More evidence that the FDA is working with Sen. Durbin to eliminate your supplement access. Action Alert! The dominoes continue to line up for Senator Dick Durbin (D-IL) and his plan to restrict your supplement access. Last week, the FDA issued a policy designed to get companies to comply with its troublesome “new supplement” guidance that threatens over 41,000 supplements. … [Read more...] about FDA Colluding with Congress on Supplements
Until recently, most Americans had little trust in the FDA. But when COVID arrived in early 2020, a scared nation deepened in tribal identity and then turned its faith and trust over to the FDA and CDC. Interestingly, during COVID, medical professionals' trust in the FDA and CDC plummeted. Let’s explore how American perceptions of the FDA have changed and what this faith has … [Read more...] about From Corrupted to Trusted: Shifting Perceptions of the FDA
Earlier this month, the FDA announced it will allow a health claim regarding magnesium and hypertension, admitting there is scientific support that magnesium helps with high blood pressure…but the evidence is “inconsistent and inconclusive.” Huh? Rather than using qualifiers to downplay the evidence for magnesium, shouldn’t the FDA, a public health agency, be more concerned … [Read more...] about FDA raising our blood pressure by downplaying benefits of magnesium
Late last week, on December 9, the FDA approved the Emergency Use Authorization (EUA) for the Pfizer COVID-19 vaccine, “authorizing the use of a single booster dose for administration to individuals 16 and 17 years of age.” The booster is to be given at least 6 months after vaccination. [...] The Pfizer vaccine is particularly dangerous for young men aged 16-17. As we … [Read more...] about FDA, CDC Back BOOSTERS For Minors After Conducting Zero Testing On Boosters For Minors
Data show a simple nasal spray can neutralize the SARS-CoV-2 virus and help alleviate symptoms of COVID disease, but the feds block any mention of these benefits. The FDA and the FTC have sent warning letters to at least five companies marketing a wide range of antiseptic nasal sprays containing xylitol, saline, povidone-iodine, or some combination of these ingredients. The … [Read more...] about Breakthrough COVID Nasal Spray Blocked
STORY AT-A-GLANCE In September 2021, a group called Public Health and Medical Professionals for Transparency (PHMPT) filed a Freedom of Information Act (FOIA) request with the FDA to obtain the documentation used to approve Comirnaty. When, after a month, the FDA had not replied, the PHMPT sued It took the U.S. Food and Drug Administration 108 days to “thoroughly and … [Read more...] about FDA Wants 55 Years to Release COVID Jab Reaction Data
EDITOR’S NOTE: Following the Oct. 26 meeting of the U.S. Food and Drug Administration’s (FDA) Vaccines and Related Biological Products Advisory Committee (VRBPAC), Children’s Health Defense argued it is time to shun the individuals — and institutions — that are selling out America’s children without even a prick of conscience. At the close of this article about the members of … [Read more...] about 14 ACIP Members Who Voted to Jab Your Young Children — and Their Big Ties to Big Pharma
Attorney Aaron Siri is a Vaccine Injury attorney, one of just a handful of such attorneys in the U.S. Since the passage of the 1986 National Vaccine Injury Compensation law, one cannot sue pharmaceutical companies for vaccine injuries and deaths. A special U.S. Vaccine Court handles all cases with select judges chosen by the U.S. Government, and there only about 100 … [Read more...] about Vaccine Injury Attorney Suing the FDA: FDA Asks Federal Judge to Grant it Until the Year 2076 to Fully Release Pfizer’s COVID-19 Vaccine Data
STORY AT-A-GLANCE According to a whistleblower who worked on Pfizer’s Phase 3 COVID jab trial, data was falsified, patients were unblinded, the company hired poorly trained people to administer the injections, and follow-up on reported side effects lagged way behind Brook Jackson was the regional director of Ventavia Research Group, a research organization charged … [Read more...] about Pfizer Whistleblower Sinks Vaccine Trial Integrity
STORY AT-A-GLANCE Mainstream media have incorrectly insinuated that ivermectin is purely a veterinary drug that could be dangerous to humans; CNN falsely stated that Joe Rogan took “horse dewormer” Rogan recently interviewed CNN’s chief medical correspondent Dr. Sanjay Gupta, getting him to admit CNN lied The FDA started the “horse dewormer” fallacy based on a … [Read more...] about Secret Documents Reveal FDA’s Attack on Ivermectin
Regulatory agencies, says Encyclopedia Britannica, are a uniquely American institution. Though conceptualized as mere advisory bodies at the time of their emergence in the late 19th century, federal regulatory agencies have since acquired comprehensive legislative powers and even quasi-judicial powers — exercising “social control through rulemaking” with “almost no supervision … [Read more...] about Think the FDA Is Looking Out for Your Health? History Tells a Different Story.
