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Business as Usual in Vaccine Industry

Posted in Ahrcanum, Secrets, Lies, & Truth, tagged , , , , , , , , , , , , , , , on February 28, 2011| Leave a Comment »

It is business as usual for the vaccine industry.  The Supreme Court heard a case last week that could have destroyed pharmaceutical companies that manufacture vaccines.  

On February 22, the court ruled 6-2 to keep the special Vaccine Court system intact. In particular, they ruled against Russell and Robalee Bruesewitz, who were suing for damages on behalf of their daughter Hannah http://genome.fieldofscience.com/2011/02/supreme-court-saves-vaccine-system.html.

You see, in America if you want to sue a vaccine manufacturer you are required to go through special arbitration, in something called The Vaccine Court.  Federal law under the National Childhood Vaccine Injury Act of 1986 ,

…says that no vaccine maker can be held liable for death or injuries arising from, “side effects that were unavoidable even though the vaccine was properly prepared and was accompanied by proper directions and warnings. http://www.washingtonpost.com/wp-dyn/content/article/2011/02/22/AR2011022206008_2.html

“The majority said that Congress found such a system necessary to ensure that vaccines remain readily available, and that federal regulators are in the best position to decide whether vaccines are safe and properly designed.”- Wapo.

Yep, you read correctly federal regulators are in the best position to make decisions on vaccine safety.  There is no tort remedy at all!  Too bad if the vaccine was not properly prepared, you have no remediation outside of The Vaccine Court.

Are you ready to roll up your sleeve?

Not surprisingly, the anti-vaccine groups like Age of Autism find this appalling,

The National Autism Association (NAA) joins parents nationwide in calling yesterday’s Supreme Court decision in the Bruesewitz case a violation of civil rights. The outcome also removes any remaining incentive for vaccine manufacturers to make their products as safe as possible. http://www.ageofautism.com/2011/02/supreme-court-ruling-abandons-vaccine-injured-children-threatens-vaccine-safety.html

Whatever your own opinion of vaccines, the entire vaccine industry is free from lawsuits in a court of law.  Wow talk about a free pass, just go and collect your $200 while you’re at it.

Except that it’s not $200.  The Pharmaceutical Research and Manufacturers of America, or PhRMA spends millions lobbying Congress. http://washingtonexaminer.com/blogs/beltway-confidential/grateful-obamacare-drug-lobby-goes-bat-harry-reid?quicktabs_1=0  Just  how happy of a dance do you think they did when the healthcare reform bill passed?

No amount of reform or vaccination is going to stop viral mutations.  It what they do, so why didn’t we all get sick and die from H1N1?  Dr. Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases of the National Institutes of Health, holder of the Presidential Medal of Freedom and the National Medal of Science says,

“Bottom line, it was luck,” Dr. Fauci says. “We were lucky.”   http://www.winnipegfreepress.com/opinion/westview/116972573.html

As luck would have it, earlier this month–

“Feb 17, 2011 (CIDRAP News http://www.cidrap.umn.edu/cidrap/content/influenza/swineflu/news/feb1711strains.html  ) – Signaling that the current flu strains are likely to persist over the next several months, the World Health Organization (WHO) today recommended sticking with the current trio of vaccine strains for the Northern Hemisphere’s next influenza season.

The WHO’s vaccine strain advisory committee met on Feb 15 and 16 and released its recommendation on the WHO’s Web site. The group recommends the following for next season’s vaccine:

  • For the H1N1 component, a strain similar to A/California/7/2009
  • For the H3N2 component, a strain similar to A/Perth/16/2009
  • For the B component, a strain similar to B/Brisbane/60/2008-like virus

Each February, WHO experts assess the flu strains circulating throughout the globe before recommending the strains for the Northern Hemisphere’s next seasonal flu vaccine. It takes about 6 months for vaccine manufacturers to grow the viruses in chicken eggs and formulate them into trivalent vaccines.”

In the case of H1N1, it took about month before anyone added up the pieces to notify the public that there was a threat, yet within months we had a vaccine in place.

Across the drink in Ireland, “In its annual report, the Irish Medicines Board (IMB) has revealed that the Swine Flu vaccination has been linked to an increase in adverse reaction reports, with an additional 900 adverse reaction reports this year, reported The Herald.

