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Posts Tagged ‘flu shot’

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Scientists to create mutant form of new bird flu virus to work out risk of it causing a deadly human pandemic
Deadly forms of H7N9 will be made in high security labs around the world
New bird virus has already infected at least 133 people in China and Taiwan
Forty-three people have died according to World Health Organisation
Scientists said it is vital to prepare for a lethal human pandemic

Bullsh*t

What a load of crap. The h1n1 swine flu virus was discovered near a lab in Mexico. Coincidence?

How about the missing vials of lord knows what, bc they don’t from Ft. Detrick. Recall it was the plague and missing animals and vials.

Bad idea people. Just wait til WHO ask you to get a vaccine for a flu that never existed until it was made in a lab.

Ck the tab above header for more info on the flu. Stay healthy friends and for heavens sake – could you wash your hands after using the bathroom?

August 8, 2013
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Novartis has begun shipments of  Fluvirin, the seasonal influenza vaccine in the United States for the 2012-2013 influenza season.

Vaccine yes_no

What are the Fluvirin Flu Vaccine Ingredients? Here is the package insert so you can view the cocktail list for yourself. http://www.fda.gov/downloads/BiologicsBloodVaccines/Vaccines/ApprovedProducts/ucm123694.pdf

FLUVIRIN® is a trivalent, sub-unit (purified surface antigen) influenza virus vaccine prepared from virus propagated in the allantoic cavity of embryonated hens’ eggs inoculated with a specific type of influenza virus suspension containing neomycin and polymyxin.” (aka antibiotics)

It is designed for protection of the following viruses:

A/Christchurch/16/2010, NIB-74 (H1N1) (an A/California/7/2009-like virus)

 A/Victoria/361/2011, IVR-165 (H3N2)

 B/ Hubei-Wujiagang/158/2009, NYMC BX-39 (a B/Wisconsin/1/2010-like virus).

It contains some trace of thimerosal, a mercury derivative.

“Each dose from the multidose vial or from the prefilled syringe may also contain residual amounts of egg proteins.,,”  Chick Embryonic Fluid is a foreign animal proteins and genetic information injected into the human body.  We’re not scientists but as we understand it, you are getting chicken DNA- is that better than the flu?

2011 Biosecurity for Birds Calendar

CLUCK. CLUCK.

…”1 mcg ovalbumin), polymyxin (3.75 mcg), neomycin (2.5 mcg), betapropiolactone (not more than 0.5 mcg) and nonylphenol ethoxylate (not more than 0.015% w/v).

The U.S. EPA says, http://www.epa.gov/ttn/atw/hlthef/propiola.html

Acute (short-term) inhalation exposure to beta-propiolactone causes severe irritation of the eyes, nose, throat, and respiratory tract in humans.  Acute dermal exposure may cause irritation of the skin, blistering, or burns in humans.  Contact with the eyes may cause permanent corneal opacification.  Burns of the mouth and stomach may occur in humans following acute exposure via ingestion.  No information is available on the chronic (long-term), reproductive, developmental, or carcinogenic effects of beta-propiolactone in humans.  Squamous cell carcinomas of the forestomach have been reported in orally exposed rats.  In dermally exposed rodents, skin tumors have been observed.  The International Agency for Research on Cancer (IARC) has classified beta-propiolactone as a Group 2B, possible human carcinogen.

PHILADELPHIA, July 31, 2012 /PRNewswire/ — GlaxoSmithKline [NYSE: GSK] announced today it has begun shipping the first lots of 2012-2013 FluLaval®(Influenza virus vaccine) and Fluarix® (Influenza Virus Vaccine) to CDC distribution centers and U.S. healthcare providers. This follows approval of this season’s GSK seasonal influenza vaccines by the U.S. Food and Drug Administration’s Center for Biologics Evaluation and Research.
PR Newswire (http://s.tt/1jyay)
 
