John Erb Report Reveals Toxic Nature of MSG

Jeffry John Aufderheide, Top Stories

John Erb Report Reveals Toxic Nature of MSG

No Comments 07 February 2010

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.
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Don’t forget folks, MSG is an ingredient in your vaccines!

  1. Link to the CDC’s vaccine ingredient webpage.
  2. Check out the MSG Truth website here.

Revised Erb Report on MSG to the WHO

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Over 250 Studies and Case Reports Your Pediatrician Likely Never Read

By Reactions, Jeffry John Aufderheide, Top Stories, Vaccine Development

Over 250 Studies and Case Reports Your Pediatrician Likely Never Read

No Comments 29 January 2010

Jeffry John Aufderheide
1/29/10

There is a massive body of vaccine literature waiting to be discovered for the budding researcher. I have pared down a list of interesting studies and case reports on the topic of vaccines.

Many, as you can see, are not in the native English language. Most of the list is starting in the 1950’s and continues to the 1970’s. As time goes on, this list will grow… hopefully accompanied with the abstracts.

Please note the abundance of them refer to post-vaccine encephalitis.

Tip: If you go to your local library they can assist in obtaining these studies. Bombs away!

http://vactruth.com/research/list-of-studies/

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Interview of Jeffry John Aufderheide on the Robert Scott Bell show

Jeffry John Aufderheide, Top Stories

Interview of Jeffry John Aufderheide on the Robert Scott Bell show

No Comments 11 January 2010

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Approved Chaos, Part I: How the WHO is Using the Swine Flu to Hogtie the US

H1N1, Jeffry John Aufderheide

Approved Chaos, Part I: How the WHO is Using the Swine Flu to Hogtie the US

10 Comments 30 November 2009

Jeffry John AufderheideJeffry John Aufderheide
vactruth.com
11/30/09

(Part I)

(vactruth.com) When President Barack H. Obama signed a national pandemic emergency on Friday, October 24th, 2009, the media barely mentioned that “a declaration of emergency for the H1N1” had been signed.  A huge red flag should have gone up: Why was there was no reference to specific act or document? Initially, not even the White House web page had information about the pronouncement. Did Obama’s emergency proclamation, under sections 201 and 301 of the National Emergencies Act, imply that martial law was imminent?[1]

To answer that question, we first must see how the World Health Organization put Obama in such a position. The answer may surprise you.

The Department of Homeland Security(DHS), Federal Emergency Management Agency(FEMA), the Department of Health and Human Services (HHS), Center for Disease Control (CDC) and United States Northern Command (USNORTHCOM) will be the focus of a future release of this series called “Approved Chaos” that will answer questions about their status, readiness preparations and participation in the H1N1 emergency including:

  • What happens when a national emergency is declared?
  • Who is really in charge?, and most importantly,
  • What does this H1N1 emergency mean for me?

Moreover, the media portrays the government as a passive participant in the swine flu pandemic. Digging deeper, it appears there is a much different story. The previous bird flu “pandemic” was, in fact, utilized to clear many legal obstacles in orchestrating the current, coordinated effort to establish global controls.

The WHO Sets Up for Control

Fowl! Bird Flu: It's Not What You Think - Book

Fowl! Bird Flu: It's Not What You Think - Book

In 2005, the threat of a killer avian flu pandemic shouted across the airwaves. The media whipped up a complete hysteria over the H5N1 virus. The Trust for America’s Health (TFAH), funded by the Rockefeller Family Fund was a big player in the frenzy.[2] Specifically, they predicted up to 1 million deaths could be caused by the H5N1 bird flu virus.[3]   Remarkably, official WHO reports document that between 2003 and 2009, only 262 people have died worldwide from H5N1 Avian Flu.

For a great review of the pandemic that never occurred, read Dr. Sherri Tenpenny’s book, FOWL: Bird Flu: It’s Not What You Think. Prophetically, it also explains 90 percent of what is happening today with the currently hyped H1N1 pandemic.
The 2005 H5N1 fear tactics worked well. Out of the panic created by TFAH and a long list of similar organizations, the WHO released a global “Pandemic Plan” that was obediently adopted by Americans and the rest of the world. In the United States, the Federal Pandemic Plan was incorporated into what is known as the the National Response Plan, under Homeland Security Presidential Directive 5.

