DON’T LET THEM LIE TO YOU ABOUT THE PFIZER JAB!

NOTHING WAS APPROVED BY FDA, ONLY FOR EMERGENCY USE!
SEE THE FULL EXTENTION: Pfizer-BioNTech COVID-19 Vaccine EUA LOA reissued August 23 2021 (fda.gov)
It appears that Pfizer is now approved for biological use, and is authorized to introduce their jab to complete their study. Which means, they are now liable when something goes wrong. They can now be sued…or so it appears they can. But it does not mean anyone can force you to take the jab. It is still a jab. You still have the right to refuse any treatment you do not want to take. They have specific dates to complete their testings for their post use. (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.” Final Protocol Submission: January 29, 2021 Study Completion: June 30, 2023 Final Report Submission: December 31, 2023).
They have a Biologics Licence Application and are now doing the post approval safety study. (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.) See: August 23, 2021 Approval Letter – Comirnaty (fda.gov)
What’s the difference between an EUA and a BLA?
A Biologics License Application, or BLA, is FDA’s standard “full approval” mechanism for biological products, including therapeutics and vaccines. A company seeking a BLA for its product must demonstrate that the product is “safe, pure, and potent,” which generally means completing robust, well-controlled clinical trials. A company receiving a BLA for their product can introduce the product into interstate commerce and market it for its approved uses. A BLA also has no defined end date — assuming no significant problems emerge, the product can stay on the market indefinitely.
So welcome to being a lab rat for the liars who deny their jabs do no harm. They are now doing their studies to see if it harms pregnant women. Pregnant moms are you up for that experiment? and to see if teens get enlarged hearts and how fast that is detected. Moms are you ready to subject your kids to that experiment? If you are hey…I hope you live well with that decision. God will be asking you why you did it. Not me. Read more of the cabal’s preplanned LOCKSTEP RESET JAB program: FDA Approves Pfizer Vaccine, Now Called Comirnaty—Here’s What FDA Approval Means | Health.com
Exploring the Legality of COVID-19 Vaccine Mandates – FactCheck.org

Even if a drug were to be approved…remember you have rights!
LIN WOOD REMINDS EVERY AMERICAN OF THEIR INFORMED CONSENT RIGHTS!
NO medical treatment can be undertaken or initiated on ANY patient without the patient’s CONSENT.
And the consent must be an INFORMED consent.
Nothing about FDA “approval” of a pharmaceutical or medical procedure impacts or alters this fundamental rule of law.
The choice to consent is the right of the patient.
Patients should choose wisely after being informed.
It is way past the time to stop the lies and illegal mandates. Mad scientists and eugenic doomsday depopulation cabal deep state operatives have gone too far and it is time to arrest all the treasonous people involved with bio warfare and the stolen election!
WHO BETRAYED AMERICA IN THE WHITE HOUSE?
It is time to remove all the traitors who signed contracts in Afghanistan agreeing to such a chaotic mess which is nothing more than a Taliban regime takeover of Kubul! And it is time to demand to publicly see these agreements that our cabal puppet Generals put together! It is time to see who signed these agreements and what they all entailed!
Expose the evil souless men who hide in the shadows! Bring them out into the light for the world to see!
Stand up and demand accountability for all their insane, upside down false flags and all of their lies about COVID-19 THAT THEY LIED ABOUT IN ORDER TO ENSLAVE THE ENTIRE WORLD!
Isn’t it time to open your eyes and see? Who is this bot they call Biden?
Who else is a puppet? Who else are not who they are telling you they are? Where did they all go? Why are you allowing them to not only steal an election, but even stealing the players too! And most of all why are you still acting like these players are who they say they are?

