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Posts Tagged ‘adjuvant’

With so many scandals and questions lingering about climategate-http://www.time.com/time/health/article/0,8599,1946082,00.html  and vaccinegate, it is disgusting Tiger Woods affairs are the lead story in the news. We thought a diversion might be in order and found this off Broadway play-  The Affair, faithfully adapted by Ronald Millar from the novel by C.P. Snow.  It played in 1962 according to the review, but would make one hell a remake. http://www.time.com/time/magazine/article/0,9171,940107,00.html#ixzz0Z6ZHdRlV

1962 was long before anyone every questioned the science behind global warming, vaccines or who our President or anyone of importance was having an affair with.  A time when one did what was told, ‘get your shots and shut up’, Coppertone was for only kids, and we were at war.   

As The Affair begins, the High Tables of the university are still rocking with an intellectual scandal that will not down with the port. Donald Howard (Keith Baxter) has been judged guilty of scientific fraud, having apparently faked a research photograph in his fellowship thesis, and a court of dons deprives him of his fellowship.

Impeccably performed, it pungently evokes its donnish milieu and nobly invokes man’s tireless quest to make justice prevail.

Will justice prevail in Copenhagen, in the truth about vaccines, or for Tiger Woods family?

 The international scandal of leaked e-mails from prominent climatologists and the pandemics push for pharmaceutical companies to release vaccines with little clinical trials before approval is familiar 47 years later.  This time it is not a play, but real life players dealing with decisions that will affect your health and living standards.  Oh yeah, your pocketbook too.

  Will justice prevail in saving lives with the use of vaccines derived from dog, kidney, monkey, He-la, and Vero cell lines? 

Ironically enough, the main character in the play was performed by Keith Howard.  In real life, a Dr. Keith Howard sits on the Scientific Advisory Committee on Genetic Modification. SACGM for short.  http://www.hse.gov.uk/biosafety/gmo/acgm/acgmcomp/index.htmCurrently Dr. Keith Howard is the Head of the Preclinical Research Group at Baxter Innovations GmbH in Orth, Austria supporting the manufacture of vaccines for interpandemic and avian influenza, and the development of new vaccines against emerging viral diseases http://www.hse.gov.uk/aboutus/meetings/committees/sacgmcu/biography.htm. Baxter has been myriad in controversy, if you have been living under a rock, type Baxter in the side search bar to learn more about them releasing live viruses, getting patents for H1N1 vaccines prior to the pandemic and other suspicious happenings.

 SACGM says of Genetically Modified things that:   

 There are no longer separate containment levels specified for work with GM animals and plants (Containment Levels A and B) – appropriate measures must be put in place to control the risks to human health and the environment. http://www.liv.ac.uk/safety/work_area_hazards/Biosafety/Genetic_Modification/Containment_and_control_measures_for_work_with_GMOs.htm

Clinical studies published by Baxter’s own scientific team suggests that adjuvants are at best useless and documented that there is no increase in antibody response, yet Baxter is manufacturing vaccines containing adjuvants for the H1N1 vaccine.  From the New England Journal of Medicine http://content.nejm.org/cgi/content/short/358/24/2573  “Results The vaccine induced a neutralizing immune response not only against the clade 1 (A/Vietnam/1203/2004) virus strain but also against the clade 2 and 3 strains. The use of adjuvants did not improve the antibody response.”From The World Health Organinzation:    http://www.who.int/vaccine_research/documents/Report_on_consultation_on_adjuvant_safety_2.pdfSeveral adjuvants have been shown to permit dose-reduction and enhanced breadth of immunity for influenza vaccines in clinical studies. In light of the recent outbreak of influenza A (H1N1)v, there may be a need in the future to immunize large population groups. Adjuvants could  potentially expand the supply of available influenza vaccines. While we have no evidence yet of  the immunological benefit of adjuvants for vaccines against the H1N1 virus, a discussion of potential safety issues at this stage will facilitate planning and clinical trial design. 

I do know that the affairs of Tiger Woods are becoming public knowledge.  Will the misguided affairs of climate change and vaccines risks have greater public awareness than Tigers? Since The Affair is long off Broadway, I think I’ll see 2012 the movie.

RELATED

https://ahrcanum.wordpress.com/2009/05/05/baxter-pharmaceutical-plant-in-mexico-ground-zero-for-flu-outbreak/#comment-4227  

https://ahrcanum.wordpress.com/2009/03/11/vaccine-drug-deadly-costs-mistakes-threaten-pandemic/

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With a rush to produce millions of H1N1 vaccines by Pharmaceutical Companies, comes the news of the first recall of the vaccine.  Will it be the last?