The States Join In

In 2005, following the WHOs lead, the United States released a final draft of a multi-year pandemic planning project. States were required to prepare pandemic plans as a condition of their federal bioterrorism preparedness grants.

A group named Association of State and Territorial Health Officials (ASTHO) assisted in molding the state response plans. ASTHO’s exclusive list of “Corporate Alliance Partners” includes vaccine manufacturing giants such as GlaxoSmithKline, Merck & Co., Henry Schein, Pfizer, Roche, and Sanofi Pasteur.[5] Their participation in the pandemic planning efforts can be seen in a 2002 document entitled, “NATURE’S TERRORIST ATTACK: PANDEMIC INFLUENZA”. [6]

The State emergency response plans were heavily guided by officials at the CDC and HHS. A comprehensive checklist was spoon-fed to state health officials who were maneuvered into compliance by the Federal “mandate”. The DHS and HHS were instructed to withhold federal grants and monies for public health initiatives if states did not act in accordance with government plans. The word ‘ransom’ should come to mind.

WHO DOC

Implications of International Health Regulations

We have now come full circle. All forms of government, federal, state and local, have adopted the World Health Organization ’s Pandemic Standard Operating Procedures. A pandemic plan in itself is not the problem. The issue is understanding the WHO’s incremental power grab via International Health Regulations.

Under the guise of preventing the international spread of disease, the Constitution of the WHO allows the World Health Assembly the authority to adopt regulations they see fit to accomplish the stated goal. By example, six diseases were originally identified by International Health Regulations for quarantine. However, in 1969 this number was reduced to three (yellow fever, plague and cholera). [7] With the current media hype surrounding the 1918 pandemic, it is especially surprising the World Health Organization to not include influenza on this list.


If we fast forward in time, major efforts can be seen to modify the scope of the Regulations from 1995 through May of 2005. On May 23rd the World Health Assembly struck gold. The language in the regulations were unified to include, “any specific disease or manner of transmission, but covering illness or medical condition, irrespective of origin or source, that presents or could present significant harm to humans”. [7] When the entire situation is put into context, the timing of a ‘killer’ bird flu pandemic was impeccable.

The International Health Regulations of 2005 were signed into force and effect in 2007. At that critical point, WHO was given authority to ‘direct’ and ‘govern’ activities “that protect the global community from public health risks and emergencies that cross international borders.” [8] The Director-General of the World Health Organization, Margaret Chan, declared a public health emergency of international concern for the first time under International Health Regulations in April, 2009. [9]

The implications of international health regulations and this emergency declaration are far reaching. International Health Regulations are legally binding agreements for all international members of the WHO. This is a major story ignored by the press and not understood by most citizens. The WHO international health regulations by-pass the checks and balances established by the U.S. Constitution and our Founders. George Washington, Thomas Jefferson, and Benjamin Franklin are rolling in their graves.

We have a serious problem as a nation. This scheme was not implemented as the media portrays: benign and harmless. It was devised incrementally by very powerful people with no input from our elected representatives. Never before has there been such an orchestrated effort to give a world organization jurisdiction over our lives in America. The WHO has emerged as the global “H1N1 Mafia” and is accountable to no one.

Part II of this series covers Obama’s H1N1 emergency declaration. Was martial law declared? Stay tuned.



REFERENCES:

[1] Declaration of a National Emergency with Respect to the 2009 H1N1 Influenza Pandemic. October 24, 2009. URL: http://www2a.cdc.gov/phlp/docs/2009H1N1%20prc%20rel.pdf

[2] Trust For America’s Health. Year in Review, 2001; 33. URL:http://healthyamericans.org/about/review2001.pdf

[3] Trust For America’s Health. “A Killer Flu?”, June 2005; 19. URL: http://healthyamericans.org/reports/flu/Flu2005.pdf

[4] School of Public Health and Health Services and the Homeland Security Policy Institute. “The H1N1 Influenza A Virus: A Test Case for a Global Response”, May 2009. URL:http://www.gwumc.edu/sphhs/about/rapidresponse/download/Rapid_SwineFlu_Final.pdf

