Yep I'd be ready to hit the road running knowing this was in the cocktail!!!!!!
71. January 2002. The anthrax vaccine manufacturer’s license to manufacture and distribute vaccine (under a new trademark, BioThrax) was approved after the FDA accepted the expedited application. A review of FDA's newly approved anthrax vaccine product label revealed systemic adverse reaction rates now published at 5 to 35% based on post-surveillance studies, which was up to 175 times or 17,500% higher than the original 0.2% on the old product label when the AVIP was announced in 1997. The new anthrax vaccine product label also listed six reported deaths including cardiac arrest, myocardial infarction, aplastic anemia, central nervous system (CNS) lymphoma. Birth defects were also listed based on a US Navy retrospective study. The FDA revised the product labeling, confirming positive risk of birth defects based on human data, and downgraded the vaccine to Category D. Approximately 40 serious adverse events were now on the product label including: cysts, sepsis, angioedema, asthma, aplastic anemia, lymphoma, leukemia, vascular disease, systemic lupus, multiple sclerosis, arthritis, Guillain-Barré syndrome, immune deficiency, seizures, tremors, facial palsy, hearing and visual disorders, meningitis, encephalitis, atrial fibrillation, spontaneous abortion, liver abscess, fatigue, mood-cognition, musculoskeletal disorder.
http://www.hspig.org/ipw-web/bulletin/bb/viewtopic.php?t=1926
Ah the good life!!!
Hog
