Tag: safety

PESTICIDES, like antibiotics, are fueling the rise of untreatable SUPERBUGS – study

In a remote Himalayan village, a polluted river reflects a grim reality: the water, once sacred, now teems with antibiotic-resistant bacteria thriving in a chemical soup of pesticides and hospital waste. This is Ground Zero for a public health crisis that scientists now trace back to industrial agriculture’s unchecked reliance on pesticides. For decades, these toxins have been hailed as saviors against crop-destroying pests, but recent studies reveal they are unwitting partners in an even deadlier crescendo—antibiotic resistance.

Key points:

  • Pesticides and antibiotics work synergistically to breed antibiotic-resistant superbugs in waterways, accelerating a global health crisis.
  • India’s contaminated water ecosystems—harboring deadly cholera pathogens and drug-resistant E. coli—exemplify a ticking time bomb of antibiotic resistance.
  • Bacteria evolve defenses like biofilms and gene-sharing plasmids to survive pesticide bombardment, creating drug-resistant strains that even modern medicine can’t combat.
  • Farmers, governments, and corporations face pressure to abandon chemical dependency in favor of organic farming or risk triggering a healthcare collapse.

Confronting a new Silent Spring

Modern medicine’s holy grail, antibiotics, are failing spectacularly, and pesticides are making it worse. Over 5 million people died from drug-resistant infections in 2019, a toll projected to surge to 10 million annually by 2050. India’s waterways, choked with runoff from agrochemical plants and sewage, have become nurseries of superbugs, warns a harrowing study. This is no accident—it’s a consequence of agriculture’s chemical war against nature, a conflict humanity is losing.

The post-World War II Green Revolution brought pesticides like DDT and BHC to India in the 1950s, promising food security through chemical might. By 1971, when regulations finally arrived, India had already built the template for 21st-century disaster: pesticides rampaging through ecosystems, duplicating insects’ resistance in microbes.

“The Green Revolution was never just about food—it was an ideological battle to conquer nature with chemicals,” says Dr. Rajeshwari Rajammal of India’s Center for Sustainable Agriculture. “But organisms adapt, and pathogens are playing catch-up faster than we can innovate.”

Today, India is the world’s fourth-largest pesticide producer, yet its farms use just 0.4 kg per hectare compared to China’s 1.83 kg—proof that scale isn’t the only problem. The chemicals India creates but doesn’t consume flow into global supply chains, spreading resistance worldwide. “You can’t binge on toxins and call it ‘growth’ forever,” Dr. Rajammal adds. “Nature always settles the bill.”

The antibiotics dumped into rivers through pharmaceutical waste (India is a top drug producer) only amplify resistance. In the Ganges River, antibiotic-resistant Vibrio pathogens cause untreatable cholera. Groundwater in Assam and Uttar Pradesh carries E. coli strains that laugh off ampicillin. Meanwhile, aquaculture in Bangladesh combines pesticides and antibiotics into a microbial arm’s race, creating monsters that even fortified drugs can’t kill.

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Johnson & Johnson Lead Scientist and Executive Admit Baby Powder Contained ‘Cancer-Causing Heavy Metals’

The O’Keefe Media Group on Friday released undercover video of a Johnson & Johnson lead scientist and executive admit that baby power contained cancer causing heavy metals.

This is the second undercover video in OMG’s series exposing Johnson & Johnson.

Joshua Rys, a Regulatory Affairs Scientist who managed Johnson & Johnson’s baby products spilled the truth to an OMG undercover journalist.

“When I started, actually I started working on the consumer group. Johnson’s was one of my brands. So I managed all the baby products. So actually, when that all happened, I was working on that,” said Joshua Rys.

Rys continued, “It wasn’t actually the product itself, it was an impurity. So naturally talc comes from mines, and the mines don’t have, I guess, 100 percent accurate standards. So the heavy metals, it’s not the talc itself that gives you the cancer, it’s the heavy metals that are in there.”

David Altman, Executive & Senior Clinical Analyst at Johnson & Johnson, said, “This is not your father’s J&J… they don’t really give a sh*t about people.”

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 Johnson & Johnson Lead Scientist Confesses J&J COVID-19 Vaccine Was ‘Not Safe and Effective,’ Reveals “Lack of Research” From Rushing to Release Vaccine: “People Wanted It, We Gave It to Them”

“We didn’t do the typical tests,” said Joshua Rys, a Lead Scientist in Regulatory Affairs for Johnson & Johnson (J&J), revealed on hidden camera that the typical clinical process was abandoned for the COVID-19 vaccine, knowingly bypassing standard testing protocols under pressure from the U.S. government and public demand. He added, “This was just, ‘let’s test it on some lab models… and just throw it to the wind and see what happens.’”