Canadian doctors have been advised not to use a batch of 170,000 swine flu vaccines after six reports of serious allergic reactions among recipients, but there are no similar reports from other countries, pharmaceuticals company GlaxoSmithKline PLC said Tuesday. via http://www.huffingtonpost.com/2009/11/24/swine-flu-recall-h1n1-vac_n_368776.html

GlaxoSmithKline has asked that the October batch of H1N1 swine flu Pandemrix be taken out of circulation because it produced serious and immediate anaphylactic reactions in one out of 20,000 vaccinations, compared with one out of 100,000 in other shipments. Most of the vaccine Manitoba received from the suspect lot had already been used by the time the province received the alert. Of the 63,000 doses shipped, only 630 remained unused by the four regional health authorities in Manitoba that received them…Pandemrix contains parts of influenza (flu) viruses that have been inactivated (killed). Pandemrix contains a flu strain called A/California/7/2009 (H1N1) v-like strain (X-179A). Pandemrix contains small amounts of haemagglutinins (proteins from the surface) of a virus called A(H1N1)v that is causing the current pandemic. The virus has first been inactivated so that it does not cause any disease. http://www.dancewithshadows.com/pillscribe/glaxosmithkline-recalls-a-lot-of-h1n1-vaccine-pandemrix-from-canada-due-to-side-effects/

Highlights from  The Summary of Product Characteristics or patient information sheet from  http://www.emea.europa.eu/humandocs/PDFs/EPAR/pandemrix/emea-combined-h832en.pdf says that Pandemrix contains:

AS03 adjuvant composed of squalene (10.69 milligrams), DL-polysorbate 80 (4.86 milligrams) tocopherol (11.86 milligrams), The vaccine contains 5 micrograms thiomersal.   6.1 List of excipients:  Polysorbate 80,  Octoxynol 10, Thiomersal, Sodium chloride (NaCl), Disodium hydrogen phosphate, Potassium dihydrogen phosphate,  Potassium chloride,  Magnesium chloride, Water for injections, Sodium chloride, Disodium hydrogen phosphate.

In clinical studies of efficacy they tested the vaccine in ferrets where all of the ferrets died and exhibited viral shedding.  Additionally:

Following influenza vaccination, false-positive serology test results may be obtained by the ELISA method for antibody to human immunodeficiency virus-1 (HIV-1), hepatitis C virus and, especially  HTLV-1. In such cases, the Western blot method is negative. These transitory false-positive results may be due to IgM production in response to the vaccine.

Translated- the vaccine contains ingredients labeled as toxic, and you might test positive for AIDS and Hepatitis!   Further info on Pandemrix is at http://en.wikipedia.org/wiki/Pandemrix.  Pandemrix has not been approved in the U.S.A.  Pandemrix date of first authorization- MAY 20, 2008, well before the current H1N1 pandemic.  Eye chiwawa!

Back up to the flu episode of 1976.  

About 200 soldiers in basic training at Fort Dix in New Jersey fell ill and at least four soldiers had pneumonia, and one died and the virus was identified as an H1N1 swine flu virus, “thought to be a direct descendant of the virus that caused the pandemic of 1918,” . “This conclusion was based on antibodies to H1N1 antigens found in survivors of the 1918 pandemic and the belief that the 1918 virus was eventually transmitted to pigs in the Midwest, where it persisted and caused sporadic human cases.”

Not only did the pandemic fail to appear, but the vaccine apparently harmed some people. Health officials suspended the vaccination campaign on Dec 16, 1976, after receiving numerous reports of Guillian-Barre syndrome (GBS), a paralyzing neurologic illness, after vaccination, according to an August 1979 report in the American Journal of Epidemiology. Nationwide surveillance detected 1,098 patients with GBS onset from October 1976 through January 1977.   Epidemiologic evidence suggested that many cases were related to vaccination, with an estimated risk of 1 case for every 100,000 vaccinations. http://www.cidrap.umn.edu/cidrap/content/influenza/panflu/news/apr2209swine.html

In a rush to judgement and fast tracking vaccine approval for not only GlaxoSmithKline PLC, are we seeing a vision of things to come for people who take the H1N1 Swine Flu vaccines?