[5] The Association of State and Territorial Health Officials (ASTHO). “2009 ASTHO Annual Report”, 2009; 28. URL: http://www.astho.org/About/09-Annual-Report/

[6] Association of State and Territorial Health Officials (ASTHO). “Preparedness Planning for State Health Officials: Nature’s Terrorist Attack: Pandemic Influenza”, November 2002. URL: http://www.astho.org/Programs/Infectious-Disease/Emerging-Infectious-Diseases/Pan-ASTHO-Pandemic-Influenza-2002/

[7] World Health Organization. “International Health Regulations, 2nd ed.”, 2005; 8. URL: http://whqlibdoc.who.int/publications/2008/9789241580410_eng.pdf

[8] World Health Organization. “Ten things you need to do to implement the IHR”. Accessed November 29th, 2009. URL: http://www.who.int/ihr/about/10things/en/

[9] School of Public Health and Health Services and the Homeland Security Policy Institute. “The H1N1 Influenza A Virus: A Test Case for a Global Response”, May 2009; 4. URL: http://www.gwumc.edu/sphhs/about/rapidresponse/download/Rapid_SwineFlu_Final.pdf

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Jeffry John Aufderheide, News, Vaccine Propaganda

“Recipe” that Fosters Influenza Vaccine Interest and Demand

No Comments 02 November 2009

Think your psychological buttons are not being pushed to get the H1N1 vaccine? Read this and think again…

http://www.ama-assn.org/ama1/pub/upload/mm/36/2004_flu_nowak02.pdf


Slide 2

“Recipe” that Fosters Higher Interest and
and Demand for Influenza Vaccine (1)
1.Influenza’s arrival coincides with immunization “season” (i.e., when people can take action)
2.Dominant strain and/or initial cases of disease are:
–Associated with severe illness and/or outcomes
–Occur among people for whom influenza is not generally perceived to cause serious complications (e.g., children, healthy adults, healthy seniors)
–In cities and communities with significant media outlets (e.g., daily newspapers, major TV stations)

Slide 3

“Recipe” that Fosters Influenza Vaccine Interest and Demand (2)
3.Medical experts and public health authorities publicly (e.g., via media) state concern and alarm (and predict dire outcomes)–and urge influenza vaccination.
4.The combination of ‘2’ and ‘3’ result in:
A.Significant media interest and attention
B.Framing of the flu season in terms that motivate behavior (e.g., as “very severe,” “more severe than last or past years,” “deadly”)

Slide 4

“Recipe” that Fosters Influenza Vaccine Interest and Demand (3)
5.Continued reports (e.g., from health officials and media) that influenza is causing severe illness and/or affecting lots of people–helping foster the perception that many people are susceptible to a bad case of influenza.
6.Visible/tangible examples of the seriousness of the illness (e.g., pictures of children, families of those affected coming forward) and people getting vaccinated (the first to motivate, the latter to reinforce)
7.References to, and discussions, of pandemic influenza–along with continued reference to the importance of vaccination.

Slide 5

Implications of “Recipe”
•A large component of consumer demand for flu vaccination is contingent upon things we can’t control (e.g., timing, severity,extent, duration of the disease and resulting illness).
•Vaccination demand, particularly among people who don’t routinely receive an annual influenza vaccination, is related toheightened concern, anxiety, and worry. For example:
–A perception or sense that many people are falling ill;
–A perception or sense that many people are experiencing bad illness;
–A perception or sense of vulnerability to contracting and experiencing bad illness.

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H1N1, Jeffry John Aufderheide, Medical Cartel, News

No Child Left Unimmunized: A Plan To Turn Every School In America Into H1N1 Vaccine Clinic

2 Comments 30 October 2009

Jeffry John Aufderheide
VACTRUTH
October 30th, 2009

(vactruth.com) Many believe that forced vaccination for the H1N1 flu is a stones throw away. Evidence is beginning to support such a hypothesis as it came to my attention that contained within the current “heath-care” bill are plans to use elementary and secondary schools as likely venues to vaccinate children with the H1N1 vaccine. (Thank you CL!)