“The committee agrees that further investigation is warranted concerning narcolepsy and vaccination against influenza (H1N1) 2009 with Pandemrix and other pandemic H1N1 vaccines,” the WHO said, quoted CBS News, which noted that the European Medicines Agency is also looking into the issue, as well. Pandemrix is not being used in the U.S. due to its immune-boosting compound that is not approved in this country.

Significantly, a CBS News Investigation in October 2009 revealed that reports from the U.S. government concerning the Swine Flu Outbreak were significantly overblown and that data from all of the United States indicated that many cases diagnosed as the swine flu were not a flu; the CDC apparently advised doctors to diagnose and count all flu-like illness as swine flu, without testing, added CBS News. http://www.newsinferno.com/pharmaceuticals/swine-flu-shots-lead-to-spike-in-irish-adverse-event-reports/ 

What?  The CDC may have advised doctors to diagnose flu-like symptoms as being H1N1, really imagine that? But wait, why then would the U.S. Food and Drug Administration announce it has issued an Emergency Use Authorization (EUA) for a another diagnostic test for the 2009 H1N1 influenza virus? https://ahrcanum.wordpress.com/2009/07/27/swine-flu-vaccine-connection-to-aids-polio-smallpox/

Because they could, can, did and just might do it again, and there is nothing you can do about it in a court of law in The United States of America.

Just a little pin prick please.

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Children’s Tylenol Recall, FDA Investigation

Posted in Ahrcanum, Secrets, Lies, & Truth, tagged , , , , , , , , , , , , , , , , , , , , , , , , , , , on May 3, 2010| 1 Comment »

Tylenol, Motrin, Zyrtec and Benadryl.  What parent doesn’t have at least one of these pain relievers in the house if they’ve got kids?  It’s time for more Spring cleaning, and that includes the medicine cabinet.  

More than 40 over-the-counter infant’s and children’s liquid medications are being recalled by McNeil Consumer Healthcare, based in Fort Washington, PA.  The recall involves 43 various children’s versions of  Tylenol, Motrin,  Zyrtec and Benadryl.

The list of recalled products is found on the McNeil website,  http://www.mcneilproductrecall.com/page.jhtml?id=/include/mpr_ndc_finder.inc  where they say: 

McNeil Consumer Healthcare is initiating this voluntary recall because some of these products may not meet required quality standards. This recall is not being undertaken on the basis of adverse medical events.

However, as a precautionary measure, parents and caregivers should not administer these products to their children.

They don’t meet quality standards? 

Tylenol, Motrin,  Zyrtec and Benadryl products met Johnson & Johnson’s McNeil Consumer Heathcare division quality standards just fine until the Food and Drug Administration showed up.  Had the FDA not done a routine  inspection in April, no one would be the wiser that there was a problem in the first place.  Was it a surprise visit?

The FDA said it was reviewing procedures at McNeil, which appears to be the sole source of the problems. “We are following through with the facility to make certain that everything has been checked,” said FDA spokeswoman Elaine Gansz Bobo.

According to McNeil and the FDA, some of the products recalled may have a higher concentration of active ingredient than is specified on the bottle. Others may contain particles, while still others may contain inactive ingredients that do not meet internal testing requirements.  Read more: http://www.nydailynews.com/lifestyle/health/2010/05/01/2010-05-01_fda_investigating_recall_of_childrens_medicine_including_tylenol_motrin_zyrtec_b.html#ixzz0msMXhTqH

Higher Concentrations? 

Particles?   What kind of particle exactly?  Particles of feces perhaps?  I call bullshit on Johnson and Johnson, McNeil, and maybe the FDA too.  Where were there own internal quality assurance people to ensure products standards? We are not talking about one product in dispute, but 43 different products that have different problems. 

The WSJ wrote that consumer complaints about certain over-the-counter children’s medications spurred the investigation that led to the recall.

