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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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Open wide, say ahhh and check out more posts from Ahrcanum including our Swine Flu report that started  in April and is updated regularly at https://ahrcanum.wordpress.com/swine-flu-report/

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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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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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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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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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cell lines

You haven’t heard it all on the H1N1 Swine Flu Vaccines. 

Growing viruses in cell cultures has allowed preparation of purified viruses for the manufacture of  vaccines.  The Salk polio vaccine was one of the first mass produced earning three scientists a Nobel Prize for a discovery of a method of growing the virus in monkey kidney cell cultures related to the polio vaccine.  Recall President Obama just recieved a Noble for “for giving the world “hope for a better future.”    https://ahrcanum.wordpress.com/2009/02/27/obama-nobel-peace-prize-nomination-for-what/

Along comes AIDS. http://www.whale.to/v/aids2.html, http://www.newdawnmagazine.com/Article/Cancer_Causing_Vaccines.html

Along comes SARS.  http://www.conspiracyplanet.com/channel.cfm?channelid=8&contentid=824

Along comes H1N1.  www.ahrcanum.com

Once again, the science of virology and pharmaceutical corporations seek out a cure and prophylaxis. There are a zillion sites for vaccine ingredients including this one, but none other than here will you learn that the H1N1 vaccine in America may have been cultured in a dog’s kidney.   

In one trial of Influenza A (H1N1) 2009 Monovalent MF59-Adjuvanted Vaccine- http://content.nejm.org/cgi/content/full/NEJMoa0907650v1 The vaccine was manufactured by Novartis it is noted that-

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.

“The federal government is encouraging manufacturers to set up production in the United States, since all companies but one, Sanofi-Aventis, now import their flu vaccines.  The government also gave $1.3 billion, spread among several manufacturers, to develop ways of producing the vaccine in vats of animal cells rather than in eggs. Cell culture is less vulnerable to contamination and the process could save at least a few weeks. 

Novartis is building a cell culture flu vaccine factory in Holly Springs, N.C., which might be ready for use in 2010 or 2011. The federal government is providing nearly $500 million in construction costs and guaranteed vaccine purchases. ” http://www.nytimes.com/2009/04/29/business/economy/29vaccine.html?_r=1&ref=health

Can you spell collusion? C O LL  U S I O N- not only will our tax dollars build the facility, but we are guaranteeing vaccine purchases that will be made in animal cells like monkeys and dogs.  Arf, Arf, to another emergeny use authorization.

First comes the egg, next comes the dog, next comes the human.  Are we barking up a tree?  We do not have a virologist on staff here, but seeing as H1N1 is a mutated virus of pigs, birds and humans and that vaccines are grown in mammalian cell cultures- the possibility that a reassortment of genetic materials sure seems plausible.   No DNA vaccine is approved for human use, although. “There are reasons that injections of a sequence of DNA encoding part of a pathogen could stimulate immunity. It was soon realized that “DNA vaccination” had numerous potential advantages over conventional vaccine approaches including inherent safety and a more rapid production time.  http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2746192&tool=pmcentrez.  We ask if a DNA vaccine  also couldn’t motivate genetic cross mutations in human species?  Would humans be suject to viruses unique to animal species? If we grew a tail, it sure wouldn’t wag.

Walter Nelson-Rees revealed the extraordinary fact that roughly one third of all the tissue cultures in laboratories around the world had been colonised and taken over by the human cancer cell line called HeLa.  http://www.aidsorigins.com/content/view/221/2/  HeLa cells are shown above.  One of the earliest human cell lines, descended from Henrietta Lacks, who died of the cancer that those cells originated from, the cultured HeLa cells shown here have been stained with Hoechst turning their nuclei blue. -wiki-

Wake up and smell the dog shit. 

Drug manufacturers are likely using cells infected with cancer, growing them in chickens, culturing them in pigs, monkeys, dogs, even plants, and then encouraging you to, “Just get your damned vaccine.”  http://www.infowars.com/just-get-your-damn-vaccine/ said. 

You have to ask yourself, don’t they realize that toxic ingredients and mishmash of species for vaccines can damage the immune system in an of itself?

Dr. Kalokerinos said, “My final conclusion after forty years or more in this business is that the unofficial policy of the World Health Organisation and the unofficial policy of ‘Save the Children’s Fund and almost all those organisations is one of murder and genocide…. They want to make it appear as if they are saving these kids, but in actual fact they don’t. I am talking of those at the very top. Beneath that level is another level of doctors and health workers, like myself, who don’t really understand what they are doing. But I cannot see any other possible explanation: It is murder and it is genocide.” http://www.whale.to/v/kalokerinos.html

He goes into detail on the vaccine conspiracy and relays a story from 1975- ” When this politician rang me up he said in an endeavor to improve the Aboriginal mortality we stepped up the vaccination campaigns. And that is what had done it. They were actually immunising sick kids. ”

The WHO, CDC and others claim that the world has no defense against H1N1 or any other virus for that matter and they are WRONG.  In the Novartis trial study:

Fifteen percent of subjects had detectable prevaccination levels of hemagglutination-inhibition antibody, consistent with results of seroepidemiologic studies.  Although we excluded subjects with previous respiratory illnesses, asymptomatic infection with influenza A (H1N1) viruses cannot be ruled out, as local activity was present during the study.

Basically, they immunized people who already had the H1N1 antibody similarly to immunising sick kids in Aboriginal territories! 

