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"FDA-approved does not mean a product is safe." Former pharmaceutical rep turned healthcare whistleblower Brigham Buhler (Brigham Buhler) abandoned his career after learning this. He breaks down the huge safety flaws in FDA approvals, and how millions of patients are dying every year due to negligence:

Danny Jones

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17,967 просмотров • 6 месяцев назад •via X (Twitter)

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Why does it seem like RFK backed down from the vaccine issue and pivoted to food? Brigham Buhler (Brigham Buhler) is a healthcare entrepreneur and advocate who has worked alongside RFK and testified on health issues around the country. He discusses the hidden strategy RFK is using to make real changes in the MAHA movement:

Why does it seem like RFK backed down from the vaccine issue and pivoted to food? Brigham Buhler (Brigham Buhler) is a healthcare entrepreneur and advocate who has worked alongside RFK and testified on health issues around the country. He discusses the hidden strategy RFK is using to make real changes in the MAHA movement:

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Peptides are one of the most powerful healing tools we have, but the FDA says they’re not needed. That’s because they’re repeating what pharmaceutical lobbyists told them. But here’s the truth: ✅ Insulin is a peptide ✅ Peptides are short-chain amino acids naturally found in the body ✅ Their safety profile is better than many drugs ✅ Their results? Incredible Brigham Buhler and I break this down in a conversation you won’t want to miss.

Gary Brecka

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Dr. Patrick Soon-Shiong just exposed a maddening FDA reality on his own approved cancer drug (Anktiva): It’s fully approved in the US for one rare form of bladder cancer… but not for the common form most patients have. So even though the same drug is already FDA-approved and sitting in their files, he can’t use it off-label for other patients without insane one-patient-at-a-time paperwork, IRB delays, and individual FDA sign-off. Meanwhile, Saudi Arabia (with their own sophisticated FDA) reviewed the exact same 1.7 million pages of data and approved it for more cancers. His blunt takeaway: Cancer is a war against time. Patients are forced to fly to Saudi Arabia for access… or wait in bureaucratic limbo while the clock runs out. “I’m completely befuddled as to why this molecule… that stimulates your NK cells is not allowed to give to people who have low NK cells.” If a drug is already FDA-approved and sitting in their own files, why the insane barriers to using it for other patients who are dying? Is this protecting people… or protecting something else?

Dr. Patrick Soon-Shiong just exposed a maddening FDA reality on his own approved cancer drug (Anktiva): It’s fully approved in the US for one rare form of bladder cancer… but not for the common form most patients have. So even though the same drug is already FDA-approved and sitting in their files, he can’t use it off-label for other patients without insane one-patient-at-a-time paperwork, IRB delays, and individual FDA sign-off. Meanwhile, Saudi Arabia (with their own sophisticated FDA) reviewed the exact same 1.7 million pages of data and approved it for more cancers. His blunt takeaway: Cancer is a war against time. Patients are forced to fly to Saudi Arabia for access… or wait in bureaucratic limbo while the clock runs out. “I’m completely befuddled as to why this molecule… that stimulates your NK cells is not allowed to give to people who have low NK cells.” If a drug is already FDA-approved and sitting in their own files, why the insane barriers to using it for other patients who are dying? Is this protecting people… or protecting something else?

Camus

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🚨The Truth About Healthcare Corruption & Why 1.7 Million Americans Die Each Year! 🚨 The healthcare system in America is broken. Chronic disease is killing 1.7 million people annually, and it’s not a coincidence. Big Pharma is making billions while insurance companies put profits over patient care. In TODAY'S episode, Brigham Buhler exposes the dark side of healthcare: why prescription drug prices are skyrocketing, how insurance companies are failing us, and why we’re paying the price for GLP-1 drugs we helped create. If you care about your health (or your wallet), you need to hear this. Watch now ⬇️ 🎙️Michael Bosstick LAURYN BOSSTICK

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The Bossticks

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Are vaccines safe? What’s actually in them? In this 2-part episode of Science in 5, WHO’s Dr. Kate O’Brien breaks down how vaccines are tested, approved, and monitored even after they reach the public. She also explains what happens if a safety concern is flagged.

Are vaccines safe? What’s actually in them? In this 2-part episode of Science in 5, WHO’s Dr. Kate O’Brien breaks down how vaccines are tested, approved, and monitored even after they reach the public. She also explains what happens if a safety concern is flagged.