Additionally, it is hardly surprising that federal funds are being dangled as carrots to an already money-starved education system in exchange for participation. There should be much concern in America especially when the director of the CDC will be calling the ’shots’, or rather, who will be getting them and which ones.

It would be likely that your child would be forced to receive the H1N1 vaccine under this provision. It is a plausible story since many folks now are outright rejecting the unproven and quick-to-market H1N1 shot.


The link to the bill can be found here: http://docs.house.gov/rules/health/111_ahcaa.pdf (page 1391)

SEC. 2524. NO CHILD LEFT UNIMMUNIZED AGAINST INFLUENZA: DEMONSTRATION PROGRAM USING ELEMENTARY AND SECONDARY SCHOOLS AS INFLUENZA VACCINATION CENTERS.

There’s also some language that sounds to me like the director of the CDC will decide which immunizations will be included under preventative care for CHIPS and Medicaid.

Subtitle B—Prevention

SEC. 1711. REQUIRED COVERAGE OF PREVENTIVE SERVICES. (Page 1043)

‘‘(B) vaccines recommended for use as appropriate by the Director of the Centers for Disease Control and Prevention; and
(1) in subsection (c)(2)(B)(i), by striking ‘‘the
advisory committee referred to in subsection (e)’’
and inserting ‘‘the Director of the Centers for Disease Control and Prevention’’;

Section 2524 is also eerily reminiscent of a recent white paper RAND Corporation published in which ‘barriers’ to mass vaccinating (low income) children were identified. One road block specifically named were parental consent laws on a state level.

A recommendation was made to Sanofi Pasteur, who coincidentally manufactures vaccines, to find a way around these state consent laws which could only be interpreted as leveraging the Federal Government to put into law such a mandate.

It would be curious to discover if there was influence on Capitol Hill to add this provision? I’m not a betting man, but I suspect there was.


1. Read the analysis on the RAND Corporation’s white paper here.

(link) http://vactruth.com/2009/08/26/rand-advises-pharmaceutical-company-on-strategies-in-vaccinating-low-income-students/

2. Learn more about vaccines at http://www.vaccinationeducation.com


SEC. 2524. NO CHILD LEFT UNIMMUNIZED AGAINST INFLUENZA: DEMONSTRATION PROGRAM USING ELEMENTARY AND SECONDARY SCHOOLS AS INFLUENZA VACCINATION CENTERS.

http://docs.house.gov/rules/health/111_ahcaa.pdf

(a) PURPOSE.—The Secretary of Health and Human
19 Services in consultation with the Secretary of Education,
20 shall award grants to eligible partnerships to carry out
21 demonstration programs designed to test the feasibility of
22 using the Nation’s elementary schools and secondary
23 schools as influenza vaccination centers.
24 (b) IN GENERAL.—The Secretary shall coordinate
25 with the Secretary of Labor, the Secretary of Education,

State Medicaid agencies, State insurance agencies, and
2 private insurers to carry out a program consisting of
3 awarding grants under subsection (c) to ensure that chil4
dren have coverage for all reasonable and customary ex5
penses related to influenza vaccinations, including the
6 costs of purchasing and administering the vaccine in7
curred when influenza vaccine is administered outside of
8 the physician’s office in a school or other related setting.

9 (c) PROGRAM DESCRIPTION.—
10 (1) GRANTS.—From amounts appropriated pur11
suant to subsection (l), the Secretary shall award
12 grants to eligible partnerships to be used to provide
13 influenza vaccinations to children in elementary and
14 secondary schools, in coordination with school
15 nurses, school health care programs, community
16 health care providers, State insurance agencies, or
17 private insurers.
18 (2) ACIP RECOMMENDATIONS.—The program
19 under this section shall be designed to administer
20 vaccines consistent with the recommendations of the
21 Centers for Disease Control and Prevention’s Advi22
sory Committee on Immunization Practices (ACIP)
23 for the annual vaccination of all children 5 through
24 19 years of age.

