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European Medicines Agency Safety Of "Swine Flu" Jab To Be Tested After Being Used

Thursday, September 17, 2009

European Medicines Agency Safety 0f "Swine Flu" Jab To Be Tested After Being Used

Paris : Earlier European Medicines Agency admitted in its report that New H1N1 Swine Flu Vaccine Contains Adjuvants.

But now the European Medicines Agency has admitted in an email that the safety and effectiveness of the "swine flu" vaccine will be monitored by "special procedures" after they are being used in the European population.

Biological experiments like this constitute crimes under domestic and international law.

European Medicines Agency press officer added : "The Agency has also set up special procedures to monitor the effectiveness and safety of pandemic vaccines after they have been authorised, once they are being used in the European population".

According to European Medicines Agency document Doc. Ref. EMEA/461476/2009 .Three of vaccines, Daronrix, Focetria and Pandemrix, contain ‘adjuvants’. These are compounds that are included with the vaccine strain to help stimulate a better response. Adjuvants are also added to pesticide spray mixtures to enhance or modify the pesticide and/or physical properties of the pesticide or the spray mix.

New H1N1 Swine Flu Vaccine Contains Adjuvants,European Medicines Agency

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