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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:įasciitis, 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.
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.
On March 1, the FDA lost the case in the District Court of Texas. 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
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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. Note: The PHMPT group, made up of dozens of academics, professors and public health professionals from prominent U.S.
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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. The plaintiffs argued that the FDA violated U.S. The PHMPT group was furious: by 2076, many of the people who made, approved, and vaccinated the vaccine had long since left the world.
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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.įollowing 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.Ī 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.Īccording 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. 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 . 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.
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