BOMBSHELL: The FDA’s emergency use authorization (EUA) for covid “vaccines” was FAKED

After Congress passed the Public Readiness and Emergency Preparedness Act (PREP Act) back in 2020, things changed for the worse at the U.S. Food and Drug Administration (FDA) in terms of the standards used to authorize and approve vaccines, biologics, and other pharmaceutical drugs. All of the certified Good Clinical Practices (GCP) that were followed prior to 2020 went out the window at the height … Continue reading BOMBSHELL: The FDA’s emergency use authorization (EUA) for covid “vaccines” was FAKED

Scientists discover some Fully Vaccinated Children are suffering Sepsis & Autoimmune Disease when exposed to Covid-19

A new study conducted by several doctors on behalf of the University of Colorado has found that Covid-19 vaccination can cause children to suffer Vaccine-Associated Enhanced Disease (V-AED), and further analysis of the confidential Pfizer documents forcibly published by court order reveals both Pfizer and the U.S. Food & Drug Administration (FDA) knew it would happen. The study, published 31st May 2022, aimed to prove that … Continue reading Scientists discover some Fully Vaccinated Children are suffering Sepsis & Autoimmune Disease when exposed to Covid-19

Breaking News: FDA Panel Recommends Moderna Two-Dose COVID Vaccine for Kids Ages 6 to 17 Despite Serious Safety Concerns

The U.S. Food and Drug Administration’s vaccine advisory panel on Tuesday voted 22 – 0 to authorize Moderna’s COVID-19 vaccines for children ages 6 to 11 and 12 to 17 despite the lack of short- and long-term safety data and no evidence children are at risk of serious illness. The U.S. Food and Drug Administration’s (FDA) vaccine advisory panel today voted unanimously to recommend Moderna’s COVID-19 vaccine … Continue reading Breaking News: FDA Panel Recommends Moderna Two-Dose COVID Vaccine for Kids Ages 6 to 17 Despite Serious Safety Concerns

Pharma and the FDA Knew Lipid Nanoparticles from the Covid Shots Go EVERYWHERE – Yes, the Brain Too!

Dr. Ryan Cole: “It was originally designed to take mRNA and or chemotherapeutic agents to organs that are hard to get to, like the brain… Scientists knew they would not stay in the arm. To have told the people of the world otherwise was a straight up scientific lie.” Continue reading Pharma and the FDA Knew Lipid Nanoparticles from the Covid Shots Go EVERYWHERE – Yes, the Brain Too!

FDA Finally Admits that Covid Vaccines DO Cause Blood Clots

The U.S. Food and Drug Administration (FDA) has altered its guidance for the Wuhan coronavirus (Covid-19) “vaccine” from Janssen (Johnson & Johnson), which the federal agency now admits causes blood clots. An FDA news release explains that the Janssen injection now has limited authorized use in individuals 18 years of age and older due to the risk of thrombosis with thrombocytopenia syndrome (TTS), “a syndrome of rare … Continue reading FDA Finally Admits that Covid Vaccines DO Cause Blood Clots

FDA Tells Doctors in 8 States to Stop Using COVID-19 Treatment

U.S. drug regulators have directed health care workers in eight states to stop using a COVID-19 treatment because it may not be effective against an Omicron coronavirus subvariant that’s rising in prevalence. The Food and Drug Administration (FDA) said sotrovimab, a monoclonal antibody used to treat COVID-19, can no longer be used in Connecticut, Maine, Massachusetts, New Hampshire, New Jersey, New York, Rhode Island, and … Continue reading FDA Tells Doctors in 8 States to Stop Using COVID-19 Treatment

COVID-19 Vaccine Massacre: 68,000% Increase in Strokes, 44,000% Increase in Heart Disease, 6,800% Increase in Deaths

by Brian ShilhavyEditor, Health Impact News The corporate media is now controlled by the interests of Big Pharma which has spent over $1 BILLION in promoting COVID-19 vaccines. See: Local, National Media Paid $MILLIONS To Push COVID-19 Vaccines Even last night’s Oscar’s show was sponsored by Pfizer and BioNTech. So when this corporate media now switches their focus to trying to convince the American public that … Continue reading COVID-19 Vaccine Massacre: 68,000% Increase in Strokes, 44,000% Increase in Heart Disease, 6,800% Increase in Deaths

Just Released Documents by Pfizer Show BioNTech Paid FDA $2,875,842.00 “Drug User Fee” for COVID-19 Vaccine Approval

