What does this FDA language even mean, “safe and effective”?
These are subjective terms repeatedly deployed as part of a propaganda campaign. The FDA provides no data to support their claims, and no qualifications concerning what they mean by “safe and effective”. FDA, CDC and the current executive branch now acknowledge that myocarditis, stroke in the elderly, seizures in children, neurologic damages, reproductive/menstruation risks in women, and a wide variety of other adverse events are associated with these modified mRNA products. Disclosure of virtually all of these adverse events has been actively suppressed and delayed by FDA, CDC and the executive branch. They assert that these are “rare” adverse events, but do not define what “rare” means, making this yet more propaganda.
Contrary to FDA denial and disinformation regarding risks of contaminating DNA fragment delivery and genotoxicity (genome damages by inserting these DNA fragments into the genome of patients), Moderna US Patent #2019/0240317 A1 discloses that Moderna is aware of the genotoxicity risks of DNA when delivered into patients by highly active non-viral lipid nanoparticle delivery systems includes the risk of genotoxicity, resulting in “problems including the possibility of insertional mutagenesis, which could lead to the activation of oncogenes or the inhibition of tumor suppressor genes”.
In contrast to the perverse obscene tragedy associated with this centralized top-down approach which has been endorsed and promoted by mandarins of finance, governments, globalist organizations and massive non-governmental organizations, the traditional “bottom up” approach of focusing on treatment of symptoms by repurposing the existing pharmacopeia to prevent disease and death from a highly inflammatory respiratory virus was far superior to the centralized top-down approach.
If nothing else, due in large part of those with the courage to speak scientific and medical truth to power, the world is increasingly becoming aware that the propaganda promoted by the vaccine manufacturers, US Government and the World Health Organization concerning the COVIDcrisis and the centralized top-down approach has been a fraud.
This list of published adverse event types stands in stark contrast to the list of over 6,000 published and curated publications which I have provided listing peer reviewed publications focusing on how to overcome vaccine hesitancy.
The adverse event publications fall into the following broad categories:
Immune issues/Auto immunity/Guillain-Barre Syndrome
Other Adverse Events, including death.
Recently, results of a study which was funded by a non-profit self-help group for the vaccine injured has become available. This privately funded “React-19” group, has provided the vast majority of funding available to treat the COVID vaccine damaged, and has now funded a study at Yale University.
React 19 membership includes over 36,000 vaccine injured Americans, members from over a dozen countries worldwide in their injured global coalition. While the Federal government has paid out just $17,000 to six people for their vaccine injuries, ACT 19 has paid out over $750,000 in medical grants. ¾ of a million dollars to the Government’s $17,000.