The CDC & FDA Deliver BAD NEWS About the Booster Shots! They May Trigger Strokes!

In addition to cardiac events, another life-threatening side effect has been associated with the Pfizer-BioNTech vaccine. When is the risk period? Does the flu shot play any role in these events? What actions should we take to better protect ourselves? Summary of Key Facts On Jan. 13, 2023, the FDA and CDC issued a joint statement that a new “safety signal” for ischemic stroke had been detected in … Continue reading The CDC & FDA Deliver BAD NEWS About the Booster Shots! They May Trigger Strokes!

CDC Aware of Hundreds of Safety Signals for COVID Jab

STORY AT-A-GLANCE In September 2022, The Epoch Times asked the U.S. Centers for Disease Control and Prevention to release its Proportional Reporting Ratio (PRR) data mining results. PRR1 measures how common an adverse event is for a specific drug compared to all the other drugs in the database. According to the standard operating procedures2,3 for the Vaccine Adverse Event Reporting System (VAERS), which is run jointly by … Continue reading CDC Aware of Hundreds of Safety Signals for COVID Jab

REVISIONIST HISTORY: FDA now claims its crusade against ivermectin was just a “recommendation” against taking it

The U.S. Food and Drug Administration (FDA) is trying to rewrite history by claiming that it never actually told Americans not to take ivermectin for the Wuhan coronavirus (Covid-19). The FDA insists it only made a “recommendation” that people not take the generic antiparasitic drug, which was first approved by the FDA for human use back in 1996. (Related: Ivermectin is also considered by the World Health Organization [WHO] … Continue reading REVISIONIST HISTORY: FDA now claims its crusade against ivermectin was just a “recommendation” against taking it

FDA Chief: Long-Awaited Opioid Review Still in the Works

A long-awaited review of prescription opioid medications, including their risks and contribution to the U.S. overdose epidemic, is still underway at the Food and Drug Administration, the agency’s commissioner said Tuesday. Dr. Robert Califf wrote in a blog entry that the FDA is still studying “what revisions are needed to support appropriate use” of opioid painkillers like OxyContin and Vicodin. The update comes as part … Continue reading FDA Chief: Long-Awaited Opioid Review Still in the Works

Doctors Suing Food And Drug Administration Over Ivermectin

A Washington law firm has filed a federal lawsuit against the Food and Drug Administration (FDA) for interfering with the use of ivermectin as a treatment for COVID-19. The lawsuit was filed by Boyden Gray & Associates on behalf of three doctors who were disciplined for prescribing human-grade ivermectin to patients. The firm’s founder, attorney Boyden Gray, is a former legal adviser to the Reagan … Continue reading Doctors Suing Food And Drug Administration Over Ivermectin

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

FDA Releases Thousands of Pages of Documents Related to the Experimental Covid-19 Vaccines through FOIA Request — Animal Studies Showed Adverse Affects

The Gateway Pundit previously reported — Texas Northern District Judge Mark Pittman made the decision to release documents after the group behind the FOIA request, Public Health and Medical Professionals for Transparency, filed a joint status report.   The FDA then reached an agreement with the government on how fast the documents will be produced. The FDA had originally asked for 75 years, but Judge Pittman shot down the ridiculous request in January, setting … Continue reading FDA Releases Thousands of Pages of Documents Related to the Experimental Covid-19 Vaccines through FOIA Request — Animal Studies Showed Adverse Affects

68,000% Increase in Strokes as FDA and NIH Secretly Study Reports of Neurological Injuries After COVID-19 Vaccines

The Epoch Times published an explosive report today stating that they have received emails that allegedly show that the U.S. Food and Drug Administration (FDA) and National Institutes of Health (NIH) have been quietly studying neurological problems that have appeared in people after they took a COVID-19 vaccine. Two U.S. agencies have been quietly studying neurological problems that have appeared in people who have had COVID-19 vaccines, … Continue reading 68,000% Increase in Strokes as FDA and NIH Secretly Study Reports of Neurological Injuries After COVID-19 Vaccines

Obama FDA Head that Allowed Opioid Crisis to Increase Confirmed to Lead the FDA Again as COVID Shots Set to Join Annual Flu Shots in Windfall for Big Pharma

Apparently Robert Califf did such a good job of helping Big Pharma shield themselves from any liabilities due to the opioid crisis that destroyed the lives of so many Americans while he was head of the FDA under President Obama, that he is being brought back to lead the FDA again to help Big Pharma continue growing in record profits and sales as they get … Continue reading Obama FDA Head that Allowed Opioid Crisis to Increase Confirmed to Lead the FDA Again as COVID Shots Set to Join Annual Flu Shots in Windfall for Big Pharma

Russia labels GMOs, while America’s government sells out to the biotech poisoners and propagandists

Monday, March 25, 2019 by: Vicki Batts (Natural News) GMO labeling laws have been a source of controversy in the United States for quite some time. Consumer advocates have called upon the federal government to protect Americans’ right to freedom of choice and to encourage transparency in the food industry, but officials seem to be more interested in defending corporate interests. Industry leaders are afraid proper … Continue reading Russia labels GMOs, while America’s government sells out to the biotech poisoners and propagandists

