FDA

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

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

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 far more devastating causes of preventable death in America. You see, while the Florida school shooting happened just once, the deaths of hundreds of Americans from FDA-approved prescription medications goes on every single day, without pause.

That’s why, according to scientific research, at least 106,000 Americans are killed each year by legal medications which are prescribed by licensed doctors. (Source: “Death By Medicine” analysis.)

Chemotherapy kills an estimated 2,700 people every day across the globe

The website PharmaDeathClock.com counts the number of people killed by toxic medicine every day, both in America and around the world. According to the site, chemotherapy alone kills an estimated 2700 people every day around the world. (See the Chemo Kills website for more details.)

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

China’s First GMO Rice Gets US FDA Approval

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– China’s First GM Rice Gets US FDA Approval:

A genetically modified (GM) rice product developed by a group of Chinese scientists has acquired the US Food and Drug Administration (FDA) approval, the first such Chinese product allowed to enter the US market.

Source: www.globaltimes.cn

However, neither China nor the US has approved mass cultivation of the rice amid low acceptance from the Chinese public for GM food.

Huahui No.1 rice, developed by the Huazhong Agricultural University, is genetically engineered to resist a wide range of insects, thus reducing the use of pesticides.

Read moreChina’s First GMO Rice Gets US FDA Approval

Ghost in the Machine, Part 2 — Success Breeds Greed That Gets in the Way of Ethics, Common Sense and Caution

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– Ghost in the Machine, Part 2 — Success Breeds Greed That Gets in the Way of Ethics, Common Sense and Caution:

By Dr. Mercola

Direct-to-consumer (DTC) drug advertising, which began in 1997, has done a lot more than make Pharma arguably the most profitable industry in the world and a Wall Street success story. It has greatly increased the number of prescription drugs that Americans take. In 1992, five years before DTC advertising began, Americans took an average of seven prescription drugs a year. A mere 15 years later that number had nearly doubled to 12 per year.1,2

To sell drugs, aggressive drug advertising whips up fears over rare diseases like exocrine pancreatic insufficiency (introduced at the 2017 Super Bowl) and make a disease out of common, nearly universal conditions to frighten and motivate people into taking prescription drugs.

Another DTC advertising tactic is convincing people to take drugs simply because they might be “at risk” of a condition. Sadly, drug advertising is not the only way Pharma gets dangerous drugs into the nation’s medicine chests. Thanks to outrageous conflicts of interest at the U.S. Food and Drug Administration (FDA) — the new FDA Commissioner, Dr. Scott Gottlieb, is a drug company consultant — drugs that would once have not been approved fly through their approvals.

Read moreGhost in the Machine, Part 2 — Success Breeds Greed That Gets in the Way of Ethics, Common Sense and Caution

FDA Just Approved ‘Smart Pill’ Antidepressant So Gov’t Can Track You As They Force Medicate You

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– FDA Just Approved ‘Smart Pill’ Antidepressant So Gov’t Can Track You As They Force Medicate You:

With the FDA recently authorizing the world’s first “smart pill”, many ethical questions are being raised by medical doctors. Forced medication by the state seems imminent.

The Food and Drug Administration (FDA) recently approved what may be the world’s first “smart pill.” Abilify MyCite, (aripiprazole) a “pill with a sensor that digitally tracks if patients have ingested their medication” was approved for sale and distribution by the FDA in mid-November. Now, a month after the drug’s approval, several of the world’s leading medical doctors are questioning the ethics surrounding the controversial drug.

Read moreFDA Just Approved ‘Smart Pill’ Antidepressant So Gov’t Can Track You As They Force Medicate You

Why the Truth Is So Important to Me (Truthstream Media Video)

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H/t reader Squodgy:

“Love this girl, her sincerity is palpable, her concerns infectious.”

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AND NOW: Ecstasy labelled a ‘breakthrough therapy’ for patients with post-traumatic stress disorder (PTSD) by the FDA

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– Ecstasy labelled a ‘breakthrough therapy’ for patients with post-traumatic stress disorder by the FDA:

ILLICIT drug ecstasy is one step away from being licensed in the US for its effectiveness in treating post-traumatic stress disorder.