Can’t seem to find the ingredient list for 2012-2013 so here’s last years data-

050126_MB_ChickenArt.jpg

Not to be left out of the zillion dollar industry

SWIFTWATER, Pa., July 9, 2012 /PRNewswire via COMTEX/ — Sanofi Pasteur, the vaccines division of Sanofi , announced today that the first lots of Fluzone vaccine began shipping to U.S. health care providers following Food and Drug Administration (FDA) licensure of the 2012-2013 formulation. This initial shipment represents the first of more than 60 million doses of seasonal influenza vaccine the company plans to deliver to health care providers in the U.S. this influenza season. http://www.marketwatch.com/story/sanofi-pasteur-begins-shipping-fluzone-influenza-virus-vaccine-in-us-for-2012-2013-season-2012-07-16?reflink=MW_news_stmp

And the ingredient list for Fluzone- Formaldehyde and http://www.rxlist.com/fluzone-drug.htm 

 

Ingredient Quantity (perdose)
Fluzone 0.25 mL Dose Fluzone 0.5 mL Dose Fluzone High-Dose 0.5 mL Dose Fluzone Intradermal 0.1 mL Dose
Active Substance: Split influenza virus, inactivated strainsa: 22.5 mcg HA total 45 mcg HA total 180 mcg HA total 27 mcg HA total
A (H1N1) 7.5 mcg HA 15 mcg HA 60 mcg HA 9 mcg HA
A (H3N2) 7.5 mcg HA 15 mcg HA 60 mcg HA 9 mcg HA
B 7.5 mcg HA 15 mcg HA 60 mcg HA 9 mcg HA
Other:
Sodium phosphate-buffered isotonic sodium chloride solution QSb to appropriate volume QSb to appropriate volume QSb to appropriate volume QSb to appropriate volume
Formaldehyde ≤ 50 mcg ≤ 100 mcg ≤ 100 mcg ≤ 20 mcg
Octylphenol Ethoxylate ≤ 75 mcg ≤ 150 mcg ≤ 250 mcg ≤ 50 mcg
Gelatin 0.05% 0.05% None None
Preservative
Single-Dose Presentations None None None None
Multi-Dose Presentation (Thimerosal) N/A 25 mcg mercury N/A N/A
a per United States Public Health Service (USPHS) requirement.
b Quantity Sufficient.
N/A not applicable

CLUCK. CLUCK.

While humans are not ideal hosts for H5N1, bird flu viruses do sometimes manage to adapt for easy transmission from human to human, and the results can be devastating. In 1918, one such transformation led to the Spanish flu pandemic, a global outbreak that claimed an estimated 50 million people.

To better understand the possibility of H5N1 making a similar transformation, two teams of scientists recently manipulated the virus until it could spread through the air from one ferret to another. If a flu virus can infect a ferret, then it could theoretically infect other mammals, including humans. http://www.nytimes.com/2012/06/26/science/the-evolution-of-bird-flu-and-the-race-to-keep-up.html?pagewanted=all

Getting back to the eggs.

Avian influenza (AI)–the bird flu–is a virus that infects wild birds (such as ducks, gulls, and shorebirds) and domestic poultry (such as chickens, turkeys, ducks, and geese). There is a flu for birds just as there is for humans and, as with people, some forms of the flu are worse than others.

From the FDA-http://www.fda.gov/Food/ResourcesForYou/Consumers/ucm085550.htm

“AI is primarily spread by direct contact between healthy birds and infected birds, and through indirect contact with contaminated equipment and materials. The virus is excreted through the feces of infected birds and through secretions from the nose, mouth and eyes.

Contact with infected fecal material is the most common of bird-to-bird transmission. Wild ducks often introduce LPAI into domestic flocks raised on range or in open flight pens through fecal contamination. Within a poultry house, transfer of an HPAI virus between birds also can occur via airborne secretions. The spread of avian influenza between poultry premises almost always follows the movement of contaminated people and equipment.

AI also can be found on the outer surfaces of egg shells and in the case of HPAI, can infect the inside of the egg which includes the yolk and albumen or the egg white. Transfer to eggs is a potential means of AI transmission. Airborne transmission of virus from farm to farm is highly unlikely under usual circumstances.

