Quinvaxem, a powerful 5 in 1 vaccine currently being distributed in India, containing live Diphtheria, Tetanus, Hib oligosaccharide (Haemophilus influenzae) & Hepatitis B viruses plus an inactivated B. Pertussis virus (heat treated or attenuated), has already caused the deaths of at least 5 children in Sri Lanka according to the WHO, 8 children in Bhutan and at least 3 children in Pakistan. Further serious adverse side effects have also been reported. More than 34 million doses of the vaccine had been distributed worldwide as at March 2008.
Sri Lankan authorities initially withdrew the vaccine in 2008 ‘after 25 serious adverse reactions that included five deaths and Bhutan stopped its use within two months of introduction in July 2009 after eight deaths.’ But in a bizarre twist Sri Lanka has recently reintroduced Quinvaxem, without any changes to the product itself, after a WHO expert panel, which investigated the events, declared that the vaccine was ‘unlikely’ to have caused the deaths.
http://sify.com/news/vaccine-may-be-killing-children-uk-report-news-national-kh4k94efdid.html
According to the British Medical Journal the World Health Organisation (WHO), in an elaborate cover-up, changed its own criteria for classifying adverse effects to say the vaccine was not responsible for the deaths in Sri Lanka,’ Jacob Puliyel, head of paediatrics at St Stephen’s Hospital in Delhi and key author, told IANS.
’20 reports of non-fatal AEFIs described as suggestive of hypotonic-hyporesponsive episode (referred to as HHE-like) following use of the pentavalent vaccine had been submitted to the Epidemiological Unit of the Ministry of Health. HHE is a recognized adverse reaction to whole-cell and acellular pertussis-containing vaccines, and to Haemophilus influenzae type b and hepatitis B vaccines. It is self-limited with no long-term sequelae.’
http://www.who.int/immunization_safety/aefi/investigation_pentavalent_Sri_Lanka/en/index1.html
Since 2006 a total of $910 Million including a $110 million grant from Unicef “to Support Vaccination Programs In The Developing World” has been awarded to Dutch biopharma company Crucell, a global biopharmaceutical company austensibly “focused on research development, production and marketing of vaccines, proteins and antibodies that prevent and/or treat infectious diseases” for their new fully liquid pentavalent vaccine QuinvaxemTM (*co-developed with Novartis Vaccines, Diagnostics of Chiron & Berna Biotech in Korea). The much touted vaccine “for protection against five childhood diseases” was prequalified by the World Health Organization in September 2006, enabling Crucell to bypass normal safety requisite procedures.
http://www.bioresearchonline.com/article.mvc/Crucell-Announces-New-Award-Of-110M-For-0001?atc~c=771+s=773+r=001+l=a&VNETCOOKIE=NO
“WHO prequalification for Quinvaxem (TM) marks an important milestone for Crucell as we pursue our strategy of becoming a leading vaccine player,” said Crucell’s CEO, Dr Ronald H.P. Brus. “The public-private partnership between the United Nations Organizations, Crucell and Novartis over the many years of its development have made this innovative vaccine a reality. We believe this vaccine will make an important contribution to pediatric vaccination programs for the developing world, and will confirm Crucell’s place as a leading supplier of such important vaccines.”
http://www.lifescience-online.com/Crucell_Announces_WHO_Prequalification_for_Quinvax,1874.html?portalPage=Lifescience+Today.News
Crucell internal data reveals a staggering formulation behind Quinvaxem: including 4 live viruses (*some contents produced in genetically engineered yeast cells) , 1 attenuated live virus, Aluminium phosphate, thimerosal & formaldehyde.
