The jabs are all problematic because the manufacturing processes used are new, as are the excipients they contain, which a team of experts from the Cholet public hospital in the west of France say “should be considered as new active substances.”
Led by Dr. Catherine Frade, a pharmacist, the research team worked with public data released by the European Medicines Agency (EMA) in relation to the injections released by Pfizer-BioNTech, Moderna, AstraZeneca, and Janssen (Johnson & Johnson). All four of these injections only have temporary authorization based on perceived need, as opposed to approval based on clinical evidence of safety and efficacy.
All of the jabs are also still subject to studies that extend out to 2024 – three years from now – and beyond. Very little is known, at this point, about the long-term side effects of the injections, though we are seeing short-term side effects in the form of serious blood clots and death.
According to the CTIAP, all four Chinese Virus injections were released for public administration before “proof of quality for the active substance and the finished product” was verified. All of the labs where the jabs are produced also obtained future deadlines to submit associated studies.
What this means, of course, is that every person who takes a Wuhan Flu shot is a human guinea pig participating in a mass pharmaceutical experiment. How vaccine recipients fare moving forward remains to be seen.
In the coming months and years, the research team warns, “variabilities, which impact the very core of the product, could even invalidate any clinical trials conducted.”
“Prudence would even dictate that, in all countries where these vaccines against COVID-19 have been marketed, all the batches thus ‘released’ should be withdrawn immediately; and that these MAs that have been granted should be suspended, or even canceled, as a matter of urgency until further notice,” they say....<<<Read The Full Article Here>>>...