It’s the latest in a spate of recall woes for J&J; in November it pulled some kinds of Tylenol Arthritis due to their moldy odor, then added more lots and products to the recall over the next few months.   As the WSJ notes, this latest recall signifies “another dent in J&J’s reputation as a model of corporate responsiveness.” The company’s handling of Tylenol poisonings in 1982 made it the subject of case studies in effective crisis management, but the recent recalls are fraying that reputation. http://blogs.wsj.com/health/2010/05/03/recall-roundup-jj-pulling-childrens-tylenol-motrin-other-meds/

There are plenty of third world countries with pharmaceutical production standards that fall far short of our standards.  Johnson and Johnson, the world leader in pharmaceuticals, medical goods and consumer products is an American company. The manufacturing plant in question is on American soil, with presumably American citizens working there.  Shame, shame for not enforcing standards, especially for children’s products and shame on the FDA as well.  Why did it take two weeks to notify the public that more than 40 children’s drugs were contaminated with yet to be named, “particles.”

Marc Boston, a McNeil spokesman, would not discuss the deficiencies cited by the FDA or say when the manufacturing facility was shut down. The company also declined to disclose the amount of products affected by the recall.  http://www.washingtonpost.com/wp-dyn/content/article/2010/05/01/AR2010050103051.html  Since when did FDA reports become sealed? It may be an ongoing investigation but I bet no one discloses anything more except when they announce that Tylenol is back in production,

The FDA regulates approximately 25 cents of every dollar spent annually by American consumers. The FDA is responsible for regulating products to ensure the safety of foods, drugs, biological products, medical devices, cosmetics, radiation-emitting devices, and more.  FDA’s Special Agents frequently investigate criminal wrongdoing by large companies. If these investigations lead to prosecution, the guilty officers and employees often receive federal prison sentences, while the company can expect to receive multimillion-dollar fines and restitution payments.  http://www.fda.gov/default.htm

Is the FDA’s Office of Criminal Investigations (OCI) looking into criminal activity?  What department of government investigates malfeasance of the FDA when it doesn’t do its job? For at least two weeks, these over the counter medicines were being used and sold, and shipped.  Did McNeil willfully ship known adulterated goods in interstate commerce? Did the FDA allow them xtra time to get there act together before notifying the public? 

To produce 43 different drugs at one facility, even if they operated at full steam means that there was a problem for a very long time.  When was the last FDA inspection?

“A $1.8 million 2006 Institute of Medicine report on pharmaceutical regulation in the U.S. found major deficiencies in the current FDA system for ensuring the safety of drugs on the American market. http://en.wikipedia.org/wiki/Food_and_Drug_Administration ”  Four years after the study, we are in the same state of affairs. 

WAPO goes on to write,

This is at least the third major recall of Tylenol products by McNeil since 2008.

In January, McNeil recalled 49 types of Tylenol products made for adults and two Tylenol products made for children after consumers complained of a mold-like odor and of temporary and minor nausea, stomach pain, vomiting and diarrhea. The company determined that some of the medicines had been contaminated by trace amounts of a chemical that is sometimes present on shipping and storage material.

In 2008, McNeil recalled 21 types of children’s and infants’ Tylenol liquid products, saying that although the products met internal standards, an unused portion of one inactive ingredient did not meet all quality standards.

“The company is conducting a comprehensive quality assessment across its manufacturing operations and has identified corrective actions that will be implemented before new manufacturing is initiated at the plant where the recalled products were made.” http://www.mcneilproductrecall.com/page.jhtml?id=/include/new_recall.inc.  According to Wiki, along with their Fort Washington plant, McNeil also has plants in Lancaster, PA and Las Piedras, Puerto Rico. 

Here’s a hard pill to swallow, Johnson and Johnson is trading up one dollar midday, on the NYSE to $65.34. http://www.nyse.com/about/listed/jnj.html. 

  CLICK HERE FOR RECALL INFORMATION ON CERTAIN INFANTS’ TYLENOL® AND CHILDREN’S TYLENOL® PRODUCTS

CLICK HERE FOR RECALL INFORMATION ON CERTAIN INFANTS’ MOTRIN® AND CHILDREN’S MOTRIN® PRODUCTS

CLICK HERE FOR RECALL INFORMATION ON CERTAIN CHILDREN’S ZYRTEC® PRODUCTS

CLICK HERE FOR RECALL INFORMATION ON CERTAIN CHILDREN’S BENADRYL® PRODUCTS

CLICK HERE FOR INFORMATION ON ALL RECALLED PRODUCTS FROM APRIL 30, 2010

UPDATED MAY 15. 2010. “This inspection report is pretty close to being the worst I’ve seen. It suggests that basically the FDA found an issue with almost every system at the plant.” 

