Many people have asked: how is the best way to stop the insanity behind the incessant vaccine narrative? The likely best approach is to start demanding the pharmaceutical companies have their liability waivers removed.
If the vaccine is safe and effective, why would the U.S. government still need to provide liability waivers from adverse vaccine outcomes?
Start pressuring legislators and elected officials to force the elimination of the waivers. Alinsky them… Make them live up to their own narrative; their own words, their own rules. If the vaccines are safe/effective, why do we need the waivers? If you want to get more people vaccinated, drop the waiver moving forward.
Eliminate those liability waivers and watch how fast every vaccine mandate is dropped, while every voice demanding vaccination goes quiet.
There is an FDA approved vaccine at this point. However, that vaccine is unavailable. The vaccine that i being used in its place has the same ingredients, so what’s the difference, right?
The difference is that they are legally separate products. So, you get a shot with a vaccine that is approved for emergency use, and the makers are shielded from liability, and the people giving out the shots don’t even understand this.
Well, wouldn’t you want a waiver if you were purposely poisoning people? What a stupid question. This is what happens when you refuse to recognize evil.
Worldwide vaccine failureDeaths hitting new highs in Singapore (85% of the population fully vaccinated – NOT adults, the entire population):
From Singapore to the Netherlands to Iceland to Vermont. And coming soon to the entire northern half of the United States.
I am afraid this is going to become common..And then they will find a way of covering it up..which most likely they have already figured out how they will ether ignore it or say it is because of other health issues..It is coming to those of all ages who took the jab..
You can count on a cover-up of long-term vaccine side effects, since the majority of *short-term* vaccine injuries and deaths were already swept under the rug.
The majority of short-term vaccine injuries occur after the first injection. These victims are not counted as vaccinated until two weeks after their SECOND shot.
HELLOOO.. When you’re dead or injured, you never get around to the second shot!
So none of these dead and injured people are counted as vaccinated? What happens when you drop dead with the syringe still in your arm? Is it still officially counted as an UNvaccinated death/injury?
When something is declared an emergency the big pharm co should have to develop and distribute any medicines at cost. No profit. This would greatly help to keep them from keeping a lie going as they are going now.
This I believe is how they are getting around lawsuits..emergency authorization..You see how happy they are that is just emergency authorization..because I was reading from an article put out by one of the vax pushers..that because it is not FDA approved they can put a disclaimer that says it is for emergency authorization and that way they don’t incur liability..
But that emergency use authorization (EUA) for *experimental* mRNA injections also means that they cannot be legally mandated! People *must* legally consent to volunteer for these Big Harma EXPERIMENTS. ? ? ?☠️
And yet the governor’s and universities and hospitals all pretend it’s now FDA approved and they can force you.
This is a well planned population wide planned culling event. They are killing us off and they know they are killing us off and they planned to be killing us off and hey have no intention of stopping in killing us off.
You’re everywhere!
If they don’t get us with vax..Wuhan is trying to create the monster virus..50 percent more deadly than COVID..Senator Rand Paul has been trying so hard t get this..murder hole to be defunded.but so far no one else is helping him..that I know of..
If the liability waivers are dropped and the providers of the vax no longer have protection, they will be withdrawn from the market and the reason will be a “need for further study”.
The question as to why an emergency can still be claimed to exist is very illuminating! In this regard, our government (at all levels), when pressed to justify its extreme measures since the very outset, has always stood on the fact that the pandemic was creating a lack of available medical services capacity. And this point hasn’t changed, and CONTINUES TO BE THE ONLY BASIS JUSTIFYING THIS EMERGENCY!
They’ve never once questioned the fact that the death rate is very small, or any similar data related to the various levels of danger to different groups and subgroups of the population. Therefore, the key insight about this pandemic as regards the role our government has played throughout by over-hyping a state of emergency born strictly of limited medical capacity (and nothing else!), and willfully conflating it with a grave danger to the general health of America citizens (not true!) is the following: our medical system has incrementally grown ossified from its adherence to a socialist model, thus losing the free enterprise vitality necessary to grow and prosper to meet the future demands of a healthy growing population.
If Republican politicians fail to state this fact prominently and forcefully, so as to identify it as the central reason why the US economy was held hostage these last 20 months, the Nation will continue to be propagandized by the same leftwing media outlets that had egregiously blamed President Trump (biggest lie ever told!) for allowing the pandemic to grow out of control.