The US Food and Drug Administration (FDA) has determined that illicit drug ecstasy is a “breakthrough therapy” in post-traumatic stress disorder (PTSD) treatment.

Methylenedioxymethamphetamine (MDMA), commonly referred to as ecstasy, could now have a faster pathway to pharmaceutical approval in the US, reports Science Alert .

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New FDA-approved Hepatitis B vaccine found to increase heart attack risk by 700%

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Additionally, the Hepatitis B vaccine is very, very harmful to the immune system, which is why they inject it into your children, whose immune system hasn’t developed yet and who are getting injected with a totally useless vaccine (even if vaccines would work properly), because children do usually not have sex, nor are they likely to ‘share’ Hepatitis B contaminated syringe’s.

“Hepatitis B is generally considered an adult disease because it’s transmitted through unsafe sex and shared needles.”

– New FDA-approved Hepatitis B vaccine found to increase heart attack risk by 700%:

A new FDA-approved Hepatitis B vaccine has been found to increase the risk of heart attacks by 700%, yet Facebook, Google, YouTube and Twitter ban any talk of vaccine dangers. There is a complete blackout of medical and scientific facts if they show vaccines to be anything less than magical, risk-less, medical utopian gifts to humanity.

This new analysis comes from Dr. Jack Wolfson, a well-informed cardiologist practicing in Arizona who dares to speak out on the truth about vaccine risks. Here’s his report:

 

Hepatitis B vaccine linked to 700% increase in heart attacks

Read moreNew FDA-approved Hepatitis B vaccine found to increase heart attack risk by 700%

Amish farmer sold herbal health products. He’s going to prison for 6 years.

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– Amish farmer sold herbal health products. He’s going to prison for 6 years:

An Amish man was sentenced Friday to six years in prison for obstructing a federal agency and for making and selling herbal health products that were not adequately labeled as required by federal law.

Samuel A. Girod of Bath County, a member of the Old Order Amish faith, was convicted in March on 13 charges, including threatening a person in an attempt to stop him from providing information to a grand jury.

U.S. District Judge Danny Reeves repeatedly asked Girod in court if he wished to make a statement but Girod refused. Girod, who represented himself, does not acknowledge that the court has jurisdiction.

“I do not waive my immunity to this court,” Girod told the judge. “I do not consent.”

Read moreAmish farmer sold herbal health products. He’s going to prison for 6 years.

Amish Man Sentenced To Six Years In Prison For Not Seeking FDA Approval

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– 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.”

Read moreAmish Man Sentenced To Six Years In Prison For Not Seeking FDA Approval

FDA Wants to Jail Sam Girod for 48 Years, for Making Salves People Love

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– FDA Wants to Jail Sam Girod for 48 Years, for Making Salves People Love:

Sam Girod is a Kentucky farmer who runs a small business selling natural skin salves made from herbs such as chickweed, which seem to help relieve a host of skin conditions, including allergic rashes,  psoriasis, poison oak and even skin cancers.

If you look up chickweed on Amazon, you will find pages of chickweed products, dozens and dozens of products, in some cases followed by glowing testimonials from users about how this or that chickweed provided relief from terrible itching, and even cured their skin cancers.

Read moreFDA Wants to Jail Sam Girod for 48 Years, for Making Salves People Love

FDA Quietly Bans Another Cheap Cancer Treatment: Intravenous Vitamin C

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… intravenous Vitamin C works as an oxidant (and not an anti-oxidant) and the generation of hydrogen peroxide is the main mechanism, why Vitamin C infusions are effective against cancer.

Related info:

– Researchers found that using vitamin C correctly (intravenously) in high doses kills cancer cells

– Clinical Guide To The Use Of Vitamin C

– FDA Quietly Bans Another Cheap Cancer Treatment: Intravenous Vitamin C:

It would be naive to think that the FDA endeavors to protect the public’s health as its primary focus. 

