Independent Alternative-News Aggregation
Source: TheEpochTimes.com
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.
Source: rwmalonemd.substack.com
From Part I – the interview left of with the big question of who is the puppet master? What’s behind all this propaganda and control over the past three years? I spoke of different theories that people had put out there, and ended with the beginning of the hypothesis that the CIA may in fact be that controlling element. Part II picks up the thesis there.
Source: AmericanThinker.com
Remdesivir may be the most despised drug in American history, earning the nickname Run Death Is Near for its lethal record during COVID. Experts claimed that it would stop COVID; instead, it stopped kidney function, then blasted the liver and other organs. Now this reviled destroyer of kidneys has been approved by the FDA for COVID treatment of kidney patients. Does anybody else feel as if the FDA is shoving its power in our faces and laughing at us?
Source: ChildrensHealthDefense.org
Emergent BioSolutions’ new anthrax vaccine contains dangerous toxins and may cause severe side effects, according to the product’s package insert.
The U.S. Food and Drug Administration (FDA), which approved the vaccine last week, posted the package insert late Friday.
“Is this a label or a cartoon?” asked Meryl Nass, M.D., a bioterrorism and anthrax expert who published an analysis of the insert on Substack. “You can’t make this stuff up,” she said.
Source: Brownstone.org
The uncritical, blind faith in vaccines is the preeminent sacred cow of modern medicine. (It happens to be its preeminent cash cow as well.) It is a quasi-religious, dogmatic article of conviction, rather than a sound scientific theory or an empirically-based clinical precept.
Vaccines have been controversial since their introduction centuries ago. Only in very recent history has there been a rigidly enforced orthodoxy of belief within the medical establishment that vaccines must be unanimously regarded as “safe and effective,” no questions asked.
Continue reading “Solutions to Vaccine Troubles in Ten Sentences – Clayton J. Baker, MD 7/24/23”
Source: ChildrensHealthDefense.org
A 13,685-page tranche of documents related to Moderna’s COVID-19 vaccine clinical trials released Tuesday contain details about the deaths of 16 trial participants, the prevalence of severe adverse events (SAEs) and other abnormalities.
Source: ChildrensHealthDefense.org
News that the World Health Organization (WHO) on Friday is expected to classify aspartame as a “possible carcinogen” has reignited a debate that has churned since the U.S. Food and Drug Administration (FDA) first approved the artificial sweetener more than four decades ago.
Source: LewRockwell.com
June 27, 2023, Robert F. Kennedy Jr. held a Health Policy Roundtable featuring a panel of health freedom advocates, including yours truly; my good friend Dr. Patrick Gentempo; Maureen McDonnell, a holistic pediatric nurse; Dr. Pierre Kory, cofounder of the Frontline COVID Critical Care Alliance (FLCCC); filmmaker Mikki Willis; Sayer Ji, founder of Greenmed.com; and Dr. Sherri Tenpenny.
Continue reading “Kennedy’s Health Policy Roundtable – Dr. Joseph Mercola 7/8/23”
Source: ChildrensHealthDefense.org
Editor’s note: This is the first in a three-part series examining key questions in the public debate on the safety of wireless radiation. Part I addresses the question, How did the FDA arrive at its position on cellphones and cancer?
Source: TheEpochTimes.com
Now that the pandemic has ended, researchers are urging regulatory agencies to consider the safety issues associated with the rapid approval of COVID-19 vaccines—and to correctly classify messenger RNA (mRNA) vaccines as gene therapy products (GTPs) to prevent pharmaceutical companies from bypassing regulatory standards.
Source: ChildrensHealthDefense.org
Story at a glance:
Source: usrtk.org
Sucralose is the most widely used artificial sweetener in the United States. Most commonly sold under the brand name Splenda, the chemical is used in over 6,000 food products. It is often found in “diet” sodas including Diet Coke with Splenda, Diet Pepsi with Splenda, as well as Gatorade’s Propel Water, low-calorie Kool-Aid, Atkins Diet products, and other low-calorie foods and drinks.
Sucralose is 600 times sweeter than sugar and itself contains no calories. Although it has been marketed as a healthy product that can help fend off obesity and diabetes, sucralose consumption has been linked to leukemia, weight gain, obesity, diabetes, liver inflammation, metabolic dysfunction and other illnesses.
Continue reading “Sucralose: Emerging Science Reveals Health Risks – Stacy Malkan 5/30/23”
Source: ChildrensHealthDefense.org
Children ages 12 to 17 who received the mRNA COVID-19 vaccine face a heightened risk of heart inflammation, according to a new U.S. Food and Drug Administration (FDA) study.