A new congressional report released Wednesday revealing the baby food industry has failed to keep products with heavy metals off the shelves spurred calls for federal authorities to enact swift action and tough limits on toxin levels. “This is what happens when you let the food and chemical companies, not the FDA, decide whether our food is safe to eat,” said Scott Faber, … [Read more...] about Congressional Report: Baby Food Industry Knowingly Sold Products Contaminated With Heavy Metals
STORY AT-A-GLANCE Jodi O’Malley, a registered nurse who works for the U.S. Department of Health and Human Services’ Indian Health Services branch in Phoenix, Arizona, is blowing the whistle on COVID jab injuries A DHHS emergency room physician admits no one is reporting COVID jab injuries, even though it’s required for emergency use medications According to media … [Read more...] about Medical Mafia Is Sinking the Health Care System
In what one major news source is calling a “major blow to vaccine efforts,” two senior U.S. Food and Drug Administration officials have suddenly turned in their resignations. Thirty-two-year FDA veteran Marion Gruber is leaving her position as director of FDA’s Office of Vaccines Research & Review (OVVR) in October, and her deputy, Dr. Philip Krause, who has worked in … [Read more...] about Two Key Senior FDA Officials Resign Over Vaccine Decisions
STORY AT-A-GLANCE Respiratory syncytial virus (RSV) — a respiratory virus that causes typically mild cold-like symptoms — is emerging out of season around the world Most children have been exposed to RSV by their second birthday and recover without incident. In rare cases, RSV can progress to pneumonia or bronchiolitis (inflammation of the small airways of the … [Read more...] about FDA Fast-Tracks RSV mRNA ‘Vaccine’
Two of the U.S. Food and Drug Administration’s (FDA) top vaccine regulators will leave the agency this fall, raising questions about the Biden administration and the way it sidelined the agency. According to an email sent by Dr. Peter Marks, director of the FDA’s Center for Biologics Evaluation and Research (CBER), to staff members Tuesday, Dr. Marion Gruber, director of the … [Read more...] about 2 Top FDA Vaccine Officials Resign, Raising Questions About Pressure From White House to Approve Boosters
The US Government regulator for drugs, the Food and Drug Administration, has just announced that it has voted full approval for the mRNA genetic vaccine of Pfizer and BioNTech, or did they? This supposed new status is being used by the Biden Administration and many states and companies to impose mandatory vaccinations. The notoriously conflicted Biden covid adviser, Tony Fauci … [Read more...] about Scandal Behind the FDA Fake Approval of Pfizer Jab
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 … [Read more...] about Here’s Why No One Can Force You to Take Pfizer’s Newly ‘Approved’ Comirnaty Vaccine
Dear Readers, Surveys show a collapse in confidence of medical professionals in the FDA and CDC. https://www.paulcraigroberts.org/2021/08/28/believing-fdas-pfizer-approval-and-getting-vaxxed-is-stupid/ It is completely obvious that the two corrupt government agencies sacrificed public health to pharmaceutical profits. The approval granted Pfizer’s “vaccine” was given … [Read more...] about FDA’s Approval of Pfizer Covid Vaccine Is Not Justified
Dear Readers, As I predicted, the corrupt US Food & Drug Administration (FDA), allegedly a regulatory agency but in actuality an agent for Big Pharma and agri-business, has, according to news reports, given final approval to Pfizer’s Covid “vaccine.” (Why only Pfizer’s? Is there favoritism at the FDA?) The FDA congratulates itself declaring the “vaccine” a “milestone as … [Read more...] about The FDA Has Proved Itself To Be A Totally Corrupt And Criminal Organization
The FDA is signaling a change in how supplements are regulated that threatens not just hemp oil, but the entire industry. Action Alert! The FDA recently rejected two “new supplement” notifications for full spectrum hemp oil products. Previously the agency targeted CBD oil, stating that CBD is not a dietary supplement. These new actions are extremely concerning since they … [Read more...] about FDA Expands Supplement Attack, Targets Hemp Oil
A few months before the first COVID-19 vaccines received Emergency Use Authorization (EUA) in late 2020, a global vaccine safety expert cautioned the rushed circumstances made it essential to “get [safety monitoring] right” by “intensively” and “robustly” scrutinizing adverse events following the experimental rollout. As this expert stated, “Deploying any new vaccine based … [Read more...] about We’ve Never Seen Vaccine Injuries on This Scale — Why Are Regulatory Agencies Hiding COVID Vaccine Safety Data?
The FDA’s recent actions against a critical supplement have spurred some in Congress to action. We must build more support on Capitol Hill to protect access. Action Alert! Over the last few months, we’ve been telling you about the FDA’s attack against N-acetylcysteine (NAC), an important antioxidant supplement. We believe the FDA is clearing the market of affordable NAC … [Read more...] about Will Congress Halt FDA’s NAC Attack?