1 (3) PARTICIPATION VOLUNTARY.—Participation
2 by a school or an individual shall be voluntary.
3 (d) USE OF FUNDS.—Eligible partnerships receiving
4 a grant under this section shall ensure the maximum num5
ber of children access influenza vaccinations as follows:
6 (1) COVERED CHILDREN.—To the extent to
7 which payment of the costs of purchasing or admin8
istering the influenza vaccine for children is not cov9
ered through other federally funded programs or
10 through private insurance, eligible partnerships re
11ceiving a grant shall use funds to purchase and ad
12minister influenza vaccinations.
13 (2) CHILDREN COVERED BY OTHER FEDERAL
14 PROGRAMS.—For children who are eligible under
15 other federally funded programs for payment of the
16 costs of purchasing or administering the influenza
17 vaccine, eligible partnerships receiving a grant shall
18 not use funds provided under this section for such
19 costs.
20 (3) CHILDREN COVERED BY PRIVATE HEALTH
21 INSURANCE.—For children who have private insur22
ance, eligible partnerships receiving a grant shall
23 offer assistance in accessing coverage for vaccina24
tions administered through the program under this
25 section.

1 (e) PRIVACY.—The Secretary shall ensure that the
2 program under this section adheres to confidentiality and
3 privacy requirements of section 264 of the Health Insur4
ance Portability and Accountability Act of 1996 (42
5 U.S.C. 1320d–2 note) and section 444 of the General
6 Education Provisions Act (20 U.S.C. 1232g; commonly re7
ferred to as the ‘‘Family Educational Rights and Privacy
8 Act of 1974’’).
9 (f) APPLICATION.—An eligible partnership desiring a
10 grant under this section shall submit an application to the
11 Secretary at such time, in such manner, and containing
12 such information as the Secretary may require.
13 (g) DURATION.—Eligible partnerships receiving a
14 grant shall administer a demonstration program funded
15 through this section over a period of 2 consecutive school
16 years.
17 (h) CHOICE OF VACCINE.—The program under this
18 section shall not restrict the discretion of a health care
19 provider to administer any influenza vaccine approved by
20 the Food and Drug Administration for use in pediatric
21 populations.
22 (i) AWARDS.—The Secretary shall award—
23 (1) a minimum of 10 grants in 10 different
24 States to eligible partnerships that each include one

1 or more public schools serving primarily low-income
2 students; and
3 (2) a minimum of 5 grants in 5 different States
4 to eligible partnerships that each include one or
5 more public schools located in a rural local edu6
cational agency.
7 (j) REPORT.—Not later than 90 days following the
8 completion of the program under this section, the Sec9
retary shall submit to the Committees on Education and
10 Labor, Energy and Commerce, and Appropriations of the
11 House of Representatives and to the Committees on
12 Health, Education, Labor, and Pensions and Appropria13
tions of the Senate a report on the results of the program.
14 The report shall include—
15 (1) an assessment of the influenza vaccination
16 rates of school-age children in localities where the
17 program is implemented, compared to the national
18 average influenza vaccination rates for school-aged
19 children, including whether school-based vaccination
20 assists in achieving the recommendations of the Ad21
visory Committee on Immunization Practices;
22 (2) an assessment of the utility of employing el23
ementary schools and secondary schools as a part of
24 a multistate, community-based pandemic response

1 program that is consistent with existing Federal and
2 State pandemic response plans;
3 (3) an assessment of the feasibility of using ex4
isting Federal and private insurance funding in es5
tablishing a multistate, school-based vaccination pro6
gram for seasonal influenza vaccination;
7 (4) an assessment of the number of education
8 days gained by students as a result of seasonal vac9
cinations based on absenteeism rates;
10 (5) a determination of whether the program
11 under this section—
12 (A) increased vaccination rates in the par13
ticipating localities; and
14 (B) was implemented for sufficient time
15 for gathering enough valid data; and
16 (6) a recommendation on whether the program
17 should be continued, expanded, or terminated.
18 (k) DEFINITIONS.—In this section:
19 (1) ELIGIBLE PARTNERSHIP.—The term ‘‘eligi20
ble partnership’’ means a local public health depart21
ment, or another health organization defined by the
22 Secretary as eligible to submit an application, and
23 one or more elementary and secondary schools.
24 (2) ELEMENTARY SCHOOL.—The terms ‘‘ele25
mentary school’’ and ‘‘secondary school’’ have the