He acknowledged that the public wasn’t informed about the shortcuts, asking, “Do you have any idea the lack of research that was done on those products?” Rys claimed, “People wanted it, we gave it to them.”

While public officials claimed the vaccines were “safe and effective,” Rys pushed back. “There’s no proof. None of that stuff was safe and effective,” he said, adding that the industry relies on a benefit-risk tradeoff to justify product launches.

Rys also pointed to government pressure through Operation Warp Speed. “The government is like, ‘We need help… You’re solving this problem,’” he said. “People panic, so they try to solve it in whatever way they think is good.”

According to a U.S. Department of Health and Human Services (HHS) spokesperson, “Even during a public health emergency, pharmaceutical companies are still required to follow strict protocols for clinical testing. For emergency use, companies must show that the benefits clearly outweigh the risks. Oversight doesn’t stop at approval — the FDA and other agencies also monitor products closely once they’re in use. That includes real-world safety tracking, independent advisory committees, and required reporting of any adverse events. These steps are in place to make sure public health decisions are based on solid science and strong safeguards — especially in emergencies.

Dr. Marty Makary and Dr. Vinay Prasad recently announced a new vaccine safety and transparency framework — one that’s built on gold-standard science, real-world data, and honest communication with the public and will require thorough safety testing before licensing. Their work is focused on strengthening trust, improving how we monitor safety after vaccines are in use, and making sure people have clear, accurate information to make informed decisions.

HHS remains committed to full transparency and evidence-based oversight — putting the safety of the American people first.”

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Why I’m Sounding the Alarm on Sprayable Intranasal COVID-19 Vaccine

Last week, Science Advances published a study on the CVXGA1 nasal COVID-19 vaccine Phase 1 trial. I was asked by The Defender to provide my thoughts on this recent development.

Excerpts from the article reveal why I’m sounding the alarm!

Investigative journalist Sonia Elijah noted that CVXGA1, which enters the mucus membranes and lungs through the nose, has the “potential for shedding viral particles through intranasal secretions, which could expose unvaccinated individuals.”

Elijah said the study didn’t examine if shed materials can be spread to others. “This raises significant safety concerns about replication and shedding risks,” she said.

The Defender highlighted my critique:

According to Elijah, the lack of a control group and the small sample size “weakens the trial’s ability to accurately assess safety and immunogenicity,” but these aren’t the only flaws.

Elijah said:

“The study lacks data on RNA detection levels and did not perform infectivity assays to confirm if shed materials can be spread to others.

The lack of specific safety and immunogenicity data for the adolescent group raises concerns about the vaccine’s effects in younger individuals.

The open-label design, where both participants and researchers knew who received the vaccine, introduces potential bias in reporting and assessing outcomes, such as adverse events.”

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USDA’s Mass H5N1 Poultry Vaccination Plan Likely to Rely on Leaky Zoetis H5N2 Vaccine

The leading candidate appears to be the Zoetis vaccine targeting H5N2 — even though the dominant strain spreading through U.S. flocks is H5N1 clade 2.3.4.4b.

The vaccine uses the N2 neuraminidase subtype deliberately to support DIVA (Differentiating Infected from Vaccinated Animals) surveillance — allowing authorities to detect field infections in vaccinated birds.

In February 2025, the USDA issued a conditional license to Zoetis for its Avian Influenza Vaccine, H5N2 Subtype, Killed Virus, specifically for use in chickens, based on a “reasonable expectation of efficacy based on serology data”. In other words, the approval rests on hope that antibody titers will translate into real-world protection—not on demonstrated effectiveness against infection or transmission.

A conditional license allows the vaccine to be used immediately, but only under specific circumstances—such as during an outbreak or in targeted populations. As of June 2025, Zoetis’s H5N2 vaccine remains the only avian influenza vaccine conditionally approved by the USDA for use in U.S. poultry. No other vaccines are currently authorized or ready for large-scale deployment.

However, according to the USDA, inactivated virus vaccines—such as the Zoetis H5N2 formulation—are non-sterilizing in the field. This means they do not prevent infection, do not eliminate viral shedding, and allow vaccinated birds to silently carry and transmit H5N1, particularly in densely populated commercial flocks.

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Nerve pain medication gabapentin possibly tied to dementia, study says

A drug used to treat seizures, nerve pain and restless leg syndrome might be linked with increased risk of dementia, a new study says.

Regular gabapentin use appeared to increase risk of dementia by 29% and mild cognitive impairment by 85%, researchers reported Thursday in the journal Regional Anesthesia & Pain Medicine.

What’s more, the risk was more than doubled in people normally considered too young to suffer from brain aging, those 18 to 64, results show.

“The findings of this study support the need for close monitoring in adult patients prescribed gabapentin to assess for potential cognitive decline,” wrote the research team led by Nafis Eghrari, a medical student at Case Western Reserve University in Cleveland.