HPAI can be spread from birds to people as a result of extensive direct contact with infected birds. Broad concerns about public health relate to the potential for the HPAI virus, such as the HPAI H5N1, to mutate, or change into a form that could spread easily from person to person. The U.S. Department of Health and Human Services is aggressively working to ensure public health is protected.”

CLUCK. CLUCK.

To address the variability in the egg supply, Sanofi Pasteur restructured its flock management so that embryonated eggs would be available to support vaccine production at full capacity throughout the year. Because embryonated eggs are themselves potentially susceptible to avian influenza, flocks associated with vaccine production are under strict contract and must be completely housed, monitored by veterinarians, and raised under biosecurity regulations. With government support, Sanofi Pasteur has also established contingency flocks as a backup against avian influenza and other risks. http://www.nae.edu/Publications/Bridge/EngineeringandVaccineProductionforanInfluenzaPandemic/Egg-BasedProductionofInfluenzaVaccine30YearsofCommercialExperience.aspx

Biosecurity chickens. Who’d have thought? Yup-  Not much security if u ask us. http://www.aphis.usda.gov/animal_health/birdbiosecurity/biosecurity/

Product names are registered trademarks of respective owners.

This article, “Flu Shot Vaccine Ingredients 2012-2013,”  is not medical advice. Educate yourself so that in making a decision where you or your child is concerned, you should take an active role in learning. http://www.anh-usa.org/main-menu/resources/position-papers/862/ and the U.S. Government at http://www.cdc.gov/flu/about/season/flu-season-2012-2013.htm#us-vaccine

Smiling is infectious, you can catch it like the flu. Someone smiled at me today, And I started smiling too.

And the number one post in our Flu Section is about an associated rash from either the flu or the vaccine. https://ahrcanum.wordpress.com/2009/10/19/swine-flu-rash-hives-symptoms/

Stay tuned and have a good day, one day it will be your last.  God Bless.

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The Swine Flu Report that began in April 2009 is at https://ahrcanum.wordpress.com/swine-flu-report

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RECALLED

MedImmune announced it is recalling it’s Nasal Spray vaccine, Flu Mist designed to maybe, prevent Swine Flu.  

“Nearly five million doses of an H1N1 swine flu vaccine were recalled today because the strength of the nasal sprays may have decreased over time and they may not be as potent as they are supposed to be, the Food and Drug Administration said. Only about 3,000 of the recalled vaccine doses produced by the MedImmune unit of drug maker AstraZeneca are believed to still be in circulation or storage. The vast majority were administered to patients in October and November, at the peak of the H1N1 vaccination process, according to a Reuters news report.” via http://www.attorneyatlaw.com/2009/12/millions-of-h1n1-vaccine-doses-recalled-due-to-potency-problem/ 

MedImmune has released a pdf with the lot numbers and additional information at http://www.attorneyatlaw.com/2009/12/millions-of-h1n1-vaccine-doses-recalled-due-to-potency-problem/

That’s millions of people who inhaled the live swine flu virus and it probably doesn’t offer any protection at all.  Want to know what else they inhaled and then breathed out on an unsuspecting population? http://www.fda.gov/downloads/BiologicsBloodVaccines/Vaccines/ApprovedProducts/UCM182406.pdf

Each pre-filled refrigerated Influenza A (H1N1) 2009 Monovalent Vaccine Live, Intranasal sprayer contains a single 0.2 mL dose. Each 0.2 mL dose contains 106.5-7.5 FFU of the live attenuated influenza virus reassortant of the pandemic (H1N1) 2009 virus: A/California/7/2009 (H1N1)v. Each 0.2 mL dose also contains 0.188 mg/dose monosodium glutamate, 2.00 mg/dose hydrolyzed porcine gelatin, 2.42 mg/dose arginine, 13.68 mg/dose sucrose, 2.26 mg/dose dibasic potassium phosphate, 0.96 mg/dose monobasic potassium phosphate, and <0.015 mcg/mL gentamicin sulfate. The vaccine contains no preservatives. 

