The Food and Drug Administration (FDA) is questioning the evidence provided by Johnson & Johnson in its application for authorization of its coronavirus booster shot, according to a document released prior to the October 15 meeting with FDA vaccine advisers.
Pfizer announced Thursday it applied to the Food and Drug Administration (FDA) for approval of its vaccine for 5-11-year-olds — a significant move, as no coronavirus vaccine has been approved for children younger than 12.
Biden Education Secretary Miguel Cardona said Thursday he not only supports mandatory Chinese coronavirus vaccines for eligible schoolchildren, he expects states to “make sure it happens.”
After a dismal week for the Biden administration on several fronts, the New York Times published a “puff piece” profile on White House press secretary Jen Psaki, which repeatedly praised her as “straightforward” and “professional,” Fox News reported Sunday.
Scott Gottlieb, the former commissioner of the Food and Drug Administration (FDA), admitted during an interview on Face the Nation that the six foot social distancing rule recommended by public health officials for months on end was actually “arbitrary in and of itself,” and he noted that “nobody knows where it came from.”
On Friday’s broadcast of CNN’s “Situation Room,” FDA Vaccines and Related Biological Products Advisory Committee member Dr. Paul Offit stated that “in many ways, the FDA and CDC were marginalized” by the Biden administration’s handling of coronavirus vaccine boosters, but
Pfizer and BioNTech are set to seek FDA approval in November for their COVID vaccine to use in children between 6 months and 5 years old.
Pfizer prefaced its upcoming presentation to the Food and Drug Administration (FDA) to discuss its application for Chinese coronavirus booster shots by asserting data shows vaccine efficacy wanes over time.
Two senior vaccine regulators, who are departing the Food and Drug Administration (FDA), published a paper blasting coronavirus booster shots, something discussed and embraced by the Biden administration and federal health officials.
Producers of the Pfizer vaccine, BioNTech, are preparing to request clearance to vaccinate children five and older, and the company is ready to begin making smaller doses for children younger than 12.
The Associated Press recently issued a correction to a report alleging that 70% of poison control cases in Mississippi were linked to the drug ivermectin.
Throughout his presidency, Joe Biden has constantly repeated the mantra that he would “follow the science” on coronavirus policy, but two Food and Drug Administration (FDA) officials have just resigned in protest of what they claim is the Biden administration perpetuating an atmosphere of pressure and intimidation to push the coronavirus booster shots.
A pair of top Food and Drug Administration (FDA) officials overseeing the review of COVID-19 vaccine applications will depart the agency this coming fall, according to a Tuesday report.
U.S. regulators are likely to greenlight a coronavirus booster vaccine for vaccinated adults beginning at the six month gap following the previous shot instead of eight-months, according to the Wall Street Journal.
Following the Food and Drug Administration’s (FDA) announcement that it had officially approved the Pfizer vaccine for the coronavirus, taxpayer-funded National Public Radio (NPR) turned to Dr. Anthony Fauci, who said there won’t be “some good control” of the virus until next year.
Data from the Centers for Disease Control and Prevention (CDC) has demonstrated what anonymous administration officials described to Politico as a “worrying drop” in coronavirus vaccine efficacy over time, leading to the Biden administration’s conclusion to push vaccine booster shots.
Hundreds of protesters gathered at the Maine State House this week to protest the state’s rule requiring healthcare workers to get vaccinated for the Chinese coronavirus.
The vast majority of Americans oppose being forced or coerced into getting a vaccine for the Chinese coronavirus, a Convention of States Action/Trafalgar Group survey released this week found.
The Food and Drug Administration (FDA) on Monday added warning labels to Johnson & Johnson’s single-dose vaccine for the Chinese coronavirus over links to a rare neurological condition.
Dr. Anthony Fauci, the chief medical adviser to His Fraudulency Joe Biden, is running around dismissing the fact that the Food and Drug Administration (FDA) hasn’t approved the China Virus vaccines as a “technicality.”
Dr. Anthony Fauci, chief medical adviser to President Joe Biden, dismissed the fact that the Food and Drug Administration (FDA) has not yet approved vaccines for the Chinese coronavirus as merely a “technical issue.”
The Food and Drug Administration (FDA) is expected to “move rapidly” to add warning labels to Pfizer and Moderna vaccines, following the emergence of heart inflammation cases — myocarditis and pericarditis — after receiving the non-traditional mRNA jabs, the agency’s Dr. Doran Fink said Wednesday.
The Food and Drug Administration (FDA) on Monday approved what it described as a “first-of-its-kind” treatment for Alzheimer’s disease, which it says “targets the fundamental pathophysiology of the disease.”
OTTAWA, Ontario (AP) – Plans to distribute the first 300,000 doses of the Johnson & Johnson COVID-19 vaccine in Canada next week are on hold after Health Canada learned part of them were manufactured at a Maryland facility that messed up the ingredients in 15 million doses bound for the U.S. market.
The Biden administration has ended the pause and will allow Johnson & Johnson to resume Chinese coronavirus vaccinations.
A Centers for Disease Control and Prevention (CDC) advisory panel recommended on Friday that the U.S. resume the use of the single-shot Johnson & Johnson coronavirus vaccine following U.S. health agencies calling for its suspension.
Leaders of the U.S. Bishops Conference (USCCB) have condemned a Food and Drug Administration (FDA) decision to cease enforcing the “in-person dispensing requirement” for chemical abortion pills during the remainder of the coronavirus public health emergency.
The Biden-Harris administration announced a reversal of Trump’s decision to end taxpayer funding for experiments using aborted babies.
U.S. Customs and Border Protection officers at Chicago’s O’Hare International Airport seized 3,200 Viagra pills from a man on a return flight from India. The man claimed the more than $96,000 worth of pills were for “his friends.” CBP officers
On Thursday’s broadcast of CNN’s “The Lead,” FDA vaccines advisory board member Dr. Paul Offit stated that teachers do not need to be vaccinated in order to return to in-person classes, many other essential workers are back to work without
The U.S. Food and Drug Administration Friday evening granted an Emergency Use Authorization (EUA) for the coronavirus vaccine developed by American company Moderna, making it the second one available in the United States.
A U.S. Food and Drug Administration (FDA) advisory panel on Thursday voted to recommend the emergency use approval of the Moderna vaccine.
Workers at Pfizer’s Michigan headquarters paused for a moment and erupted into a round of applause early Sunday morning as the first shipments of the coronavirus vaccine were being moved to a loading dock.
The Food and Drug Administration (FDA) on Friday night approved the first coronavirus vaccine for emergency use in the United States, several media outlets reported, clearing the way for U.S. officials to begin vaccinating millions of Americans as early as next week.
President Donald Trump expressed impatience Friday with the Food and Drug Administration’s delayed approval of the Pfizer coronavirus vaccine.
The CDC warned Wednesday that the Chinese coronavirus would make the next few months “the most difficult” in U.S. “public health history.”
On Monday’s broadcast of the Fox News Channel’s “Bill Hemmer Reports,” Fox News Medical Contributor Dr. Marty Makary stated that the FDA is “too bureaucratic, taking too much time” on the coronavirus vaccine and they should be able to turn
The pharmaceutical company Moderna is applying today for emergency authorization from the FDA to produce a vaccine for the coronavirus.
Three more Democrat governors join CA Gov. Gavin Newsom in saying they will not trust a virus vaccione approved while Trump is in office.
WASHINGTON (AP) — FDA approves remdesivir, the first drug for treating COVID-19.
