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Posts Tagged ‘vaccine package insert’

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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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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Pneumonia kills more young children than any other disease, but an investment of $39 billion, or just $12.9 per child, could save 5.3 million lives in developing countries by 2015, the U.N. said.  http://www.reuters.com/article/latestCrisis/idUSLT408568

November 2nd, is the first ever World Pneumonia Day www.worldpnuemoniaday.org  to bring into focus the leading killer of children worldwide.  More on the day at: http://www.huffingtonpost.com/dr-orin-levine/are-you-smarter-than-the_b_307986.html

Our proposal is that if America is going to be blackmailed by the United Nations or the World Health Organization;  forgo dropping $10 billion on the The Climate Treaty Bill.

While pneumonia is life threatening,  we believe that there is evidence showing that the PNEUMOVAX ®  vaccine (approved the USA) does not protect against pneumonia and it’s toxic ingredient phenol could equally be hazardous to your health as contracting pneumonia.

We’ve already hashed the topic on a prior post  https://ahrcanum.wordpress.com/2009/10/10/h1n1-swine-pneumonia-pneumococcal-vaccine-mf59/ that lists vaccine ingredient phenol and associated risks as with most vaccines. 

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Gardasil and Cervarix vaccines will do little to reduce cervical cancer rates, according to the drugs lead researcher in the development of two human papilloma virus vaccines, says Dr. Diane Harper. The outspoken researcher also weighed in last month on a report published in the Journal of the American Medical Association that raised questions about the safety of the vaccine, saying bluntly: “The rate of serious adverse events is greater than the incidence rate of cervical cancer.”  http://thebulletin.us/articles/2009/10/25/top_stories/doc4ae4b76d07e16766677720.txt

 The Food and Drug Administration has approved the use of the Gardasil vaccine in boys and men ages 9 to 26, and a new HPV vaccine, Cervarix, for girls and women ages 10 to 25. http://health.usnews.com/blogs/on-women/2009/10/19/hpv-vaccine-women-now-have-a-choice-between-cervarix-and-gardasil.html 

Gardasil is manufactured by Merck. The patient insert can be found at  http://www.merck.com/product/usa/pi_circulars/g/gardasil/gardasil_ppi.pdf.  The home page for Gardasil http://www.gardasil.com/gardasil-product-information/index.html says:  GARDASIL may not fully protect everyone…What are the ingredients in GARDASIL? The ingredients are proteins of HPV Types 6, 11, 16, and 18, amorphous aluminum hydroxyphosphate sulfate, yeast protein, sodium chloride, L-histidine, polysorbate 80, sodium borate, and water for injection.

tween80

image from chinesemol.com

Polysorbate 80  is commercially also known as Tween 80, a registered trademark of ICI Americas, Inc.  On January 2, 2008, AkzoNobel completed the acquisition of Imperial Chemical Industries PLC (ICI) http://www.akzonobel.com/ From the Material Data Safety Sheet on Tween 80 http://www.coleparmer.com/catalog/Msds/40200.htm, ” Adverse reproductive effects have been reported in animals.”

The  U.S. Approved, Influenza A (H1N1) 2009 Monovalent Vaccine, also contains Polysorbate 80 as does Celvapan, the second influenza vaccine made in a mammalian cell line that has been approved in the UK.. 

According to Annals of Allergy, Asthma and Immunology, Volume 95, Number 6, December 2005 , pp. 593-599(7), “it is of current relevance as a ‘hidden’ inductor of anaphylactoid reactions”, and “Polysorbate 80 was identified as the causative agent for the anaphylactoid reaction of nonimmunologic origin in the patient. Conclusions: Polysorbate 80 is a ubiquitously used solubilizing agent that can cause severe nonimmunologic anaphylactoid reactions.”

Put 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

Natural News noted in January 2009, http://www.naturalnews.com/025411.html  that the HPV Vaccine Shot Causes 500 Percent Increase in Allergic Reactions Compared to Other Vaccines.  A 1993 study on rats at http://www.ncbi.nlm.nih.gov/pubmed/8473002 also found significant fertility issues.

CDC recommendations on the flu shots?  Why of course, women and children first. 

Could this vaccine and all the others that contain Polysorbate 80, be a subversive method for population control?  Does the inequitable distribution of wealth begin with unwitting sterilizations from these approved vaccines?   We asked back in January, well before the H1N1 Pandemic ever came to light if  the government is currently conducting subversive population control on women and vagina’s, and its leader may be Nancy Pelosi.  https://ahrcanum.wordpress.com/2009/01/26/pelosis-population-control/ 

“The worst thing you or I can so for the planet is to have children” writes the Guardian’s Alex Renton, who advocated in a Sunday column an ambiguous system of system of carrots and sticks to get the developed world to stop reproducing. http://papundits.wordpress.com/2009/10/27/guardian-columnist-wants-to-cull-the-developed-world-to-stop-global-warming/

Maybe a clean bill of health may not in the best interest for all, after all.