Also on the patient insert- The following adverse reactions have been identified during postapproval use of FluMist. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to vaccine exposure. Congenital, familial and genetic disorder: Exacerbation of symptoms of mitochondrial encephalomyopathy (Leigh syndrome). Gastrointestinal disorders: Nausea, vomiting, diarrhea
Immune system disorders: Hypersensitivity reactions (including anaphylactic reaction, facial edema and urticaria)

Nervous system disorders: Guillain-Barré syndrome, Bell’s Palsy

Respiratory, thoracic and mediastinal disorders: Epistaxis

Skin and subcutaneous tissue disorders: Rash

Our most visited page on the Ahrcanum site is all about the Swine Flu Rash!  https://ahrcanum.wordpress.com/2009/10/19/swine-flu-rash-hives-symptoms/

Last week CDC announced that nearly one million does of H1N1 Swine Flu Vaccines intended for children were being recalled that were manufactured by Sanofi Pasteur, Inc..  http://www.cdc.gov/h1n1flu/vaccination/syringes_qa.htm    

“Despite the recall, the vaccine is safe and effective; parents need not worry about unusual side effects or having their children re-vaccinated,” says Anne Schuchat, director of the Centers for Disease Control and Prevention’s Center for Immunization and Respiratory Diseases. “There’s no need for parents to call pediatricians. We think the doses given are protective and safe,” she says. http://www.usatoday.com/news/health/2009-12-15-swine-flu-vaccine_N.htm       

“We think?,” she said, We think she hasn’t a clue and neither does anyone else about these fast tracked Swine Flu vaccines.  Our take on that recall is at https://ahrcanum.wordpress.com/2009/12/16/h1n1-swine-flu-vaccine-for-children-recalled/  In November, we wrote about the Canadian Vaccine Recall from GlaxoSmith Kline at https://ahrcanum.wordpress.com/2009/11/25/h1n1-swine-flu-vaccine-pandemrix-recall/  

Will the third time be the charm that changes people’s mind about getting the Swine Flu Shot or Nasal Spray now that is it generally available to the public? 

Anyone taking bets that this is not the last of the Swine Flu Vaccine recalls?

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Our most precious of resources for the future is our children.  It will be their dreams that may will solve the numerous maladies affecting mankind.  From exploring space, to exploring Earth’s own oceans, to just maybe finding a cure against diseases like cancers and viruses like the flu.  It is our children who are exposed to a myriad of vaccines that are so toxic, they should be labeled hazardous materials.   

Say nothing of the suspected links to auto-immune disorders, almost all world governments and health organizations are advocating children receive the H1N1 Swine Flu Shot, even though little clinical testing has been done on them.  You’ll recall, “Shut up and just get your damned flu shot.”      

   

 Yesterday, the CDC announced that nearly one million does of H1N1 Swine Flu Vaccines intended for children are being recalled that were manufactured by Sanofi Pasteur, Inc..  http://www.cdc.gov/h1n1flu/vaccination/syringes_qa.htm    

“Despite the recall, the vaccine is safe and effective; parents need not worry about unusual side effects or having their children re-vaccinated,” says Anne Schuchat, director of the Centers for Disease Control and Prevention’s Center for Immunization and Respiratory Diseases. “There’s no need for parents to call pediatricians. We think the doses given are protective and safe,” she says. http://www.usatoday.com/news/health/2009-12-15-swine-flu-vaccine_N.htm      

 The U.S. Government has evaluated only these vaccines that are licensed by the U.S. Food and Drug Administration. They are, with patient information links:       

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

Influenza A (H1N1) 2009 Monovalent Vaccine (Novartis Vaccines and Diagnostics Limited) gttp://www.fda.gov/BiologicsBloodVaccines/Vaccines/ApprovedProducts/ucm181973.htm   

Influenza A (H1N1) 2009 Monovalent Vaccine (Sanofi Pasteur,Inc.)http://www.fda.gov/BiologicsBloodVaccines/Vaccines/ApprovedProducts/ucm181971.htm  Recalled lots!     