In addition, the FDA said some drums used to transport raw materials to the Fort Washington facility were contaminated with a bacteria identified as B. cepacia.  http://money.cnn.com/2010/05/14/news/companies/tylenol_recall_plant_conditions/

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Open wide, say ahhh and check out more posts from Ahrcanum!      

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

Shaking, rattling and rolling into the conspiracy, truth and science of EARTHQUAKES, HAARP, EISCAT, Tesla, etc., with more posts at https://ahrcanum.wordpress.com/earthquakes-haarp/       

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Baxter Flu Vaccine Contaminated, TV Investigative Report

Posted in Ahrcanum, Secrets, Lies, & Truth, Swine Flu, tagged , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , on November 13, 2009| 4 Comments »

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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Baxter Vaccine Patent for H1N1, Two Years Before Pandemic

Posted in Ahrcanum, Secrets, Lies, & Truth, Swine Flu, tagged , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , on July 23, 2009| 42 Comments »

1918 mass graves from Spanish Flu

1918 mass graves from Spanish Flu

Baxter Pharmaceutical files for patent on H1N1 Vaccine two years before first Swine Flu, H1N1 case is reported.

Swine Flu H1N1 cases are supposedly increasing so fast that the WHO, World Health Organization is no longer keeping a record of the number of cases. 

The U.N. agency, which declared an H1N1 influenza pandemic on June 11, said last week it was the fastest-moving pandemic ever and now pointless to count every case.  It told countries to stop reporting individual cases and concentrate on mitigation measures and detecting any unusual patterns of disease or spike in rates of absenteeism.” http://www.reuters.com/article/marketsNews/idUSLL47029320090721

While most cases appear to be mild, governments around the world are still pushing vaccine manufacturers to develop a preventative vaccine for an H1N1 virus that his killed all of 700 people.  By comparison to the avian ,” Spanish flu” of 1918, which killed perhaps 50 million people worldwide, including more than 500,000 in the United States. http://abcnews.go.com/Health/Flu/story?id=1173856

From A Virus of Our Own Hatching, http://birdflubook.com/a.php?id=5 :

In 1918, “They brought out their dead. Corpses were carted away in anything, wheelbarrows—even garbage trucks. Often, though, the bodies were just pushed into corners and left to rot for days. People too sick to move were discovered lying next to corpses. All over the country, farms and factories shut down and schools and churches closed. Homeless children wandered the streets, their parents vanished. The New York Health Commissioner estimated that in New York City alone, 21,000 children lost both parents to the pandemic.  Around the world, millions were left widowed and orphaned.” 

By the grace of God, better sanitation, better access to health care or whatever, this is not happening in 2009.  The cause of 1918’s influenza was not found until years later, when a British research team finally isolated and identified the viral culprit, recreated in in the lab and then posted the genetic markers on the internet for some smart terrorist to possible recreate.

Bloomberg  says, “Companies working on swine flu vaccines include Sanofi- Aventis SA, based in Paris, GlaxoSmithKline Plc and AstraZeneca Plc, both based in London, CSL Ltd. of Melbourne and Novartis AG, based in Basel, Switzerland.  And of course, Baxter International Inc. , based in Deerfield, Illinois, has contracts with five countries for 80 million doses and has stopped taking new orders that it may not be able to fill….The swine flu pandemic will be a boon to the company this year and mutations in H1N1 and other strains may create a lasting new business for the company, he said. http://www.bloomberg.com/apps/news?pid=20601202&sid=asQokqEhf.fg  No shit, “a boon to the company?”

Baxter’s stock is performing well even though ,”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/  Another accidental release, as in 900o vials of God knows what is missing from Fort Detrick? http://www.washingtonpost.com/wp-dyn/content/article/2009/06/17/AR2009061703271.html

As in the case of AIDS- “The Kenyan lady minister, winner of the Nobel peace prize 2004, was quoted as having expressed the conviction that the AIDS virus was not a natural phenomenon but happened to be man-made. She went on to imply that the spreading of the AIDS virus over vast areas of the African continent, too, was a deliberate act (accident/conspiracy?) http://pakobserver.net/200907/23/Articles01.asp 

As possible proof H1N1 was created in the lab, Baxter seems to have the upper hand in Pandemic game of life in death filing patents for vaccines prior to the known existence of mutated viruses as  Bloomberg is reporting, “Baxter has received pre-approval for its vaccine production method, and additional tests of the vaccine in humans will be necessary.”

