(Julian Conradson) On Thursday, a Federal Judge “soundly” rejected the FDA’s panicked request for permission to produce hundreds of thousands of documents related to Pfizer and the Covid vaccines at a rate of 500 pages per month after the agency was ordered to comply with a Freedom of Information Act (FOIA) request last month.
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Admits Pfizer’s Antiviral Drug Paxlovid Causes Life-Threatening Reactions When Taken With Common Medicines
(Matthew Davis) The antiviral oral drug, paxlovid, that was developed by Pfizer to treat the Wuhan coronavirus (COVID-19) can cause severe or life-threatening effects when used with common medications. The pill is also not recommended for people with severe kidney or liver disease.
Biden’s Pick for FDA Chief Formerly Worked as a Big Pharma Consultant, Has Millions in Big Pharma Investments
(B.N. Frank) The Food and Drug Administration (FDA) is supposed to protect Americans from unsafe products. They have a long history of not doing so. One glaring example, earlier this year, the agency approved an Alzheimer’s drug that
FDA Authorizes Pfizer’s COVID-19 Booster for 12- to 15-Year-Olds, CDC Still Must Decide To Recommend
(Just The News) Boosters were already are recommended for those 16 and older
Non-Profits Petition Health and Human Services Dept and FDA to Declare Wireless Radiation as “Imminent” Health Hazard
(B.N. Frank) Decades of peer-reviewed research have determined that exposure to wireless “Wi-Fi” radiation is biologically and environmentally harmful (see 1, 2). Some countries have already recognized exposure risks and government agencies have taken action to warn and protect the public. In the U.S., the Federal Communications Commission (FCC) and other “captured” regulatory agencies continue to dismiss research proving harm.
FDA Gives Green Light to Pfizer’s Antiviral Covid-19 Pill
(100 Percent Fed Up) Could this be a game-changer as Omicron spreads across the United States? A milestone in the fight against the pandemic as the first at-home treatment Covid-19 treatment gets FDA authorization.
FDA Should Need Only ‘12 Weeks’ to Release Pfizer Data, Not 75 Years, Plaintiff Calculates
(Seth Hancock) The nonprofit group suing the U.S. Food and Drug Administration for the release of documents related to the approval of Pfizer’s Comirnaty vaccine calculated it should take the agency only 12 weeks with 19 reviewers working full-time to review and produce the documents.
“Reprehensible and Reckless:” Noted Cardiologist Blasts the FDA For Downplaying Vaccine-Induced Myocarditis and Approving Experimental Jab For Children – Says An “Extraordinary Number” of Young People Will End Up With “PERMANENT Heart Damage”
(Julian Conradson) Last week, Dr. Peter McCullough appeared on Brett Weinstein’s ‘DarkHorse’ podcast to sound the alarm over what he calls “Reprehensible and Reckless” actions by the US public health bureaucracy when it comes to their deployment of the experimental Covid-19 Vaccines – especially the FDA’s recent decision to approve the jab for children aged 5-11.
FDA Ordered Google To Remove COVID Videos From YouTube Because Agency Didn’t Like Their Message
(Ethan Huff) It has come to light that back in April, the U.S. Food and Drug Administration (FDA) sent a letter to a Google lobbyist demanding that a slew of videos on YouTube about the Wuhan coronavirus (Covid-19) be censored and removed because the federal agency did not approve of their content.
Gilead Recalls Two Lots of Remdesivir Due to Glass Contamination
(Daniel G) On December 3rd, the FDA announced that Gilead voluntarily recalled thousands of remdesivir vials due to the presence of glass particulates.
Pfizer Documents Reveal Over 1,200 Vaccine Deaths Over 90-Day Trial Period
(Cullen McCue) The Food and Drug Administration (FDA) has released the first batch of documents related to Pfizer’s COVID-19 vaccine program after a federal judge ordered that they must comply with a massive FOIA request.
The FDA Slaps Major Warning About Pfizer Drug as Vaccine Reactions Come Under Scrutiny
(Kyle Becker) The FDA has recently admitted there is now major concern over another Pfizer product. It is now slapping a warning on a class of anti-inflammatory treatments called JAK inhibitors.
Court Orders FDA To Comply With FOIA and Release Information On Pfizer EUA – First Batch of Documents Shows Over 1,200 Vaccine Deaths WITHIN FIRST 90 DAYS
(Julian Conradson) The Food and Drug Administration (FDA) released the first batch of documents related to Pfizer’s Covid-19 vaccine after a federal judge ordered that they must comply with a massive Freedom of Information Act (FOIA) request that was filed by a government accountability group called Public Health and Medical Professionals for Transparency.
FDA Tells the Courts: Sure, Americans See Data Used to Justify Vaccine Mandates… in 55 YEARS
(Kyle Becker) The U.S. government has made one excuse after another for why it no longer has to provide transparency to the American people — even when it comes to federal vaccine mandates that infringe on human rights and violate citizens’ most personal decisions over their own bodies.
VAERS Analysis Exposes CDC, FDA for Covering Up Hundreds of Serious Adverse Events Associated With COVID Vaccines
(Ethan Huff) A researcher named Albert Benavides conducted a data analysis on Vaccine Adverse Event Reporting System (VAERS), which is maintained by the Centers for Disease Control and Prevention (CDC) and the Food and Drug Administration (FDA). And what he found is that there are hundreds of serious adverse events associated with Wuhan coronavirus (COVID-19) vaccines that these two federal agencies are concealing from the public.