Influenza A (H1N1) 2009 Monovalent Vaccine (MedImmune LLC) http://www.fda.gov/BiologicsBloodVaccines/Vaccines/ApprovedProducts/ucm181970.htm      

 Influenza A (H1N1) 2009 Monovalent Vaccine (ID Biomentical) Influenza A (H1N1) 2009 Monovalent Vaccine (ID Biomedical Corporation of Quebec) and owned GlaxoSmithKline PLC     

On December 7, Sanofi Pasteur notified CDC and FDA that the potency in one batch (called a “lot”) of pediatric syringes that had been distributed was later found to have dropped below a pre-specified limit. As a result of this finding, Sanofi Pasteur tested additional lots and found that three other lots that had been distributed also had an antigen content that, while properly filled at the time of manufacturing, was later measured to be below pre-specified limits.    

For eight additional days, children were still receiving the flawed vaccine.  The Beatles sang “Eight days a week, I love love love you,” I see no love from the CDC in waiting eight days to begin a recall.    Pasteur’s approval was based on it’s Fluzone approved seasonal flu vaccine that was studied in all of 19 children according to their own patient insert on page 7. – link provided above-   

Ingredients on page 11- Influenza A (H1N1) 2009 Monovalent Vaccine, an inactivated influenza virus vaccine, for intramuscular use, is prepared from influenza viruses propagated in embryonated chicken eggs. The virus-containing allantoic fluid is harvested and inactivated with formaldehyde. Influenza virus is concentrated and purified in a linear sucrose density gradient solution using a continuous flow centrifuge. The virus is then chemically disrupted using a non-ionic surfactant, polyethylene glycol p-isooctylphenyl ether (Triton ® X-100), producing a “split virus”. The split virus is further purified and then suspended in sodium phosphate-buffered isotonic sodium chloride solution    

Influenza A (H1N1) 2009 Monovalent Vaccine is formulated to contain 15 mcg hemagglutinin (HA) of influenza A/California/07/2009 (H1N1) v-like virus per 0.5 mL dose. Gelatin 0.05% is added as a stabilizer. Each 0.5 mL dose may contain residual amounts of formaldehyde (not more than 100 mcg), polyethylene glycol p-isooctylphenyl ether (not more than 0.02%), and sucrose (not more than 2.0%).    

There is no thimerosal used in the manufacturing process of the single-dose presentations of Influenza A (H1N1) 2009 Monovalent Vaccine. The multi-dose presentation of Influenza A (H1N1) 2009 Monovalent Vaccine contains thimerosal, a mercury derivative, added as a preservative. Each 0.5 mL dose of the multidose presentation contains 25 mcg mercury   

Pregnancy Category C, found on page 10 : Animal reproduction studies have not been conducted with Influenza A (H1N1) 2009 Monovalent Vaccine or Fluzone vaccine. 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.    

Some doctors around the world have managed to draw attention to these untested vaccines.  In Israel one doctor wrote- “The combination of squalene and polysorbate 80 in a buffered solution has been shown to be an excellent anti-fertility combination, in anti-fertility research performed by scientists for the W.H.O., who were assigned the job of developing anti-fertility vaccines to reduce world population. Giving these vaccines to our young population is tantamount to sterilizing them.”  http://www.theflucase.com/index.php?option=com_content&view=article&id=1611%3Adoctors-protest-israels-decision-to-give-toxic-focetria-and-pandemrix-jabs-to-people&catid=1%3Alatest-news&Itemid=64&lang=en  Offering supporting evidence- (Fertility Impairing Vaccine And Methods of Use’ This application claims the benefit of U. S. Provisional Application No. 60/070,375, filed January 2,1998, U. S. Provisional Application No. 60/071,406, filed January 15,1998).    