On the same day that 17 children were murdered in a Florida high school, almost 300 Americans were killed by FDA-approved prescription medications

(Natural News) On the same day that 17 students and staff were killed in a Florida high school shooting, nearly 300 Americans were killed by FDA-approved prescription medications. Yet no one cried a single tear, and the (pharma-funded) news didn’t even mention the tragedy. When children are killed by guns, the news is emotionally multiplied with pseudojournalism “theatrics” to push for gun control while ignoring the … Continue reading On the same day that 17 children were murdered in a Florida high school, almost 300 Americans were killed by FDA-approved prescription medications

FDA Declares ‘Virtually All’ Drug Products Labeled As Homeopathic Are Illegal

The Food and Drug Administration (FDA) has reportedly declared that “virtually all” homeopathic drugs are illegal. Reports that the FDA is cracking down on the use of natural medicines have been circulating for a while. However, in a recently released “guidance document,” the FDA is now quoted as saying that homeopathic drugs are considered “new drugs” that are allegedly being sold illegally. The FDA released … Continue reading FDA Declares ‘Virtually All’ Drug Products Labeled As Homeopathic Are Illegal

Is Rand Paul the only U.S. Senator who opposes Big Pharma’s racketeering and price monopolies?

(Natural News) Truth be told, the best type of conservative is one who is capable of not only sticking to his or her principles, but also able to articulate those principles in a bold and fearless manner. And when it comes to shrinking the size of government and standing up to Big Pharma, Kentucky Senator Rand Paul reminds us time and time again that he … Continue reading Is Rand Paul the only U.S. Senator who opposes Big Pharma’s racketeering and price monopolies?

New FDA-approved “trackable” pill transmits information — it will tattle on you if you don’t take your meds

(Natural News) The U.S. Food and Drug Administration (FDA) recently approved a digital pill embedded with a sensor designed to inform physicians whether their patients are taking their medications. The federal approval marks a growing trend towards addressing drug non-adherence among patients, according to a New York Timesreport. The pill, called Abilify MyCite, is a modified version of Otsuka Pharmaceutical’s drug Abilify that is used in the treatment of schizophrenia, bipolar … Continue reading New FDA-approved “trackable” pill transmits information — it will tattle on you if you don’t take your meds

BIG PHARMA BIAS: FDA GRANTS ‘BREAKTHROUGH’ STATUS TO ECSTASY FOR PTSD WHILE PROHIBITING CANNABIS

If there’s one refrain we hear from politicians more than anything else, it’s “I support the troops.” However, their definition of “support” changes with the political wind, and more often than not is a farce. One example is the ongoing denial of medical cannabis to war veterans suffering from a range of conditions, from chronic pain to post-traumatic stress disorder (PTSD). Despite plenty of evidence—both scientific … Continue reading BIG PHARMA BIAS: FDA GRANTS ‘BREAKTHROUGH’ STATUS TO ECSTASY FOR PTSD WHILE PROHIBITING CANNABIS

Here’s why you should NEVER reuse your plastic water bottles

(Natural News) Would you lick a toilet seat? Hey, don’t worry, you can just drink out of your used plastic bottle instead. Researchers have suggested that refilling plastic bottles and drinking from them causes more harm than good, with the item essentially becoming a breeding ground for bacteria. The study was conducted by Treadmill Reviews and analyzed the water bottles used by an athlete after each … Continue reading Here’s why you should NEVER reuse your plastic water bottles

FDA now wants to eliminate side effect warnings from drug ads in latest collusion with Big Pharma

Natural News) We’ve all seen those drug commercials on TV with pleasant-looking grandparents frolicking in a grassy field with an adorable puppy, living life to the fullest while an announcer talks about how Big Pharma’s latest poison is going to make your life every bit as joyful. Then comes the obligatory rushed reading of a list of side effects. When the commercial is over, the … Continue reading FDA now wants to eliminate side effect warnings from drug ads in latest collusion with Big Pharma

Schumer calls on FDA to regulate ‘snortable chocolate’ such as Coco Loko

U.S. Sen. Charles Schumer is urging federal regulators to look into a “snortable chocolate” powder, saying he’s worried that it could prove harmful and is being marketed like a drug. In a letter Saturday, the New York Democrat asked the Food and Drug Administration to investigate the use of caffeine in inhalable food products such as so-called Coco Loko. It’s gotten buzz in recent weeks. … Continue reading Schumer calls on FDA to regulate ‘snortable chocolate’ such as Coco Loko

AMISH MAN SENTENCED TO SIX YEARS IN PRISON FOR NOT SEEKING FDA APPROVAL

Kentucky — “I am not a creation of state/government, as such I am not within its jurisdiction.” Those words were written by Samuel Girod in a document filed in a Kentucky federal court in June. Girod is an Amish farmer who was convicted in March of selling herbal health products that, as reported by the Lexington Herald-Leader on Friday, “were not adequately labeled as required by federal law.” According to the … Continue reading AMISH MAN SENTENCED TO SIX YEARS IN PRISON FOR NOT SEEKING FDA APPROVAL