As the news cycle continues to focus on the Ukraine situation, the FDA complied with a court order to begin releasing 55,000 pages of Pfizer data per month that was used to authorize their COVID-19 vaccine produced with BioNTech, with the first batch quietly released yesterday, March 1st. There are 150 documents that the public can now download here. One of the documents released was the … Continue reading Just Released Documents by Pfizer Show BioNTech Paid FDA $2,875,842.00 “Drug User Fee” for COVID-19 Vaccine Approval

2,809 Dead Babies in VAERS Following COVID Shots as New Documents Prove Pfizer, the FDA, and the CDC Knew the Shots Were Not Safe for Pregnant Women

The latest data dump into the U.S. Government’s Vaccine Adverse Events Reporting System (VAERS) happened yesterday (12/3/21) and covers data through 11/26/2021. There are now 927,740 cases reported to VAERS following COVID-19 shots for the past 11 months, out of the total of 1,782,453 cases in the entire VAERS database filed for the past 30+ years. That means that 52% off ALL vaccine adverse reaction cases in VAERS for the past … Continue reading 2,809 Dead Babies in VAERS Following COVID Shots as New Documents Prove Pfizer, the FDA, and the CDC Knew the Shots Were Not Safe for Pregnant Women

Breaking: U.S. Pauses Johnson & Johnson Vaccine, Citing ‘Rare’ Blood Clots

The CDC and FDA called for a temporary but immediate halt to the use of J&J’s COVID vaccine while they investigate at least six cases of potentially dangerous blood clots in people who received the vaccine. Federal agencies today said they will stop using the single-shot Johnson & Johnson (J&J) COVID vaccine at mass vaccination sites while they investigate the vaccine’s possible link to potentially dangerous blood … Continue reading Breaking: U.S. Pauses Johnson & Johnson Vaccine, Citing ‘Rare’ Blood Clots

FDA Issues Emergency Use Authorization for Another Experimental COVID-19 Vaccine

The FDA today issued an emergency use authorization (EUA) for Janssen Biotech’s adenovirus experimental COVID-19 vaccine. Janssen Biotech, Inc., is a subsidiary of the Johnson and Johnson multi-national corporation, which has paid out BILLIONS in criminal settlements, which is ongoing due to the opioid crisis. You can read their criminal rap sheet here. The Johnson and Johnson experimental COVID vaccine is not an mRNA vaccine, it … Continue reading FDA Issues Emergency Use Authorization for Another Experimental COVID-19 Vaccine

Dangerous Levels Of Toxic Heavy Metals In Baby Food, Congressional Report Finds

Several baby products made by the country’s largest baby food manufacturers contain harmful amounts of toxic heavy metals, including arsenic, lead, cadmium and mercury, that can harm infant neurological development, according to a congressional report released Thursday.  After receiving reports claiming high toxic heavy metal levels in baby foods, the House Subcommittee on Economic and Consumer Policy requested Nov. 6, 2019, seven of the largest … Continue reading Dangerous Levels Of Toxic Heavy Metals In Baby Food, Congressional Report Finds

Lawsuit Challenging FDA Approval Of Novel Genetically Engineered Color Additive That Makes Impossible Burger “Bleed” Moves Forward

FDA Fails to Demand Needed Tests, Its Approval Not Based on “Convincing Evidence” as Required by Law (Washington, D.C.) — Yesterday, Center for Food Safety (CFS) filed a legal brief in its challenge to the U.S. Food and Drug Administration’s (FDA) 2019 approval of soy leghemoglobin (“heme”), a color additive used to make Impossible Foods’ eponymous plant-based burger, the Impossible Burger, appear to “bleed” like real meat. The novel … Continue reading Lawsuit Challenging FDA Approval Of Novel Genetically Engineered Color Additive That Makes Impossible Burger “Bleed” Moves Forward

FDA Shuts Down Natural Pain Relief Options

FDA-approved pain medicines are dangerous, but the government is systematically attacking safer, non-addictive natural treatments. Action Alert! A recent study in Switzerland found that acetaminophen poisoning increased by 40% following the approval of 1,000mg doses. This is just the latest data to indicate the public health problems caused by this commonly used pain drug, which is the active ingredient in Tylenol. Despite the dangers of FDA-approved pain drugs, … Continue reading FDA Shuts Down Natural Pain Relief Options

The Little-Known Sordid History of Psychiatry

STORY AT-A-GLANCE Dr. Peter Breggin, a psychiatrist, is frequently referred to as “the conscience of psychiatry” because he’s been able to successfully reform the psychiatric profession, abolishing lobotomies and other experimental psychosurgeries Breggin refers to lobotomies as a rape of the soul, the permanent mutilation of an individual’s selfhood, as damage to one area of the brain will harm the integration of the whole brain … Continue reading The Little-Known Sordid History of Psychiatry

FDA issues warning letter for not including the most serious risks in advertisement for medication-assisted treatment drug

