Which leads me to wonder about this -->
which leads to this which from Sept 4, 2021---> Current Fiesta Mood...🥳🥳🥳
Which leads to wonder:
Drop 55
Look to Twitter:
EXACTLY THIS: "My fellow Americans, the Storm is upon us......."
God bless.
Which leads me to wonder about this -->
which leads to this which from Sept 4, 2021---> Current Fiesta Mood...🥳🥳🥳
Which leads to wonder:
Drop 55
Look to Twitter:
EXACTLY THIS: "My fellow Americans, the Storm is upon us......."
God bless.
Some highlights:
"Molnupiravir was developed for the treatment of Influenza. According to whistleblower complaint Molnupiravir has mutagenic properties and may change your DNA. Now, Molnupiravir has been repurposed for COVID-19. Merck has entered into agreements with Indian manufacturers and has also announced $5 million of donations to enter into Indian market. Here is all you need to know about Merck’s Covid pill Molnupiravir."
Molnupiravir may change your DNA
"In April 2020, Rick Bright, who was removed as head of the Biomedical Advanced Research and Development Authority (BARDA) before the approval of the drug, submitted a whistleblower complaint asserting that Ridgeback pressured BARDA to provide funding to manufacture EIDD-2801 despite Bright’s concerns that similar drugs in its class have mutagenic properties."
"A previous company, Pharmasset, that had investigated the Molnupiravir’s active ingredient had abandoned it over similar concerns."
"In genetics, a mutagen is a physical or chemical agent that permanently changes genetic material, usually DNA, in an organism and thus increases the frequency of mutations above the natural background level."
"exerts its antiviral action through introduction of copying errors during viral RNA replication."
What could go wrong? scrambling your own code maybe? What would that look like? Rise of the Mutants.
Anyone notice the obsession with trying to alter DNA lately?
Follow the money ---> "In June 2021, the U.S. Department of Health and Human Services committed to buy US$1.2 billion worth of molnupiravir (approximately 1.7 million courses) from Merck if it received an emergency use authorization (EUA) or approval from the U.S. Food and Drug Administration (FDA)."
