Showing posts with label FDA. Show all posts
Showing posts with label FDA. Show all posts

Thursday, August 23, 2018

US Gov't Moves To Allow Greater Access To Medicines Without Doctor Visit But It's Not What You Think

US Gov't Moves To Allow Greater Access To Medicines Without Doctor Visit But It's Not What You ThinkBrandon Turbeville
Natural Blaze
August 10, 2018

If the US government and the FDA have their way, Americans may soon have more access to medications and prescription drugs without having to first see a doctor. This is undoubtedly a positive step in the right direction. Unfortunately, it’s not exactly what you might think.

For those who are unaware, in the United States, an allegedly free country, American citizens no longer have the option to decide what medications they believe they need or wish to take and simply purchase those medications from a pharmacy as in times past or as in many other countries today. Instead, they are forced to make an appointment with a doctor who is considered (and considers himself) the ultimate authority on what a patient can consume, regardless of the patient’s choices. Of course, the patient has to pay for that visit and he/she may not even be prescribed the proper medicine even after begging the doctor’s permission to access it. The patient then has to go to the pharmacy and prove that he has his hall pass (prescription) in order to be receive his medication.

Now, a new draft guideline from the FDA seems to be heading in the opposite direction but “seems” is the operative word here. The FDA is looking into to how it can “lower healthcare costs” and one of the options may be opening up certain medications to potential purchase without a doctor’s visit.

But before anyone gets the idea that America is inching its way back to freedom, you might want to slow down. Independent thought and individual choice is not on the menu just yet.

One idea is that patients could answer questions on a mobile-phone app to help determine whether or not they should be able to have access to a medication without needing a prescription.


Friday, February 9, 2018

FDA Tries To Kill FOIA On Alter Of GMOs

FDA FOIA GE SalmonBrandon Turbeville
February 8, 2018

In a surprising turn of events, a U.S. federal court has ruled in favor of the public interest. Even more surprising, the court ruled against the FDA which has been pushing the approval of GE salmon for human consumption.

The approval of the GE salmon, which is made from the DNA of Pacific Chinook Salmon, Atlantic Salmon and Deepwater Ocean Eel Pout, took place in 2015. However, the battle has been raging long before and after that date. The FDA, while launching a jihad against natural supplements and kratom, became the first government agency in the world to approve a GM animal for commercial sale and consumption.

Apparently the “every possible danger must be hyped, examined and exploited for a ban” methodology only applies to harmless substances and those that improve the health and livelihoods of the average American. When it comes to those substances which could potentially harm large amounts of people, or eradicate entire species of animals, the FDA takes a hands-off approach.

This time around, many experts have expressed concern with GE salmon, including biologists at U.S. Wildlife agencies who work with fish and wildlife, criticizing the FDA for not properly investigating the potential impacts. The FDA while jumping on the bandwagon of every distorted story in regards to kratom and natural supplements, ignored these professionals with real concerns. As a result, on March 2016, Earth Justice filed a lawsuit against the FDA. The lawsuit required the FDA to compile a record of research and documents that led up the FDA decision to approve GE salmon. The lawsuit requires a complete record.

At the time of the writing of this article, the FDA has refused to release most of the documents related to its decision despite a number of clients requesting those documents under FOIA. As Earth Justice states,


Saturday, December 23, 2017

FDA Sets Sight On Homeopathy, Part Of Larger Big Pharma Jihad

Brandon Turbeville
December 21, 2017

After years of accusing homeopathics as being worthless placebos, the FDA is going after homeopathics as though they are dangerous materials

It seems the FDA is doubling down in its wild jihad against natural and alternative health products, individual choice and anything that threatens Big Pharma’s profits and control.

After years of claiming that homeopathy is an ineffective placebo, the FDA is now claiming that it’s dangerous. The FDA has announced plans to crack down on the sale of a number of homeopathic products.

“In recent years, we’ve seen a large uptick in products labeled as homeopathic that are being marketed for a wide array of diseases and conditions, from the common cold to cancer,” FDA Commissioner Scott Gottlieb said in a statement announcing the new policy.

“In many cases, people may be placing their trust and money in therapies that may bring little to no benefit in combating serious ailments, or worse — that may cause significant and even irreparable harm because the products are poorly manufactured, or contain active ingredients that aren’t adequately tested or disclosed to patients,” Gottlieb says.


Friday, November 17, 2017

FDA, DEA Launch Massive Assault On Kratom – Drug War For Miracle Plant Ramping Up

attack on kratom - kratom drug warBrandon Turbeville
Natural Blaze
November 16, 2017

To no one's surprise, the U.S. government, after hysterically declaring a "national emergency" over America's opioid crisis, is once again setting its sights on Kratom, the non-addictive natural plant that has helped thousands of Americans wean themselves off opioids.

In 2015, the DEA announced its plans to place Kratom on the list of Controlled Substances (in the same scheduling level as heroin to be exact) but, amid public outcry, the agency backed off, deferring to FDA "review" and "advice." Many optimistic  Kratom activists were tempted to rest on their laurels, trusting that the FDA would prove to be more reasonable in relation to Kratom and hoping the testimonials, overwhelming public support for Kratom, and the science itself would win the day.

