Organization Sues FDA for Failing to Protect Public from Biologically and Environmentally...
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ICAN OBTAINS FDA REPORT WHICH SHOWS SHOCKING CONDITIONS AT MODERNA VACCINE FACTORY
The US Food and Drug Administration has approved the first injectable medication to treat frostbite.
The psyop to throw the public off the trail of the next engineered pandemic is very real. A new bat lab is constructed in Ft. Collins, Colorado.
The FDA has granted clearance for the first AI-powered handheld medical device to assist physicians in detecting all three common skin cancers: basal cell carcinoma, squamous cell carcinoma, and melanoma.
In an effort to encourage the discovery of more treatment and diagnostic options in the medical field, the U.S. Food and Drug Administration (FDA) has finalized a rule allowing certain clinical trials to operate without obtaining informed consent fro
The U.S. Food and Drug Administration (FDA) is seeking to persuade a federal court to dismiss a lawsuit challenging its repeated advisories against using ivermectin to treat COVID-19.
"Shot Dead The Movie," tells the heartbreaking stories of children who died after receiving COVID-19 shots. Their parents are left behind to pick up the pieces, wondering how and why a shot they were assured was safe took the lives of their child
The US Food and Drug Administration has warned wholesalers, retail pharmacies, health care practitioners, and patients about counterfeit versions of Novo Nordisk's diabetes drug Ozempic.
U.S. health officials are investigating whether three brands of recalled cinnamon apple puree and applesauce that left dozens of American children sickened may have been intentionally contaminated with lead.
When the pandemic was in full swing and the world was scrambling to find an effective way to treat COVID-19, two promising treatments emerged: ivermectin and hydroxychloroquine (HCQ).
Under Operation Warp Speed, the Food and Drug Administration (FDA) hastily approved experimental mRNA technology and sold it under the label "vaccine."
...found in at least some of the COVID-19 shot vials!! The latest from Dr. Joseph Ladapo, Florida's Surgeon General - Serious questions demanded of the CDC and the FDA.
In an effort to protect its farming industry, its economy, and the health of its citizens, Italy recently became the first country to officially ban cultivated meat.
The recent findings of DNA fragments in the Pfizer and Moderna Covid-19 vaccines has led many to question why the FDA, which is responsible for monitoring the quality and safety of the vaccines, has failed to sound the alarm.
The U.S. Food and Drug Administration (FDA) has a long history of NOT protecting Americans from unsafe products – some that have even been banned elsewhere for decades.
Dr. Robert Malone, the inventor of mRNA and DNA vaccines, slammed health regulatory agencies for not informing people about potential plasmid DNA contamination in mRNA COVID-19 vaccines.
Neuralink has FDA clearance to start messing with people's heads--and not just figuratively.
Most Americans are familiar with the fun, dinosaur-shaped chicken nuggets popularized by food manufacturers like Tyson.
Federal regulators are warning Americans not to use 26 over-the-counter eye drop products that they said could lead to eye infections -- and partial vision loss or blindness.
A bit of knowledge about "public health" can be a dangerous thing when financially conflicted partisans control the executive branch...
The U.S. agencies that clear and recommend vaccines should disclose when they learned that COVID-19 vaccines may cause seizures and convulsions in children, a U.S. senator says.
Pfizer's COVID-19 vaccine is adulterated due to the undisclosed presence of a DNA sequence, experts say.
September 11, 2023, the U.S. Food and Drug Administration announced1 it had approved reformulated monovalent COVID shots by Pfizer and Moderna for use in individuals 12 years of age and older.
In 2017, the US Food and Drug Administration (FDA) entered into a memorandum of understanding (MOU) with the Bill & Melinda Gates Foundation.
Sudafed, Mucinex, Allegra, Dayquill 'Fail to Outperform Placebo Pills'
The agency was sued after rejecting Freedom of Information Act requests