World Health Organization (WHO)

77,028 просмотров • 1 год назад

🚨 The FDA created a loophole that’s been allowing Big Food to approve their own chemicals to use in our foods “FDA has been deceiving Americans with the safety of chemical additives in food — Over a thousand chemical additives currently used in processed food were neither safety reviewed nor tested by the FDA, which includes natural flavors According to a longstanding FDA ruling from the 1950s, food companies can conclude in their own the new chemical additives are generally recognized as safe for their intended use, and then use that additive in food without notifying the FDA. If companies voluntarily choose to submit the GAS notice to the FDA, the FDA will issue a no questions asked approval. Once the chemical is designated as GRAS "Generally Recognized as Safe" and used in food, the FDA does not regulate it or reevaluate it As a result, 98.7% of all food chemicals that entered the marketplace since 2000 were only reviewed and tested by the food and chemical companies that created them as the fourth most common ingredient on food labels.” Every single American needs to watch this video start to finish, the amount of poison that’s being legally allowed is beyond comprehension. THIS is what everyone is overweight and full of chronic diseases in America

🚨 The FDA created a loophole that’s been allowing Big Food to approve their own chemicals to use in our foods “FDA has been deceiving Americans with the safety of chemical additives in food — Over a thousand chemical additives currently used in processed food were neither safety reviewed nor tested by the FDA, which includes natural flavors According to a longstanding FDA ruling from the 1950s, food companies can conclude in their own the new chemical additives are generally recognized as safe for their intended use, and then use that additive in food without notifying the FDA. If companies voluntarily choose to submit the GAS notice to the FDA, the FDA will issue a no questions asked approval. Once the chemical is designated as GRAS "Generally Recognized as Safe" and used in food, the FDA does not regulate it or reevaluate it As a result, 98.7% of all food chemicals that entered the marketplace since 2000 were only reviewed and tested by the food and chemical companies that created them as the fourth most common ingredient on food labels.” Every single American needs to watch this video start to finish, the amount of poison that’s being legally allowed is beyond comprehension. THIS is what everyone is overweight and full of chronic diseases in America

Wall Street Apes

135,267 просмотров • 1 год назад

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Lila Rose

17,307 просмотров • 4 месяцев назад

THERE IT IS 🚨 The FDA is admitting they have no idea what’s being used in our food The FDA admits they have no idea about 10,000+ chemicals allowed into our foods introduced WITH NO SAFETY STUDIES because they were self approved by Big Food “The real issue here is that the FDA commissioner, as we sit here today, does not know what's in our food. Most Americans, most moms would assume that the ingredients in our food have been subjected to safety studies. That is not true. For the past 40 years, the food industry's taken advantage of a loophole where they can ‘Generally recognize a food as safe GRAS.’ And 95 % of food ingredients now in our food supply have been self-identified as safe with no safety studies. Once you designate that loophole, you do not have to submit the ingredient or safety studies to the FDA and that loophole use has led to the FDA not knowing what's in our food. It could be 2,000 ingredients, it could be 10,000. We don't know. There is no safety study on food” READ THAT AGAIN The FDA is finally announcing GRAS Reform, “Generally recognized as safe.” The Trump Admin is finally closing this loophole, this is a massive deal This loophole has been exploited so bad that 98.7% of all food chemicals that entered the marketplace since 2000 were only reviewed and tested by the food and chemical companies that created them No FDA studies, no safety studies. Just straight into our food

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Wall Street Apes

526,199 просмотров • 1 месяц назад

$IBRX oh my god, PLEASE you gotta watch this: On the Cuomo show last night with Dr. Pat Soon-Shiong as a guest, an ex-FDA exec basically spilled everything: Total CONFIRMATION of the CHAOTIC MESS INSIDE the FDA and how deep BIG PHARMA’S INFLUENCE really runs. Uncoordinated and bureaucratic is still an understatement — it’s practically by design at this point. And then there’s the bit about Merck and why Keytruda got approved… fascinating, if not a little too telling: “Multibillion dollar company with floors of people that understand the science in very subtle ways and what the most direct streamline path will be to get an FDA novel.” Admittedly there’s supposedly a new way of thinking now within the FDA - the talk of “collaboration,” “accelerated approvals,” etc. But, also, in this round it’s confirmed: real change will still take a while. Meanwhile, patients are still running out of time - this program made that painfully clear (see tweets of patients reports)