Japanese health ministry officials will fly to Canada by early December, to study the Canadian authorities decision to hold off on using a batch of its swine flu vaccine Pandemrix, reports said quoting a Japanese newspaper said.  Japanese health ministry’s decision comes in the wake of its plan to import GlaxoSmithKline’s flu vaccine Pandemrix to cover 37 million people in the year ending March.  However, there’s no change to Japan’s plan to import Glaxo’s flu vaccine Pandemrix. http://www.dancewithshadows.com/pillscribe/japanese-health-officials-to-fly-canada-no-change-in-plan-to-import-h1n1-swine-flu-vaccine-pandemrix/ 

Will they reconsider?  Will you reconsider getting any flu shot even as governments around the world are encouraging you to do so?

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preganantmother

It is safe for pregnant women to use any licensed swine flu vaccine, whether it contains a “booster” substance known as an “adjuvant” or not, the World Health Organisation said today.  The WHO’s advisory panel on immunisation said while there had been a “few worrisome reactions” to the vaccine, the safety of the medicines were proving similar to the normal seasonal flu vaccines.  “Some adverse events following vaccination have been notified, but they are well within the range of those seen with seasonal vaccines, which have an excellent safety profile,” the panel said. reported via http://www.irishtimes.com/newspaper/breaking/2009/1030/breaking39.htm

Has pregnancy robbed you of your rational thinking to believe this? 

1. There is no evidence based science that H1N1 vaccine prevents serious complication/death from H1N1.
2. There is no evidence based science that H1N1 vaccine prevents infection with H1N1.
3. There is no evidence based science that H1N1 vaccine is safe for fetuses.
4. There has been NO safety data released by any of the manufacturers of the H1N1 vaccine.

For that matter, there is no large randomized clinical trial on the influenza vaccine and whether it prevents death.

Marc Silberman, M.D. via http://onthescene.blogs.foxnews.com/2009/10/28/the-h1n1-vaccine-and-pregnant-women/

Still not convinced?  Read the patient inserts for the U.S. Approved H1N1 Swine Flu at  https://ahrcanum.wordpress.com/2009/09/27/h1n1-swine-flu-vaccine-package-insert-warnings/

Influenza A (H1N1) 2009 Monovalent Vaccine (CSL Limited)http://www.fda.gov/BiologicsBloodVaccines/Vaccines/ApprovedProducts/ucm181975

8.1 Pregnancy

Pregnancy Category C: Animal reproduction studies have not been conducted with Influenza A (H1N1) 2009 Monovalent Vaccine or AFLURIA. It is also not known whether these vaccines can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Influenza A (H1N1) 2009 Monovalent Vaccine should be given to a pregnant woman only if clearly needed.

Every day, bad things happen to people. When you vaccinate a lot of people in a short period of time, some of those things are going to happen to some people by chance alone,” said Dr. Daniel Salmon, a vaccine safety specialist at the Department of Health and Human Services. http://www.philly.com/philly/wires/ap/features/health/20090927_ap_swineflushotintensetrackingforsideeffects

That’s some consolation for death.

Forget about the seasonal flu vaccine too. 

CDC’s website for the ingredients of FLUVIRIN® , from Novartis, 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)

From Novartis’ own study, 13 NONCLINICAL TOXICOLOGY. 13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility.  FLUVIRIN® has not been evaluated for carcinogenic or mutagenic potential, or for impairment of fertility.http://www.novartis-vaccines.com/downloads/diseases-products/fluvirin_vial_syringe.pdf

We suggest waking up in the hospital with a healthy baby by not getting taking the Swine Flu Shot.  BTW, your baby will begin receiving vaccinations immediately upon birth unless you do not give permission to vaccinate in advance. 

Image via healthjockey.com

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Vaccinestamp

“Delays in the release of H1N1 flu shots show that the United States is too dependent on other countries for the manufacture of vaccines and that the technology to make them must be improved,” said HHS Secretary Kathleen Sebelius. http://www.google.com/hostednews/ap/article/ALeqM5hDG1Y2pO9MZlJLNboKJOSSY9xWTwD9BFOG0O4 

Oh shut up.  Sebelius is appealing for more money for the pharmaceutical industry plain and simple, and is doing so at the risk of every single man, woman, child animal, and insect population on Earth.   

