Covid-19 Pfizer Releases Court Ordered Test Results.
Posted by Sandy on March 5, 2022 · Leave a Comment
I previously wrote two stories (1) Tuskegee Experiment (2) Aids Epidemic. I wrote the stories knowing it would lead to the third story concerning Covid and attempted to reveal a dark place in American history and what the government is capable of if not watched with a close eye. Thankfully we have people who are willing to do that for us.
Using fear as a means of manipulating the masses, people agreeing to give up the rights to manage their own bodies and health, forced to carry vaccine card’s and allowing themselves to be injected with a vaccine with unknown long term consequences.
One of my favorite quotes: “Truth is like a lion, you need not defend it. Let it loose and it will defend itself!” St. Augustine.
Full disclosure
I did not want, or accept the vaccine for Covid. Here’s my explanation for the decision I made.
I am in excellent health, with the exception of a knee that needed replacement, take no prescribed medication, but take vitamins and minerals daily. I still manage my home and continue to edge, weed-wack and mow my own lawn, although what used to take me 3-4 hours are spread out over 2 days.
On my 65th. birthday I became eligible for Medicare and was advised to find a doctor. I did. On my first visit he asked if I had received a flu shot. I had not, so he gave me one. It took all of 2 day’s before I became violently ill, and it lasted 7-10 days. I attributed it to the flu shot.
Second year the doctor said he was going to give me a fly shot, and I refused the vaccine. When he questioned me I told him how sick I was after receiving it previously. His response was “think how much sicker you would have been had you not received it” I relented and held my arm out for the second flu shot, with the same devastating results.
Third year he insisted I take the flu shot, I insisted I needed a doctor who would listen to me, left his office and never looked back. My new doctor listened and understands, doesn’t insist, and explained he has to ask if I want the flu and pneumonia shot. I just smile at him.
For over two years we have listened to MSM (main stream media) report on Carona and the wonderful vaccine developed that would save lives if we consented to receiving it. Many like myself were not willing and we were considered villainous, a danger to society, not welcome if we couldn’t produce a Vaccination Card.
President Biden and Fauci appeared on TV and quoted in MSM, that was the information we received.
Media appeared never to question it, just accepted what was told to them and reported the news as given.
I have two people in my life, one an old friend who advises me on stories I want to write on WPB Watch. He shows me the other side of the coin. Many times he is right, and when we don’t agree he is fine with it. You know who you are, and I thank you for your patience.
The other is a new friend who finds information and is willing to share it with me, as he has done for this story. I thank you for your trust, and you know who you are. Let the journey begin.
12/21/2020 ” President-elect Joe Biden received his first dose of the Pfizer and BioNTech coronavirus vaccine on live television and reassured Americans of the vaccine’s safety.”
1/11/2021 – “Joe Biden on Monday received the second dose of the Pfizer/BioNTech Covid-19 vaccine on camera, as part of an effort by the President-elect’s incoming administration to reassure the country of the safety of the vaccines.”
9/27/2021 “President Joe Biden received a Covid-19 booster shot Monday, in accordance with the latest guidance from the Centers for Disease Control and Prevention.”
The President of the United States is one of the most protected people in the world, and Americans are expected to believe Biden received a vaccine developed by Pfizer, the first to receive emergency use authorization from the Food and Drug Administration (FDA) in under a year not knowing the long term effects. It worked, people began rolling up their sleeves. One friend told me she trust the science, I replied the science is what Fauci and the CDC tells you it is.
We received daily reports on people who died from Carona, millions admitted to hospitals and placed on ventilators. One man was shot in the head and his reported cause of death was Carona virus. The media picked up on the story and received an apology, a mistake was made.
Sen. Scott Jensen, R-Minn., a physician in Minnesota, was interviewed by “The Ingraham Angle” host Laura Ingraham on April 8 on Fox News and claimed hospitals get paid more if Medicare patients are listed as having COVID-19 and get three times as much money if they need a ventilator.
Jensen said, “Hospital administrators might well want to see COVID-19 attached to a discharge summary or a death certificate. Why? Because if it’s a straightforward, garden-variety pneumonia that a person is admitted to the hospital for – if they’re Medicare – typically, the diagnosis-related group lump sum payment would be $5,000. But if it’s COVID-19 pneumonia, then it’s $13,000, and if that COVID-19 pneumonia patient ends up on a ventilator, it goes up to $39,000.”
Jensen clarified in the video that he doesn’t think physicians are “gaming the system” so much as other “players,” such as hospital administrators, who he said may pressure physicians to cite all diagnoses, including “probable” COVID-19, on discharge papers or death certificates to get the higher Medicare allocation allowed under the Coronavirus Aid, Relief and Economic Security Act. Past practice, Jensen said, did not include probabilities.” Read the entire story below:
December 18, 2021 Wait what? FDA wants 55 years to process FOIA request over vaccine data
Freedom of Information Act requests are rarely speedy, but when a group of scientists asked the federal government to share the data it relied upon in licensing Pfizer’s COVID-19 vaccine, the response went beyond typical bureaucratic foot-dragging.
As in 55 years beyond.
That’s how long the Food & Drug Administration in court papers this week proposes it should be given to review and release the trove of vaccine-related documents responsive to the request. If a federal judge in Texas agrees, plaintiffs Public Health and Medical Professionals for Transparency can expect to see the full record in 2076. Read the entire story below:
“January 7, 2022 Score one for transparency. Judge orders FDA to hasten release of Pfizer vaccine docs.”
“A federal judge in Texas on Thursday ordered the Food and Drug Administration to make public the data it relied on to license Pfizer’s COVID-19 vaccine, imposing a dramatically accelerated schedule that should result in the release of all information within about eight months.