Moreover, unless this point is understood, we will fail to comprehend the contributory facts that created our avoidable predicament. Indeed, to avoid similar events in the future, we need to return to the principles that had once made our nation great, i.e. decentralized government that relies on the free enterprise system to create abundant goods and services , not limited, strictly controlled, government sponsored goods and services such as occurs in our current medical system.
For me, that’s the biggest lesson concerning our government’s rationale for invoking emergency powers! It certainly wasn’t due to health risks, and it can’t be over-emphasized that the government never actually claimed it was, although they clearly allowed the two issues to be conflated in the minds of the public.
Shame!
Not only that the ‘emergency’ has run it’s course, but it is also my understanding that an EUA can only be issued by the FDA when there are no *other* FDA-approved alternatives.
Guess what? We have an FDA-approved alternative!
Now that the FDA officially “approved” Pfizer’s COMIRNATY, shouldn’t all the other EUA’s cease to exist? WHY is Big Harma still allowed to use the other (EUA) Pfizer injection, the EUA Moderna injection and any other EUA injections, with all of them under liability shields, no less?
Since COMIRNATY is approved, all the other EUA’s should end now, correct? It isn’t necessary, nor is it prudent, to continue *experimenting* on humans now that there is an official, “FDA approved” alternative!
PS: I noticed that spell check no longer recognizes COMIRNATY. I guess the powers-that-be would prefer we stop referring to it anymore.. since it is mysteriously “approved” but ..just as mysteriously.. nowhere to be found? ?
When I just searched it to check my spelling, it came up as “Pfizer Comirnaty 2024.”
2024? What the heck is *that* all about?
Under the Commiraty approval document by the FDA, there are still a number of studies that still need to be administered through 2025. Here’s the reference:
Part 1 of 2 comments due to size:
The FDA and Pfizer in rushing approval for the Comirnaty vaccine are committing crimes against humanity because of what they themselves admit in the FDA’s original approval letter for the Pfizer Comirnatyvaccine – here’s a link to it from the FDA’s website:
https://www.fda.gov/media/151710/download
I have excerpted and condensed the parts from the above PDF link – all of these safety and effectiveness studies are all set to be completed in future years – does that make sense to you? Would you let your children get injected with this jab??
But it’s worse than that – you’ll notice they want studies on adults as well since they never bothered with those in the first place.
In their own words:
BioNTech Manufacturing GmbH August 23, 2021
Attention: Amit Patel
Pfizer Inc.
235 East 42nd Street
New York, NY 10017
We are deferring submission of your pediatric studies for ages younger than 16 years for this applicationbecause this product is ready for approval for use in individuals 16 years of age and older, and the pediatric studies for younger ages have not been completed.
1. Deferred pediatric Study C4591001 to evaluate the safety and effectiveness of COMIRNATY in children 12 years through 15 years of age.
Study Completion: May 31, 2023
Final Report Submission: October 31, 2023
2. Deferred pediatric Study C4591007 to evaluate the safety and effectiveness of COMIRNATY in infants and children 6 months to <12 years of age.
Study Completion: November 30, 2023
Final Report Submission: May 31, 2024
3. Deferred pediatric Study C4591023 to evaluate the safety and effectiveness of COMIRNATY in infants <6 months of age.
Final Protocol Submission: January 31, 2022
Study Completion: July 31, 2024
Final Report Submission: October 31, 2024
We have determined that an analysis of spontaneous postmarketing adverse events reported under section 505(k)(1) of the FDCA will not be sufficient to assess known serious risks of myocarditis and pericarditis and identify an unexpected serious risk of subclinical myocarditis. Furthermore, the pharmacovigilance system that FDA is required to maintain under section 505(k)(3) of the FDCA is not sufficient to assess these serious risks.
Therefore, based on appropriate scientific data, we have determined that you are required to conduct the following studies:
4. Study C4591009, entitled “A Non-Interventional Post-Approval Safety Study of the Pfizer-BioNTech COVID-19 mRNA Vaccine in the United States,” to evaluate the occurrence of myocarditis and pericarditis following administration of COMIRNATY.
We acknowledge the timetable you submitted on August 21, 2021, which states that you will conduct this study according to the following schedule:
Monitoring Report Submission: October 31, 2022
Interim Report Submission: October 31, 2023
Study Completion: June 30, 2025
Final Report Submission: October 31, 2025
5. Study C4591021, entitled “Post Conditional Approval Active Surveillance Study Among Individuals in Europe Receiving the Pfizer-BioNTech Coronavirus Disease 2019 (COVID-19) Vaccine,” to evaluate the occurrence of myocarditis and pericarditis following administration of COMIRNATY.