The new strain of swine flu, A/H1N1 includes genetic material from swine, poultry and human variants, and underscores the contribution of high densities of farmed animals serving as Petri-dishes for the evolution of zoonotic diseases, compounded by human proximity, international travel, and trade, especially in live animals. The US government will spend $2 billion of public funds in contracting drug companies to fast-track vaccine production to combat this new influenza strain, a policy decision based on fear and ignorance, if not also pandering to corporate interests regardless of the potential risks, questionable need and effectiveness of such a vaccine. Vaccinations will be given without adequate testing for safety and effectiveness, and the Government has ruled that manufacturers are immune from law suits over adverse reactions. Michael W. Fox  BVetMed, PhD, DSc, MRCVS http://www.twobitdog.com/DrFox/specialreport_Article.aspx?ID=ffaa40af-5973-400d-9655-e25eec3d946e

Sebelius knows damned well that vaccine technology does exists for an updated vaccine-making process.   The problem comes from the lies of  governments on how vaccines are currently made and opening Pandora’s box of mutated viruses.  

 st judes

This patent won approval in 1998, outlining a a  means of vaccine development…  http://www.patentstorm.us/patents/5824536/description.html  and pdf a thttp://www.patentstorm.us/patents/pdfs/patent_id/5824536.html from the Saint Jude Children’s Research Hospital:

At present, many viral vaccines other than influenza are produced using primary trypsinized cells, including cells from monkey kidneys, and the kidneys of rabbits and hamsters. Primary diploid cell (sic- aborted fetus) cultures have certain advantages such as easy preparation using simple media and bovine sera and sensitivity to a wide-range multiple viruses. However, primary diploid cells suffer from disadvantages, such as contamination by various adventitous agents, variable quality and sensitivity; and difficulty in obtaining suitable tissue for cultivation

For example, primary diploid cell cultures obtained from monkey kidneys of wild animals usually contain endogenous viruses.

Furthermore, only MDCK cells, (sic- dog kidney) among the continuous cell lines tested, have been reported to support potentially sufficient growth and isolation of viruses (Frank et al., J. Clin. Microb. 10:32-36 (1979); Schepetink & Kok, J. Virol. Methods 42:241-250 (1993)). However, this line has been found to produce tumors and has thus not been certified for vaccine production, as not substantially free of adventitious agents.

The technology exists.  The question arises, do you want to be injected with a virus that was grown in a mammal that is not human?  Have you already been injected with a vaccine that was cultivated from a mammal like the polio vaccine was?   Dr. Robert B. Strecker, M.D., Ph.D back in 1982 warned of AIDS and recombinant retroviruses like H1N1 in a report he called “The Bioalert Attack.”    https://ahrcanum.wordpress.com/2009/09/24/swine-flu-aids-vaccine-control-by-world-health-org/ 

But the fact is, you are not being told the truth by the government or the so-called AIDS experts. The media, for reasons of their own, will not present information contradicting the official propaganda. So you can choose to go along with the same people who gave us brain cancer (SV-40 virus) as a result of their contaminated polio vaccines in the early 1960’s, a polio-like disease from their contaminated Swine Flu Vaccine in the 1970’s; and AIDS from their smallpox and hepatitis B vaccines; or, you can at least make yourself aware of the clear and present dangers that we all face by watching The Strecker Memorandum. http://sonic.net/~doretk/ArchiveARCHIVE/Aids/6.Strecker%20Memo.html

 novartis

In one trial of Influenza A (H1N1) 2009 Monovalent MF59-Adjuvanted Vaccine- by Novartis http://content.nejm.org/cgi/content/full/NEJMoa0907650v1 

The seed virus was grown in Madin–Darby Canine Kidney (MDCK) cell culture by means of standard processes similar to those used for the development of Optaflu vaccines against interpandemic influenza. The vaccine was formulated and produced by Novartis (Marburg, Germany) as an inactivated surface-antigen H1N1 vaccine…Our vaccine was produced from a classical egg-derived seed virus propagated in a MDCK cell line..

Optaflu®  is the first influenza vaccine made in a mammalian cell line, rather than chicken eggs.

 Calling for approval of new technology calls into question the safety of using viruses in humans and other mammals as this study GM Vaccines Recombine into Unpredictable Hybrid shows the chaos that can be created when playing God.

 In what may be the first experiment of its kind, scientists infected cell cultures with two related viruses….  A single virus multiplied into hundreds of thousands of viruses in a few hours, with unpredictable consequences. Since the marker gene in the transgenic virus was not present in some of the newly formed hybrid viruses, it would not be possible to track transgenic viruses as the origin of the hybrids, if they were found in the wild.