Dianne
UPDATE: 11:48 PM AUGUST 24, 2021
According to the Pfizer Vaccine Fact Sheet for Healthcare Providers, the vaccine is still an Emergency Use Authorization. They pulled a fast one to deceive the public.
The US Food & Drug Administration redacted some very important information about the Pfizer vax approval. They tried to trick you again. (That’s a nice way of saying they lied to you again. The words taken out of the grey redactions….said the following:
“The licensed vaccine has the same formulation as the EUA-authorized vaccine and the products can be used interchangeably to provide the vaccination series without presenting any safety or efectiveness concerns. The products are legally distinct with certain differences that do not impact safety or effectiveness.”
LEGALLY IT IS NOT FDA APPROVED AND THEY STILL ARE NOT LIABLE FOR ANY DAMAGE THIS DRUG DOES!
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Thank You my brother in Christ, I have not been worried (stressed a little) but not worried. God is my savior: my help and my salvation. Glory be to God. Thank you for some great advice!
Take a look at today’s biden bot. He has an attached earlobe on the his right AND a hanging earlobe on his left. When you watch his fake speeches look at him when he turns his head. One is attached and the other not. I’ve noticed this since CNN’s townhall and took pictures of each side.
We’re duped every day.
This is whats funny to me how everyone is afraid of FDA approval like it was some mandate. Do you know how many drugs FDA approves of and we are not mandated to take them? Are you mandated to take wayfarin or prosac, etc.? If you were mandated you would have to take who knows what from your doctor. Dont let these idiots lie about the vaccine being approved or that its mandated- they are losing their narratives and are scrambling to keep their plans intact.
They have to keep us scared by telling us they can mandate it now.
Well you how much Satan loves for people to FEAR no matter what side you are on.
VERSE OF THE DAY INSPIRATIONAL IMAGE – AUGUST 24, 2021
https://www.kingjamesbibleonline.org/Inspirational-Images/large/Romans_1-16.jpg
https://jasonofgod.files.wordpress.com/2012/07/armorofgod-31.jpg?w=1100
https://i.pinimg.com/originals/ba/25/82/ba25824aa80397d4058aa64644d69efa.jpg
Verse of the Day for Tuesday, August 24, 2021
✟
“For I am not ashamed of the gospel of Christ: for it is the power of God unto salvation to every one that believeth…”
Romans 1:16 (KJV)
https://www.fda.gov/media/151710/download
The so-called vaccine was approved. The facts are important, if you want to fight you must have truth on your side.
I don’t believe it ever should have been and I pray that people become more informed and refuse it at all costs!
We have mixed docs floating out there and mixed messages, as you say. The fact is they are approved for a biological use…and introduced to complete their study. They have specific dates to complete their testings for their post use. (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.” Final Protocol Submission: January 29, 2021 Study Completion: June 30, 2023 Final Report Submission: December 31, 2023).
They have a Biologics Licence Application and are now doing the post approval safety study. (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.)
What’s the difference between an EUA and a BLA?
A Biologics License Application, or BLA, is FDA’s standard “full approval” mechanism for biological products, including therapeutics and vaccines. A company seeking a BLA for its product must demonstrate that the product is “safe, pure, and potent,” which generally means completing robust, well-controlled clinical trials. A company receiving a BLA for their product can introduce the product into interstate commerce and market it for its approved uses. A BLA also has no defined end date — assuming no significant problems emerge, the product can stay on the market indefinitely.
Now, I wonder if they can be sued if something goes bad? Is there any difference betweent the two?
We need a miracle From GOD in the name of JESUS and a GREAT AWAKING. 8 months of a clown show. America is a laughing stock .And it is sad.
Not to add to the confusion, but WHY did BioNTech Manufacturing GmbH submit a biologics license application for COMIRNATY (COVID-19 Vaccine, mNRA) when the FDA Fact Sheet for Recipients and Caregivers states on page one that “COMIRNATY (COVID-19 Vaccine, mRNA) is an FDA-approved COVID-19 vaccine MADE BY PFIZER for BioNTech”? The footnotes to the Fact Sheet clearly says that COMIRNATY and the Pfizer-BioNTech COVID-19 vaccine, which has been received by millions, are different – “The products are legally distinct with certain differences that do not impact safety or effectiveness.” FDA may say they are interchangeable under the Emergency Use Authorization, but the vaccine taken by millions is NOT approved by the FDA. Is any COMIRNATY vaccine available anywhere?
Everyone should listen to your 2 Plandemic Documents that were posted yesterday at 5:05 PM.
I love your work and I continue to study History and the Bible. It’s amazing the times we live in… God Bless You Dianne
I was hoping I could post a jpg. Perhaps someone could teach me how to do it. “Be Just And Fear Not” Warren
I think the eligibility criteria that Jarrin states in the video is for participation in the clinical trial studies. I don’t think it’s the criteria to reject the vaccine. I am researching to find something concrete to combat an employer mandating the vaccine when they come down with it…which they will…eventually. There is so much evil in the world.
An employer can NOT mandate you to take a vaccine or any medical treatment. If you quit…you have no legal claim. If you let them fire you, then you have a legal claim that will hold up and win in court and you are eligible for unemployment. You have to have them fire you. Or kick you out of school, or deny you whatever they are denying you. No one can force you to take medical treatment, NOT EVEN YOUR DOCTOR. IT applies to every American citizen.
Thank you. I am researching for a friend. I already told him not to quit. I just thought I saw a resource previously that had sample letters you could use, etc. I just cannot remember where I saw that.
The CEO of Gab has them on there. The Frontline docs might have them also.
All sorts of help here, Vicki
https://americasfrontlinedoctors.org/legal/vaccines-the-law/
I work at a Native American owned casino on sovereign land and seems they can do what they want. But I know the drill, DON’T QUIT.
Liberty Counsel has free printable legal forms on their website. Here’s the link to their action page. https://lcaction.org/vaccine
gab.com has some good stuff
Thank you Dianne!! You empower us to keep pushing into the kingdom! Prayers and blessings!
I am sick about all this. It is disgusting what is happening the the American people
The EUA is supposedly only for kids aged 12 to 15yo. I read this document as well. IDK