This is what happens when you combine the desire for speed with politicized regulators. All have been due to failures of testing or failures in manufacturing processes. Most of these tragedies occurred even before vaccine manufacturers were given virtually complete protection from liability in 1987. With the duration of patent exclusivity determining how much new products earn, products are rushed to market as quickly as possible, most using a shortened path for FDA review. Recalls and market removals of approved products are much more common than they used to be. We can only expect more of these disasters in the future, especially if the products are mandated for everyone. The adverse effect profile of drugs and vaccines is generally not well known until millions of people have received the drug or vaccine. New federal legislation (21st Century Cures Act of 2016 etc.) that speeds up licensing of vaccines, and removes liability from the manufacturers for all vaccines placed on the childhood schedule, all vaccines recommended by CDC for pregnant women, and new, potentially unlicensed products used during declared emergency situations — increases the potential risk of vaccines.
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