$IBRX oh my god, PLEASE you gotta watch this: On the Cuomo show last night with Dr. Pat Soon-Shiong as a guest, an ex-FDA exec basically spilled everything: Total CONFIRMATION of the CHAOTIC MESS INSIDE the FDA and how deep BIG PHARMA’S INFLUENCE really runs. Uncoordinated and bureaucratic is still an understatement — it’s practically by design at this point. And then there’s the bit about Merck and why Keytruda got approved… fascinating, if not a little too telling: “Multibillion dollar company with floors of people that understand the science in very subtle ways and what the most direct streamline path will be to get an FDA novel.” Admittedly there’s supposedly a new way of thinking now within the FDA - the talk of “collaboration,” “accelerated approvals,” etc. But, also, in this round it’s confirmed: real change will still take a while. Meanwhile, patients are still running out of time - this program made that painfully clear (see tweets of patients reports)

Berlinergy

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On Wednesday, Robert F. Kennedy Jr will testify before the Senate Finance Committeee. The chair of that committee, Senator Mike Crapo , gave a powerful testimony to our Roundtable last year defining the stakes. He talked about being let down by the current healthcare system, taking matters into his own hands by consuming books and podcasts, and experimenting with a WHOLE FOOD diet to radically improve his biomarkers (and thus his health, happiness, and longevity). He talked about how the current FDA and CMS regulations disincentivized him on this journey of wellness by preventing access to preventative monitoring. Our country would be RADICALLY TRANSFORMED if more Americans embarked on Senator Crapo’s path of curiosity to spur awe of the inter-connectivity of our human bodies and implement common sense actions to reverse disease. Let’s not forget the monumental stakes of this nomination. Senator Ron Johnson Casey Means, MD Jillian Michaels Dr Jordan B Peterson Max Lugavere Brigham Buhler Marty Makary MD, MPH Vani Hari Grace Price Mikhaila Peterson Courtney Swan Jason H. Karp

On Wednesday, Robert F. Kennedy Jr will testify before the Senate Finance Committeee. The chair of that committee, Senator Mike Crapo , gave a powerful testimony to our Roundtable last year defining the stakes. He talked about being let down by the current healthcare system, taking matters into his own hands by consuming books and podcasts, and experimenting with a WHOLE FOOD diet to radically improve his biomarkers (and thus his health, happiness, and longevity). He talked about how the current FDA and CMS regulations disincentivized him on this journey of wellness by preventing access to preventative monitoring. Our country would be RADICALLY TRANSFORMED if more Americans embarked on Senator Crapo’s path of curiosity to spur awe of the inter-connectivity of our human bodies and implement common sense actions to reverse disease. Let’s not forget the monumental stakes of this nomination. Senator Ron Johnson Casey Means, MD Jillian Michaels Dr Jordan B Peterson Max Lugavere Brigham Buhler Marty Makary MD, MPH Vani Hari Grace Price Mikhaila Peterson Courtney Swan Jason H. Karp

Calley Means

160,963 просмотров • 1 год назад

For too long, 340B has been a system of abuse. Now, U.S. Senators are cracking down—reforming the program to ensure every dollar serves patients, not profits. This is how we restore fairness and accountability in healthcare.

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4,919,530 просмотров • 11 месяцев назад

🚨New Information on UFOs, Big Pharma & Human Experiments🚨 In this insane episode Brigham Buhler (Brigham Buhler) and I cover big Pharma’s insane history and how it overlaps with UFO secrecy: 1. Rockefeller → Flexner (1910): Rockefeller commissions a report that ensures total control over petrochemical based medicines. Natural/holistic medicinal schools and practices get wiped out. AMA/FDA power is locked in. 2. War Crimes to Pharma: Horrific Japanese Unit 731 human experimentation data immunized and absorbed post-WWII. Bayer’s Third Reich entanglements… then later payouts and scandals. 3. Agent Orange → Roundup: Monsanto’s evolution from wartime chemistry to a food system saturated with glyphosate. Court cases and controversy follows. 4. MK-Ultra never really ended: The CIA’s ORD (Office of Research and Development) picks up the torch. The Scientific Engineering Institute is privatized, becomes G.D. Searle (chaired by Donald Rumsfeld), then sold to Monsanto. Government black labs bleed into Big Pharma. 5. Follow the incentives: 2011–2019 saw 356 “blockbuster” drugs. According to Brigham, Big Pharma originated ~0–2 of them; taxpayers funded the rest before industry scooped them at Phase III. 6. Suppressed modalities: Red light, hyperbaric, EMF-based therapies, peptides, biologics—anything not easily patented or insurer-friendly gets sidelined. 7. DOE’s double life: The agency tied to UFO/nuclear stories also ran the Human Genome Project. If you’re looking for the nexus of biology and secrecy, start there. If you’ve ever wondered how the UFO cover-up culture merged with healthcare capture, this episode connects the dots and provides the receipts. Full episode live now!👇

