Hi Folks!
I haven’t written much about the covid shot lately, so thought it was time. The linked article is from vaersanalysis.info, and gives tons of graphs about the ACTUAL Safety & Efficacy of the covid shot. It is NOT from the CDC. The data is from the CDC, but this blog actually analyzes it and makes it understandable.
Interestingly enough, the CDC shut down their VAERS (Vaccine Adverse Events) Safety Signal Reporting system on September 29, 2023. What that means is, they no longer are tracking AEs from the covid shot. Note to self: that is a felony.
That is a complete dereliction of duty. Did I mention COMPLETE…? Below is what the CDC SAID they would do:
I worked at a pharmaceutical company doing research for 10 years, so I’ll give you a little background on how drugs are lawfully required to be approved. It helps to know the process, so you know how poorly the mRNA shots have been handled.
There is a step-wise process to studying a drug, and each Phase must be approved by the FDA before moving to the next Phase.
PRECLINICAL TRIALS - a compound researchers consider a candidate for becoming a useful drug will be tested in vitro on human cell clumps or in animals. If the compound has positive results and proves NONtoxic to cells or animals, it moves on to being tested in humans.
Next come Clinical Trials. Some writers are calling Phase 0 through Phase III trials “clinical trials.” They are not.
I looked up Clinical Trials to be sure I was talking the same language that is used today, and the verdict is out. What I mean is, when I was working for pharma, “clinical trials” included only those studies done specifically for SAFETY & EFFICACY. They were done in trained clinic sites, that were instructed rigorously to document EVERY adverse event, from hangnail to DEATH FOR ANY REASON. Even a death that might not seem drug-related, like being attacked by a tiger or falling off a cliff still had to be documented as “study related”, because it occurred during the study.
In addition, Clinical Trial refers only to studies done in a large population of up to 3,000 people. Study data are reported on standardized Case Report Forms, you can’t just jot stuff down on a cocktail napkin or bits of toilet paper. These CRFs are monitored regularly by the pharmaceutical company research team and usually an independent audit committee.
Bottom line: A Clinical Trial RIGOROUSLY shows Safety & Efficacy of a compound.
Two to 3 years is normal for Clinical Trials. The mRNA shots went from lab to mandate in less than a year. Hm.
The term “clinical trials” seems to be more fluid these days. Some sources I looked at consider Phase 0 through Phase III to be “clinical trials.” Were that the case, one could argue that the mRNA shots DID go through Clinical Trials, which insinuates they were tested for Safety and Efficacy. They were not.
So. Now I’ll explain the different trial phases, and let you draw your own conclusions.
PHASE 0 - Includes giving the compound to 15 or less healthy adult, nonpregnant humans. This usually is done in males, which could be problematic these days since some people out there don’t know what a man or woman actually is, but I digress. This phase establishes:
a tiny dose is given
signs of toxicity are noted and recorded
if toxicity is noted the drug goes BACK TO THE LAB
PHASE I - Includes giving the compound to 20 - 80 healthy nonpregnant humans, again usually males. This phase establishes:
the highest dose that can be given without “significant” side effects (side-effect parameters must be defined before the study; it’s not a shoot-from-the-hip decision)
correct route of dosage, i.e. oral, injection, intravenous, topical, etc.
some non-specific parameters of efficacy
some non-specific parameters of safety
PHASE II - Includes several hundred participants who actually have the disease for which the compound is being tested, who are given the compound in the dosage amount and route established in Phase I, and requires several months or years. This phase establishes:
if the dosage amount and route are correct
gives more specific parameters for safety & efficacy, but still is not adequate to fully establish safety & efficacy
helps establish protocols for Phase III studies
PHASE III - Includes several thousands of participants who actually have the disease for which the compound is being tested, being given the compound in the dosage amount and route established in Phase II, and often requires several years.
compound is evaluated for safety & efficacy against other known treatments
participants are blindly randomized to treatment with the testing compound or placebo treatment
neither patient nor researcher know which treatment a patient is receiving
because of the larger number of patients and longer duration of the study, rare and long-term adverse events are more likely to be noted
At this point the voluminous data is ready to be analyzed, criticized, re-analyzed, written up and submitted to the FDA for possible approval. To be approved, the data MUST SHOW the new compound is at least as effective as other current treatments.
Herein lies the rub for mRNA shots. It was never tested against other vaccines for being as effective against covid as, for example, the polio vaccine is against polio. Ruh roh. In addition, the mRNA shot should have been tested against ANY KNOWN TREATMENTS for covid. That includes hydroxychloroquine, ivermectin, dexamethasone, remdesivir, etc.
IF actual Safety & Efficacy Clinical Trials had been done the deadly adverse event profile of the drug would have been known before people got hideously sick and/or died from it.
One can argue that in light of the “pandemic” we needed to move faster than it would take for years of research to establish true Safety & Efficacy. One can argue that. However, we are looking at a disease that at the time was KNOWN to be 98.5% recoverable. Hm.
So what if lots of people got it? Ninety-eight point five percent of them got over it and returned to normal daily life. It’s called Mean-flu. Nasty, but highly recoverable. We didn’t need a freaking “vaccine”!!!!
Here’s the real rub: The Pfizer data coming out is showing that Pfizer KNEW how deadly the shot could be. They found that out in the Phase II studies. HOWEVER, they incorrectly called adverse events that were causing hospitalization “non-serious”, then dropped the patient from the study so no further incriminating follow up data could be recorded. Their files show that they KNEW the shots could be deadly.
As furious as that makes me, let me explain why it’s so serious. Well, other than the fact they were releasing a deadly product they knew would be forced on the world population. There is that.
In addition, there are things called GCPs, Good Clinical Practices, that are written down for pharmaceutical companies to follow when doing research for submission to FDA to approve a new drug. To disregard those GCPs is a felony. Of course, killing people is a felony, too, but I digress. To disregard LOTS of those GCPs constitutes LOTS of felonies. If elephants ate felonies, the study of the mRNA shots would cause massive elephant obesity around the globe for a long, loooooong time. Those gluttonous pachyderms would be grounded like beached whales.
The drug companies KNEW what they were doing.
There’s also the possibility the mRNA shots were only distributed by drug companies, but were researched and manufactured by the Department of Defense. But that’s for another time.
Stay as far away from the shots as you can and use the spike protein degradation protocol I put in an earlier post if you did take it. It’s proven to be pretty effective.
Okay, I’m done for now. I hope this explained some important stuff to you. These shots have NEVER gone through Clinical Trials nor have they been tested for Safety & Efficacy. The drug companies and the FDA have committed an astounding number of felonies, including murder. And they knew the drug was murderous while they tested it. Oh, the humanity!
One day they will be held accountable. If not here, then in the afterlife.
Rest assured. And remember Philippians 4:19 -
“And my God will meet all your needs according to His GLORIOUS Riches in Christ Jesus.”
True that.
Thank you.