“The kinds of viral research going on today, including applications in biowarfare, are primarily driven to develop new vaccines to market in the name of ‘preventive’ human and veterinary medicine. You didn’t think your pet was safe did you? What is injected into our farm animals for human consumption? Since the first vaccine was licensed in 1979, a total of 79 genetically engineered biologics have been licensed; all but 20 are still being produced.  Now there are 2,379 active product licenses for these animal vaccines and other biologics and 110 licensed manufacturers’.”  http://www.twobitdog.com/DrFox/specialreport_Article.aspx?ID=273f53f4-bcdc-474f-a189-cca1d1a81c38 

What about the ingredients that U.S. Vaccine suppliers have to adhere to, including the fact that no vaccine approved so far.(only thimerosal/mercury) will contain adjuvants like MF-59 in the U.S.?  In Canada, they are making special provisions for pregnant women to receive a non-adjuvanted vaccine while the rest of the population gets the adjuvanted one. http://www.cbc.ca/health/story/2009/10/16/ontario-pregnant-women-vaccine496.html?ref=rss The Swiss government is doing the same.  German soldiers will receive a different vaccine that contains no mercury or thimerosal- often linked to autism.https://ahrcanum.wordpress.com/2009/10/15/baxter-h1n1-vaccine-celvapan-to-german-soldiers/

The U.S. government has awarded a $487 million contract to Novartis for a plant in North Carolina that will make flu vaccine by growing the virus inside animal cells, preferably from mammals. The plant is expected to be up and running by 2011 or 2012. http://www.nytimes.com/2009/04/29/business/economy/29vaccine.html?_r=2&ref=health

 Also, Protein Sciences Corp. of Meriden, Conn., landed a five-year, $147 million contract to develop a vaccine using its recombinant technology — flu proteins grown in insect cells. The hope is that the first doses would be available within 12 weeks of the beginning of a pandemic. That is about twice as fast as flu vaccine produced from eggs.  Biotechnology company Vical Inc. said Thursday its developing swine flu vaccine prompted “robust” immune responses in 100 percent of animals infected with distinct strains of the virus.  Vical is developing its vaccine under an agreement with the U.S. Navy. It is currently working the U.S. Navy to secure funding in order to advance the vaccine candidate to human studies.http://blog.taragana.com/n/vical-says-its-developing-swine-flu-vaccine-prompts-immune-responses-in-mice-rabbits-164849/

“I think you’re going to see these new technologies come on board rapidly, especially given what’s happened this year,” said Paul Radspinner, president and chief executive of FluGen Inc., a Madison, Wis., company working on several new vaccine technologies of its own.http://blog.taragana.com/n/production-of-swine-flu-vaccine-is-way-behind-schedule-50-year-old-technology-is-blamed-202650/

The U.S. government and scientists are going  buggy!  To think that no one can figure why we are seeing cross species mutations in virus is absolutely asinine based on vaccine technology of intermingling cell species. 

“The only safe vaccine is one that is never used.—-No vaccine can be proven safe before it is given to children.”—statements by the late James A. Shannon, while serving as Director of the US National Institutes of Health.   

Related post https://ahrcanum.wordpress.com/2009/10/12/h1n1-swine-flu-vaccine-grown-in-dog-cells/

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We do not provide medical advice, see your health care practitioner when appropriate. ® logos by respective owners.

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 PD*10352192

image props via http://www.clevelandleader.com/node/10778

Swine flu, the virus of the novel A H1N1 flu strain-the never before seen mixture of viruses typical among pigs, birds and humans now has vaccine and a flu mist drug approval from the U.S. federal government.  The first of the cases of flu were being reported from the outskirts of Mexico City, Mexico in February 2009.  Six months later, the swine vaccines are manufactured, approved and ready for the government mass vaccination programs!

First WHO declared a Phase 6 alert level and the CDC followed suit declaring the H1N1 flu pandemic a public health emergency. This  allowed the FDA to authorize drug companies to fast track experimental vaccines skipping over the usual required testing and clinical studies.

The dirty little secret is that it appears the drug manufacturers may have held patents on the mutated Swine H1N1 Flu vaccine before it ever began its trek across the world.

Novartis of Switzerland is expected to supply nearly half of the vaccines in the U.S. and applied for it’s Swine Flu vaccine patent on November 6, 2006.  The United States Patent and Trademark Office (USPTO) accepted and granted the application,  US 20090047353 for a “Split Influenza Vaccine with Adjuvants” in February 2009, just about the time the flu was beginning to spread.