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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.

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The CDC is saying that one out of five children in the U.S. have probably already had H1N1 Swine Flu, long before any vaccine was available.  http://www.cdc.gov/flu/weekly/  Maine Republican Senator Susan Collins said, “It now appears that much of the vaccine could arrive only after many people have already been infected with H1N1.  http://abcnews.go.com/Health/WireStory?id=8932595&page=2

Whether you blame the vaccine makers or government’s distribution process, it looks likely that there is going to be a lot of unused vaccines leftover. 

David Fedson, Former Director of Medical Affairs, Aventis Pasteur MSD and a former consultant to the World Health Organization, said in a September interview with CFR- The Council on Foreign Relations:
 
H1N1, or so-called swine flu virus, has not disappointed us at all. It’s now in virtually every country of the world and managed to make that move in just a matter of a couple of months. After six weeks or so, it became quite evident that overall, the effects of infection in populations were rather mild, and in general no more severe than a seasonal [flu]. What we’ve seen is a mild illness overall that’s infecting a very large number of people and communities in a rather short period of time.
 
What we’ve been witness to, is how good the propaganda machine called government heathcare is in America.   The World Health Organization and the World’s health experts knew that H1N1 was no more severe than the seasonal flu, but forgot to tell anyone.  
America’s reaction was to spend $1.5 billion for the 250 million swine flu vaccines that the government has ordered so far and will be distributing free to doctors, pharmacies and schools. In addition, Congress has set aside more than $10 billion this year to research flu viruses, monitor H1N1’s progress and educate the public about prevention. http://abcnews.go.com/Business/big-business-swine-flu/Story?id=8820642&page=1  
 
As to what to do with the left over flu shots, the ingredients in the vaccine probably qualify as hazardous waste.  Spending money in the name of research is one thing; spending tax dollars hazzardly on a vaccine that may not work according to the patient inserts and after the fact, is quite another. 

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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.

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H1N1 Swine Flu, The Global Pandemic to rival the 1918 Outbreak has so far not mutated into a catastrophic event, unless of course you are one of the 1000 dead in the U.S.  http://news.yahoo.com/s/ap/20091023/ap_on_he_me/us_med_swine_flu . Worldwide, more than 5,000 people have reportedly died from swine flu since it emerged this year and developed into a global epidemic, the World Health Organization said Friday. Since most countries have stopped counting individual swine flu cases, the figure is considered an underestimate .http://www.katu.com/news/national/65903407.html  Although the death rate has been rather minimal, the influenza infection rate is rising and spreading. 

It has become painfully obvious that neither governments or the pharmaceutical industry are able to deal with any sort of a pandemic, let alone one more serious than H1N1, like SARS. 

pinkfloydwall2

O.K.
Just a little pin prick.
There’ll be no more aaaaaaaaah!
But you may feel a little sick.
Can you stand up?
I do believe it’s working, good.
That’ll keep you going through the show
Come on it’s time to go.

There is no pain you are receding
A distant ship’s smoke on the horizon.
You are only coming through in waves.
Your lips move but I can’t hear what you’re saying.
When I was a child
I caught a fleeting glimpse
Out of the corner of my eye.
I turned to look but it was gone
I cannot put my finger on it now
The child is grown,
The dream is gone.
but I have become comfortably numb. Pink Floyd lyrics via http://www.sing365.com/music/lyric.nsf/Comfortably-numb-lyrics-Pink-Floyd/6F30EBDB86AD066C482568A100060594 with photo props to http://atlasshrugs2000.typepad.com/atlas_shrugs/2006/04/pink_floyds_ant.html

Unlike the song, “I cannot put my finger on it now,” we have a pretty good idea of where to put our finger.  Which finger and where to point it is the question.

