FDA for use in vaccines distributed in the U.S. yet, although squalene is an adjuvant used in vaccines distributed in Europe and other countries.

GlaxoSmithKline’s proprietary formula ASO3™ and Novartis’ MF59™ are two examples of squalene adjuvants.

As damaging as the neurotoxin mercury is, it’s important to realize that aluminum is also a neurotoxin and aluminum-based adjuvants are estimated to be even MORE toxic than mercury.

GREAT NEWS — No Squalene Allowed in US Swine Flu Vaccines!

Fortunately, Americans can draw a sigh of relief as it pertains to squalene — one of the most controversial of the adjuvants — at least for now.

Although vaccine manufacturers were pushing to be allowed to use squalene in many of the swine flu vaccines, and the US Department of Health and Human Services purchased spent more than $400 million of tax payers’ money to stockpile the oil-based adjuvant, their efforts have been unsuccessful so far.

In order to legally allow unlicensed squalene adjuvants to be included in licensed H1N1 vaccines, the US government would have had to issue an Emergency Use Authorization (EUA).

There have been small H1N1clinical trials in which experimental squalene adjuvants were included and tested, which have been reported by various media sources, fueling the questions about its use. But that is different from an FDA licensed vaccine that is made available for general public use.

To date, no EUA has been issued, so the swine flu vaccines licensed for use in the US do NOT contain squalene. However, it is still unclear whether the National Emergency declaration issued by President Obama on October 23, 2009, will cover adding novel adjuvants like squalene, or whether a separate EUA must be issued to allow the use of unlicensed adjuvants.

The best way to confirm the existence of vaccine components is to consult the vaccine product manufacturer inserts. Below, you will find links to the inserts for the four H1N1 vaccines licensed for use in the US.

You may also want to review the transcript of the July 23, 2009 meeting of the FDA Vaccines & Related Biological Products Advisory Committee for more information on the discussion about whether the FDA should issue an EUA and allow unlicensed adjuvants in US vaccines.

Thankfully, so far, the FDA has declined to approve squalene adjuvants for US H1N1 vaccines, but that does not mean that the drug companies will not continue to press for approval in the future.

Beware: European Vaccines May Contain Squalene

Unfortunately, vaccine manufacturers have persuaded countries in Europe and elsewhere to add squalene to seasonal influenza and H1N1 vaccines, so if you live outside the US, you will need to do some further research to determine which vaccines may contain squalene.

A recent article in the English version of the German news source The Local, for example, warns that the German Defense Ministry has ordered a special stock of H1N1 vaccines for their troops that will contain neither mercury nor adjuvants, whereas the general public will be given vaccines containing both.

When checking for squalene, beware that the ingredient called MF59™ is an oil-in-water emulsion of squalene, Tween™80 (polyoxyethylene sorbitan monooleate), and sorbitan trioleate.

MF59 is approved for human use in Europe, but not in the U.S.

Four Swine Flu Vaccines have Gained US FDA Approval

Below I will review the list of ingredients for the four swine flu vaccines that gained U.S. FDA approval on September 15. (As of this writing, GlaxoSmithKline is the only contracted vaccine manufacturer that has not yet gotten their swine flu vaccine approved.)

Please note that there may be additional anti-virals available that are being used to treat swine flu, and/or swine flu vaccines on the market in other countries, but this article only covers the following four vaccines that have received FDA approval for use in the US:

* MedImmune (intranasal spray)
* Novartis
* Sanofi-Pasteur
* CSL

These companies, along with GlaxoSmithKline, have all been awarded contracts by the U.S. Department of Health and Human Services (HHS) for development and production of more than 195 million doses of swine flu vaccine.

For more information, warnings and side effects of each ingredient, please follow the hyperlinks provided.

MedImmune

MedImmune, which is a subsidiary of London-based AstraZeneca, offers an intranasal spray that contains live attenuated virus. The package insert for MedImmune’s intranasal vaccine can be found here.

Please note that the adverse reaction information for MedImmune’s vaccine is based on studies conducted with the seasonal flu version known as FluMist.

Please review the insert for numerous warnings, contraindications, and adverse reactions.

Of special note are the warnings that it should not be administrated to children and adolescents (2-17 years of age) receiving aspirin therapy or aspirin-containing therapy, because of association of Reye’s syndrome.