Indeed, that would be a conflict of interest, as it serves its master, the pharmaceutical industry.

Has the Food and Drug Administration engineered a shortage of intravenous vitamin C as part of an overall attack on natural and non-toxic approaches to healing that compete with prescription drugs?

Read moreFDA Quietly Bans Another Cheap Cancer Treatment: Intravenous Vitamin C

Here we go again: FDA Commissioner in pocket of Big Pharma

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– Here we go again: FDA Commissioner in pocket of Big Pharma:

by Jon Rappoport

April 17, 2017

The excellent medical reporter, Martha Rosenberg, has written a piece at Salon: “The FDA Now Officially Belongs to Big Pharma.” Here are a few highlights:

It is hard to believe only four senators opposed the confirmation of [the new FDA Commissioner]…[he] received money from 23 drug companies including the giants like Johnson & Johnson, Lilly, Merck, Schering Plough and GSK…”

Read moreHere we go again: FDA Commissioner in pocket of Big Pharma

FDA quietly bans powerful life-saving intravenous Vitamin C

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– FDA quietly bans powerful life-saving intravenous Vitamin C:

It would be naive to think that the FDA endeavors to protect the public’s health as its primary focus. Indeed, that would be a conflict of interest, as it serves its master, the pharmaceutical industry. Has the Food and Drug Administration engineered a shortage of intravenous vitamin C as part of an overall attack on natural and non-toxic approaches to healing that compete with prescription drugs? An analysis by Natural Blaze would suggest that the answer is yes.

Natural Blaze claims that a critical shortage of IV bags in general followed an FDA ban on the mass production of intravenous vitamin C. The FDA limited the availability of IV-C and the pharmaceutical industry halted production of injectable vitamins and minerals, after a 60 minute story about the miraculous recovery of a swine flu patient on life support. Because of the shortage of IV-C, doctors called upon compounding pharmacies to produce it. But the FDA began to limit compounding pharmacies after injectable steroids produced by the New England Compounding Center were contaminated with a fungus that caused a deadly outbreak of meningitis. Here is an example of an entire industry being punished for the dubious practices of one compounding pharmacy.

Read moreFDA quietly bans powerful life-saving intravenous Vitamin C

Giving a FluLaval shot to a 200 pound man is 79,365.587 times greater than the FDA recommendations

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USDA Allows Non-GMO Label for Some GMO Fed Animal Products

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– USDA Allows Non-GMO Label for Some GMO Fed Animal Products:

The United States Department of Agriculture’s Food Safety Inspection Service (FSIS) informed Sustainable Pulse on Monday that they will allow multi-ingredient products, which include GMO fed animal products, such as eggs, meat or poultry, to be labeled Non-GMO.

Sustainable Pulse requested further details on the FSIS guidelines published in August, due to ‘confusing’ language regarding which products will be able to be labeled non-GMO.

Read moreUSDA Allows Non-GMO Label for Some GMO Fed Animal Products

FDA Finds Glyphosate Residues in Oat Cereals for Babies

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quaker-oats

– FDA Finds Glyphosate Residues in Oat Cereals for Babies:

The U.S. Food and Drug Administration, which is quietly starting to test certain foods for residues of a weed killing chemical linked to cancer, has found the residues in a variety of oat products, including plain and flavored oat cereals for babies.

Source: www.huffingtonpost.com By Carey Gillam

Data compiled by an FDA chemist and presented to other chemists at a meeting in Florida showed residues of the pesticide known as glyphosate in several types of infant oat cereal, including banana strawberry- and banana-flavored varieties. Glyphosate was also detected in “cinnamon spice” instant oatmeal; “maple brown sugar” instant oatmeal and “peach and cream” instant oatmeal products, as well as others. In the sample results shared, the levels ranged from nothing detected in several different organic oat products to 1.67 parts per million, according to the presentation.