Amish man slapped with six-year prison sentence for growing and selling his own herbal remedies

(Natural News) On the morning of June 30 2017, a federal judge sentenced an Amish man to six years in prison. His crimes: making and selling herbal health products that were not “adequately labeled”, and obstructing a federal agency. According to TheDailySheeple.com, the farmer, one Samuel A. Girod of Bath County in Kentucky, was convicted last March 13 for growing, manufacturing, and selling herbal supplements without approval … Continue reading Amish man slapped with six-year prison sentence for growing and selling his own herbal remedies

Alert: Maine approves three types of GMO potatoes

(Natural News) Maine just became the last state in the nation to approve the use of three new types of genetically modified (GM) potatoes – the Innate Generation 2 Russet Burbank, the Ranger Russet and the Atlantic potato varieties. The Maine Board of Pesticides Control approved the new potatoes, which were developed by the Idaho-based J.R. Simplot Co., in early May. The company claims that … Continue reading Alert: Maine approves three types of GMO potatoes

Science-based GMO website filters out corporate propaganda

(Natural News) In 1992, scientists at the Federal Drug Administration (FDA) made a ruling that has forever changed our world. Over a quarter of a century ago, the FDA sold out to corporations and boldly proclaimed that genetically modified organisms (GMOs) were a safe and efficient means of food production. At the time they stated, “the agency is not aware of any information showing that foods derived … Continue reading Science-based GMO website filters out corporate propaganda

FDA to use millions in taxpayer dollars to promote GMO propaganda

(Natural News) You might not be willing to buy GMO foods, but you’ll still be spending money on them thanks to a new congressional bill that allocates $3 million of taxpayer dollars to “consumer outreach and education regarding agricultural biotechnology.” A Pew study recently discovered that 39 percent of people in the U.S. think GMOs are bad for your health, and now the FDA – … Continue reading FDA to use millions in taxpayer dollars to promote GMO propaganda

FDA approves clinical trial of ecstasy for possible treatment of PTSD

(NaturalNews) Could ecstasy soon be hitting a pharmacy near you? The FDA recently approved of a large-scale, Phase 3 clinical trial of MDMA for post-traumatic stress disorder. The approval follows a series of small-scale studies that have indicated that small amounts of the drug can provide effective treatment for the illness. While it may sound like a fun time, for those who suffer with PTSD, … Continue reading FDA approves clinical trial of ecstasy for possible treatment of PTSD

Superbugs: Big Pharma to blame for coming death of 700,000 people annually

(NaturalNews) As new guidelines set forth by the U.S. Food and Drug Administration (FDA)to curb antibiotic overuse and abuse on factory farms slowly come into effect, the drug industry is apparently setting its greedy sights elsewhere – towards countries where restrictions on antibiotic use are looser, or simply where “anything goes.” Livestock are the single biggest consumers of antibiotic drugs in the U.S. – not … Continue reading Superbugs: Big Pharma to blame for coming death of 700,000 people annually

Human-Animal Hybrids Are a Violation of Human Dignity

Human-animal hybrids? No longer is it simply the stuff of science fiction. On August 4th, the National Institutes of Health (NIH) released a proposed policy that would lift the longstanding moratorium on the taxpayer funding of certain experiments creating embryos that are part human, part animal, known as “chimeras,” and even letting them grow into adult form. NIH solicited comments on their proposal, and FRC signed on … Continue reading Human-Animal Hybrids Are a Violation of Human Dignity

The FDA Just Crapped On Your Sushi By Approving GMO Salmon

Yep, this is actually happening. GMO Salmon is now approved by the FDA. So go ahead folks, eat your science lab fishy with that peaceful safe and secure feeling you eat regular fish that was made by nature with. Because that just makes all the sense in the world. The FDA Approves AquAdvantage Salmon. The FDA has approved AquaBounty Technologies’ application for AquAdvantage Salmon, an … Continue reading The FDA Just Crapped On Your Sushi By Approving GMO Salmon

FDA Prepares to Fast Track New Vaccines Targeting Pregnant Women

Vaccines Kill! Vaccines are Dangerous! Following is a public comment made by Barbara Loe Fisher, NVIC Co-founder & President, at the Nov. 13, 2015 meeting of the FDA Vaccines & Related Biological Products Advisory Committee (VRBPAC) on proposed changes to FDA requirements for licensure of vaccines intended for use during pregnancy Birth defects, chromosomal damage, premature birth, low birth weight, pregnancy complications and sudden infant … Continue reading FDA Prepares to Fast Track New Vaccines Targeting Pregnant Women

FDA approves experimental GMO salmon for human consumption despite lack of adequate safety studies

(NaturalNews) Just as we predicted, the U.S. Food and Drug Administration (FDA) has brazenly betrayed the public’s trust by approving the world’s first genetically modified (GM) animal in direct defiance of science – a transgenic salmon branded “AquAdvantage”that has never been proven safe for human consumption or the natural environment. The New York Times (NYT) reports that AquAdvantage, a product of AquaBounty Technologies, has received … Continue reading FDA approves experimental GMO salmon for human consumption despite lack of adequate safety studies