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CDC Adds Dangerous Bivalent COVID Shots to their Childhood Immunization Schedule...

Introduction by Fabio Giuseppe Carlo Carisio ITALIAN VERSION The Covid vaccines have also been included among those scheduled in immunization ordinary plan for 15-month-old children by...

VITAL! Pfizer mRNA Vaccines: Risks of Pulmonary Embolism, Myocarditis, Blood Clots....

by Fabio Giuseppe Carlo Carisio VERSIONE IN ITALIANO In the lates weeks the British Medical Journal blamed the Food and Drug Administration because had concealed the...

Horrific Confessions From 2 Pfizer Officials

In November 2022, recently retired head of vaccine R&D at Pfizer, Kathrin Jansen, said “we flew the aeroplane while we were still building it. We couldn’t wait for data, we had to do so much at risk.” Pfizer compressed its vaccine development timeline from 10 years to a mere nine months by simultaneously developing and testing the product in human trials.

“COVID: Logic, Reasoning and Scientific Evidence Disappeared with Fauci-Gates’ Dangerous Vaccines”...

The COVID-19 pandemic is one of the most manipulated infectious disease events in history, characterized by official lies in an unending stream lead by government bureaucracies, medical associations, medical boards, the media, and international agencies.

British Medical Journal’s BOMB: “US FDA Hides Data on Serious Adverse...

Introduction by Fabio Giuseppe Carlo Carisio An explosive article was published a few days ago by the British Medical Journal but was not prominent in the media...

“Myocarditis in Young People and Embolism in Women Growing after Vaccination...

In 2021, the difference in myocarditis coincided with the vaccination campaign in young individuals.

CDC Pushed for COVID-19 Boosters Without Clinical Trials. Disturbing Emails: “Pfizer...

The U.S. Centers for Disease Control and Prevention (CDC) pressured U.S. regulators to clear COVID-19 boosters without clinical trial data, according to newly released emails.

FDA bans ‘Trrrump’ antibody treatment (at gunpoint?)

RT: The US Food and Drug Administration (FDA) has revoked its emergency use authorizations for two kinds of monoclonal antibodies treatments produced by Regeneron and Eli Lilly. The regulator said the two therapeutics were “highly unlikely to be active against the omicron variant.”

FDA Approves Injectable Naloxone for Opioid Overdoses

Opioid-related overdose deaths are one of the leading causes of death in the United States.

On the Horizon: A Pill to Treat COVID-19?

Molnupiravir would be the first oral medication to treat COVID-19.

Blockbuster: It wasn’t Wuhan, despite Rand Paul’s ‘Lie Soup’, COVID’s Home...

A SARS-like cluster of circulating bat coronaviruses shows potential for human emergence

FDA gives full approval on Pfizer vaccine

Jim W. Dean - The main vax boost will come from businesses that did not want to risk getting sued for terminating employees for refusing to get a vaccine still in the experimental stage.

Do not drink, cook with, sell, or serve “Real Water” alkaline...

Consumers, restaurants, and retailers should not drink, cook with, sell, or serve “Real Water” alkaline water, until more information is known about the cause of the illnesses.

Ongoing Clashes Between the FDA and HHS

A personnel shake-up driven by ongoing clashes between the agency and the HHS department that oversees it.

FDA Approves Emergency Use Authorization for Pfizer/BioNTech COVID-19 Vaccine

The rollout of Covid-19 vaccine could then begin in the United States in a matter of days

Livestream of FDA Advisory Committee to Discuss Pfizer/BioNTech COVID-19 Vaccine Candidate

FDA has scheduled a meeting of its Vaccines and Related Biological Products Advisory Committee (VRBPAC) on Dec. 10

Watch Meeting of Advisory Committee on COVID-19 Vaccine Held 10/22

The development of safe and effective vaccines to prevent SARS-CoV-2 infection and/or COVID-19 is essential to help bring the pandemic under control.

How the FDA Stood Up To Trump

FDA and Scientists Say 'No' to Trump Pandemic Instructions https://twitter.com/nytimes/status/1318733786448908288?s=20 Health Editor's Note: As VT has reported, Trump has openly accused the FDA of trying to...

Trump Attempts to Rebrand ‘Emergency Authorization’ for COVID-19 Vaccine

The administration proposed labeling a Covid-19 vaccine authorization a ‘pre-licensure,’ which FDA says would undermine its procedures.

Supply for Antiviral Remdesivir is Meeting U.S. Demands

Beginning October 1, Gilead will be responsible for distributing Veklury in the United States upon conclusion of the previous distribution agreement with the U.S. Federal government.

Trump, Butt Out of the COVID-19 Vaccine Process

These actions are eroding the public’s confidence.

Recalls on Peaches: Possible Salmonella Risk

Check to see where your peaches are coming from

Trump’s MMS (Fake COVID-19 Cure) Scammers Charged in Miami Federal Court...

Defendants Allegedly Attempted to Avoid Government Regulation by Selling Products Through a Company They Deceptively Named Genesis II Church

FDA To Release Guidelines for COVID-19 Vaccine Approval

More than 100 vaccines are being tested worldwide

FDA Gives Emergency Authorization for Use of Siemens Total Antibody Test

Siemens Healthineers Receives FDA Emergency Use Authorization for its SARS-CoV-2 Total Antibody Test that Delivers Superior Clinical Performance Siemens  Tarrytown, NY |  Jun 01, 2020 • Total antibody test...

FDA Imposes Very Strict Guidelines on HCQ, Chloroquine, and AZM

Health Editor's Note: Read this FDA communication listing restrictions for the use of hyroxychloroquine, chloroquine, and azithromycin. The use of these medications may cause...