As is typically the case in life, the optimists were sorely disappointed.

The FDA, long known to be essentially run by Big Pharma, has now joined the ranks of the DEA (which also placed CBD oil on the list of controlled substances on the same level as heroin) in a scathing attack on Kratom, signalling that the end may be nigh for the miracle plant if activists do not succeed in fighting back both behemoth agencies who act as the enforcement arms of Big Pharma, the private prison industry, and the police state.

As the Washington Post reported,

The Food and Drug Administration issued a strong warning Tuesday to consumers to stay away from the herbal supplement kratom, saying regulators are aware of 36 deaths linked to products containing the substance.

Thursday, July 27, 2017

Herbal Coffee Controversy Reveals Fragility Of American Health

coffee viagraBrandon Turbeville
July 21, 2017

A new story is sweeping the news regarding a controversial “herbal coffee.”

Recently, New of Kopi Jantan Tradisional Natural Herbs Coffee, which was marketed as a male enhancement product has come under fire by the FDA for including undisclosed ingredients. the most notable ingredient not mentioned on the label is desmethyl carbodenafil, a compound that is structurally similar to the active ingredient to Viagra.

In addition, the coffee product also contains milk, although it is not listed as an ingredient on the packaging.

So before anyone rises up in arms against the FDA, it appears the agency is actually doing its job for once, i.e., ensuring that consumers know what they are consuming.

Regardless of how the FDA intends to pursue the issue, most reasonable people would not argue that Bestherbs Coffee LLC should not be able to sell its product with both milk and Viagra-like ingredients. Most reasonable people would also argue that they should inform consumers that their product contains these ingredients.

Bestherbs has voluntarily recalled the product nationwide, and the FDA is mostly concerned with the fact that desmethyl carbodenafil could pose a number of health issues when mixed with nitrates. Unfortunately many men with diabetes, heart disease, high blood pressure and high cholesterol are prescribed nitrates to deal with their illness. The FDA is also concerned that the presence of milk could affect consumers with dairy allergies.


Tuesday, July 11, 2017

We’re Not Joking: Sen Schumer Wants The FDA To Crack Down On Raw Cacao

Brandon Turbeville
July 10, 2017

Senator Chuck Schumer (D-NY) appears to be a man with way too much time on his hands. Either that, or he has grown temporarily bored with promoting the disproven conspiracy theories of Russian hacking.

Something is obviously amiss. What other explanation can there be for the Senator’s recent ridiculous campaign to force the FDA to begin regulating chocolate?

Schumer launched his initiative on Saturday in order to enlist the FDA in a fight to regulate “snortable chocolate” powder that is being used by some in clubs for euphoria and energy.

Schumer specifically targeted products like Coco Loko whose product is marketed as raw cacao snuff. The product includes powder that is made from raw cacao beans which contain caffeine.

Coco Loko also specifically contains other substances including taurine, guarana and ginkgo biloba.

While informing consumers of a potential risk if it exists is by no means a bad thing, it’s obvious that Schumer is simply following the same path as fellow idiot Jeff Sessions in promoting yet another extension to the drug war. Either that or his obsession compulsion with regulating, taxing, banning and bombing has become an actual psychosis.

Don’t believe me? Here’s a brief list of things that Chuck Schumer has tried to ban:


Tuesday, August 30, 2016

Truth on the Tracks with Brandon Turbeville - August 30, 2016

Brandon Turbeville
BrandonTurbeville.com
UCY.TV
August 30, 2016

Truth on the Tracks with Brandon Turbeville - August 30, 2016

Brandon discusses the Turkish invasion of Syria, the creation of Buffer Zones, the FDA attack on Natural supplements, 43 points and this week's marching orders.

ACCESS THE PROGRAM HERE

ACCESS THE TRUTH ON THE TRACKS ARCHIVES HERE





Thursday, April 30, 2015

Truth on the Tracks with Brandon Turbeville - April 26, 2015

Truth on the Tracks with Brandon Turbeville - April 27, 2015

Brandon interviews Isabel Perkins - a Young Living distributor in the Columbia, South Carolina area, as well as an activist and organizer with Moms Across America and March Against Monsanto.

Brandon also discusses what the March Against Monsanto, anti-GMO movement needs to move forward and achieve a real effect in the way of demands. Brandon discusses Neil Young, vaccines, and more reasons not to stand with Rand.

Isabel Perkins' Young Living website can be found here : https://www.youngliving.org/isabelperkins

Isabel Perkins: Moms Across America : http://www.momsacrossamerica.com/izzysoils

Young Living Essential Oils With Isabel Perkins Facebook Page: https://www.facebook.com/pages/Young-Living-Oils-with-Isabel-Perkins/778778762168421?fref=ts

March Against Monsanto Columbia SC facebook page: https://www.facebook.com/MAMColumbiaSC?fref=ts

www.MomsAcrossAmerica.com

www.March-Against-Monsanto.com