Baxter is nothing, if not prepared for the swine flu outbreak if the wording in this 2008 US patent application is anything to go by from http://www.theoneclickgroup.co.uk/news.php?start=2760&end=2780&view=yes&id=3581#newspost :

See Baxter Vaccine Patent Application US 2009/0060950 A1 FILED AUGUST 28, 2007

“In particular preferred embodiments the composition or
vaccine comprises more than one antigen…..such as
influenza A and influenza B in particular selected from of one
or more of the human H1N1, H2N2, H3N2, H5N1, H7N7, H1N2,
H9N2, H7N2, H7N3, H10N7 subtypes, of the pig flu H1N1,
H1N2, H3N1 and H3N2 subtypes, of the dog or horse flu H7N7,
H3N8 subtypes or of the avian H5N1, H7N2, H1N7, H7N3,
H13N6, H5N9, H11N6, H3N8, H9N2, H5N2, H4N8, H10N7, H2N2,
H8N4, H14N5, H6N5, H12N5 subtypes.”

“Suitable adjuvants can be selected from mineral gels,
aluminium hydroxide, surface active substances, lysolecithin,
pluronic polyols, polyanions or oil emulsions such as water in
oil or oil in water, or a combination thereof. Of course the
selection of the adjuvant depends on the intended use.
E.g. toxicity may depend on the destined subject organism
and can vary from no toxicity to high toxicity.”

“Three different influenza strains, two A-strains Hiroshima
(HR, H3N2), a New Calcdonia (NC, H1N1) and a B-strain,
Malaysia (MA), were produced in Vero cell cultures. After
virus propagation the infectious virus harvest is inactivated
prior to purification….”

Read that last paragraph again-

BAXTER produced H1N1 cell cultures nearly two years before the pandemic! 

 Today 7/23/09, “the Vaccines and Related Biological Products Advisory Committee will hear about the status of H1N1 vaccine production, as well as the FDA’s plans for evaluating vaccines in time for the fall flu season, when public health officials expect to see resurgent H1N1 infections.” http://www.medpagetoday.com/ProductAlert/DevicesandVaccines/15170.  The meeting will be held at Hilton Hotel Washington DC North/Gaithersburg,  620 Perry Parkway, Gaithersburg, Maryland 20877 – http://www.fda.gov/AdvisoryCommittees/Calendar/ucm170908.htm,  as  one of our finest taxpayer funded government office buildings wouldn’t due for such a meeting!  CIDRAP- The Center for Infectious Disease Research usually posts follow ups here  http://www.cidrap.umn.edu/cidrap/content/influenza/swineflu/index.html 

Want to bet Baxter will be one of the presenters?

U.S. health officials are considering a fall immunization campaign that could involve an unprecedented 600 million doses of vaccine for the currently circulating H1N1 swine flu vaccine.http://www.forbes.com/feeds/hscout/2009/07/21/hscout629120.html

And, just like Baxter predicted human testing, “The University of Maryland School of Medicine’s Center for Vaccine Development will be one of 10 centers in the nation to test a swine flu vaccine on adults and children.  The clinical trial, slated to begin next month, will enroll up to 1,000 adults and children to evaluate whether the vaccine is safe and effective in preventing the virus known as H1N1, which public health officials fear could mutate into a deadlier strain this fall.http://www.baltimoresun.com/health/bal-swinefluvaccine-0722,0,755431.story  Other city medical Iowa City, Iowa; St. Louis; Nashville; Seattle; Atlanta; Cincinnati and Houston reportshttp://www.nationalterroralert.com/updates/2009/07/22/u-s-looks-for-volunteers-for-swine-flu-vaccine-test/ .

