Vaccine Maker Admits on FDA Website That DTaP Vaccine Causes Autism
A HUGE hat tip and shout out goes to Mike Adams, the Health Ranger, for finding pharmacological admittance and written proof that at least one vaccine causes autism as an adverse reaction.
According to the U.S. FDA’s online Biologics Blood Vaccines publication, Sanofi Pasteur’s Diphtheria, Tetanus Toxoids and Acellular Pertussis Vaccine Adsorbed (DTaP) package insert information under the section for Adverse Reactions, which runs from page 6 to page 11, we find the following declared admission that DTaP caused autism “during post-approval use of Tripedia vaccine.” See the copy and paste information below. So, why all the denials that a vaccine hasn’t or can’t cause autism?
Parents, here’s your proof!
Diphtheria and Tetanus Toxoids and Acellular Pertussis Vaccine Adsorbed
Tripedia
Additional Adverse Reactions
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. Events were included in this list because of the seriousness or frequency of reporting. Because these events are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequencies or to establish a causal relationship to components of Tripedia vaccine.2 [1]
The reference 2 above refers to Sanofi Pasteur Inc., Data on File – 072503. [2] Personally, I’d love to examine that Data on File 072503!
It should be noted that
Acellular Pertussis Vaccine Concentrates (For Further Manufacturing Use) are produced by The Research Foundation for Microbial Diseases of Osaka University (BIKEN), Osaka, Japan, under United States (US) license, and are combined with diphtheria and tetanus toxoids manufactured by Sanofi Pasteur Inc. Tripedia vaccine is filled, labeled, packaged, and released by Sanofi Pasteur Inc. [3]
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