1 meanings given such terms in section 9101 of the
2 Elementary and Secondary Education Act of 1965
3 (20 U.S.C. 7801).
4 (3) LOW-INCOME.—The term ‘‘low-income’’
5 means a student, age 5 through 19, eligible for free
6 or reduced-price lunch under the National School
7 Lunch Act (42 U.S.C. 1751 et seq.).
8 (4) RURAL LOCAL EDUCATIONAL AGENCY.—
9 The term ‘‘rural local educational agency’’ means an
10 eligible local educational agency described in section
11 6211(b)(1) of the Elementary and Secondary Edu12
cation Act of 1965 (20 U.S.C. 7345(b)(1)).
13 (5) SECRETARY.—Except as otherwise speci14
fied, the term ‘‘Secretary’’ means the Secretary of
15 Health and Human Services.
16 (l) AUTHORIZATION OF APPROPRIATIONS.—To carry
17 out this section, there are authorized to be appropriated
18 such sums as may be necessary for each of fiscal years
19 2011 through 2015.

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Jeffry John Aufderheide, News

CEO of vaccine company gives presentation on product pipeline and relationships with CDC and academia

1 Comment 22 October 2009

Jeffry John AufderheideJeffry John Aufderheide
VACTRUTH
10/22/09

(vactruth.com) How many times have you pondered wondered what the intimate picture of the world of vaccines and pharmacology look like? VACTRUTH has received a video of the CEO of a local Colorado vaccine company that is giving a rather candid presentation on its humble beginnings.

The acoustic and visual quality of the video is rather poor. However, this engaging piece of evidence is merely a drop in the bucket compared to the likes of GlaxoSmithKline, Novartis, Sanofi Pasteur, and Merck. In the beginning minutes one will clearly see the intimate relationship between the Center for the Disease Control, academia, off shore manufacturing, private sector funding, and ambitions to likely vaccinate vast hundreds of millions of men, women and children.

I won’t play much of a spoiler, but suffice to mention somewhere in the presentation are plans to put genes from the (Yersinia pestis) Plague and smallpox into a single vaccine. Is this a good strategy? I have no idea.

This is called a recombinant vaccine or recombinant vaccine technology. FDA oversight will likely be scant as the manufacturing of the vaccine will likely appear to be taking place in India. I almost forgot about the part about the World Health Organization and GAVI…. oh yeah, no spoiling!

Most importantly, this video is incredibly relevant to the socio-political climate surrounding the current influenza and H1N1 vaccine debate. According to a company press release in June,

“Based on its ongoing avian influenza vaccine research, Inviragen is designing vaccines to protect against multiple influenza strains, including seasonal influenza and the recently emerged H1N1 influenza strain……Inviragen will leverage its success in designing avian influenza vaccines to identify vaccine candidates that protect against pandemic and seasonal influenza viruses.”

I am sure the folks at the CDC and Inviragen have the best intentions. Keep in mind Inviragen is a small fish in a big ocean, for now. The blatant conflicts of interest between government (Center for Disease Control), research and development, funding, and manufacturing must be put into the proper light so all may make better informed decisions.

Sit back, relax and enjoy the presentation, folks. The full version is coming soon…

Full Version

CEO of vaccine company gives presentation on product pipeline and relationships with CDC and academia from VACTRUTH on Vimeo.

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By Reactions, Dr. Andrew Moulden, Jeffry John Aufderheide, News

Revolutionary Video Shows How All Vaccines Are Damaging The Brain

1 Comment 08 October 2009

Jeffry John Aufderheide
VACTRUTH
10/08/2009

(vactruth.com) A newly launched video by Dr. Andrew Moulden is available on his Brainguardmd.com website. The movie is self explanatory. If you are truly interested in understanding how every single vaccine is affecting you and your loved ones, watch and learn with your very own eyes what is happening to our children.

Moreover, Dr. Andrew Moulden provides a ’see for yourself’ format in which parents can see the damage with their very own eyes.

Be patient as the video takes time to load.
Dr. Moulden’s website is http://brainguardmd.com.

