Thursday, March 31, 2016

Confidential GSK report reveals that INFANRIX Hexa causes brain damage, anal leakage, autism and more

From this page.....

http://republicbroadcasting.org/news/italian-court-rules-mercury-and-aluminum-in-vaccines-cause-autism-us-media-continues-total-blackout-of-medical-truth/

Also presented as evidence was a 1,271-page confidential GSK report revealing that the drug giant knew full well from human clinical trials that INFANRIX Hexa causes autism, but the company chose to release the vaccine anyway. At least five known cases of autism arising from the jab are listed in the report on page 626, in fact:


http://ca.gsk.com/media/537989/infanrix-hexa.pdf

At the conclusion of this damning report, GSK admits that INFANRIX Hexa can cause a wide range of deadly illnesses but insists that its risk-benefit profile “continues to be favourable.” Listed among INFANRIX Hexa’s adverse events are:

• Anemia hemolytic autoimmune disease (premature destruction of red blood cells)
• Thrombocytopenia (low blood platelet count)
• Thrombocytopenia purpura (blood clots in small blood vessels)
• Autoimmune thrombocytopenia (immune system destroys blood platelets)
• Idiopathic thrombocytopenic purpura (excessive bruising or bleeding from lack of platelets)
• Hemolytic anemia (red blood cells destroyed and removed from bloodstream prematurely)
• Cyanosis (skin discoloration caused by lack of oxygen at skin’s surface)
• Injection site nodules, abscesses and injection site abscesses
• Kawasaki’s disease (inflammation of arteries)
• Encephalitis (inflammation of the brain)
• Encephalopathy (abnormal brain function)
• Hematochezia (passage of blood through the anus)
• Allergic reactions (including anaphylactic and anaphylactoid reactions)
• Death


The Daily Messenger: Boom! FDA Document Admits Vaccines Are Linked to Autism...

The Daily Messenger: Boom! FDA Document Admits Vaccines Are Linked to Autism...





Click here for the document on the FDA website.
http://www.fda.gov/downloads/BiologicsBloodVaccines/Vaccines/ApprovedProducts/UCM101580.pdf

Page 11 of 13

Causes of deaths included seven SIDS, and one of each of the following: enteritis, Leigh Syndrome, adrenogenital syndrome, cardiac arrest, motor vehicle accident, and accidental drowning. All of these events occurred more than two weeks post immunization.2 The rate of SIDS observed in the German case-control study was 0.4/1,000 vaccinated infants. The rate of SIDS observed in the US open-label safety study was 0.8/1,000 vaccinated infants and the reported rate of SIDS in the US from 1985-1991 was 1.5/1,000 live births.34 By chance alone, some cases of SIDS can be expected to follow receipt of whole-cell pertussis DTP35 or DTaP vaccines.

Adverse events reported during post-approval use of Tripedia vaccine include idiopathic thrombocytopenic purpura, SIDS, anaphylactic reaction, cellulitis, autism, convulsion/grand mal convulsion, encephalopathy, hypotonia, neuropathy, somnolence and apnea.