It is important to remember that these are EXPERIMENTAL “vaccines” and the only mRNA “vaccines” to receive an “emergence” approval as “safe”. ALL PREVIOUS mRNA “vaccines” have FAILED in ANIMAL TRIALS. These “vaccines” SKIPPED ANIMAL TRIALS. The Humans are now the Animal of Choice for Big Pharma.
Please make use of quotes around the word ‘vaccine’ when referencing the cited shots.
j/k (or not).
These shots are NOT vaccines. The propaganda is both infuriating and nauseating (the latter pertaining to the level of hysteria by sheeple).
You should have overheard the conversation in my earshot while performing work in a hospital. These were doctors discussing the coronavirus ‘vaccines’. Almost word-for-word, they were spouting federal propaganda while discussing continued masking & ‘social distancing’. It was rather pathetic to hear (yet not unexpected for purveyors of AMA dogma).
Thanks.
The mRNA elicited an immediate immune response before it could enter the animal's (mouse) cells where it was supposed to initiate transcription of the viral antigen. Drew Weissman, MD, PhD, a professor of Infectious Diseases in Penn’s Perelman School of Medicine, and Katalin Karikó, PhD, an adjunct associate professor at Penn and a senior vice president at BioNTech, together discovered that exchanging one of the four building blocks of messenger ribonucleic acid (mRNA) molecules could overcome this. The modified nucleoside ( pseudouridine or 5-methylcytidine) allowed the mRNA strand to avoid the immediate immune attack and; thereby, sneak into the host cell where it could produce the viral antigen protein (in this case, the Covid spike).
This modified nucleoside trick is the game changer that makes this technology work as well as it does.
We understand there are concerns the vaccine was developed quickly, but Kati (Karikó) and I developed our enabling technology fifteen years ago, and we and other scientists have been working on how to use it to develop mRNA ever since,” Weissman said. “This isn’t brand new—scientists have been studying vaccines using this mRNA platform for at least six or seven years. Based on all of the data available to date, these mRNA vaccines have shown a good safety profile. Clinicians always consider risk–benefit scenarios whenever we recommend a new treatment or a new vaccine to patients and to the public, and with this vaccine there’s no comparison—the benefit is huge and there’s really little to no risk.”
It is important to remember that these are EXPERIMENTAL “vaccines” and the only mRNA “vaccines” to receive an “emergence” approval as “safe”
what specific safety concerns do you have?