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FDA Approves Experimental H1N1 Swine Flu Vaccine Prior to Children Safety Trials Beginning

By Reactions, H1N1, Jeffry John Aufderheide, Vaccine Development

FDA Approves Experimental H1N1 Swine Flu Vaccine Prior to Children Safety Trials Beginning

8 Comments 16 September 2009

Jeffry John AufderheideJeffry John Aufderheide
VacTRUTH
09/16/09

(vactruth.com) In a stunning move, the FDA has approved four monovalent Swine Flu vaccines for the following companies: CSL Limited, MedImmune LLC, Novartis Vaccines and Diagnostics Limited, and Sanofi Pasteur, Inc. Adding to the confusion is the fact that purported ’safety trials’ for the Swine Flu vaccine haven’t even begun, in some instances.

By example, Novartis is just starting vaccine safety trials for three to eight year old children supposedly as of 09/15/09 as reported in the last article I wrote entitled, “Ingredients Found in Spermicides, Cleaners, and Cosmetics along with Thimerosal, and Squalene Present in Experimental H1N1 Vaccine“. One can only wonder as to what head FDA officials are thinking when they approved the vaccine on the same day. Yet, according to the newly released package inserts, we now know exactly why this decision was made.

The document concerning the Novartis trial becomes a pivotal piece in discerning what is happening behind closed doors. Generally speaking, all four package inserts communicate the same message and are structured similarly. Therefore, we will select quotes from the Novartis insert for the purposes of this article.

—-For the reader’s edification, here are links to information concerning the vaccine by manufacturer—-

PAST STUDIES ARE THE JUSTIFICATION FOR APPROVAL

How does a vaccine get approved without being properly tested for safety? The press release entitled “FDA Approves Vaccines for 2009 H1N1 Influenza Virus” which can be read here gives us our first clue…

“Based on preliminary data from adults participating in multiple clinical studies, the 2009 H1N1 vaccines induce a robust immune response in most healthy adults eight to 10 days after a single dose, as occurs with the seasonal influenza vaccine.”

“Clinical studies under way will provide additional information about the optimal dose in children. The recommendations for dosing will be updated if indicated by findings from those studies. The findings are expected in the near future.”

Needless to say there is a fair amount of assuming going on by high government officials and those that are practicing ‘evidence based medicine.’ The main assumption of course that this vaccine is perfectly safe. “Where is Novartis and others receiving their information from,” one may ask?  The package insert for Novartis clearly states,

“Safety data were collected in a total of 2768 adult and geriatric subjects (18 years of age and older) who have received FLUVIRIN in 29 clinical studies since 1982.” (pg 6)

“In 9 clinical studies since 1997, among 1261 recipients of FLUVIRIN, 745 (59%) were women; 1211 (96%) were White, 23 (2%) Asian, 15 (1%) Black and 12 (1%) other; 370 (29%) of subjects were elderly (≥65 years of age). All studies have been conducted in the UK, apart from a study run in the US in 2005-2006 where FLUVIRIN was used as a comparator for an unlicensed vaccine.” (pg 6)

“In 1987 a clinical study was carried out in 38 ‘at risk’ children aged between 4 and 12 years (17 females and 21 males)…Three clinical studies were carried out between 1995 and 2004 in a total of 520 pediatric subjects (age range 6 – 47 months).” (pg 10)

Are they implying no testing has been completed for this new experimental H1N1 Swine Flu vaccine? I can see the logic of someone believing that the experimental H1N1 Swine Flu vaccine is safe predicated on the fact it is created with the same ‘technology’ as past shots. Moreover, when official bodies of government reiterate a sound byte, it sure is easier to believe.

If the aforementioned studies in the vaccine insert indicate vaccine safety, it doesn’t make much sense to have safety trials. Even more so, wouldn’t the clinical studies performed would be totally useless if, by example, different formulations were different? It appears what is being said and what is being done are  entirely different matters altogether.