🚨New Information on UFOs, Big Pharma & Human Experiments🚨 In this insane episode Brigham Buhler (Brigham Buhler) and I cover big Pharma’s insane history and how it overlaps with UFO secrecy: 1. Rockefeller → Flexner (1910): Rockefeller commissions a report that ensures total control over petrochemical based medicines. Natural/holistic medicinal schools and practices get wiped out. AMA/FDA power is locked in. 2. War Crimes to Pharma: Horrific Japanese Unit 731 human experimentation data immunized and absorbed post-WWII. Bayer’s Third Reich entanglements… then later payouts and scandals. 3. Agent Orange → Roundup: Monsanto’s evolution from wartime chemistry to a food system saturated with glyphosate. Court cases and controversy follows. 4. MK-Ultra never really ended: The CIA’s ORD (Office of Research and Development) picks up the torch. The Scientific Engineering Institute is privatized, becomes G.D. Searle (chaired by Donald Rumsfeld), then sold to Monsanto. Government black labs bleed into Big Pharma. 5. Follow the incentives: 2011–2019 saw 356 “blockbuster” drugs. According to Brigham, Big Pharma originated ~0–2 of them; taxpayers funded the rest before industry scooped them at Phase III. 6. Suppressed modalities: Red light, hyperbaric, EMF-based therapies, peptides, biologics—anything not easily patented or insurer-friendly gets sidelined. 7. DOE’s double life: The agency tied to UFO/nuclear stories also ran the Human Genome Project. If you’re looking for the nexus of biology and secrecy, start there. If you’ve ever wondered how the UFO cover-up culture merged with healthcare capture, this episode connects the dots and provides the receipts. Full episode live now!👇

Jesse Michels

41,231 просмотров • 11 месяцев назад

REPORT: The FDA official who fast-tracked COVID vaccine approvals has just been hired by Eli Lilly. Former vaccine chief Peter Marks left his government post only months ago—and now he’s cashing in with the same industry he helped enrich. This is the same man who sidelined FDA scientists, buried vaccine injury data, and told Americans the shots were “safe and effective.” A Midwestern Doctor notes Peter forced rapid approvals to keep Biden’s mandates on track, even after his own experts warned no more corners could be cut. Now, he’s pocketing millions as Eli Lilly’s new head of infectious disease research—joining the endless parade of officials who sold out to Big Pharma. Nine of the last ten FDA commissioners have done the same. From Pfizer to Moderna to the WHO, the pattern is undeniable: public health isn’t about protecting you—it’s about protecting profits. 's explosive report reveals what this move means for the next phase of the agenda. Watch the full episode:👇

REPORT: The FDA official who fast-tracked COVID vaccine approvals has just been hired by Eli Lilly. Former vaccine chief Peter Marks left his government post only months ago—and now he’s cashing in with the same industry he helped enrich. This is the same man who sidelined FDA scientists, buried vaccine injury data, and told Americans the shots were “safe and effective.” A Midwestern Doctor notes Peter forced rapid approvals to keep Biden’s mandates on track, even after his own experts warned no more corners could be cut. Now, he’s pocketing millions as Eli Lilly’s new head of infectious disease research—joining the endless parade of officials who sold out to Big Pharma. Nine of the last ten FDA commissioners have done the same. From Pfizer to Moderna to the WHO, the pattern is undeniable: public health isn’t about protecting you—it’s about protecting profits. 's explosive report reveals what this move means for the next phase of the agenda. Watch the full episode:👇