USPTO Class 424, Drug, bio-affecting and body treating compositions inventions-“Influenza virus strains used in vaccines change from season to season. In the current inter-pandemic period, trivalent vaccines are typical, including two influenza A strains (H1N1 and H3N2) and one influenza B strain. The invention can be used with inter-pandemic strains of this type, but can also be used with viruses from pandemic strains (i.e. strains to which the vaccine recipient and the general human population are immunologically naïve), such as H2, H5, H7 or H9 subtype strains (in particular of influenza A virus), and influenza vaccines for pandemic strains may be monovalent or may, for instance, be based on a normal trivalent vaccine supplemented by a pandemic strain. Depending on the season and on the nature of the antigen included in the vaccine, however, the invention may protect against one or more of influenza A virus HA subtypes H1, H2, H3, H4, H5, H6, H7, H8, H9, H10, H11, H12, H13, H14, H15 or H16. The invention may protect against one or more of influenza A virus NA subtypes N1, N2, N3, N4, N5, N6, N7, N8 or N9….

“For pandemic strains, administration to all age groups is preferred.”

It is a coincidence that a split influenza vaccine is granted its patent just as a split influenza virus is infection thousands?  Is it beyond reason that Novartis could have released the mutated virus as a boon to profitize on the patent?  Is it plausible that Swine Flu did not occur due to a freak in nature?  Why would Novartis suggest that administration of the vaccine is for all age groups and pregnant women?

As to what ingredients is in the approved Swine Flu vaccine-Celtura Novel H1N1 Swine Flu Vaccine Novartis -it is still any one’s guess, although the adjuvant MF59 is in it and numerous tests show adjuvnats cause significant side effects.  MF59 has never been approved by the FDA. Drug ingredients can usually be found herehttp://www.rxlist.com/script/main/srchcont_rxlist.asp?src=swine+flu+vaccinee  but no listings yet on the flu vaccine.

Reuters reported August 5, 2009- http://www.reuters.com/article/pressRelease/idUS112167+05-Aug-2009+MW20090805 that Novartis will be providing 30 million doses of Fluvirin® vaccine in the U.S., to support the annual seasonal influenza vaccination campaign for 2009-2010.  The vaccine contains antigens to the three influenza virus strains for this year’s vaccine recommended by the World Health Organization (WHO):
—  A/Brisbane/59/2007, IVR-148 (H1N1)
—  A/Uruguay/716/2007, NYMC X-175C (H3N2) (an A/Brisbane/10/2007-like
    virus)
—  B/Brisbane/60/2008

CDC’s website for the ingredients of FLUVIRIN® , from Novartis, 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)

We at Ahrcanum are no scientists, but could the Fluvrin vaccine itself help prompt the further mutation of Swine flu: as Novartis notes it’s flu vaccine has not been evaluated for mutagenic potential, let alone fertility?  Why are there still trace amounts of mercury in the ingredients with ties to causing autism and autoimmune diseases? WTF is the Vaginal spermicide Octoxynol 9 -used to prevent conception an ingredient?http://www.drugs.com/mmx/octoxynol-9.html

From Novartis’ own study,

13 NONCLINICAL TOXICOLOGY. 13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility.  FLUVIRIN® has not been evaluated for carcinogenic or mutagenic potential, or for impairment of fertility.http://www.novartis-vaccines.com/downloads/diseases-products/fluvirin_vial_syringe.pdf

  Again from Novartis: https://www.novartisvaccinesdirect.com/Fluvirin/FluvirinAbout

 

 The study also makes reference to H1N1 as early as 1998. see Table 5.

 Important safety information
Serious allergic reactions, including anaphylactic shock, have been observed in people receiving Fluvirin influenza virus vaccine. Fluvirin vaccine should not be administered to individuals with a history of systemic hypersensitivity reaction to eggs or egg proteins or other components of Fluvirin vaccine, including thimerosal, or to anyone who has had a life-threatening reaction to previous influenza vaccination

Baxter International, is not without it’s own vaccination conspiracy,  but it will not be supplying swine flu vaccine to the U.S.  The company “is not able to distribute pandemic vaccine in the U.S., because the U.S. government requires license for a seasonal vaccine first, and Baxter doesn’t currently have that license,” says Chris Bona, a spokesman for Baxter Biosciences.  Baxter is is producing all its H1N1 vaccine at facilities in Austria and the Czech Republic. They applied for a US Vaccine Patent Application US 2009/0060950 A1 FILED AUGUST 28, 2007.  TWO YEARS BEFORE SWINE FLU.