Similar statements can be found regarding CSL’s AFLURIA, and Norvartis’ FLUVIRIN and are recapped in a previous post at https://ahrcanum.wordpress.com/2009/09/27/h1n1-swine-flu-vaccine-package-insert-warnings/   

In the U.K., they too are unsure of just how many shots is necessary – 

In line with adults children will be given just one dose of the vaccine, rather than the two that was originally thought might be necessary for younger age groups. However, preliminary data from two newly released trials published in the Lancet suggest that a single vaccine may not offer children sufficient immunity against the virus. Since the pandemic began earlier this year 17 children under five have died after contracting swine flu, as well as 266 older children and adults. Tests on versions of the vaccine produced by nine different manufacturers show that some offered protection to as few as 45 per cent of children under three. http://www.telegraph.co.uk/health/swine-flu/6817459/Swine-flu-giving-young-children-one-dose-of-vaccine-may-not-protect-them.html       

 In November, we wrote about a Canadian Vaccine Recall from GlaxoSmith Kline at https://ahrcanum.wordpress.com/2009/11/25/h1n1-swine-flu-vaccine-pandemrix-recall/ :       

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.       

The Political Jungle summed it up nicely at  http://takeastandagainstliberals.blogspot.com/2009/12/swine-flu-vaccine-recall.html “Already used and they have no idea why the vaccine changed, or lost potency. No clue. What else do they have no clue about?”       

At least the expired Tamiflu for Oral Suspension hasn’t lost it’s potency!  Back up to July2009, The FDA authorized 4 lots of Tamiflu for Oral Suspension for use beyond their labeled expiration dates. FDA is now authorizing additional lots in an effort to ensure that Tamiflu for Oral Suspension is available for patients during this public health emergency. The lots of Tamiflu for Oral Suspension that are being authorized are part of the Strategic National Stockpile and have been tested through the federal government’s Shelf-Life Extension Program (SLEP). http://www.fda.gov/Drugs/DrugSafety/PostmarketDrugSafetyInformationforPatientsandProviders/DrugSafetyInformationforHeathcareProfessionals/ucm184770.htm       

From cases of anaphylactic shock and low potency levels, this recall is another setback for vaccine manufacturers who continue to profess that their products are safe, even as they have been given full immunity from prosecution in the U.S. Perhaps these recalls will have the advantage to educate and warn parents not to vaccinate in the first place.    

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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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In it’s infinite wisdom,  The U.S. Food and Drug Administration (FDA) approved yet another seasonal flu vaccine on Friday, November 27, 2009. Agriflu, manufactured by Novartis Vaccines and Diagnostics in Siena, Italy, was approved for people ages 18 years and older to prevent the seasonal flu (influenza virus subtypes A and B). It is not effective against the H1N1 Swine flu.  The approval of the new seasonal influenza vaccine, Agriflu, is an important step in adding to the production capacity to enhance the supply of vaccine for the United States for future influenza seasons,” said Karen Midthun, M.D., acting director of the FDA’s Center for Biologics Evaluation and Research.http://www.examiner.com/x-9696-SF-Senior-Care-Examiner~y2009m11d28-New-seasonal-flu-vaccine-approved-Agriflu

The symptoms of H1N1 are similar to those of regular seasonal flu. Virtually all the flu now in this country is H1N1 and not the seasonal flu, although there are other flu-like viruses that cause many illnesses.  Nationally, in the first six months since the arrival of H1N1, an estimated 22 million Americans became ill with H1N1, 98,000 were hospitalized, and 3,900 died, said Dr. Anne Schuchat, director of the National Center for Immunization and Respiratory Disease. via http://www.buffalonews.com/home/story/859656.html

Whether it is caving to pharmaceutical pressure or what, America now has Agriflu added to its list of acceptable vaccines, further opening the door to allow Novartis to produce variated swine flu or some other pandemic vaccine in the future.  The U.S. requires that H1N1 manufacturers be licensed for the seasonal flu first- which is why Baxter Pharmaceutical and others were not permitted to have access to millions of patients in America.  Seeing as there is no seasonal flu so to speak of, my antenna are up.

