The Never-Ending Pandemic...
New Medications Engineered To Create New Variants...
Nearly three years into the Covid-19 pandemic and we’re still seeing the approval of new medications for “Emergency Use Authorization” (EUA). Why do government officials keep extending the “state of emergency”? How is it that this particular illness has functioned completely differently than any other illness in the history of the world? The fast-tracking of questionable medications may be playing a role in the continued existence of this “pandemic”. Not only are the vaccines causing all kinds of irreparable harm, but there are also other new treatments being used upon the unsuspecting masses to keep the public deeply entrenched in the throes of a never-ending wave of endemic illness and death, all in the name of “science”. Today, we’re going to examine a relatively new pharmaceutical product that has been approved for EUA by the FDA. The name of the drug is Molnupiravir, which also goes by the brand name, Lagevrio. This drug has some very concerning properties that make little sense in light of the fact that there are other therapeutics available to help alleviate some of the more serious symptoms associated with this malady. But, despite that fact, the powers that be have to keep rolling the ball forward, and keep the fear narrative alive and well to “get more shots in arms”. What is this new medication, which is being touted as a “miracle drug” by some? Let’s look at its description and history, shall we? “Molnupiravir is a prodrug of the synthetic nucleoside derivative N4-hydroxycytidine and exerts its antiviral action by introducing COPYING ERRORS during viral RNA replication.” Let me translate for you, essentially, it works by causing mutations in the RNA sequence of cells infected with viral proteins, ostensibly stopping the virus from replicating itself. But, let’s look at a further description of its mechanism of action. “Molnupiravir inhibits viral reproduction by promoting WIDESPREAD MUTATIONS in the replication of viral RNA by RNA-directed RNA polymerase…”“This causes more MUTATIONS in all downstream copies than the virus can survive, an effect called viral ERROR CATASTROPHE or LETHAL MUTAGENESIS.” So, in theory, the drug causes the infected cells to mutate and therefore stop the virus from replicating (and, although it is possible that this can cause mutagenic damage to healthy cells as well, they don’t tell you that). This drug was originally developed as an experimental influenza treatment at Emory University’s Drug Innovation Ventures at Emory (DRIVE) company, but its development was abandoned for MUTAGENICITY concerns. It was since acquired by Ridgeback Biotherapeutics, who then partnered with Merck to further development with help from grants by the Defense Department, and was given authorization for EUA in December of 2021. It is what they call an “Investigational” oral antiviral. That means it’s experimental, folks. It passed Emergency Use Authorization bu a very narrow margin (13-10) because of its questionable efficacy (only 30% effective) and concerns that “Molnupiravir’s MUTAGENIC EFFECTS COULD CREATE NEW VARIANTS THAT EVADE IMMUNITY AND PROLONG THE COVID-19 PANDEMIC.” You read that right, there are serious scientifically valid concerns that this new “wonder-drug” could turn human beings into to walking variant factories, producing new, novel diseases that evade immunity. And here we are. The eugenics program has gone from passive mode into full frontal operational mode, right in public view, and people still refuse to accept the fact that this whole “pandemic” situation is all part of a larger population reduction program instigated by an international “elite” to cull the population of whom they call, “the useless eaters” (their words, not mine). Links to pertinent material will be provided below. I hope you find value in this article. If you do, please consider checking out some of my other work (links also below). Thank you for reading. Cheers!
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