For Immediate Release:December 11, 2019 The U.S. Food and Drug Administration today posted a warning letter to Alkermes, Inc. of Massachusetts, for misbranding the drug Vivitrol (an extended-release injection formulation of naltrexone) by omitting warnings about the most serious risks associated with the drug from promotional materials. Vivitrol is approved for the prevention of relapse to opioid dependence, following opioid detoxification and should be part of a … Continue reading FDA issues warning letter for not including the most serious risks in advertisement for medication-assisted treatment drug

‘ALARMING’ Number of People Received Restricted Fentanyl, study says

An “alarming” number of US patients received a highly potent form of opioid that is 100 times more powerful than morphine and that they never should have been prescribed, according to a new study.The research, published Tuesday in JAMA: The Journal of the American Medical Association, found that the US Food and Drug Administration and opioid manufacturers failed at multiple levels to adequately monitor the restricted … Continue reading ‘ALARMING’ Number of People Received Restricted Fentanyl, study says

FDA Shocking Study: Cells Used In Vaccines Contaminated With Serious Viruses Including Cancer

The U.S. Food and Drug Administration (FDA) has published shocking results which found that cells used in the manufacturing of numerous childhood vaccines are often contaminated with serious viruses including cancer. The FDA study looked at vaccines that are made from living cells, or replicated cell substrates that some manufacturers are investigating to create. According to research, these cells are oftentimes contaminated with hidden viral fragments which … Continue reading FDA Shocking Study: Cells Used In Vaccines Contaminated With Serious Viruses Including Cancer

BP Med Warning! If You Take This, You Need To Speak To Your Doctor To Change It. It Can Cause Cancer.

KEY POINTS A pharmacy warns the FDA that it found a chemical believed to cause cancer in a widely used blood pressure medication, according to a filing. Valisure told FDA that high levels of dimethylformamide were found in valsartan, a drug produced by Novartis and other pharmaceutical companies. A pharmacy warned the Food and Drug Administration that it found a chemical believed to cause cancer in a … Continue reading BP Med Warning! If You Take This, You Need To Speak To Your Doctor To Change It. It Can Cause Cancer.

Leaked FDA Study: Toxic “Forever Chemicals” Contaminate Many Foods

The Food and Drug Administration (FDA) has quietly revealed some troubling information about a class of toxic chemicals that the agency found in significant levels in our food supply. At a recent scientific conference, the FDA shared the findings of its first broad testing of food for a worrisome class of nonstick, stain-resistant industrial compounds called per- and polyfluoroalykyl substances, or PFAS. The FDA has not … Continue reading Leaked FDA Study: Toxic “Forever Chemicals” Contaminate Many Foods

WARNING: This Diabetes Drug Could Cause Dangerous Body Infection

Prior to reading this, understand that Diabetes Type II can be easily reversed and completely controlled with perfect double digit blood sugars by eating the right foods.  A note to you is to never stop your medications without the express knowledge of your medical provider (who hopefully is a naturopathic MD).  Before it’s too late, make an appointment with a nutrition friendly physician.  These dangers … Continue reading WARNING: This Diabetes Drug Could Cause Dangerous Body Infection

FDA: Ambien Is Making People Kill Themselves While Asleep

The FDA says sleeping pills are linked to falls, burns, limb loss, poisoning, drowning, car crashes, and even suicide. New Warning Sleep medications including Ambien have become infamous for prompting people to act bizarrely in a semi-sleeping stupor — but now the U.S. Food and Drug Administration (FDA) will require sleeping pill manufacturers to post warnings on labels, according to The New York Times. Harrowing incidents related to sleeping … Continue reading FDA: Ambien Is Making People Kill Themselves While Asleep

FDA cracks down on fluoride levels but still allows the neurotoxin to be DELIBERATELY added to bottled water

The U.S. Food and Drug Administration (FDA) is now cracking down on fluoride levels and has set a new legal limit for the neurotoxin in bottled water. The previous standard allowed manufacturers to add .8 to 1.7 milligrams of fluoride per liter. The FDA’s new regulation will cap fluoride levels at .7 milligrams per liter. While the new regulation is a step in the right direction … Continue reading FDA cracks down on fluoride levels but still allows the neurotoxin to be DELIBERATELY added to bottled water

FDA inspections reveal that factories in China and India produce CARCINOGEN-TAINTED blood pressure and heart medications. Is YOUR Medication Tainted?

A shocking investigation has just revealed serious contamination issues for blood pressure medications made in foreign factories. Drugs made at plants located in China and India are tainted with carcinogenic substances, according to a report from the FDA. Estimates suggest that one out of every three American adults takes a blood pressure medication. How many people will be affected by this recall is currently unknown. … Continue reading FDA inspections reveal that factories in China and India produce CARCINOGEN-TAINTED blood pressure and heart medications. Is YOUR Medication Tainted?