Source: ChildrensHealthDefense.org
New evidence suggesting public health officials knew early in 2021 that COVID-19 vaccines posed a heightened risk of myocarditis in young men — but withheld that information from the public — raises questions about whether federal health agencies violated any laws.
Source: ChildrensHealthDefense.org
Describing it as a “long-sought scientific achievement,” the U.S. Food and Drug Administration (FDA) on Wednesday approved Arexvy, the first vaccine for respiratory syncytial virus (RSV).
GlaxoSmithKline Biologicals (GSK) developed Arexvy under the FDA’s Priority Review designation. The FDA approved it for people ages 60 and older.
Source: GMWatch.org
The US Food and Drug Administration (FDA), which regulates genetically modified organisms (GMOs) for food safety, has written a letter to manufacturers and developers of new plant varieties who intend to transfer genes for proteins that are food allergens (including allergens from foods identified as major food allergens) into new plant varieties used for food. The FDA cautions these developers to consider the food safety risks posed by such allergens and plan early in development to manage the risks.
Source: petermcculloughmd.substack.com
I would have never thought five years ago that I would be using advanced monoclonal antibodies to treat acute viremia in a potentially fatal illness to help a patient avoid hospitalization or death. Yet, early research done by Dr. Ralph Baric who conceived SARS-CoV-2 in his 2015 papers also anticipated the development of a countermeasures such monoclonal antibodies directed against SARS-CoV-2.
Source: LewRockwell.com
Dr. Mercola Interview Begins at 3:40 Video Link
September 12, 2022, U.S. President Joe Biden signed an “Executive Order on Advancing Biotechnology and Biomanufacturing Innovation for a Sustainable, Safe and Secure American Bioeconomy.”1
This executive order makes biotechnology a national priority across agencies and branches of government. As noted in this order, biotechnology will also be used to “improve” food security, sustainability, and agricultural innovation in the U.S.:
Continue reading “Executive Order Lays Foundation for Lab-Created Foods – Dr. Joseph Mercola 4/5/23”
Source: ChildrensHealthDefense.org
Infants and children 6 months through age 4 who received the three-dose primary series of the Pfizer-BioNTech COVID-19 vaccine are now eligible for a fourth dose — Pfizer’s bivalent booster shot.
The U.S. Food and Drug Administration (FDA) on Tuesday amended the Emergency Use Authorization (EUA) of Pfizer bivalent COVID-19 booster vaccine for the younger age group, but only for those children who received the three-dose series before the FDA authorized Pfizer’s bivalent Omicron booster as the third shot in the primary series.
Source: ChildrensHealthDefense.org
Story at a glance:
Source: ChildrensHealthDefense.org
The U.S. Food and Drug Administration approved Recombivax HB, the hepatitis B vaccine for newborns, based on clinical trials performed on only 147 infants and children who were monitored for just five days.
Source: ChildrensHealthDefense.org
Amid tens of thousands of lawsuits that are pending in state courts all across the U.S., a new report based on evidence discovered in these court cases reveals Big Pharma giant GlaxoSmithKline (GSK) had, for decades, concealed evidence showing that Zantac could cause cancer.
Source: TheEpochTimes.com
The U.S. Food and Drug Administration (FDA) changed the end date of a study it is requiring Pfizer to conduct because Pfizer requested a delay, the agency says.
“The company requested an extension from FDA for completion, which the agency granted,” an FDA spokesperson told The Epoch Times via email.
Source: ConservativeReview.com
Imagine not only having injected 5.5 billion people with multiple doses of the failed COVID shots, but destroying lives and denying humane treatment on account of them. Now imagine knowing everything we know about the efficacy and safety of these novel therapies and still forging ahead with more doses and now RSV and flu shots built upon the same platform. Bad enough, right? Well, it gets even worse. Fauci now concedes that all respiratory viral vaccines are garbage, including those for flu, coronavirus, and RSV. Yet the policies never match the new admissions, as they race to accelerate the new flu and RSV shots within months.
Source: TheEpochTimes.com
Top U.S. health officials were concerned with an “adverse event issue” concerning COVID-19 vaccines being injected during pregnancy, according to newly disclosed emails.
On May 14, 2021, officials with the U.S. Food and Drug Administration (FDA) and U.S. Centers for Disease Control and Prevention (CDC) were exchanging emails about language concerning the co-administration of COVID-19 vaccines with other vaccines during pregnancy.