Baxter’s Many Lethal “Accidents”
Bioweapons Lawsuit: “In criminal charges filed against Baxter on April 8th, 2009 at the Vienna City Prosecutor’s office, Landesgerichtstr 11, 1080 Vienna, Austria by Jane Burgermeister, a resident of Vienna, Austria, it was alleged that Baxter unlawfully, wilfully and knowingly, in the period between December 2008 and February 2009, employed manipulative and deceptive devices and contrivances in violation of national and international laws on the manufacturing, possession, release and dissemination of biological weapons of mass destruction and on organised crime, to manufacture and distribute a biological agent that is classified as a bioweapon among the population in order to profit from the pandemic.”
Alarming News about Baxter International
On February 27, 2009, various news agencies, including Helen Branswell in the Canadian Press, reported:
Baxter International that “released contaminated flu virus material from a plant in Austria confirmed (today) that the experimental product contained live H5N1 avian flu viruses.” The WHO said the incident occurred at the company’s research facility in Orth-Donau, Austria, but claimed “that public health and occupational risk is minimal” thus far. What’s not known, however, “are the circumstances” behind the incident that, according to some, raise suspicions while others call it a willful criminal act. More on that below.
The contaminated product, “a mix of H3N2 seasonal flu viruses and unlabelled H5N1 (Avian Flu) viruses, was supplied to an Austrian research company…. Avir Green Hills Biotechnology.” It then “sent portions of it to sub-contractors in the Czech Republic, Slovenia and Germany.”
The problem was discovered when The Czech Republic company discovered that ferrets innoculated with the product died. “Ferrets shouldn’t die from exposure to human H3N2flu viruses.”
Public health authorities called it a “serious error” that showed “the H5N1 virus in the product was live.” But Baxter “has been parsimonious about the amount of information it has released about the event.” Christopher Bona, the company’s global bioscience communications director, did confirm that the material was a “live….experimental virus” made at the Orth-Donau research laboratory.
Security experts expressed alarm that something this serious could happen, calling the co-mingling (or reassortment) of human H3N2 with H5N1 avian viruses a dangerous practice that should never occur because of the potentially devastating effects to human health. “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 hybrid virus able to transmit easily to and among people,” who, in turn, could transmit it to enough others to potentially cause a pandemic. So far, nothing this extreme has happened, but a future threat remains.
As Medical Director of the Natural Solutions Foundation, Dr. Rima Laibow warns about dangerous, toxic drugs and vaccines. On March 6, 2009, she posted a “Pandemic Flu Emergency Action eAlert on her healthfreedomusa.org web site stating:
“World media (outside America) are reporting that Baxter Pharmaceuticals has admitted that it ‘accidently’ contaminated various vaccine batches with Avian Flu viruses. These batches were shipped to 18 countries. Clearly, either 1. stupidity and incompetence (are to blame) or 2. intentional contamination of flu vaccine lots was at work.”
Many Avian Flu vaccines compete with each other, yet they’re “profitable ONLY if used in huge numbers.” Although “Avian Flu has been slow to be become pandemic by ‘jumping the species barrier’ to humans in large numbers,” might Baxter’s
“accident” be a way to do it? If so, Big Pharma will score “One of the biggest wins in history.”
In fact, it already has after the Center for Infectious Disease Research & Policy (CIDRAP) reported that Congress (in mid-June) “approved $7.65 billion for battling pandemic influenza, more than three times what the House and Senate had earlier proposed.” Unsurprisingly, it was part of “a $106 billion (Iraq and Afghanistan war) supplemental appropriation bill” to open a new front at home in the form of dangerous vaccines – perhaps to be mandated for everyone.
Laibow sees a “manipulated disaster of unprecedented magnitude precipitated by unprecedented avarice and greed,” and adds that “Baxter International Inc. is no stranger to recalls and lethal contaminations.” Its record includes producing faulty infusion and volumetric pumps, HIV-2 tainted Albumin Buminate 5 percent, faulty dialysis machine tubing and blood-cleaning filters, and various other products that should make everyone leery of its soon-to-be-released Swine Flu vaccine. Along with similar ones from other pharmaceutical companies, these drugs cause serious autoimmune diseases and absolutely should be avoided, even if mandated.
Laibow expresses great alarm in stating:
“Baxter mixed a virus which has a hard time infecting people (H5N1 Avian flu) with one that infects them easily (“Seasonal Flu”) in a medium which can promote mutations of the H5N1 virus into a type which can infect us easily. What will be in the vaccine you are forced/coerced/threatened into allowing into your body? Who knows?”
What is known are our constitutional and Nuremberg Code rights. The Fifth Amendment protects against abusive government authority in stating that “No person shall….be deprived of life, liberty, or property, without due process of law….” The Eight Amendment prohibits “cruel and unusual punishments.” Depriving someone of health is tantamount to the latter as well as life by harming and potentially shortening it.
The Nuremberg Code requires voluntary consent of human subjects without coercion, fraud, deceit, and with full disclosure of known risks. It also affirms that experiments should avoid “all unnecessary physical and mental suffering and injury,” and should never be conducted if there’s “an a priori reason to believe death or disabling injury will occur” or harm to human health.
Was the viral contamination intentional?
The shocking answer is that this couldn’t have been an accident. Why? Because Baxter International adheres to something called BSL3 (Biosafety Level 3) – a set of laboratory safety protocols that prevent the cross-contamination of materials.
As explained on Wikipedia (http://en.wikipedia.org/wiki/Biosaf…):
“Laboratory personnel have specific training in handling pathogenic and potentially lethal agents, and are supervised by competent scientists who are experienced in working with these agents. This is considered a neutral or warm zone. All procedures involving the manipulation of infectious materials are conducted within biological safety cabinets or other physical containment devices, or by personnel wearing appropriate personal protective clothing and equipment. The laboratory has special engineering and design features.”
Baxter and HIV Infected Blood Products
Main article: Contaminated haemophilia blood products
A cite from http://www.haemophilia-litigation.com/, access date 31.05.2006:
“After 1978, there were four major companies in the United States engaged in the manufacture, production and sale of Factor VIII and IX: Armour Pharmaceutical Company, Bayer Corporation and its Cutter Biological division, Baxter Healthcare and its Hyland Pharmaceutical division and Alpha Therapeutic Corporation, which have been or are defendants in certain lawsuits.
The plaintiffs allege that the companies manufactured and sold blood factor products as beneficial “medicines” that were, in fact of likely to be contaminated with HIV and/or HCV. This resulted in the mass infection and/or deaths of thousands of haemophiliacs worldwide.
It is believed that three of these companies, Alpha, Baxter, and Cutter, recruited and paid donors from high risk populations, including prisoners, intravenous drug users, and blood centers with predominantly homosexual donors, to obtain blood plasma used for the production of Factor VIII and IX. Plaintiffs allege that these companies failed to exclude donors, as mandated by federal law, with a history of viral hepatitis. Such testing could have substantially reduced the likelihood of plasma containing HIV and/ or HCV entering plasma pools.”