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Data quietly published by a host of countries across Europe reveals that excess deaths among children are still occurring at an alarming rate as we enter the spring of 2024. The deaths cannot be blamed on COVID-19 because the data has proven the alleged virus and disease rarely harms children, if at all. And the terrible trend only began when the European Medicines Agency extended Emergency Use Authorisation (EUA) of the COVID-19 vaccines to children in the middle of Spring of 2021. Before this. excess deaths among children among children were in negative figures. With the year 2020, the height...

Doctors are free to prescribe ivermectin to treat COVID-19, a lawyer representing the U.S. Food and Drug Administration (FDA) said this week.“FDA explicitly recognizes that doctors do have the authority to prescribe ivermectin to treat COVID,” Ashley Cheung Honold, a Department of Justice lawyer representing the FDA, said during oral arguments on Aug. 8 in the U.S. Court of Appeals for the 5th Circuit.The government is defending the FDA’s repeated exhortations to people to not take ivermectin for COVID-19, including a post that said “Stop it.”The case was brought by three doctors who allege the FDA unlawfully interfered with their...

The Department of Defense (DOD) is mulling moving forward with discharges for some servicemembers who did not seek exemptions to the COVID-19 vaccine mandate, according to a Feb. 24 letter from the Office of the Secretary of Defense viewed by the Daily Caller News Foundation. As of Friday, the services have rescinded their vaccination orders as required by Congress. “It’s very important that our service members go and follow orders when they are lawful,” Under Secretary of Defense for Personnel and Readiness Gilbert Cisneros told Republican Rep. Jim Banks of Indiana Tuesday. The military is considering discharging servicemembers who did...

Mis- and disinformation have been prevalent throughout the COVID-19 pandemic, but in recent months anti-vax activists and conspiracy theorists have latched on to a new phrase to help their cause: “died suddenly.” Anti-vaxxers hoping to convince people that COVID vaccines are linked to sudden deaths among younger people have invoked the term while trying to exploit tragic events like the death of soccer journalist Grant Wahl, or Damar Hamlin suffering a cardiac arrest during an NFL game. Though that theory has no scientific evidence to support it, the “died suddenly” rhetoric has gained a lot of traction on social media....

Pfizer and BioNTech said Monday they are seeking Emergency Use Authorization for an updated COVID-19 bivalent booster vaccine for children ages 6 months to 4 years old, but critics said the vaccines are obsolete and too risky.Pfizer and BioNTech are seeking Emergency Use Authorization (EUA) for an updated COVID-19 bivalent “booster” vaccine for children ages 6 months to 4 years old.Pfizer on Monday said if the bivalent booster receives EUA, children in this age group will receive two doses of the original COVID-19 vaccine, followed by a dose of the “updated” vaccine targeting Omicron subvariants BA.4 and BA.5.Previously, children under...

On January 24, 2022, The FDA revoked Emergency Use Authorizations (EUAs) for two COVID monoclonal antibody (McAb) treatments, bamlanivimab and etesevimab (administered together) and REGEN-COV (casirivimab and imdevimab), made by Eli Lilly and Regeneron respectively. Again on March 25, the FDA revoked the EUA for sotrovimab, which is no longer authorized for use at this time in specified states and territories due to its ineffectiveness against the prevalence of Omicron sub-variants, such as BA.2 in those regions, brought in from overseas. Even these state-of-the-art McAbs can’t keep up with the rapidly mutating, highly transmissible COVID-19 variants. In doing so, the...

Idaho Gov. Brad Little has vetoed legislation that would make it illegal for most businesses to require the coronavirus vaccine. ... Last year, Montana became the first state in the nation to ban most businesses from requiring vaccines as a condition of employment. That law, like the one proposed in Idaho, cited “discrimination” as the reason. ... Idaho's bill, dubbed the “Coronavirus Pause Act,” would have subjected public and private employers to a misdemeanor charge punishable by a $1,000 fine if they require vaccines as a condition of employment or service. It includes exemptions for situations involving federal law, existing...

I can't find any news regarding an expectation of the Emergency Use Authorization expiration on 1/7/2022. Has it expired ? Has it been reauthorized ? Or is it now permanent ?

It took about 4 days for David Boulware, MD, MPH, to write the FDA emergency use authorization (EUA) application for fluvoxamine. Yes, a doctor wrote an EUA application -- a task that has typically been relegated to pharmaceutical companies -- and yes, it was for a generic drug that physicians could technically prescribe off-label. But Boulware, of the University of Minnesota, who is involved in a trial that's investigating fluvoxamine and other repurposed drugs -- along with a handful of other doctors and researchers -- took it upon themselves to apply because they believe the data substantiate its use in...

Following Wednesday’s story in which The Ohio Star reported that Pfizer is currently still shipping it’s Emergency Use Authorization (EUA) COVID-19 vaccine, the Ohio Department of Health (ODH) won’t say which version of the vaccine it is distributing. ODH is responsible for acquiring and distributing at least some of the state’s supply of COVID-19 vaccines, though Alicia Shoults of the ODH’s Office of Public Affairs told The Star by phone Thursday afternoon that some healthcare providers procure the vaccine directly from the federal government. The Star asked Shoults which version of the Pfizer vaccine ODH was procuring – Comirnaty or...

