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WHO, BioNTech Pfizer and FDA EMA Knew Everything at the End of 2019
In this episode of ICIC, Dr. Reiner Fuellmich talks to Italian researcher and biochemist Dr. Gabriele Segalla about the mRNA injections, who proves with his descriptive information material and his groundbreaking published studies that the manufacturer of the Pfizer-BioNTech COMIRNATY substance knew about the dangers of the so-called „vaccines“ already in the run-up to their release, and tried to cover up this fact.
What is the qualitative-quantitative composition of the substances? Also the difference between a solution and a colloidal suspension, the size of the nanoparticles, why the coalescence of the flocculants plays an important role and how great the danger of an overdose or an ineffectiveness is, are presented and explained in detail in this context.
Dr. Segalla’s presentation proves that the manufacturer was aware of stability problems and formulation difficulties, and goes on to explain what these stability and formulation problems were. Based on an FOI release document, it is clear that these were the very first factors that the manufacturer tried to cover up and censor.
Also, the manufacturer was aware of the adverse side effects of the substances and that they could cause health problems, which are confirmed by epidemiological statistics, such as Allergic or anaphylactic reactions, cardiovascular diseases, myocarditis, pericarditis, thrombotic phenomena, ischemic strokes, paresthesias, sudden metastasis, autoimmune diseases, key reactions of various kinds, alteration of the menstrual cycle, activation of herpes zoster, neurological and hepatic diseases, eye diseases, thyroid diseases, sudden death, etc.
There is no doubt that this is a formulation that is obviously unstable and yet was approved by the EMA a year later.