**UPDATE May, 2022**
Despite the court victory, it now appears that the documents being released are raising questions about how frequently adverse events were reported as “unrelated” to the ‘vaccine.’ Serious yet supposedly “unrelated” adverse events included (Source):
- Acute asthma exacerbation
- Aortic aneurysm (listed as a pre-existing condition)
- Appendicitis (requiring hospitalization)
- Atrial defibrillation
- Cardiac arrest and acute respiratory failure, requiring hospitalization, sustained by a patient who then was “lost” (could not be located for continued participation in the trial)
- Chest pain (requiring hospitalization, later listed as cardiac ischemia)
- Coronary artery occlusion (listed as both serious and life-threatening)
- Injuries sustained from a fall
- Intermittent non-cardiac chest pain (requiring hospitalization)
- Left breast cancer (listed as a pre-existing occult malignancy)
- Neuritis (peripheral nerve Injury), listed as “unrelated” to the vaccine but related to the blood draw during vaccination
- Pulmonary embolism and bilateral deep venous thrombosis
- Respiratory failure (requiring hospitalization)
- Right ureteropelvic junction obstruction (requiring hospitalization, listed as congenital)
- Small bowel obstruction, listed as “unplanned,” and a panic attack
Only ONE adverse event is clearly specified as being related to the shot: psoriatic arthritis, with no prior history of the condition.
The large number of serious adverse events, often requiring hospitalization, that were all deemed “unrelated” to the shot definitely raises eyebrows as well as the fact there were many discrepancies in the recording of these events.
https://aaronsiri.substack.com/p/instead-of-fdas-requested-500-pages
INSTEAD OF FDA’S REQUESTED 500 PAGES PER MONTH, COURT ORDERS FDA TO PRODUCE PFIZER COVID-19 DATA AT RATE OF 55,000 PAGES PER MONTH!
A great win for transparency that removes a stranglehold “health” authorities have had on data independent scientists need to offer solutions and address serious issues with the vaccine program.
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On behalf of a client, my firm requested that the FDA produce all the data submitted by Pfizer to license its Covid-19 vaccine. The FDA asked the Court for permission to only be required to produce at a rate of 500 pages per month, which would have taken over 75 years to produce all the documents.
I am pleased to report that a federal judge soundly rejected the FDA’s request and ordered the FDA to produce all the data at a clip of 55,000 pages per month! (See link for article & Judge’s order)
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Important quote:
No person should ever be coerced to engage in an unwanted medical procedure. And while it is bad enough the government violated this basic liberty right by mandating the Covid-19 vaccine, the government also wanted to hide the data by waiting to fully produce what it relied upon to license this product until almost every American alive today is dead. That form of governance is destructive to liberty and antithetical to the openness required in a democratic society.
It’s important to note:
- NONE of the documents used to allegedly evaluate the safety & efficacy of the COVID shots have been released to the public who paid for them
- The federal government has absolved Pfizer, medical services workers who administer the shot, and itself of any legal liability for injuries
- Pfizer pays mainstream media which is a conflict of interest. Take a look at the creepy Pfizer commercial aimed at kids: http://
- The federal government is still using every means possible to force the entire population to get injected with experimental products which have shown the highest rate of injury and death than any other “vaccine” in the entire history of VAERS
- The shots contain genetic information that forces the body to make antigenic components, namely the spike protein of the now no-longer-circulating Wuhan strain of SARS-CoV-2
- Researchers have found numerous contaminants and a toxic spike protein in the injection vials as well as a substance that appears to be ‘self aware,’ nanoparticles which are not biocompatible, parasites, graphene hydroxide & heavy metals
- A Lancet study showed that protection against symptomatic COVID-19 declined such that by six months, some of the more vulnerable “vaccinated” groups were at greater risk than their unvaccinated peers. Doctors are calling this phenomena in the repeatedly ‘vaccinated’ “immune erosion” or “acquired immune deficiency”, accounting for elevated incidence of myocarditis and other post-vaccine illnesses that either affect them more rapidly, resulting in death, or more slowly, resulting in chronic illness. In short, they develop VAIDS (“vaccine” acquired immune deficiency syndrome)
For more:
- https://madisonarealymesupportgroup.com/2021/11/19/fda-asks-judge-to-grant-it-until-2076-to-fully-release-pfizers-covid-vaccine-data/
- https://madisonarealymesupportgroup.com/2022/01/03/bidens-fda-chief-pick-used-to-work-as-big-pharma-consultant-has-millions-in-pharma-investments/
- https://madisonarealymesupportgroup.com/2021/12/06/fda-foia-shows-over-1200-deaths-within-1st-90-days-of-covid-jab-but-cdc-still-overcounting-covid-deaths-undercounting-deaths-after-covid-shots/
- https://madisonarealymesupportgroup.com/2021/11/22/boosters-for-all-but-the-acip-fda-cdc-have-no-data-with-all-the-vaxxed-doctors-dead-or-fired-whos-working-in-hospitals/
- https://madisonarealymesupportgroup.com/2018/02/28/corruption-in-fda-states-constitutional-attorney/
- https://madisonarealymesupportgroup.com/2021/12/17/fdas-suspicious-timing-on-wanting-more-information-on-nac-which-helps-covid-lyme-msids/
Dr. José Luis Sevillano proposes a preventive treatment for Panamanian colleagues who at a conference were very interested in treating patients with zinc, glutathione, and N-acetylcysteine (NAC). These antioxidants have been found to help the body detoxify graphene, which experts have discovered in the PCR swabs, face masks, and the COVID injections. More on graphene here.
Madison Area Lyme Support Group 