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Approves Vaccine After Admitting It Has No Safety Testing

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Approves Vaccine After Admitting It Has No Safety Testing
« on: Mar 25, 2018, 07:01:31 am »
 

EvadingGrid

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Shocking Video: US Advisory Committee Approves Vaccine After Admitting It Has No Safety Testing
http://govtslaves.info/2018/03/shocking-video-us-advisory-committee-approves-vaccine-after-admitting-it-has-no-safety-testing/





'In regards to vaccines, would you assume that when a new vaccine is being added to the schedule, there would be lengthy discussions, regarding proof of safety testing, so that the committee members would all feel very confident that this was a vaccine that should be added to the vaccine program?

Well you might find yourself in disbelief after viewing this short video of a recent meeting regarding the HEPLISAV-B, a new Hepatitis B vaccine by the Advisory Committee On Immunization Practices, and instead, you may feel very concerned that these committee members really do not seem to care that there isn’t any proof that it is indeed safe for use. Spam_A Spam_B HEPLISAV-B, the vaccine in question, is the first new vaccine for Hepatitis B ‘prevention’ in 25 years in the USA and is made by the company Dynanax Technologies. This vaccine contains two new adjuvants, called HBsAgand CpG 1018, and they have never been used in any other vaccines before.

Interestingly, when you take a look at the vaccine insert for the HEPLISAV-B, it states that 5 clinical trials were carried out on this vaccine, yet they only shared 3 of the 5 trials data on it’s insert.Where is the data on the other two trials? Why wasn’t it included?

The post safety data was carried out between 1 week to 13 months after the first vaccine was given. It is important to note there is also no information in the insert on how many participants had more than one dose of this vaccine yet, it is recommended that two doses are given to each adult.

Just under 10,000 people took part in these 5 trials. 18 deaths were reported out of the 3 trials data which was included on the insert. This also begs the question, with the missing two trials data, how many deaths were recorded, none, or many? What other adverse reactions were recorded? Without seeing this data, of course one must pose a question like this. It is disturbing that we just don’t know what else happened.'













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