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.  Celtura is the Novel H1N1 Swine Flu Vaccine produced by Novartis. For more on the patent conspiracy https://ahrcanum.wordpress.com/2009/09/18/swine-flu-vaccine-patent-conspiracy/

Here is the patient insert for Novartis Agriflu http://www.fda.gov/downloads/BiologicsBloodVaccines/Vaccines/ApprovedProducts/UCM192127.pdf with the usual toxic ingredients.  Although manufactured and formulated without thimerosal, it contains

Each 0.5 mL dose may contain residual amounts of egg proteins (<0.4 mcg), formaldehyde (10 mcg), polysorbate 80 (50 mcg), and CTAB (12 mcg). Each dose may also contain residual amounts of neomycin (0.02 mcg by calculation) and kanamycin (0.03 mcg by calculation), which are used during the initial stages of manufacture.

13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility AGRIFLU has not been evaluated for carcinogenic or mutagenic potential, or for impairment of male fertility.

Deranged w/ Swine? Buy This $5,000 Chair!

Male Fertility?  OMG, Fall out of your chair here, as no other patient insert that I have read has even bothered to mention male fertility.  If any reader finds one- post it it the comment section, please.   The document goes on with the usual and notes that there are, ” no adequate and well-controlled studies in pregnant women. Because animal reproduction studies are not always predictive of human response, AGRIFLU should be given to a pregnant woman only if clearly needed.”

If you are one of the sleeping sheeples who has no idea what Polysorbate 80 is, time to wakie upie and backtrack to this post- https://ahrcanum.wordpress.com/2009/10/28/gardasil-vaccine-doesnt-work-contains-tween-80/ that highlights in plain English, polysorbate 80 can affect your immune system and cause severe anaphylactic shock which can kill.  The study included a pregnant woman who suffered anaphylactic shock after being given a IV drip of multi-vitamins containing polysorbate 80. http://infertility.suite101.com/article.cfm/polysorbate_80_causes_infertility

Do you see a pattern as to why AGRIFLU and numerous other vaccines have not been recommended for pregnant women?  Yet, the CDC has pregnant women in the front of the line to recieve seasonal and H1N1 vaccines!

 The 2009-2010 seasonal influenza vaccine is available for use in the United States and through six brand names and manufacturers:  http://www.fda.gov/ForConsumers/ConsumerUpdates/ucm100139.htm

• Afluria, by CSL Limited
• Fluarix, by GlaxoSmithKline Biologicals
• FluLaval, by ID Biomedical Corp of Quebec.
• Fluvirin, by Novartis Vaccines and Diagnostics Limited
• Fluzone, by Sanofi Pasteur Inc.
• FluMist, by MedImmune, LLC

 The vaccine for 2009-2010 seasonal influenza contains the following:

 • an A/Brisbane/59/2007 (H1N1)-like virus
• an A/Brisbane/10/2007 (H3N2)-like virus
• a B/Brisbane/60/2008-like virus

I take exception to the use of the term LIKE VIRUS.  LIKE WHAT THE F**k U TALKING ABOUT?  Which one of the “like viruses” would be nice to be identified to the citizens of the U.S. on behalf of it’s govenernment, don’t ya think?  Why would two year old viruses still be the most prevelent in these vaccines when since April we’ve all known H1N1 was going to do the most damage?

The FDA announced the formation of a Transparency Task Force to recommend ways to improve the openness and transparency of the agency’s information. This will help make useful and understandable information about FDA activities and decision making more readily available. http://www.fda.gov/ForConsumers/ConsumerUpdates/ucm163900.htm.  Once again the transparency of a  H1N1 like virus that won’t protect you from the H1N1 virus becomes victim to the obscenity of authorizing yet another vaccine laden with toxins into the population.

Centers for Disease Control and Prevention (CDC) on November 30th on cases of H1N1 symptoms show that the spread of the virus has definitely peaked, and seems to be on the decline.  The report is current through Week 46, November 15-21, 2009. via http://www.examiner.com/x-18331-Natural-Health-Examiner~y2009m11d30-H1N1-Swine-Flu-symptoms-peaked–on-decline-CDC-statistics-update-11302009.