”Baxter sent vaccines contaminated with deadly live H5N1 avian flu virus to 18 countries (including the Czech Rep)before someone caught the mistake and the vaccine got injected thousands of people.   Baxter just missed creating its own pandemic then by mixing  deadly H5N1 virus with a mix of H3N2 seasonal flu viruses, or did they?  By possibly creating the pandemic, maybe Baxter already has the cure and that is why WHO has deemed them the appropriate pharmaceutical company to lead the way for a swine flu vaccine. https://ahrcanum.wordpress.com/2009/07/23/baxter-vaccine-patent-h1n1/

We happened upon  the World’s Most Ethical Companies list done annually by Ethisphere. http://ethisphere.com/wme2009/  This year, 99 companies made the cut including:

AstraZeneca  UK/Sweden • Pharma & Biotech

Novo Nordisk Denmark • Pharma & Biotech

Novartis Switzerland • Pharma & Biotech

Novozymes Denmark • Pharma & Biotech

Baxter International USA • Medical Devices

Disclaimer-Swine Flu Conspiracy theories can sometimes be triggered by real world events.

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Open wide, say ahhh and check out these posts on the A/H1N1 Swine Flu from Ahrcanum, where the conspiracy spreads as fast as the virus itself.

https://ahrcanum.wordpress.com/swine-flu-report/

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In case you missed it…scientists are exhuming bodies from 1919 and the outbreak of the Spanish Flu.  

The body of an aristocrat who died nearly 90 years ago has been exhumed in the hope that it will help scientists combat a future flu pandemic. http://news.bbc.co.uk/2/hi/uk_news/england/humber/7617968.stm

WHO and most countries declared a pandemic and state of emergency thanks to the novel H1N1 Swine Flu months ago.  The future pandemic they would have us believe in is now.  Finality will decide if it is the vaccine or the virus that kills more.

What else are they going to dig up?  The truth?

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Open wide, say ahhh and check out these posts on the A/H1N1 Swine Flu from Ahrcanum, where the conspiracy spreads as fast as the virus itself.

https://ahrcanum.wordpress.com/swine-flu-report/

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How dare they? 

The U.S. health officials approved vaccines from four drug makers to help prevent the H1N1 swine flu, ensuring there will be enough to inoculate Americans who want the protection. http://www.reuters.com/article/domesticNews/idUSTRE58E6D720090915 

Conclusions In preliminary analyses, the monovalent influenza A (H1N1) 2009 MF59-adjuvanted vaccine generates antibody responses likely to be associated with protection within 14 days after a single dose is administered. (ClinicalTrials.gov number, NCT00943358 [ClinicalTrials.gov] .) and at http://content.nejm.org/cgi/content/full/NEJMoa0907650

Seeing as we spent millions buying something that didn’t exist, is there any wonder the vaccines got aproved?

There will be vaccines for everyone,” said Sebelius at a hearing of the U.S. House of Representatives Energy and Commerce Committee.

Yipee.  The U.S. Food and Drug Administration approved vaccines from Sanofi-Aventis SA, CSL Ltd, Medimmune and Novartis AG forSwine H1N1 strain of influenza.  The MedImmune vaccine is the swine flu version of FluMist, which is a nasal spray. The other three vaccines are traditional flu shots. Novartis is expected to supply nearly half of the U.S. supply calling the vaccine Celtura.

FDA approval was expected claiming the vaccines are made the same way as seasonal flu vaccines. The FDA has previously said it considers the swine flu vaccine merely a strain change from the seasonal flu vaccine, avoiding the lengthy approval process that new vaccines must go through.http://www.webmd.com/cold-and-flu/news/20090915/swine-flu-vaccines-get-fda-nod?src=RSS_PUBLIC

Apparently neither the FDA nor any other governmental acronym for BS aka Bull $hit, does not take offense at the use of adjuvants that had not been approved for human use until the declaration of emergency.  The FDA  now permits adjuvant use in the approved Swine Flu Vaccine and adjuvant MF59 is apparently in the vaccine from Novartis.  With suspicions of ties to causing autoimmune disorders, these fine squalene ingredients can be found in the Swine Flu Vaccines now approved by the FDA and being paid for with your tax dollars.