In addition, it’s important to realize that safety has not been established in individuals with underlying medical conditions predisposing them to influenza complications.

MedImmune’s vaccine also should not be administered to any individual with asthma, or children under the age of 5 with recurring wheezing because of the potential for increased risk of wheezing post vaccination.

Lastly, please note that some viruses contained in this and other intranasal vaccines CAN spread from the vaccinated person to others. Hence, if a person has a compromised immune system, he or she could be placed at risk of infection from people who have been vaccinated. The ease of transmission appears to vary from strain to strain.

Dosing Instructions for MedImmune Intranasal Spray vaccine:

* Children 0-2 years: Not approved
* Children 2-9 years: 2 doses, 0.2 ml each, approximately one month apart
* Children and adults between the ages of 10-49 years: 1 dose, 0.2 ml
* Adults 50-65: Not approved, as FluMist was found to have no demonstrable effectiveness in this age group
* Seniors 65 and over: Not approved
* Pregnant women: Not recommended

Ingredients include:

* Live, attenuated virus
* Monosodium glutamate. MSG is a known neurotoxin and excitotoxin.
* Egg proteins
* Sucrose (table sugar)
* Dibasic potassium phosphate
* Monobasic potassium phosphate
* Gentamicin sulfate (antibiotic)

Intranasal vaccines do not contain thimerosal (mercury).

Questionable Efficacy…

According to the insert, FluMist has demonstrated a mere 44.5 percent reduction in influenza rate when looking at all strains, compared to active controls (other flu vaccines).

Novartis

The package insert for Novartis’ Influenza A(H1N1) 2009 Monovalent vaccine can be found here.

Again, the adverse reaction information for this swine flu vaccine is based on studies conducted with the seasonal flu vaccine Fluvirin, not the A(H1N1) vaccine itself.

It is worth noting that the safety data for Fluvarin (upon which the safety data for the swine flu vaccine is based), was collected from 29 clinical studies over the past 27 years that included no more than 2,768 adults.

In these studies, the subjects were observed for 30 minutes after vaccination, and were instructed to complete a diary card for the three days following immunization, to collect local and systemic reactions.

So, keep in mind that the “safety data” for this vaccine is based on studying human subjects for FOUR DAYS. Not weeks, months, or years, to see if problems occur down the line.

Please review the insert for numerous warnings, contraindications, and adverse reactions.

Dosing Instructions (intra-muscular injection):

* Children 0-4: Not recommended
* Children 4-9: Two 0.5 ml doses one month apart
* Children 9-17: One 0.5 ml dose
* Adults, 18 and over: One 0.5 ml dose

Ingredients include:

* Inactivated A/California/7/2009(H1N1)v-like virus derived from cell-cultures using dog kidneys. Physorg.com http://www.physorg.com/news175767804.html recently reported that a Swiss authority overseeing medicine and therapeutical products had found bacterial contamination in test batches of the vaccine — a charge that Novartis has denied.
* Single-dose vials contain 1 mcg of mercury per 0.5 ml dose
* Multi-dose vials contain 25 mcg of mercury per 0.5 ml dose
* Egg proteins
* Polymyxin (antibiotic)
* Neomycin (antibiotic found in many topical medications). Neomycin is in the FDA pregnancy category D. This means that it is known to be harmful to fetuses.
* Beta-propiolactone (a disinfectant). According to the EPA: “No information is available on the chronic (long-term), reproductive, developmental, or carcinogenic effects of beta-propiolactone in humans. The International Agency for Research on Cancer (IARC) has classified beta-propiolactone as a Group 2B, possible human carcinogen.”
* Nonylphenol ethoxylate (NPE) (a toxic cleaning agent)

Sanofi-Pasteur

The package insert for Sanofi-Pasteur’s Influenza A(H1N1) 2009 Monovalent vaccine can be found here.

The adverse reaction information for Sanofi-Pasteur’s vaccine is based on studies conducted with the seasonal flu version known as Fluzone. The safety data for infants under the age of 3 is based on adverse reactions of 19 children, reported within a mere three days of vaccination.
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Please review the insert for numerous warnings, contraindications, and adverse reactions.