“Moreover, this provides a foundation to further research whether gabapentin plays a causal role in the development of dementia and cognitive decline,” the researchers added.

Gabapentin has become increasingly popular for the treatment of chronic pain because it’s not nearly as addictive as opioids, researchers said in background notes.

But concerns have been growing that gabapentin might contribute to cognitive decline, since it works by suppressing communication between nerve cells, researchers said.

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US Orders “Immediate Shutdown” Of Mexican Cattle Trade After Cross-Border Parasitic Fly Threat

U.S. Agriculture Secretary Brooke Rollins has ordered the immediate suspension of all live cattle, bison, and horse imports from Mexico via the southern border. The move comes in response to a newly confirmed case of New World Screwworm in Mexico—a highly destructive parasite that poses a massive threat to U.S. livestock and the broader food supply chain.

“I have ordered an immediate shutdown of live cattle, bison, and horse trade through the southern U.S.–Mexico border,” Rollins wrote on X, adding, “This decisive action comes after Mexico confirmed another case of New World Screwworm in Veracruz. As promised, @USDA remains vigilant to ensure the protection of America’s livestock and food supply.” 

She quoted a U.S. Department of Agriculture press release that announced the trade suspension, which signals heightened biosecurity concerns within the USDA and reflects a zero-tolerance posture toward potential cross-border parasitic threats.

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Weight loss jab patients facing deadly organ failure risk, experts warn

  • A nurse warns that weight-loss injections like Mounjaro are prescribed without crucial blood tests, risking pancreatitis, organ failure, and death.
  • UK regulators are investigating more than 560 reports of pancreas inflammation and ten deaths linked to GLP-1 agonist drugs.
  • Mandatory blood screening could identify high-risk patients, but corporate providers prioritize profits over safety, skipping safeguards.
  • Post-market data reveals severe risks, including contraceptive failure, muscle wasting, and blindness, yet manufacturers downplay dangers.
  • Experts demand stricter regulations, pre-screenings, and holistic obesity care instead of profit-driven pharmaceutical shortcuts.

A medical whistleblower has exposed a life-threatening oversight in the booming weight loss injection industry, revealing that thousands of patients are being prescribed potent GLP-1 agonist drugs like Mounjaro without critical blood tests that could prevent pancreatitis, sepsis, and fatal organ failure.

As UK regulators investigate more than 560 reports of pancreas inflammation and ten deaths linked to these “miracle” injections, frontline healthcare workers are demanding immediate reforms to protect vulnerable patients from Big Pharma’s reckless profit-driven protocols.

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Vaccine advisory board votes to remove controversial mercury-based compound from flu vax

In a win for the Make America Healthy Again (MAHA) movement, the Advisory Committee on Immunization Practices (ACIP) voted 5-1 to limit flu vaccines to only those free of thimerosal. The mercury-containing preservative, largely phased out of childhood vaccines by 2001, still lingers in some multi-dose flu shots. But with 96% of U.S. flu vaccines for the 2024-2025 season already thimerosal-free, single-dose options are not hard to come by.

The committee, freshly revamped by Health and Human Services (HHS) Secretary Robert F. Kennedy Jr., also voted 5-1 to mandate thimerosal-free flu vaccines for children 18 and under and pregnant women. 

The effort to remove thimerosal began in the late 1990s, sparked by growing public and scientific scrutiny of mercury exposure. In 1997, the FDA Modernization Act prompted a review of mercury in medical products, including thimerosal, a mercury-based preservative used since the 1930s to prevent microbial contamination in multi-dose vaccine vials.

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Disturbing Study Suggests Living Near Golf Course Can Increase Parkinson’s Risk 126% Due to Pesticides

An alarming study claims living near a golf course, often considered prime real estate, can significantly increase one’s risk of developing Parkinson’s, a neurodegenerative disease characterized by the gradual loss of motor control.

Patients who lived within one to three miles of a course were most affected, according to the study.

The study, published in JAMA, compared data from 419 people with Parkinson’s from southern Minnesota and Western Wisconsin to a control group between 1991 to 2015. 

The data led researchers from the Barrow Neurological Institute in Arizona and the Mayo Clinic to suspect pesticides sprayed throughout the expansive courses, which may seep into groundwater, could be to blame.

“After adjusting for patient demographics and neighborhood characteristics, living within 1 mile of a golf course was associated with 126% increased odds of developing PD [Parkinson’s Disease] compared with individuals living more than 6 miles away from a golf course,” the study states.

“Additionally, individuals living in water service areas with a golf course in vulnerable groundwater regions had 82% greater odds of developing PD compared with those in nonvulnerable groundwater regions,” the study states.

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