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Washington, DC, March 03, 2022 (GLOBE NEWSWIRE) — In a 55,000-page set of documents released Tuesday, the U.S. Food and Drug Administration’s (FDA) Center for Biologics Evaluation and Research (CBER) clears for the first time the public has access to data that Pfizer submitted to the FDA from its clinical trials in support of a COVID-19 vaccine license. This follows U.S. District Judge Mark T. Pittman’s January 6 ruling to deny the FDA’s request to suppress data for the next 75 years that the agency said was necessary, in part due to its “limited resources”.
A 38-page report included in the documents has an appendix, “LIST OF ADVERSE EVENTS OF SPECIAL INTEREST,” which lists 1,291 different adverse events after vaccination. The list includes acute kidney injury, acute flaccid myelitis, sperm antibody positive, brainstem embolism, brainstem thrombosis, cardiac arrest, heart failure, cardiac ventricular thrombosis, shock cardiogenic, central nervous system vasculitis, neonatal death, deep vein thrombosis, brainstem encephalitis, hemorrhagic encephalitis, frontal lobe epilepsy, foaming mouth, epileptic psychosis, facial paralysis, fetal distress syndrome, gastrointestinal amyloidosis intestinal seizures, generalized tonic-clonic seizure, Hashimoto encephalopathy, hepatic vascular thrombosis, herpes zoster reactivation, immune-mediated hepatitis, interstitial lung disease, jugular vein embolism, juvenile myoclonic epilepsy, liver injury, low birth weight, inflammatory syndrome multisystemic in children, myocarditis, neonatal convulsion, pancreatitis, pneumonia, stillbirth ance, tachycardia, temporal lobe epilepsy, testicular autoimmunity, thrombotic cerebral infarction, Type 1 diabetes mellitus, neonatal venous thrombosis, and vertebral artery thrombosis among 1,246 other medical conditions after vaccination.
“It’s a bombshell,” said Mary Holland, president and general counsel of Children’s Health Defense (CHD). “At least we now know why the FDA and Pfizer wanted to keep this data secret for 75 years. These findings should put an immediate end to Pfizer COVID vaccines. The potential for serious harm is very clear, and people injured by vaccines are barred from suing Pfizer for damages. »
The US government has already purchased 50 million doses of the Pfizer vaccine for children under five to deliver by April 30, 2022, although the FDA has yet to grant emergency use authorization. (USA) for this age group. The risk of serious injury or death from COVID for healthy children is virtually zero and so far the vaccine is not effective when used in young children.
According to The GuaRdian, “Pfizer made almost $37bn (£27bn) in sales from its Covid-19 vaccine last year – making it one of the most lucrative products in history – and predicted another bumper year in 2022, with a big boost coming from his Covid-19 Paxlovid pill.President Biden announced Paxlovid in his State of the Union address on Tuesday, the same day the data from Pfizer were made public. “We’re launching the ‘Test to Treat’ initiative so people can get tested at a pharmacy and, if positive, receive antiviral pills on the spot at no cost,” Biden said. during his speech.
From mid-December 2020 to February 18, 2022, the U.S. government database, the Vaccine Adverse Events Reporting System (VAERS), received 1,134,984 reports of adverse events, including 24,402 deaths, following vaccination against the COVID. Additionally, there have been 4,021 cases of myocarditis and pericarditis in the United States, including 2,475 cases associated with Pfizer, 1,364 cases with Moderna, and 171 cases with J&J’s COVID vaccine. These include 643 reports of myocarditis and pericarditis in children aged 12 to 17 years.
“It would be criminal to expose infants and young children to this extremely risky product,” Holland said. “VAERS data shows the catastrophic effects of the vaccine on the health of millions of people, yet Pfizer and other vaccine makers are raking in billions of dollars without fear of being held liable for injuries and deaths from their vaccines. “
The FDA’s attempt to suppress this data supporting the pharmaceutical industry’s findings is not a new phenomenon in this country’s public health system. For more information on pharmaceutical corruption and the industry’s close relationship with government regulatory agencies, read The Real Anthoby Fauci: Bill Gates, Big Pharma and the Global War on Democracy and Public Health by CHD Chairman and Senior Counsel Robert F. Kennedy, Jr.
Children’s Health Defense is a 501(c)(3) non-profit organization. Its mission is to end child health epidemics by working aggressively to eliminate harmful exposures, hold those responsible accountable, and establish safeguards to prevent future harm. For more information, visit ChildrensHealthDefense.org.
Rita Shreffler Children's Health Defense 202-599-1461 [email protected]
Source: Children’s Health Defense