We would definitely give our thumbs down at governments ineptitude to precipitate any remedy or vaccine remediation for its people.  Consider H1N1 a test of the emergency broadcast system that has failed.  The people who want bring government health care to millions can not even manage to stockpile vaccines or antivirals.  They authorized expired Tamiflu to be distributed to children after it sat on shelves for years! https://ahrcanum.wordpress.com/2009/10/08/tamiflu-expired-children-to-reciev/

We would give thumbs up if we were to succumb to the theory of big pharmaceutical and government collaboration and collusion.  Much evidence points H1N1 to being lab created.  Wherever H1N1 originated from, it is a viral mutation from animals that has jumped into the human species.  No virologist can predict the mutation of H1N1. No vaccine in the U.S. contains adjuvants, just a little injury causing mercury.  Also,  no cell line from African Green Monkey has been revealed in vaccine manufacturing for the U.S.  (at least that we know of)

Pink Floyd’s Animals album was born from Roger Waters concept, where the human race was reduced to dogs, pigs, and sheep. The concept was borrowed from George Orwell‘s Animal Farm, but in Waters’ version the sheep eventually rise up to overpower their oppressors.wiki-

Waters and Orwell weren’t too far off. If we are the sheeples, are we the damned?  Are people waking up from the dream coma and illusion of safety by the government, World Health Organization and World Bank?  Are the sheep rising up in knowledge and mistrust in everything from the financial bailouts to a campaign to vaccinate with little clinical testing. We think we’ll give them middle finger. 

We will also give the middle finger to Thomson Reuters PULSE Health care Survey at http://www.reuters.com/article/pressRelease/idUS108985+23-Oct-2009+PRN20091023  saying:

“It’s astounding, with all the information being distributed about swine flu, that only a third of the population expects to get vaccinated,” Pickens said. “There is also a group of people who are very concerned about swine flu, but not likely to get the flu shot. Presumably, they experience some type of barrier to care. They are mostly young adults, less educated, lower income, and female.”

We presume, they do not want a Swine Flu Vaccines because they are other wise healthy.  Any differences in education, income, or access to health care, “people who are concerned about Swine Flu,” are smart enough to know when the sheep of the wool is being pulled over their eyes.  Lumping in the female perspective- perhaps women who may be pregnant do not want to pass toxins on to their fetus.  Every source cites the fact that there no clinical studies on fertility from taking the H1N1 or seasonal flu vaccines.

The list of U.S. Approved H1N1 Vaccines with patient package insert warnings is here- https://ahrcanum.wordpress.com/2009/09/27/h1n1-swine-flu-vaccine-package-insert-warnings/

Now the Discovery Channel and MYTHBUSTERS have teamed up with the United States Department of Health and Human Services to help inform the public about ways to protect themselves and prevent the spread of the H1N1 flu virus. www.discovery.com You can see the disgusting sneeze spreading airborne pathogens at http://www.youtube.com/watch?v=dCzbw4or19g&feature=player_embedded

Cover your mouth, roll up your sleeve, it’s just a little pinprick.  Come on its time to go.

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The Centers for Disease Control(CDC) believes that up to 12 million fewer doses of H1N1 vaccine than expected will be available by month’s end. Availability will be limited for the next week or two due to manufacturing delays. The CDC had hoped 40 million doses would be available by end of October, but this is very unlikely. http://www.huliq.com/8059/87759/h1n1-swine-flu-production-slower-expected

2009 H1N1 Influenza Vaccine Supply Status

Aggregate Totals
Posted October 16, 2009, 12:00 PM ET
Doses Allocated as of 10/14/09* 11,422,900
Doses Ordered as of 10/14/09 7,971,800
Doses Shipped as of 10/14/09** 5,885,900
*Doses allocated to project areas for ordering are those that are at the distribution depots and ready for project areas to order.
Vaccine is allocated to each project area in proportion to its population (pro rata).

**There is a lag time between allocation, ordering, and shipment of doses as project areas place orders and those orders are processed and shipped.

Project areas reflect CDC Public Health Emergency Response (PHER) Grantees.

http://www.cdc.gov/h1n1flu/vaccination/vaccinesupply.htm

Dr. Anne Schuchat, CDC’s director of the National Center for Immunization and Respiratory Diseases reported on Friday that manufacturers are making unprecedented amounts of vaccine, but difficulties growing the vaccine, as well as time-consuming potency and purity testing, are contributing to the delay. “We are not cutting any corners in the safety of the production of the vaccine or the testing and oversight of the vaccine” Schuchat explained.

Let us explain. The 2009 H1N1 Vaccine should be labeled as toxic waste.  Here are the patient inserts on each of the approved vaccines in the U.S. https://ahrcanum.wordpress.com/2009/09/27/h1n1-swine-flu-vaccine-package-insert-warnings/  All were given fast track approval based on how previous seasonal vaccines were manufactured.  All have legal immunity from any lawsuits that might arise due to injury.  Quite simply, the CDC has cut corners.

 

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