Lazy eyes listen
Following release of the Covid-19 vaccine, numerous adverse reactions have been discovered, some of which include: fever, muscle soreness, dermatitis amongst others.
Recently, Pfizer vaccine were forced to release real vaccine data, including a 9-page report on “adverse reactions to Pfizer vaccines” which immediately went viral on Twitter.
On March 1, the U.S. Food and Drug Administration (FDA) lost the lawsuit filed against them by the Public Health and Medical Professionals for Transparency (PHMPT), a nonprofit organisation who first filed a lawsuit against them in the U.S. District Court for the Northern District of Texas last September, Questioning the FDA’s decision to withhold data related to Pfizer and BioNTech’s 2019 COVID-19 vaccine .
In November last year, the PHMPT organization asked the FDA to fully disclose the vaccine review data, but the FDA did not respond prompting the lawsuit against them.
Following the FDA’s defeat, the court mandated them to release a 329,000-page review document for Pfizer’s new crown vaccine by this summer ; the FDA has now released the first batch of the documents.
A total of 150 documents are currently published on the FDA’s website for free download but they have not released a statement to address the latest development.
According to our source The FDA petitioned a federal judge to disclose only 500 pages of important documents a month. hence, it will take 55 years to fully disclose the 329,000 pages of information, until 2076.
The PHMPT group was furious: by 2076, many of the people who made, approved, and vaccinated the vaccine had long since left the world.
The plaintiffs argued that the FDA violated U.S. federal law, that “once a license is obtained, the data and information of a biological product in the process of license approval can be immediately disclosed to the public,” which is in line with the FDA’s commitment to “complete transparency” before and after the approval of the new crown vaccine The opposite.
Note: The PHMPT group, made up of dozens of academics, professors and public health professionals from prominent U.S. universities, allege that independent scientists could not conduct proper analysis until the full documents Pfizer submitted to the FDA for approval of its COVID-19 vaccine were made public. There is no way to ensure that critical vaccines that millions of Americans either voluntarily or are required by their employers will be safe and effective
On March 1, the FDA lost the case in the District Court of Texas. From that day on, a large number of review documents related to the “safe and effective” of Pfizer’s vaccine must be released one after another.
The document includes a 9 page report which details over 1,000 adverse reactions to Pfizer’s Vaccine which got many internet users talking the adverse reactions in the document include:
Fasciitis, swollen eyes, facial paralysis, alopecia areata, anaphylactic shock, anaphylaxis during pregnancy, acute cardiomyopathy, acute respiratory failure, injection site vasculitis, epilepsy, blood clots, arrhythmias, arthritis, asthma, bronchospasm, heart Sudden arrest, heart failure, chest discomfort, asphyxia, acute cutaneous lupus erythematosus, acute encephalomyelitis, acute kidney injury, acute outer macular retinopathy, aplastic anemia, chronic autoimmune glomerulonephritis, chronic cutaneous lupus erythematosus , chronic spontaneous urticaria, hemolytic anemia, colitis, dermatitis, diabetes, embolic cerebral infarction, endocrine disorders, neonatal myasthenia gravis, myelitis, non-infectious oophoritis, thyroiditis, ulcerative proctitis, ocular pruritus, genital herpes, glossopharyngeal nerve palsy, hemorrhagic vasculitis, cervicitis, lupus cystitis, lupus encephalitis, multiple sclerosis, etc.
The released documents contain pages marked as “priority review requests” which consist of more than 100 pages of anonymous security-related data sheets, some pages show reports on unidentified participants’ gender, age and BMI tables; which are some Typical drug or vaccine application documents.
Another page shows Pfizer payed the FDA nearly $2.9 million in standard user fees; fast-track designation letter (usually not published); non-clinical confidential summary of vaccine; vaccine trials not randomized list of anonymous subjects, etc.
It is not certain if the disclosed documents will provide new findings on the safety or efficacy of the vaccine. however, the representative of the non-profit organization (PHMPT) said, “Our job is to obtain these documents, and the real situation is left to scientists and other professionals to analyze.”
The released documents generated mixed reactions from internet users on twitter:
“Of the 46,000 participants in the Pfizer trial, 42,000 had adverse reactions and 1,200 died. The FDA rule is that only one person dies within 30 days of receiving an experimental drug to end the trial. It never happened 7and we need to ask why”– One twitter user wrote.
“France is removing mandatory vaccines, many wonder if this has anything to do with Pfizer’s release of data.”
” Reports show 1,229 healthy people died from vaccines.”
“Nine pages of side effects that they want to hide for 75 years.”
“Millions of people will get sick or die from the vaccine, and no one can know what will happen in the next few years.”
“Side effects after vaccination.”
“A week after the vaccination, I have contractile muscle pain in my thigh that has been going on for over a month..”
On the flip side, some people said that all vaccines may have side effects, and Pfizer has released the actual data, “then it is the ‘safest’ vaccine” ↓