Read moreFDA Finds Glyphosate Residues in Oat Cereals for Babies

Not just marijuana: The FDA has always denied the existence of therapeutic benefits associated with ALL plants

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Medicinal-Plants-Roots

– Not just marijuana: The FDA has always denied the existence of therapeutic benefits associated with ALL plants:

Those who support the nationwide legalization of marijuana for therapeutic use, were disappointed by the Food and Drug Administration’s (FDA) recent failure to reclassify marijuana’s status from that of a Schedule I drug to another more appropriate classification.

Since 23 states have now legalized marijuana for medical use, and since numerous studies have confirmed its value as medicine and have proven that it is safe, it seemed the logical next step to begin relaxing the laws at the federal level.

Read moreNot just marijuana: The FDA has always denied the existence of therapeutic benefits associated with ALL plants

DEA Has Deliberately Blocked Marijuana Research For 40 Years, Generating Massive Profits From The ‘Drug War’

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marijuana-cannabis

– DEA blocked marijuana research for 40 years, generating massive profits from the ‘drug war’ while committing heinous acts against growers:

The medicinal value of cannabis cannot be ignored. This healing plant has successfully been used for treatment of pain, insomnia, rheumatoid arthritis, Parkinson’s, multiple sclerosis, seizure disorders, and even cancer.

Despite its long history of medicinal use throughout the world, cannabis has remained an illegal, controlled substance in the US, aggressively pursued by government agents for many decades. The US Drug Enforcement Administration (DEA) gained significant authority over cannabis after the Controlled Substances Act of 1970 was signed into law. Once enacted, the DEA created a scheduling system that classified different substances according to their potential for addiction and abuse. Without any scientific backing, the DEA put cannabis at the top of the list – a schedule one drug with the greatest potential for addiction, with no medicinal value whatsoever.

Read moreDEA Has Deliberately Blocked Marijuana Research For 40 Years, Generating Massive Profits From The ‘Drug War’

Top 7 alarming food modifications you should avoid at ALL COSTS

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Business-Man-Junk-Food-Healthy-Bridge

– Top 7 alarming food modifications you should avoid at ALL COSTS:

There are many ways corporations modify food products with chemicals in order to increase sales. They use toxic chemicals to extend shelf life, make food look more attractive, kill bugs in the fields, stave off mold and mildew, kill fungus and bacteria, add flavor back in after chemicals kill the taste, and actually make people depressed and anxious to fuel the chemical medicine industry. Most of it’s nothing new, and has been going on since WWII. GMOs have been in existence for 30 years now, though few people are aware of that.

The cumulative effect of poisons in the body is something you can’t sue one food manufacturer for, or one doctor, or one chemical company. The corporate food industry in America is sinister and insidious. They know they can’t be held accountable for long-term chronic sicknesses from which so many Americans suffer. The FDA could care less about Americans’ health and well-being.

Read moreTop 7 alarming food modifications you should avoid at ALL COSTS

Big Pharma’s medical research papers are total bunk… hundreds were fraudulently ghostwritten by a P.R. firm called ‘DesignWrite’

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Scientist-Research-Results-Lab

– Big Pharma’s medical research papers are total bunk… hundreds were fraudulently ghostwritten by a P.R. firm called ‘DesignWrite’:

Even though the big revelations about Big Pharma’s science paper research fraud came out years ago, most people are still not aware of this. Here’s the scoop: Drug companies routinely pay P.R. firms to ghostwrite clinical science papers which are published in medical journals and forwarded to the FDA to “prove” the drugs are safe and effective. But it’s all a farce: The papers are pure fiction, dreamed up by what are essentially marketing firms for the sole purpose of getting drugs approved even when they don’t work.

“In 2009, around fourteen thousand women who developed breast cancer while taking Prempro, a hormone replacement therapy (HRT), sued the drug’s manufacturer, Wyeth,” wrote Rupert Sheldrake in an extraordinary book called Science Set Free.

Read moreBig Pharma’s medical research papers are total bunk… hundreds were fraudulently ghostwritten by a P.R. firm called ‘DesignWrite’