Glaxo Smith Kline’s  (NYSE: GSK)  previously accepted orders of FLUARIX® (Influenza Virus Vaccine) for the 2008-2009 influenza season through the company’s direct ordering Web site, www.GSKvaccinesdirect.com, but has apparently been left out of this year’s Swine Flu approval of vaccines- at least so far.

Preparations for influenza A (H1N1) 2009 vaccination programs are under way, but the optimal formulation is unknown. http://content.nejm.org/cgi/content/full/NEJMoa0907650

Sebelius also said that no additional treatments are expected to be necessary to help boost the vaccine.”There are some back up plans if things took a terrible turn for the worse,” she said. 

Since she did not expand on back up plans if things took a terrible turn for the worse with the approved Swine H1N1 Flu vaccine –antenna are UP!  Quarantines, Forced Vaccinations, Fema Camps, Border Closures, Martial Law, New World Order, etc?   Just what are the back up plans that the U.S. government, big pharma, and the health care industry have in store for us? What a perfect time for health care reform!

Sourced from  http://thebirdflupandemic.com/archives/german-swine-flu-vaccine-trial-participant-coughs-up-blood A participant in German swine flu vaccine trials has come forward with startling allegations that he experienced serious adverse side effects after taking the swine flu vaccine – including coughing up blood. …The original German article containing Axel’s story here (it is in German though):http://www.merkur-online.de/nachrichten/muenchen/schweinegrippe-impfung-testpatient-packt-meta-451084.html  Hit the translate button on Ahrcanum side bar topside for translation.

Some swine flu patients are still infected with H1N1 virus that they can transmit to other people eight to 10 days after their symptoms strike, researchers say. The finding suggests that the CDC’s recommendation for people with flu-like illness to avoid others until at least 24 hours after they are free of fever may not go far enough.“Three days after your fever subsides, you’re probably still contagious with H1N1 [swine] flu,” says Gaston De Serres, MD, PhD, a medical epidemiologist at the National Institute of Public Health in Quebec.  De Serres tells WebMD that it’s not yet known exactly when it is safe to go back to school or work. “But a couple of days [after symptoms strike] is likely to be insufficient. You’re probably contagious for about a week.”  http://www.webmd.com/cold-and-flu/news/20090915/swine-flu-how-long-are-you-infectious

As if the threat of Swine Flu isn’t enough- “An analysis of 50 shower heads from nine U.S. cities found that about 30 percent harbored high levels of Mycobacterium avium — a group of bacteria that can cause lung infections when inhaled or swallowed. Researchers from the University of Colorado at Boulder found the levels of Mycobacterium avium were 100 times higher than those found in typical household water.  http://www.reuters.com/article/lifestyleMolt/idUSTRE58E03U20090915

The biggest threat from Swine Flu?  Drowning. “Tests on about 100 Americans who died from swine flu virus found that they had infections deep in their lungs, which caused acute respiratory distress syndrome. Often fatal, it fills the air sacs with fluid, starves the blood of oxygen and leaves patients gasping for breath. Basically, patients suffocate or drown”http://blogs.usatoday.com/ondeadline/2009/09/cdc-swine-flu-causing-deadly-lung-infections-like-avian-virus.html?csp=34 

Sheessh, you might survive the flu, the vaccine and finally feel better,,,, enough to take a shower and you get something other bacteria that will kill you.

The Youtube video featuring a Dr. Marc Girard condemns the swine flu vaccine as ‘badly developed’. Declaring ‘on French TV that the “swine flu” vaccine could cause 60,000 deaths in France, especially among young people, children and pregnant women. It’s in French and translates to you are fukced and here at  http://bimchat.wordpress.com/2009/09/15/breakdown-of-swine-flu-vaccine/ 

“A vaccine is being developed in conditions of amateurism such as I have never seen. Lets take the pessimistic hypothesis: one death among every 1000 patients. There are plans to vaccinate 60 million people, and you so you already have 60,000 deaths, and this time, young people, children, pregnant women.”“What you are saying is serious because many people are getting ready to get the vaccine and you, you are saying, You must not get a vaccination!”

…”some patients with swine flu (h1n1) virus tend to suffer worse symptoms compared to those with a normal seasonal flu. http://www.swinefluheadlines.com/2009/09/how-swine-flu-works-it-infects-cells-deep-in-the-lungs/ 

No shit sherlock?

Stay dirty and stay the hell away.

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Open wide, say ahhh and check out these posts on the A/H1N1 Swine Flu from Ahrcanum where the conspiracy spreads as fast as the virus itself.

https://ahrcanum.wordpress.com/swine-flu-report/

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