Quinvaxem™composition per 1 dose (0.5 ml):
• Diphtheria toxoid ³ 30 IU
• Tetanus toxoid ³ 60 IU
• inactivated B. pertussis ³ 4 IU
• Hib oligosaccharide 10 μg, conjugated to ~25 μg of CRM197
• Hepatitis B surface antigen 10 μg • Aluminium phosphate 1.36 mg
* Contains traces of thimerosal as a residue from manufacturing process. Antigen production:
• Diphtheria toxoid, Tetanus toxoid
Prepared from C. diphteriae and C. tetani cultures by
inactivation of the toxins with formaldehyde and purification
• Inactivated B. pertussis
Prepared from inactivated and purified B. pertussis cultures
• CRM-Hib
Purified H. influenzae capsular oligosaccharides are
conjugated to CRM197, a detoxified mutant of diphtheria toxin
Antigen production:
• Hepatitis B surface antigen (HBsAg)
Produced in genetically engineered yeast cells (Hansenula
polymorpha) carrying the relevant gene of the HBsAg
Process steps:
– growth of cells
– disruption of cells
– inactivation
– purification of HBsAg
Sources of antigens:
• Diphtheria toxoid, Tetanus toxoid, Pertussis suspension:
Novartis Behring, Marburg, Germany
• CRM-Hib:
Novartis Siena, Siena, Italy
• HBsAg:
Berna Biotech Korea Corp. (BBKC), Yongin, Korea
All antigens are shipped to Berna Biotech Korea Corp. for
formulation, filling and packaging of the product
QuinvaxemTM: quality (as of May 29, 2006):
• BBKC serves as a model for Korean authority (KFDA) in
terms of quality systems and cGMP
• production in BBKC is fulfilling international standards
• recently inspected by WHO, with overall favourable
conclusion
• The collaboration between Crucell/Berna Biotech and Novartis Vaccines resulted in the successful development of the new fully liquid pentavalent vaccine QuinvaxemTM
http://www.salsoc.org.ar/Berna/presentaciones/5_Quinvaxem_Spyr.pdf
‘”For 2008 we see sales of Quinvaxem significantly higher than in 2007,” Crucell’s Chief executive officer Ronald Brus told analysts but did not give a specific figure. In 2007 Crucell sold 21.3 million units Quinvaxem, up from 6.3 million in 2006.’
http://www.reuters.com/article/idUSWEB483020080212
Dr. Russell Blaylock, one of the world’s foremost brain surgeons has pointed out that multiple live viruses, when combined in a single dose vaccine, frequently result in auto-immune failure & severe neurological distress, Ischemia and in some circumstances even death.
“Some vaccines, including the MMR, smallpox, and chickenpox vaccines, contain live viruses. By giving three and sometimes four live viruses together, the risk of developing a lifetime viral infection (a persistent viral infection) increases tremendously. This is especially so with the MMR vaccine, which contains two live viruses known to suppress the immune system for months.”
Dr.Russell L. Blaylock M.D.
“Heavy metals & viruses in vaccines cause abnormal development in brain, long-term changes that put a child at high risk of neuro-degenerative diseases ie. Parkinson’s & Alzheimer’s for the rest of their life; also they become hyper-sensitive to environmental toxins (Pesticides, Herbicides). Live viruses in vaccines are incorporated into your genetic material & passed on to your children. Many rare forms of cancer are now very common ie Pancreatic cancer. Lymphoma is now the number one malignancy in 30 year olds and rising. Asthma has seen a ten fold increase over last 2 decades. Type 1 Diabetes has also been linked to auto-immune disorder caused by vaccines.” Dr. Russell Blaylock
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VRM Live – 01/28/11: Vaccine Resistance Movement founder Joel Lord discusses Synthetic Genomics, cloned cell vaccine technology & the death of natural immunity, gutter journalism & Dr. Wakefield’s imminent vindication with ‘Truth to Power’ host Paul Mabelis.
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VRM Live – 11/04/10: Vaccine Resistance Movement founder Joel Lord lays out the whole vaccine process with Paul Mabelis; including heavy metal toxicity, synergy, pregnancy issues & the basic principles of natural health at risk.
http://www.blogtalkradio.com/show.aspx?userurl=empradio&year=2010&month=11&day=05&url=truth-to-power-thursday
VRM Live – 09/24/10: Vaccine Resistance Movement Founder Joel Lord & activist/radio host Jesse Calhoun lay it all out tonite. Topics include the VRM Worldwide Autism Study, Scientific/Medical dictatorship, Natural Rights & Vaccine Industry fraud exposed. Special thanks to host Paul Mabelis.
http://www.blogtalkradio.com/empradio/2010/09/24/truth-to-power-thursday
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