New HepB Vaccine Approved For Testing On General Population.

This new HEP B vaccine was approved for use on pregnant women. It includes an entirely new synthetic DNA adjuvant that will trigger a part of the immune system science discovered in the past decade. There was limited study information, so instead post-marketing data gathered to determine if there are any issues. The US Vaccine Advisory Panel called the Advisory Committee on Immunization Practices (ACIP), is the group that approves vaccines for public use in the United States. Most members have connections to the pharmaceutical (aka vaccine) industry. Vaccines are approved for use and included in CDC recommendations by this organization. An adjuvant is a substance added to produce a high antibody response using the smallest amount of virus (antigen) possible. By definition adjuvants are considered to be “pharmacologically active drugs.” They are designed to be “inert without inherent activity or toxicity” and yet they are required to “potently augment effects of the other compounds” in the vaccines. [8] It is difficult to explain how a substance can be defined as pharmacologically active and at the same time be described as inert and have no activity or toxicity. With this newly approved vaccine with a brand new adjuvant, the initial study 19 people had heart issues – 16 DIED! The panel approved 100% to use on the general public. Safety of the product will be measured with post-marketing data. What exactly does that mean? Uninformed mothers will be the experiment, any negative outcomes will be recorded to determine if the safety of the vaccine. No one will be liable or accountable for the negative outcomes that include harm, injury or death.

Those who believe that science is settled and thoroughly studied – is this your definition of science?