Not to be outdone- “Nurse Luiza Duszynski flicks her syringe, squeezes a few drops of clear liquid from the needle and pushes it into Tara Seaton’s arm. With that, she became one of the world’s first recipients of a vaccine for swine flu. Seaton is among the 240 healthy adult volunteers in Australia who CSL Ltd. began injecting today with its experimental vaccine against H1N1, the new virus strain that sparked the first influenza pandemic in 41 years”.- http://www.bloomberg.com/apps/news?pid=20601124&sid=aadm7_AYSmKo

Don’t forget, “Vaccine makers and federal officials will be immune from lawsuits that result from any new swine flu vaccine, under a document signed by Secretary of Health and Human Services Kathleen Sebelius.”http://www.google.com/hostednews/ap/article/ALeqM5hjdCHrP82YTFser5vD6CzTK1az6wD99GH8580

If you feel comfortable relying on your government, get the latest from the CDC http://www.cdc.gov/h1n1flu/. 

News on Baxter’s approved Celvapan Vaccine regarding German Soldiers.  https://ahrcanum.wordpress.com/2009/10/15/baxter-h1n1-vaccine-celvapan-to-german-soldiers/

Updated 11-13-09- Baxter Admits Vaccines Contaminated at https://ahrcanum.wordpress.com/2009/11/13/baxter-flu-vaccines-contaminated-tv-report/

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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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Vaccine & Drug Deadly Costs, Mistakes Threaten Pandemic

Posted in Ahrcanum, Secrets, Lies, & Truth, Swine Flu, tagged , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , on March 11, 2009| 3 Comments »

The multi billion merger pending from pharmaceutical companies Merck with a $41.1 billion purchase of Schering-Plough Corp. probably won’t be the last big drug-industry merger.  The amount of money is staggering and the lack of regulation apparent.

The deal, which comes on the heels of Pfizer Inc.’s $68 billion bid for Wyeth in January and Roche Holding AG’s $45.7 billion offer for U.S. partner Genentech Inc. last week, will spur other drug makers fearful of falling behind into action…Sanofi-Aventis SA may next target Bristol-Myers Squibb Co., which sells the French company’s Plavix blood-thinner and the Avapro hypertension treatment in the U.S. Alternatively, Bristol- Myers may be a potential merger partner for U.K. diabetes drug partner AstraZeneca Plc.  Johnson & Johnson may make a counter bid for Schering-Plough.  http://www.bloomberg.com/apps/news?pid=20601087&sid=a.JuaqqzcDMY&refer=home

There is money to be made and lives to be saved, but human drug testing in the highest expense to bringing new drugs to market.  Many trade their bodies for the cash drug trial offers. More than 800 drug tests are taking place in India alone.  The FDA has only checked into 8 of them according to a special report http://www.tampabay.com/specials/2008/reports/india/ .

For every 5000 drugs tested in the lab, only 5 will make it to clinical trials and only 1 will pass and make it to the shelves.  It is expensive and America bears the brunt tangible costs with big pharma passing along the costs to her citizens with our disastrous medical system that by some accounts, is still the best in the world.  

In New Zealand, the use of human subjects including children as young as 6 years old, in trials of a novel GE {Genetically Engineered} food is being condemned by scientists internationally and by GE Free NZ (in food and environment).  GE ‘golden rice’ has been promoted as a solution to malnutrition, despite other readily-available sources of vitamin A.  Deficiencies of the vitamin are a cause of blindness among the poor.

“‘Pharming’ will blur the distinction between food and chemicals, disrupting our brand image far more significantly than the recent melamine contamination in milk powder in China.  Allowing human feeding trials of this experimental rice is highly concerning and  a frightening breach of human rights,” says Jon Carapiet from GE-Free New Zealand.  http://www.scoop.co.nz/stories/WO0902/S00328.htm

No where in mainstream media, is this report out about American pharmaceutical company Baxter- sending to Chech Republic, Slovenia and Germany bird flu vaccines that were found to contain actual deadly flu virus instead of the vaccine!  Baxter flu vaccines contaminated with H5N1 – otherwise known as the human form of avian flu, one of the most deadly biological weapons on earth with a 60% kill rate – were received by labs in the Czech Republic, Germany, and Slovenia.  http://www.torontosun.com/news/canada/2009/02/27/8560781.html
 
Of course, Baxter invoked trade secrets and refused to reveal how the vaccines were contaminated with H5N1, finally admitting that pure H5N1 batches were sent by accident.  On Friday {March 6, 2009}, the company’s director of global bioscience communications confirmed what scientists have suspected. “It was live,” Christopher Bona said in an email.   The contaminated product, which Baxter calls “experimental virus material,” was made at the Orth-Donau  research facility. Baxter makes its flu vaccine — including a human H5N1 vaccine for which a license is expected shortly — at a facility in the Czech Republic. 

