In a hard hitting editorial, the Indian Journal of Medical Ethics (IJME) has accused the WHO of promoting Pentavalent vaccine “by stating falsely that no adverse event following immunization (AEFI) has ever been reported with the vaccine.” The journal says this is contrary to facts.
...investigation into the deaths of children in Bhutan, Sri Lanka, India and Vietnam following use of Pentavalent vaccine. This vaccine combines the Diphtheria, Pertussis, Tetanus or DPT vaccine — long used in national immunization programs – with Hepatitis-B and H influenza-b or Hib vaccine.
Did you know that the Dept. of HHS is the patent holder on the HPV vaccine, and receives royalty checks on every dose of Merck's Gardasil and GSK's Cervarix?" "HHS owns the patent through NIH, licenses the vaccine through FDA, recommends the vaccine through CDC, and is its own judge in vaccine injury cases through HRSA."
YOU HAVE TO READ THE WHOLE SORDID STORY...
http://adventuresinautism.blogspot.com/2013/03/testimony-on-maine-ld-672-act-relating.html
Adventures in Autism: Testimony on Maine LD 672 An Act Relating to Exemption from Immunization...
...investigation into the deaths of children in Bhutan, Sri Lanka, India and Vietnam following use of Pentavalent vaccine. This vaccine combines the Diphtheria, Pertussis, Tetanus or DPT vaccine — long used in national immunization programs – with Hepatitis-B and H influenza-b or Hib vaccine.
The IJME editorial says that On 4 May 2013 the Ministry of Health of Viet Nam suspended Quinvaxem - the Pentavalent combination used in that country — after 12 deaths and 9 other non-fatal serious adverse events. According to local news reports, all the babies who died were in good health prior to vaccination and had serious trouble breathing before dying shortly afterwards.
The WHO, which investigated the incident, said the deaths were not vaccine-related and claimed that “Quinvaxem was prequalified by WHO and no fatal adverse event following immunization has ever been associated with this vaccine.”
The editorial points out that WHO had not disputed the death of 12 children soon after immunization and “therefore it is patently wrong and misleading for it to conclude that no fatal AEFI have ever been associated with the vaccine.”
This combination vaccine is not licensed for use by the U.S. Food and Drug Administration nor is it used in other developed countries, the editorial says. But the WHO recommends this Pentavalent vaccine in developing countries, by piggy backing the Hepatitis-B and Hib vaccines on the well accepted DPT to increase uptake of Hepatitis B and Hib according to a write up on the GAVI web site.
Serious adverse reactions and deaths have now been reported with Pentavalentvaccine produced by other manufacturers and in a number of countries, the journal says. Bhutan. Sri Lanka and Pakistan have stopped using the vaccine, “following unexplained deaths soon after immunization.”
This leads is to an important question...
Why would HHS not want to disclose accurate risk information to parents?
C) HHS does not disclose that it is the patent holder on the HPV vaccine, and receives royalty checks on every dose of Merck's Gardasil and GSK's Cervarix.
HHS owns the patent through NIH, licenses the vaccine through FDA, recommends the vaccine through CDC, and is its own judge in vaccine injury cases through HRSA.
YOU HAVE TO READ THE WHOLE SORDID STORY...
http://adventuresinautism.blogspot.com/2013/03/testimony-on-maine-ld-672-act-relating.html
Adventures in Autism: Testimony on Maine LD 672 An Act Relating to Exemption from Immunization...
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