The Vigilant Fox 🦊

92,432 просмотров • 11 месяцев назад

Americans have been sold out to chemical companies. Barack Obama brought on the lawyer for Monsanto to Head the FDA “The guy who determined what the FDA calls safe as food was the Vice President of Monsanto. Name is Michael Taylor — Michael started working for the FDA in the early 90s, but before that he was a lawyer at Monsanto. So he writes the rules for food safety, then goes to work as vice president for Monsanto. Then comes back under Barack Obama at the FDA for 6 more years, gains further rules on what is considered safe to eat. While Michael was in charge, he told Congress the FDA could not confirm that the chemicals in our food are safe for human consumption. For instance, the same growth hormone that he approved for cows in the United States is banned in Canada, banned in Japan, banned in Australia, banned in Europe. But somehow that growth hormone is safe for you and your American kids. FDA is not interested in protecting Americans. They are interested in protecting the special interest and lobbyists that pay them. This isn't new though. Even big pharma has lobbied hard to make the FDA literally their henchmen always have to look at where the money is and where the money goes. So if you're wondering why 60%, or quite frankly, more Americans are dealing with chronic disease, just look at the money trail. And right now the money trail says that the FDA is working hard to make corporations profitable. Let me know your thoughts in the comments.”

Americans have been sold out to chemical companies. Barack Obama brought on the lawyer for Monsanto to Head the FDA “The guy who determined what the FDA calls safe as food was the Vice President of Monsanto. Name is Michael Taylor — Michael started working for the FDA in the early 90s, but before that he was a lawyer at Monsanto. So he writes the rules for food safety, then goes to work as vice president for Monsanto. Then comes back under Barack Obama at the FDA for 6 more years, gains further rules on what is considered safe to eat. While Michael was in charge, he told Congress the FDA could not confirm that the chemicals in our food are safe for human consumption. For instance, the same growth hormone that he approved for cows in the United States is banned in Canada, banned in Japan, banned in Australia, banned in Europe. But somehow that growth hormone is safe for you and your American kids. FDA is not interested in protecting Americans. They are interested in protecting the special interest and lobbyists that pay them. This isn't new though. Even big pharma has lobbied hard to make the FDA literally their henchmen always have to look at where the money is and where the money goes. So if you're wondering why 60%, or quite frankly, more Americans are dealing with chronic disease, just look at the money trail. And right now the money trail says that the FDA is working hard to make corporations profitable. Let me know your thoughts in the comments.”

Wall Street Apes

42,133 просмотров • 6 месяцев назад

This is a pretty big deal as it rolls out.. 🚨 HHS Secretary RFK Jr is eyeing to CLOSE the GRAS Loophole To give you an idea of how absolutely explosive this is, let’s look at the history: In 1958, the U.S Government created the designation “Generally Recognized as Safe” or (GRAS), so we can make common ingredients like salt or baking soda exempt from testing. But over the decades, GRAS has been widely abused by food companies and cooperative legislators, and regulators are now determining if a substance is “safe”. In European nations, EVERY ingredient is required to be proven safe before becoming a food ingredient. —— in America, it’s just the opposite, and food ingredients are not deemed unsafe until after millions of Americans are harmed. - Kennedy highlights a stark contrast: Europe permits only about 400 legal food ingredients under rigorous standards. - In the US, he states that HHS and the FDA do not even know the precise number of ingredients in American food, with estimates varying widely between 4,000 and 10,000. He has directed the FDA to explore rulemaking that would eliminate the self-affirmed GRAS pathway, which currently allows companies to declare new food ingredients "Generally Recognized as Safe" without notifying the FDA or providing safety data publicly. This change would require mandatory notification and transparency for all ingredients.

This is a pretty big deal as it rolls out.. 🚨 HHS Secretary RFK Jr is eyeing to CLOSE the GRAS Loophole To give you an idea of how absolutely explosive this is, let’s look at the history: In 1958, the U.S Government created the designation “Generally Recognized as Safe” or (GRAS), so we can make common ingredients like salt or baking soda exempt from testing. But over the decades, GRAS has been widely abused by food companies and cooperative legislators, and regulators are now determining if a substance is “safe”. In European nations, EVERY ingredient is required to be proven safe before becoming a food ingredient. —— in America, it’s just the opposite, and food ingredients are not deemed unsafe until after millions of Americans are harmed. - Kennedy highlights a stark contrast: Europe permits only about 400 legal food ingredients under rigorous standards. - In the US, he states that HHS and the FDA do not even know the precise number of ingredients in American food, with estimates varying widely between 4,000 and 10,000. He has directed the FDA to explore rulemaking that would eliminate the self-affirmed GRAS pathway, which currently allows companies to declare new food ingredients "Generally Recognized as Safe" without notifying the FDA or providing safety data publicly. This change would require mandatory notification and transparency for all ingredients.

MJTruthUltra

245,224 просмотров • 7 месяцев назад