What remains to peak my imagination are the increasing numbers of Hemmoragic Pneumonia, rising death rates, and why the imperfect timing of approving a seasonal flu vaccine, when there is no seasonal flu?

 Your thoughts?

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Baxter Pharmaceutical, makers of H1N1 Swine Flu Vaccines has admitted that they were involved with contaminating vaccines, a Polish television station has reported.  In May 2009, we reported:

Baxter sent vaccines contaminated with deadly live H5N1 avian flu virus to 18 countries 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.  Keep in mind- Just 50 miles from the H1N1 ground zero outbreak in Mexico City, lies Baxter’s manufacturing plant in Cuernavaca, Mexico. https://ahrcanum.wordpress.com/2009/05/05/baxter-pharmaceutical-plant-in-mexico-ground-zero-for-flu-outbreak

Is the H1N1 Swine Flu the excuse that pharmaceutical companies needed to sell vaccines that were patented well before the outbreak occurred?  Like Sarah Palin, we might say, “You Betcha.”  The rush for approval based on previous manufacturing process is nothing short of a ploy for the probability that it is a weapon for population reduction.  Targeting pregnant women and young children first, they are being injected with toxic laden chemicals including spermicides to inhibit future fertility.  

In Eastern Europe, Ukraine has reacted to H1N1 by closing all schools for three weeks and banning public events and closing cinemas across the country. The bans may continue into 2010. https://ahrcanum.wordpress.com/2009/11/01/swine-flu-quarantine-in-ukraine-border-closed/  In four months national elections in Ukraine are due.  Among rival candidates are Prime Minister Yulia Tymoshenko and her chief rival, Arseniy Yatseniuk.  Will voting be delayed as well?

Not only is the Ukrainian government apparently using fears of Swine Flu pandemic to change the domestic political calculus, and President Barack Obama using the fears to impose an unnecessary state of emergency. Now it comes out that the responsible German health authorities are caught in a corrupt conflict of interest with the very pharma giants profiting from government decisions on “anti-swine flu” vaccines- via blogger Tamiflu Stop Flu at http://digg.com/d319v7g.

Baxter Pharmaceutical Company has been approved to provide upwards of 250,000 doses of Celvapan, a different H1N1 Swine Flu vaccine for German soldiers than German citizens. https://ahrcanum.wordpress.com/2009/10/15/baxter-h1n1-vaccine-celvapan-to-german-soldiers/

…the more compatible vaccine for the soldiers will not contain any contended additives nor will it contain any mercury preservatives, has been reported by the Bielefelder “Westfalen-Blatt” under reference to military sources. Its about the Serum Celvapan manufactured by Baxter, original source in German http://de.news.yahoo.com/2/20091012/tts-soldaten-bekommen-angeblich-besonder-c1b2fc3.html  and highlighted by 
http://www.fightbackh1n1.com/2009/10/german-soldiers-to-receive-different.html 

Baxter does not have a license in the U.S. to provided the seasonal or H1N1 vaccine, even though they have a patent that was granted two years before the Pandemic.  https://ahrcanum.wordpress.com/2009/07/23/baxter-vaccine-patent-h1n1/   Baxter though, isn’t the only one to hold a patent on an H1N1 vaccine before the pandemic.  Turn your head to Novartis’ vaccine approved in the U.S.A.,  https://ahrcanum.wordpress.com/2009/09/18/swine-flu-vaccine-patent-conspiracy/.

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.

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)

Likely no press in the U.S. will ever investigate or make the connections that we have tried to make, and authenticate here at Ahrcanum.  Sad to see Lou Dobbs go, he would have been the one person left who could have presented this to the American people.  Jane Burgermeister’s claim to Austrian authorities regarding a vaccine ‘conspiracy’ has been apparently dismissed.  What is not so easily dismissed, is that citizens from Poland to the four corners of the world are beginning to take notice and refuse to vaccinate.  Funny how all the vaccine manufactures are immune from lawsuits in the U.S.

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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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