People familiar with biosecurity rules are dismayed by evidence that human H3N2 and avian H5N1 viruses somehow co-mingled in the Orth-Donau facility. That is a dangerous practice that should not be allowed to happen, a number of experts insisted.   Accidental release of a mixture of live H5N1 and H3N2 viruses could have resulted in dire consequences. Ya think?  Did they send it regular mail or on an airplane with 200 happy people going on vacation?  Was it labeled as hazardous medical so a terrorist could know what to steal?  Mind numbing ignorance.

While H5N1 doesn’t easily infect people, H3N2 viruses do. If someone exposed to a mixture of the two had been simultaneously infected with both strains, he or she could have served as an incubator for a hazardous mixed virus able to transmit easily to and among people.   That mixing process, called reassortment, is one of two ways pandemic viruses are created. 
 
“This was seemingly an attempt to quickly change the story and hide the fact that the accidental contamination of a vaccine with a deadly biological agent like avian flu is virtually impossible and the only way it could have happened was by willful gross criminal negligence,” said Dr. Orly Taitz at http://defendourfreedoms.us/2009/03/10/meeting-with-scalia-and-coordinated-cyber-attack.aspx

The contamination incident came to light when the subcontractor in the Czech Republic inoculated ferrets with the product and they died. Ferrets shouldn’t die from exposure to human H3N2 flu viruses.  Imagine if they had inoculated infants rather than ferrets.

Baxter International Inc.(NYSE: BAX)  “develops, manufactures and markets products that save and sustain the lives of people with hemophilia, immune disorders, infectious diseases, kidney disease, trauma, and other chronic and acute medical conditions. http://www.baxter.com/  The company has no mention of this mistake of epic proportion on their website.

According to the Baxter site they have two products on the market: a vaccine against tick-borne encephalitis (TBE) and a vaccine against group C meningococcal meningitis.  http://www.baxtervaccines.com/?node_id=312 I think we can all agree how happy we are that this “mixing process,” didn’t affect these two vaccines already widely in use. 

According to the recommendations of the World Health Organization (WHO) three virus strains, usually two type A and one type B, are selected each year before flu vaccine production starts. This is done after a careful investigation of the circulating strains and their mutations and they pick and choose the most likely to populate. 

The CDC recommends getting vaccinated now to protect against late-circulating flu viruses and provides state pandemic Web site information at http://www.pandemicflu.gov/whereyoulive/index.html.  From all accounts the last time it was updated for the heavily populated state of New York was in 2006. http://www.health.state.ny.us/diseases/communicable/influenza/pandemic/docs/pandemic_influenza_plan.pdf  Check your state here http://www.pandemicflu.gov/plan/states/stateplans.html.

I wonder if pandemic planning activities include all the FEMA camps and train rides? 

The CDC has a list of the number of vaccines recommended for children and adults from the eradicated Polio to the newly identified diseases like Cervical Cancer who’s prevention for a few of the strains lies in the vaccine Gardasil; which is now mandated by the U.S. Government for all female immigrants.  http://www.cispimmunize.org/ 

The alleged link between thimerosal and autism has spawned numerous investigations, including a fantastic Rolling Stone article by Robert F. Kennedy Jr. that claims that the government was/is engaged in a medical cover-up. http://www.rollingstone.com/politics/story/7395411/deadly_immunity/

“All parents and patients should be informed about the risks and benefits of preventive and therapeutic procedures, including vaccination. In the case of vaccination, federal law mandates this discussion.”  http://www.cispimmunize.org/pro/pdf/RefusaltoVaccinate.pdf Physicians are also mandated to keep records of patients who refuse.  If you refuse to vaccinate your children, will your doctor enforce the Child Abuse Prevention and Treatment Act which gives states the right to literally steal your children for up to 48 hours — the time they have to prove child neglect OR abuse and then vaccinate them?

Does big pharma operate with the morals to prevent mortality? 

Someday, you will die.

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