That’s roughly 75 years and four months faster than the FDA said it could take to complete a Freedom of Information Act request by a group of doctors and scientists seeking an estimated 450,000 pages of material about the vaccine.” Read the entire story below:
“Under the PREP Act, companies like Pfizer and Moderna have total immunity from liability if something unintentionally goes wrong with their vaccines.
The quickest vaccine ever developed was for mumps. It took four years and was licensed in 1967. Pfizer’s Covid-19 vaccine was developed and cleared for emergency use in eight months — a fact that has fueled public mistrust of the coronavirus inoculation in the U.S.” Read the entire story below:
https://www.cnbc.com/2020/12/16/covid-vaccine-side-effects-compensation-lawsuit.html
Discovery of Ivermectin A National Historic Chemical Landmark Dedicated at Merck & Co., Inc., on December 2, 2016.
“The story is so improbable it defies belief: a soil sample from Japan stops suffering in Africa. It starts when a scientist discovers a lowly bacterium near a golf course outside Tokyo. A team of scientists in the United States finds that the bacterium produces compounds that impede the activity of nematode worms. It is developed into a drug that wards off parasites in countless pets and farm animals, averting billions of dollars in losses worldwide. Extraordinarily, the drug also prevents or treats human parasitic diseases that would otherwise cause blindness and other severe symptoms in hundreds of millions of people in many of the poorest countries on Earth”
https://www.acs.org/content/acs/en/education/whatischemistry/landmarks/ivermectin-mectizan.html
COVID Patient in Coma Gets Ivermectin After Court Order: (Nurije Fype)
“A 68-year-old woman with COVID-19, who has been in intensive care in an Illinois hospital for a month, started receiving the controversial drug ivermectin this week after her family sued the hospital to have someone administer it.
Fype’s daughter said her mother has been a patient at Elmhurst Hospital since April 7, was put on a ventilator on April 28, and is now in a coma.
The FDA has warned against ivermectin’s use for treating COVID-19, but a high-profile group of doctors has spoken passionately in favor of it. The National Institutes of Health said there is not enough data to recommend either for or against its use in treating COVID-19.
Three days later, according to the Daily Herald, the lawyer for the hospital, Joseph Monahan, argued the hospital could not find a hospital-affiliated doctor to administer the ivermectin.
In a follow-up hearing on Tuesday, Monahan told Orel that the hospital asked 20 doctors and 19 other health care workers, including nurses and pharmacists, to administer the medication and they all declined.
When Fype’s doctor was unable to administer it, the legal team found another doctor, Alan Bain, DO, to do it. Monahan said Bain was granted credentials to work at the hospital so he could administer it Monday evening.”
https://www.webmd.com/lung/news/20210506/covid-patient-in-coma-gets-ivermectin-after-court-order
For 20 days, Dr. Alan Bain of Chicago drove to Elmhurst Hospital, usually after a full work day, to administer ivermectin to a critically ill woman named Nurije Fype, whose daughter, Desareta, sought and won two court orders for the COVID treatment. Dr. Bain had been asked to give the drug after other hospital physicians declined, despite the court’s orders, to give the FDA-approved medication.
She said her mother is expected to return home late this week.”
The courts have been busy allowing families to sue hospitals and doctors for refusing to administer ivermectin which they believed would save their loved one’s.
March 1,2022 FDA started releasing the Court ordered Pfizer documents.
March 2,2022 I received FDA documents containing 38 pages, the last 9 pages contained a “LIST OF ADVERSE EVENTS OF SPECIAL INTEREST” I contacted a member of the media and asked if they were interested in viewing the documents. No response.
Why is the media not interested in these documents? That was the question that bothered me. I can only think of one reason. Turn on your TV and what you see/hear is advertising for a drug that will change your life, check with your doctor.
Can you imagine how many millions are made by the media for running the ad’s?
Next ad could be from Attorney’s who ask if you have taken the drug that will change your life and it has—for the worst, call me—I’m here to help.
I suppose the old adage applies “Follow the Money” may apply.
If I could suggest any reading material to subscribers it would be Robert F.Kennedy Jr’s book “The Real Anthony Fauci” A true eye opener and explains how we got to this point.
Court ordered Pfizer documents released can be read below: If your unable to open, please try a different browser.
38 pages released by FDA below.
I also received the documents below.
“BioNTech Signs Collaboration Agreement with Pfizer to Develop mRNA‐based Vaccines for Prevention of Influenza.
BioNTech will receive $120 million in upfront, equity and near‐term research payments from Pfizer and will be eligible to receive up to $305 million in potential development, regulatory and commercial milestone payments and up to double‐digit royalties.” 3 page Contract below:
20180816_Pfizer_BioNTech_Press-Release_EN
COVID-19 mRNA Vaccine (BNT162/PF-07302048)
Part 1 of the Original Submission – Rolling Biologics License Application (BLA)
Request for Priority Review Designation
Dear Dr. Gruber,
“Please find enclosed Part 1 of the Original Submission of the rolling Biologics License
Application (BLA) for the BNT162b2 vaccine candidate developed by BioNTech and Pfizer
under BB-IND 19736 for the prevention of COVID-19 caused by SARS-CoV-2 in
individuals ≥16 years of age. This vaccine was granted Fast Track Designation for
individuals >18 years of age on 07 July 2020. The Grant Fast Track Designation Letter is
provided in Module 1.7.4. Submission of this BLA as a rolling application was agreed during
the teleconference of 16 April 2021” 6 pages of documentation released by the FDA
Pfizer A wire transfer for $2,875,842.00 was made
For years I have heard fake news, fake news, fake news I never realized it was coming from my own government.
Please take a moment to say a prayer for innocence citizens of Ukraine.
The end