Dosing Instructions (intra-muscular injection):

* Children 0-5 months: Not approved
* Children 6-35 months: two 0.25 ml doses, approximately one month apart
* Children 36 months to 9 years: two 0.5 ml doses, approximately one month apart
* Children 10 years and older: one 0.5 ml dose
* Adults: one 0.5 ml dose

Ingredients include:

* Inactivated A/California/7/2009(H1N1)v-like virus propagated in embryonated chicken eggs
* Prefilled pediatric syringes and single-dose vials are mercury-free
* Multi-dose vials contain 25 mcg of mercury per 0.5 ml dose
* Formaldehyde (up to 100 mcg). Formaldehyde is classifed as a probable human carcinogen by the U.S. Environmental Protection Agency, and as a known human carcinogen by the International Agency for Research on Cancer.
* Triton-X 100 (Polyethylene glycol P-isooctylphenyl ether) is a toxic detergent
* Sodium phosphate
* Sodium chloride (table salt)
* Gelatin
* Sucrose (table sugar)

CSL Biotherapies, Inc.

The package insert for CSL’s Influenza A(H1N1) 2009 Monovalent vaccine can be found here.

The adverse reaction information for CSL’s vaccine is based on studies conducted with the seasonal flu version known as Afluria.

Here the safety data is based on adverse reactions reported within 21 days of vaccination. It’s also worth noting that the safety assessment studies were done using mercury-containing placebos, which may significantly skew the data as the control group would most likely experience similar side effects of the thimerosal as those receiving the actual vaccine.

Additionally, tucked away on page 10 it states that:

“No controlled clinical studies demonstrating a decrease in influenza disease after vaccination with Afluria have been performed.”

Please review the insert for numerous warnings, contraindications, and adverse reactions.

Dosing Instructions (intra-muscular injection):

* Adults only, 18 years and older: one 0.5 ml dose

Ingredients include:

* Inactivated A/California/7/2009(H1N1)v-like virus propagated in embryonated chicken eggs
* Single-dose vials are mercury-free
* Multi-dose vials contain 24.5 mcg of mercury per 0.5 ml dose
* Polymyxin (antibiotic)
* Neomycin (antibiotic found in many topical medications). Neomycin is in the FDA pregnancy category D. This means that it is known to be harmful to fetuses.
* Sodium chloride (table salt)
* Monobasic sodium phosphate
* Dibasic sodium phosphate
* Monobasic potassium phosphate
* Potassium chloride
* Calcium chloride
* Sodium taurodeoxycholate (detergent)
* Egg proteins (ovalbumin)
* Beta-propiolactone (a disinfectant). According to the EPA: “No information is available on the chronic (long-term), reproductive, developmental, or carcinogenic effects of beta-propiolactone in humans. The International Agency for Research on Cancer (IARC) has classified beta-propiolactone as a Group 2B, possible human carcinogen.”

How Effective is the H1N1 Vaccine, Really?

“Specific levels of HI antibody titers post-vaccination with inactivated influenza virus vaccine have not been correlated with protection from influenza virus. In some human studies, antibody titers of 1:40 or greater have been associated with protection from influenza illness in up to 50% of subjects.”

You will find that paragraph in all the vaccine inserts.

What that paragraph says, is that the vaccine only works in half, or less, of those individuals who attain the specified level of seroconversion after vaccination. The FDA defines seroconversion as achieving an antibody titer of 1:40.

This means that if a vaccine was 100 percent effective at achieving this level of seroconversion, it would protect up to 50 percent of the recipients of the vaccine.

But none of the vaccines are 100 percent effective at achieving seroconversion.

CSL’s vaccine insert, for example, (see pages 11-12), states that their H1N1 vaccine provides seroconversion for:

* 48.7 percent of people aged 18-65
* 34 percent for seniors, 65 and older

That means that, at best, their vaccine works in one out of every four people! (49 percent of 50 percent).

Which, of course, means that the vaccine does NOT work in three out of every four people…
swine flu posters

Is it REALLY worth it?

Final Thoughts

Hopefully, this compilation of data will help you weigh the risks and benefits, to make a more educated decision for yourself and your family.

You can also print out these fact-filled posters that we created. Feel free to share them any way you like around your community, at local stores, offices, and schools.

Lastly, please remember to bookmark the special section of my site devoted to all the latest H1N1 Swine Flu Alerts. It’s an excellent go-to source to stay updated on all the new swine flu developments.

Related Links:

Common Links in Swine Flu Deaths…

Swine Flu — One of the Most Massive Cover-ups in American History

Obama Declares Swine Flu Emergency

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