We acknowledge the timetable you submitted on August 21, 2021, which states that you will conduct this study according to the following schedule:
Interim Report 1 Submission: March 31, 2022
Interim Report 2 Submission: September 30, 2022
Interim Report 3 Submission: March 31, 2023
Interim Report 4 Submission: September 30, 2023
Interim Report 5 Submission: March 31, 2024
Study Completion: March 31, 2024 Final Report Submission: September 30, 2024
Part 2 of 2 comments due to size:
6. Study C4591021 substudy to describe the natural history of myocarditis and pericarditis following administration of COMIRNATY.
We acknowledge the timetable you submitted on August 21, 2021, which states that you will conduct this study according to the following schedule:
Final Protocol Submission: January 31, 2022
Study Completion: March 31, 2024
Final Report Submission: September 30, 2024
7. Study C4591036, a prospective cohort study with at least 5 years of follow-up for potential long-term sequelae of myocarditis after vaccination (in collaboration with Pediatric Heart Network).
We acknowledge the timetable you submitted on August 21, 2021, which states that you will conduct this study according to the following schedule:
Final Protocol Submission: November 30, 2021
Study Completion: December 31, 2026
Final Report Submission: May 31, 2027
8. Study C4591007 substudy to prospectively assess the incidence of subclinical myocarditis following administration of the second dose of COMIRNATY in a subset of participants 5 through 15 years of age.
We acknowledge the timetable you submitted on August 21, 2021, which states that you will conduct this assessment according to the following schedule:
Study Completion: November 30, 2023
Final Report Submission: May 31, 2024
9. Study C4591031 substudy to prospectively assess the incidence of subclinical myocarditis following administration of a third dose of COMIRNATY in a subset of participants 16 to 30 years of age.
We acknowledge the timetable you submitted on August 21, 2021, which states that you will conduct this study according to the following schedule:
Final Protocol Submission: November 30, 2021
Study Completion: June 30, 2022
Final Report Submission: December 31, 2022
We acknowledge your written commitments as described in your letter of August 21, 2021 as outlined below:
10. Study C4591022, entitled “Pfizer-BioNTech COVID-19 Vaccine Exposure during Pregnancy: A Non-Interventional Post-Approval Safety Study of Pregnancy and Infant Outcomes in the Organization of Teratology Information Specialists (OTIS)/MotherToBaby Pregnancy Registry.”
Study Completion: June 30, 2025
Final Report Submission: December 31, 2025
11. Study C4591007 substudy to evaluate the immunogenicity and safety of lower dose levels of COMIRNATY in individuals 12 through <30 years of age.
Study Completion: November 30, 2023
Final Report Submission: May 31, 2024
12. Study C4591012, entitled “Post-emergency Use Authorization Active Safety Surveillance Study Among Individuals in the Veteran’s Affairs Health System Receiving Pfizer-BioNTech Coronavirus Disease 2019 (COVID-19) Vaccine.”
Study Completion: June 30, 2023
Final Report Submission: December 31, 2023
13. Study C4591014, entitled “Pfizer-BioNTech COVID-19 BNT162b2 Vaccine Effectiveness Study – Kaiser Permanente Southern California.”
Study Completion: December 31, 2022
Final Report Submission: June 30, 2023
While the MSM condemns the use of ivermectin, the most populated state in India just declared they are officially COVID free after promoting widespread use of the safe, proven medicine. In addition to this, Ivermectin attaches to covid spikes and prevents them from binding to ACE2. Get your Ivermectin today while you still can! https://ivmpharmacy.com
How do you know how much to take ? Have you ordered from this place in India ?
While the MSM condemns the use of ivermectin, the most populated state in India just declared they are officially COVID free after promoting widespread use of the safe, proven medicine. In addition to this, Ivermectin attaches to covid spikes and prevents them from binding to ACE2. Get your Ivermectin today while you still can! https://ivmpharmacy.com
If you were pushing poison, would you want to be liable for it? Meanwhile: ONE child dies and Peloton recalls its ENTIRE line of treadmills – yet when thousands of children die from vaccines, there’s no recall, no lawsuits and no government oversight. This stuff is poison, Liability? The stockholders wouldn’t stand for it!