Secret British MMR Vaccine Files Forced Open By Legal Action

Secret British MMR Vaccine Files Forced Open By Legal Action

The UK’s Daily Mail newspaper reports today that the British government was desperately trying to prevent secret files on the proven dangerous Pluserix MMR vaccine from being released publicly under the UK’s Freedom Of Information laws.  In a recent case they have been forced to open the files up to scrutiny:-

And here is some of what will be discovered.

British Government’s Reckless Disregard for Child Health Safety

The UK’s Department of Health and others appear to have been reckless as to the safety of British children over the manner in which Glaxo company, Smith Kline & French Laboratories Ltd’s Pluserix MMR was introduced and used on British Children in 1988

  • the problems with Pluserix MMR were known to the supplier, Glaxo company Smith Kline & French Laboratories Ltd from the experience of its introduction to Canada, in 1986, where Pluserix was marketed under the name “Trivirix”
  • Trivirix (Pluserix) was withdrawn from use in Canada in 1988 because it was dangerous, causing high levels of adverse reactions in children
  • the high levels of British adverse reactions to the vaccine were apparent and known about at British Ministerial level in 1990, as shown by ministerial correspondence
     

  • Pluserix/Trivirx are the identical vaccine manufactured in the identical Smith Kline factory in Belgium and with the exact same component parts and constituents
     

  • despite the Canadian position and contemporaneously with the final withdrawal of Pluserix/Trivirix in Canada the UK signed the contract to purchase Pluserix MMR from Glaxo company, Smith Kline & French Laboratories Limited in July 1988, even though it was known by then to be too dangerous for use on our children
     

  • SK&F was provided with a blanket indemnity in that contract by the NHS Procurement Directorate
     

  • the contract was signed up by the backdoor through the North East Thames Regional Health Authority as agent for the NHS Procurement Directorate rather than being a contract directly entered into with the NHS Procurement Directorate which negotiated the contract or the NHS Executive of the time
     

  • there was no Parliamentary scrutiny of this and it seems to have been effected in a manner Ministerially deniable
     

  • similar problems were experienced in Japan with the Japanese MMR vaccine which, in common with Pluserxi/Trivirix, contained the Urabe strain of mumps virus
     

  • the Japanese MMR was also withdrawn by 1992 on safety grounds having caused high levels of adverse reactions
     

  • the British government continued the licence for Pluserix MMR after 1992, which enabled it to be supplied overseas
     

  • even today, because it is cheaper than safer alternatives, organisations like UNICEF continue supplying urabe strain containing MMR vaccine to the more adverse reaction vulnerable and less well nourished third world children
     

  • since 1998, statistical paper after paper has been published in a blaze of publicity, claiming no evidence of an association between the MMR vaccine and autism, but when all the noise has died down, on subsequent careful examination, each one has been found to be flawed
     

  • other than the Royal Free’s paper, no clinical studies of the MMR child litigants were undertaken or published
     

  • after being put under financial pressure by the British Government, in 2005 the Oxford based Cochrane Collaboration published a systematic review of all prior papers and its authors claimed to conclude the MMR vaccine was safe:-
       

    • it was shown the authors had violated the standards of evidence-based medicine and
    • their conclusions were not supported by the body of the review
    • and it later was discovered that the British Department of Health had increased the funding for Cochrane’s Oxford administration by £1 million per annum and extended the contracts of its British groups.

 

 

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