A federal district court judge rejected a claim by the U.S. Department of Defense that the Pfizer-BioNTech COVID-19 vaccine being administered under Emergency Use Authorization is interchangeable with Pfizer’s fully licensed Comirnaty vaccine. A federal district court judge has rejected a claim by the U.S. Department of Defense (DOD) that the Pfizer-BioNTech COVID-19 vaccine being administered under Emergency Use Authorization is interchangeable with Pfizer’s Comirnaty vaccine, which in August was fully licensed by the U.S. Food and Drug Administration (FDA).In an order issued Nov. 12 in Doe et al. v. Austin, U.S. Federal District Judge Allen Winsor of the U.S....

Why isn't Dr. Anthony Fauci in jail yet? Dr. Jane Ruby details his crimes in this segment with Stew, laying out 5 specific felonies the head of the NIAID has committed, and, she calls for an end to emergency use authorizations (EUAs), along with Big Pharma's blanket immunity. https://rumble.com/vp4y4j-faucis-5-felonies-exposed-congress-must-act-end-eua-and-pharma-immunity.html

Novavax Inc (NVAX.O) and partner Serum Institute of India said on Monday they received emergency use authorization for their COVID-19 vaccine in Indonesia, making it the first approval anywhere in the world for Novavax.

Senator Ron Johnson, R-Wisc., claimed that the U.S. still doesn’t have an FDA-approved vaccine as he exposed what was really approved by the government agency on “Fox News Primetime.”SEN. RON JOHNSON: We do not have an FDA–approved vaccine being administered in the U.S. The FDA played a bait and switch. They approved the Comirnaty version of Pfizer drugs. It’s not available in the U.S. They even admit it. I sent them a letter three days later going 'What are you doing?'"What they did is they extended the emergency use authorization for the Pfizer drug vaccine that’s available in the U.S.,...

Two active-duty staff sergeants of US Armed Forces—one Army, one Marine—filed a class-action lawsuit on August 17 against the leaders of the Department of Defense (DoD), the Department of Health and Human Services (HHS), and the Food and Drug Administration (FDA) for being forced to receive a COVID-19 vaccine despite having had and recovered from COVID and acquiring natural immunity to SARS-CoV-2. The lead plaintiffs in the lawsuit, Staff Sergeant Daniel Robert, US Army, and Staff Sergeant Holli Mulvihill, USMC, maintain US Sec. of Defense Lloyd Austin “ignored the DOD’s own regulations and created an entirely new definition of ‘full...

On Aug. 23, the U.S. Food and Drug Administration (FDA) issued its approval (also known as a license) for Pfizer’s Comirnaty COVID vaccine. The FDA documents related to the vaccine’s approval are as difficult to understand as the new brand name is to pronounce. According to the FDA, although Pfizer’s Comirnaty vaccine is now approved, considerable amounts of the vaccine will remain under Emergency Use Authorization (EUA). Also, the approval of the Comirnaty vaccine was limited to adults over age 16 receiving their first two doses. Vaccination with the EUA Pfizer-BioNTech or the Comirnaty vaccine in the 12- to 15-year...

If you recall early on before the jabs were "released" under EUA I pointed out that some of the early study work had odd results that I could not reasonably explain a purpose to, and they bothered me a lot.One of the most-glaring was the wildly higher antibody titers produced by them as opposed to natural infection. I mused at the time that this could easily be explained by the truncation (or simply ignorance of) the usual dose-ranging studies that are done on all drugs; those require time, of course, and when you're after Warp Speed time is something you...

Sen. Ron Johnson: 5 Questions for FDA About Pfizer Vaccine ApprovalSen. Ron Johnson (R-Wis.) on Thursday sent a letter to Dr. Janet Woodruff, acting commissioner of the U.S. Food and Drug Administration (FDA), demanding answers to five questions pertaining to the FDA’s approval of the Pfizer Comirnaty COVID vaccine. The FDA on Aug. 23 granted full approval to Pfizer’s vaccine, over the objections of some scientists who pointed out that full approval was based on only six months’ worth of data — despite clinical trials designed for two years — and that there was no public discussion of the data....

The Food and Drug Administration’s “full authorization” for the Pfizer-BioNTech vaccine for Covid-19 was announced with a fair amount of hooplah and fanfare. The President of the United States announced the monumental development and touted it as rationale for the vaccine mandates to commence in the private sector, throughout the government, and in the U.S. military. President Joe Biden was on the spot Monday morning with a quick reaction to the FDA’s “full authorization” of the Covid-19 vaccines. But a closer examination of the “full authorization” documents has some Americans feeling deceived. There is the matter that Pfizer-BioNTech still appears...

What is going on here? Are we being lied to? Specifically check page 2 and page 12. Page 2: On August 23, 2021, having concluded that revising this EUA is appropriate to protect the public health or safety under section 564(g)(2) of the Act, FDA is reissuing the August 12, 2021 letter of authorization in its entirety with revisions incorporated to clarify that the EUA will remain in place for the Pfizer-BioNTech COVID-19 vaccine for the previously-authorized indication and uses, and to authorize use of COMIRNATY (COVID-19 Vaccine, mRNA) under this EUA for certain uses that are not included in...