SWINE FLU VACCINE TRIAL CONTRADICTS ‘OFFICIAL STORY’

Looking at the CDC’s website for the ingredients of FLUVIRIN, we see it contains the following ingredients:

“Beta-Propiolactone , Egg Protein, Neomycin, Polymyxin B, Polyoxyethylene 9-10 Nonyl Phenol (Triton N-101, Octoxynol 9), Thimerosal (multidose containers), Thimerosal* (single-dose syringes)” (page 2)

Yet if we look at what is being tested in the trial we can abundantly see the two vaccines are not the same. Please look at page 2 of 13 of the experimental swine flu vaccine paperwork.

“MF59 is an adjuvant which is used in influenza vaccines licensed for adults and/or elderly in many countries worldwide, but it is not contained in any vaccines currently approved in the United States.”

If the MF59 adjuvant is approved for adults and elderly in different countries, but not approved in the United States, and at the same time we are having clinical trials on children now, how valid are those referenced studies in the FDA-approved-vaccine-inserts? That doesn’t appear to be evidence based to many in the scientific communities.

Nonoxynol-9 (which is a spermicide) mentioned on page 8 of the vaccine trial document is not mentioned as an ingredient in FLUVIRIN, according to the CDC’s website. Additionally, just because a vaccine has been manufactured by using the same process as the H1N1 vaccine insert implies, does not mean it has the same ingredients as past vaccines. Therefore, we cannot be presumptuous that all is well in the land of neurology or immunology.

Moreover, it appears that the Novartis Swine Flu vaccine insert is mostly a copied and pasted from the FLUVIRIN insert. Both inserts indicate that the vaccine is not for use for children under four years of age. Yet, Novartis is having a trial as I write this on three year old boys and girls. Even harder to grasp is the CDC’s recommendation that pregnant women and children 6-months of age are being shoved to the front of the line for  being vaccinated.

The cruel irony on page 2 of the Novartis Swine Flu vaccine insert remarks,

“Safety and effectiveness of Influenza A (H1N1) 2009 Monovalent Vaccine have not been established in pregnant women, nursing mothers or children less than 4 years of age. (8.1, 8.3, 8.4)

UNIVERSAL DECLARATIONS

I seem to recall not too long ago the FDA engaging in a witch hunt to prevent any alternative treatments for the H1N1 Swine Flu. In a press release, “FDA Warns Web Sites against Marketing Fraudulent H1N1 Flu Virus Claims” the FDA boldly declared,

“…the FDA warned consumers regarding products related to the 2009 H1N1 flu virus offered on the Internet. The products involved are those that are promoted and marketed to diagnose, mitigate, prevent, treat, or cure the 2009 H1N1 flu virus but are not approved, cleared, or authorized by the FDA. The agency advised operators of offending Web sites that they must take immediate action to ensure that they are not marketing products intended to diagnose, mitigate, prevent, treat, or cure the 2009 H1N1 flu virus that have not been cleared, approved, or authorized by the FDA.”

“The FDA will consider further civil or criminal enforcement action against those Web sites that fail to resolve the violations cited in warning letters. Actions could include seizure, injunction, and criminal prosecution.”

Let’s get this straight. The powers that be at the FDA asserts unequivocally that the experimental vaccines are safe and effective while some safety trials for the vaccines have not even been started. The formulations are clearly not the same from past flu vaccines although they are being treated as such. Additionally, testing is being conducted on children who are younger than the recommended ages in the vaccine inserts. Lastly, pregnant women and infants are FIRST in line for this vaccine. It almost all seems a bit criminal, doesn’t it?

When the FDA states that it will consider civil or criminal enforcement against blatantly falsified information, perhaps they can look no further than their own backyard.

FDA Warns Web Sites against Marketing Fraudulent H1N1 Flu Virus Claims


VacTRUTH Editor’s Note:

1. A great resource for readers to understand how vaccines are made and information about them can be located at: http://www.trackingvaccinations.com/ (HIGHLY RECOMMENDED!!!)

2. The swine flu vaccine will have 25 mcg of thimerosal. A good read on the topic can be found here: http://katysexposure.wordpress.com/2009/07/30/washington-post-swine-flu-vaccine-will-contain-mercury-toxin-linked-to-autism-and-neurological-disorders/

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Jeffry John Aufderheide, Video

Chris Yankowski’s InTheoryTV interviews Jeffry John Aufderheide

No Comments 15 September 2009

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