Help us build support in Congress to save homeopathy from the FDA’s overreach. Action Alert! We’ve been telling you over the last few years about the recent FDA guidance that threatens the future of homeopathic medicines in the US. Upending decades of safe regulation, FDA released a draft guidance in 2017 that essentially stated that all homeopathic drugs are illegal. … [Read more...] about Pressure Congress on Homeopathy
What became of Senator Dick Durbin’s (D-IL) attempt to pass more regulations on dietary supplements. Action Alert! Recently we alerted ANH members about another supplement sneak attack from Senator Durbin that would institute a mandatory listing requirement for dietary supplements. The good news is that Sen. Durbin has, so far, held off on introducing this legislation, so … [Read more...] about Supplement Sneak Attack: Update
The Biden Administration has signaled its next move as part of the White House’s full court press to pressure Americans into taking COVID-19 vaccines. It seems the White House intends to strong arm the Food and Drug Administration (FDA) into fully approving COVID vaccines, while completely dismissing evolving safety and efficacy concerns in the process. It began during a … [Read more...] about Politics over Science: Biden Admin Signals Intent to Force FDA Approval of COVID Vaccines
N-acetyl-L-cysteine (NAC) has been on the market as a supplement for decades—why is the FDA attacking it now? Action Alert! A few weeks ago, we told you about the FDA’s recent actions threatening NAC supplements—products which the FDA has allowed on the market for decades. The question is, why now, after all these years, is the FDA doing this? Digging a bit deeper, it seems … [Read more...] about Why the FDA is Attacking NAC Supplements?
Help us build support in Congress to ensure you can access the customized medicines you rely on. Action Alert! As part of its effort to implement the Drug Quality and Security Act of 2013, the FDA is poised to implement a bad policy that will limit the amount of medicines like bioidentical hormones such as estriol that compounding pharmacies can send out of state, even when … [Read more...] about Update on FDA Compounding Catastrophe
(Natural News) Drug giants Merck & Co. and Sanofi are about to unleash a new six-in-one (hexavalent) vaccine for children called Vaxelis that could kill them, and yet the federal government is fully on board. Despite prolific scientific evidence to suggest that Vaxelis is too much for a young immune system to handle, both the Food and Drug Administration (FDA) and the … [Read more...] about CDC, FDA ready to inject children with deadly six-in-one vaccine
Since the mid-1980s, the number of childhood shots on the Centers for Disease Control and Prevention (CDC) vaccine schedule has more than quadrupled. When parents express reluctance about turning their little ones into perpetual pin cushions, drug makers and doctors have a ready answer — combination vaccines that “simplify” the schedule by decreasing the number of injections … [Read more...] about CDC, FDA Prepare Mass Distribution of a Merck/Sanofi Six-in-One Vaccine for Kids, Turning Blind Eye to Safety Signals
(Natural News) All of a sudden, the Food and Drug Administration (FDA) is reversing course on the validity of antibody tests for the Wuhan coronavirus (Covid-19), which the agency says are no longer valid, even after “vaccination.” After earlier declaring antibody tests to be a gold standard in identifying the presence of the Chinese Virus, Tim Stenzel, M.D., Ph.D., director … [Read more...] about QUACKERY: After granting EUA to covid vaccines for antibody response, FDA now says antibodies are useless
(Natural News) The Food and Drug Administration (FDA) drew criticisms after granting Alzheimer’s disease drug Aduhelm a conditional approval. It allows the drug scientifically known as aducanumab to be prescribed and used while its maker Biogen conducts a post-marketing, phase 4 confirmatory study that could take years to complete. Aduhelm is the first Alzheimer’s medication … [Read more...] about ICER: FDA failed to protect patients from unproven Alzheimer’s treatment with known harms
(Natural News) As they say, the proof is in the pudding. COVID-19 shots have been the deadliest inoculations ever documented, by far, and that’s according to the CDC’s very own data. More people have died from Covid vaccines (approaching 5,000 now) than all vaccine deaths totaled since the 1950s. No wonder why. They couldn’t even reach the EAU (emergency authorized use) 50 … [Read more...] about Absolutely NOT safe and NOT effective: FDA and CDC lied about vaccine efficacy to obtain ’emergency authorized use’ (EAU) for highly-suspect human medical experiment using mRNA
A newly discovered document reveals the FDA was aware of the dangers of COVID-19 “vaccines” from the very beginning of the COVID-19 outbreak, but they hid them from us by omitting any mention of them in their public documents. The document is an SEC Registration submitted by a German company, BioNTech SE, on December 31, 2019. Like Moderna and Pfizer, BioNTech SE produces an … [Read more...] about Newly discovered document reveals the FDA was aware of dangers of COVID-19 “vaccines” but hid them from us
Earlier this year, I reported that carcinogenic N-nitrosodimethylamine (NDMA) had been found in certain blood pressure, heartburn and diabetes medications. As of February 2020, drugs recalled due to contamination with this poison included:1 Valsartan, losartan and irbesartan (high blood pressure medications) Zantac2 and Axid (heartburn medications) Metformin … [Read more...] about How Did Carcinogenic Generic Pill Get Past the FDA?