In a different study out of Spain, released October 2009, suggests that some people born before 1950 have residual immunity against the influenza A H1N1 subtype (both seasonal and pandemic) http://www.ncbi.nlm.nih.gov/pubmed/19814966?ordinalpos=14&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum.  How do these people have immunity?  

“Certainly the government learned a lesson about swine flu in the mid ‘70s because they did vaccinate everyone, and there were a lot of instances of Guillain-Barre syndrome,” he said. “But hopefully they learned those lessons, and certainly the flu shots we have in this day and age have no major evidence of any major side effects.” said Dr. Michael Serlin, the chief of infectious diseases at North General Hospital in New York City. http://jta.org/news/article/2009/05/05/1004932/before-getting-the-swine-flu-vaccine-consider-sam-goldstein  from the article, What they didn’t tell Samuel Goldstein in 1976 about the swine flu vaccine killed him.

He died of pneumonia, a complication of Guillain-Barre a side effect from the Swine Flu on Jan. 15, 1977. 

From the Pharmacy Group H1N1 vaccine side effects recap, “In 1976, a certain type of influenza (swine flu) vaccine was associated with Guillain-Barré© Syndrome (GBS). Since then, flu vaccines have not been clearly linked to GBS. However, if there is a risk of GBS from current flu vaccines, it would be no more than 1 or 2 cases per million people vaccinated. This is much lower than the risk of severe influenza, which can be prevented by vaccination.” http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=meds&log$=drug_bottom_one&part=a607017 

One in a million indeed. 

Are you willing to be that one?

Keeping in disclosure-, “None of the approved influenza A 2009 (H1N1) monovalent vaccines or seasonal influenza vaccines contains adjuvants.”  (in the U.S.) http://www.ncbi.nlm.nih.gov/pubmed/19816398?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum  As for dog kidney cells, just maybe.

Not all research centers around vaccines, with some hope for cures >> Researchers identify mechanism that helps bacteria avoid destruction in cells – http://www.physorg.com/news174400147.html 

Thanks for visiting.

related- https://ahrcanum.wordpress.com/2009/07/27/swine-flu-vaccine-connection-to-aids-polio-smallpox/

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The U.S. Government has evaluated only these vaccines that are licensed by the U.S. Food and Drug Administration. They are-

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) http://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

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

Lot release information will be updated weekly.  Last update: 9/24/2009.  http://www.fda.gov/BiologicsBloodVaccines/GuidanceComplianceRegulatoryInformation/Post-MarketActivities/LotReleases/ucm181956.htm

Manufacturer Total Number of Lots Released by FDA
MedImmune LLC 9
Novartis Vaccines and Diagnostics Limited 3
Sanofi Pasteur, Inc. 3

From the CSL package insert: Influenza A (H1N1) 2009 Monovalent Vaccine,  Manufactured by CSL Limited, Suspension for Intramuscular Injection, Initial U.S. Approval: 2007 [sic- approved TWO YEARS AGO!)

From the CSL package insert

Vaccination with Influenza A (H1N1) 2009 Monovalent Vaccine may not protect all individuals.

5.4 Limitations of Vaccine Effectiveness

Neurological disorders temporally associated with influenza vaccination, such as encephalopathy, optic neuritis/neuropathy, partial facial paralysis, and brachial plexus neuropathy, have been reported.

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.

8.3 Nursing Mothers

Neither Influenza A (H1N1) 2009 Monovalent Vaccine nor AFLURIA has been evaluated in nursing mothers. It is not known whether Influenza A (H1N1) 2009 Monovalent Vaccine or AFLURIA is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when Influenza A (H1N1) 2009 Monovalent Vaccine is administered to a nursing woman.

8.4 Pediatric Use

   Neither Influenza A (H1N1) 2009 Monovalent Vaccine nor AFLURIA has been evaluated in children. Safety and effectiveness in the pediatric population have not been established.

Similar warnings from the Novartis inserthttp://www.fda.gov/downloads/BiologicsBloodVaccines/Vaccines/ApprovedProducts/UCM182242.pdf

 8.3 Nursing Mothers-It is not known whether FLUVIRIN or Influenza A (H1N1) 2009 Monovalent Vaccine is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when Influenza A (H1N1) 2009 Monovalent Vaccine is administered to a nursing woman

 

 8.4 Pediatric UseSafety and effectiveness in pediatric subjects below the age of 4 years have not been established. [see ADVERSE REACTIONS (6) and CLINICAL STUDIES (14)] 

Pregnancy Category C: Animal reproduction studies have not been conducted with Influenza A (H1N1) 2009 Monovalent Vaccine or FLUVIRIN. It is also not known whether Influenza A (H1N1) 2009 Monovalent Vaccine or FLUVIRIN 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.

The government is starting an unprecedented system to track possible side effects as mass flu vaccinations begin next month. The idea is to detect any rare but real problems quickly, and explain the inevitable coincidences that are sure to cause some false alarms.

“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.html

Just how did CSL Limited, Suspension for Intramuscular Injection get Initial U.S. Approval in 2007?????? TWO YEARS before the explosion of H1N1 around the world.  These patient inserts appear to be from the respective manufacturers of the seasonal flu vaccine, only adding the text for H1N1 with no large clinical studies.

US officials say the first swine flu vaccine will be available on Oct. 5. http://www.presstv.ir/detail.aspx?id=107252&sectionid=3510210  Women and children first please. 

Do not sign on the dotted line. 

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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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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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