Addicts Are Hurting Their Pets to Get Access to Opioids

Addiction take your God given personality away from you and turns you into a monster… even a monster who would harm your own beloved pets in order to get drugs!  It doesn’t get much lower than that.  Perhaps today will be the day that you choose detox and get better! ~NationalAddictionNews.com People are hurting their pets in order to get their hands on opioids prescribed by … Continue reading Addicts Are Hurting Their Pets to Get Access to Opioids

RECALL: Peaches, Plums, And Nectarines Could Be Tainted With Listeria

Yet another recall has hit the shelves of a store near you. This time, it’s something really surprising. It’s fresh fruit. The FDA has announced that peaches, nectarines, and plums sold in more than a dozen states could potentially be tainted with Listeria monocytogenes. Jac. Vandenberg, Inc. of Yonkers, New York has recalled 1,727 cartons of peaches, 1,207 cartons of nectarines and 365 cartons of plums. The fruit … Continue reading RECALL: Peaches, Plums, And Nectarines Could Be Tainted With Listeria

Opioid Expert Accuses FDA of ‘Willful Blindness’ After It Approves Powerful New Painkiller

An expert tasked with helping the Food and Drug Administration weigh potential new opioid drug approvals is openly calling out the agency for what he alleges are its continued missteps in handling the opioid crisis. In an interview with the Guardian Thursday, Raeford Brown claimed that the FDA has failed to learn from its past mistakes by approving the drug Dsuvia last year, the tablet form of … Continue reading Opioid Expert Accuses FDA of ‘Willful Blindness’ After It Approves Powerful New Painkiller

FDA Advisory Panels: Asking Doctors to Prescribe Naloxone With Opioid Painkillers

The labels of prescription opioid painkillers should advise doctors to consider simultaneously prescribing the opioid overdose antidote naloxone, two U.S. Food and Drug Administration advisory panels recommend. The 12-to-11 vote during a joint meeting of the committees was described by several members as a message to the federal government to make naloxone more widely available, easier to obtain, and cheaper, the Washington Post reported. Although not required to … Continue reading FDA Advisory Panels: Asking Doctors to Prescribe Naloxone With Opioid Painkillers

FDA Says Certain Antibiotics Could Rupture Main Artery

They’re certain antibiotics, known as fluoroquinolones. Popular brand names include Avelox, Cipro, and Levaquin. Now, the U.S. Food and Drug Administration says these antibiotics “can increase the occurrence of rare but serious events of ruptures or tears in the main artery of the body,” the aorta. The FDA says these ruptures “can lead to dangerous bleeding or even death.” The FDA is requiring drug makers to add … Continue reading FDA Says Certain Antibiotics Could Rupture Main Artery

Triclosan: Is this Hazardous Toxin in Your Toothpaste, Beauty Products, Soap & Toys?

Triclosan is a “super chemical” meant to fight the spread of germs, but with the emergence of drug-resistant superbugs, the question is whether it really fights the good fight or just creates bigger problems. The answer is pretty straightforward. Triclosan is a major player when it comes to the problem of antibiotic resistance, which is becoming more common and more deadly with each passing year. … Continue reading Triclosan: Is this Hazardous Toxin in Your Toothpaste, Beauty Products, Soap & Toys?

WHAT??????? In The Midst of a Sweep of Death from Opioids, the FDA Just Approved a New Opioid 500 Times as Potent as Morphine! Are They Serious?

I truly believe this is all about POPULATION CONTROL designated by the elite!  Don’t accept a prescription for any opioid, but NEVER EVER accept a prescription for Dsuvia.  It will be automatic suicide for you and homicide from your doctor.  So, if you choose any opioids, plan your funeral and write out your eulogy.  You’ll need to! ~NationalAddictionNews.com There are concerns over a new, even … Continue reading WHAT??????? In The Midst of a Sweep of Death from Opioids, the FDA Just Approved a New Opioid 500 Times as Potent as Morphine! Are They Serious?

FDA takes action against 21 websites marketing unapproved opioids as part of agency’s effort to target illegal online sales

The U.S. Food and Drug Administration today announced it has warned four more online networks, operating a total of 21 websites, illegally marketing potentially dangerous, unapproved, and misbranded versions of opioid medications, including tramadol. The warning letters issued by the FDA to each of the networks state that they must immediately stop illegally selling these products to American consumers. “The illegal online sale of opioids … Continue reading FDA takes action against 21 websites marketing unapproved opioids as part of agency’s effort to target illegal online sales