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Note: Explore our full index to revealing excerpts of key major media news articles on dozens of engaging topics. And read excerpts from 20 of the most revealing news articles ever published.

A Ninth Circuit panel on Wednesday rolled back the Environmental Protection Agency's approval of the use of the pesticide streptomycin sulfate on citrus groves to fight citrus disease. The underlying lawsuit was brought by farmworkers and other interest groups, which argued the EPA had greenlit streptomycin sulfate for use on citrus plants without adequately considering potential harms from the chemical. The panel, consisting of U.S. Circuit Judges Ronald Gould and Johnnie Rawlinson ... and Daniel Bress ... partially ruled in favor of the EPA – determining there was substantial evidence for the EPA's assessment concerning risks which could lead to antibiotic resistance. However, they said, the EPA's assessment concerning risks to bees and other pollinators was incomplete. In a statement after the ruling, the Center for Biological Diversity, one of the groups involved in the suit, applauded the Ninth Circuit's decision. The rollback of streptomycin approval "is a significant win for public health, farmworker safety and endangered species," [said attorney] Hannah Connor. Streptomycin sulfate is used as an antibiotic to treat serious illnesses but has also found use as a pesticide. The Center for Biological Diversity claims spraying streptomycin on citrus trees to combat citrus greening disease is "highly ineffective" and argues that its use as a pesticide violates the Endangered Species Act because it causes long-term health effects to endangered animals and plants.

Note: For more along these lines, see concise summaries of deeply revealing news articles on health and government corruption from reliable major media sources.

When the U.S. Government entered into its Covid vaccine agreement with Pfizer, which was acting on behalf of the BioNTech/Pfizer partnership, in July 2020, the agreement encompassed a minimum of 100 million doses of a "vaccine to prevent COVID-19" and a payment of at least $1.95 billion. The Government declared that we were "at war" with a catastrophically dangerous virus. In keeping with the declaration of war, it was a military framework that was used for acquiring the aspirational products that became known as Covid mRNA vaccines. The Government side to the agreement with Pfizer was the Department of Defence (DoD), represented by a convoluted chain of parties, each operating as a subcontractor, or co-contractor, for the next. In fact, agencies governing civilian and public health, like the NIH, NIAID and HHS, do not have the authority to grant certain types of special acquisition contracts, which is why the Covid vaccine contracts had to be overseen by the Department of Defence. Emergency Use Authorisation (EUA) ... is a very special way to authorise a medical countermeasure in very specific types of emergencies. EUA was meant for dire situations of warfare or terrorism, not to protect the entire population from naturally occurring pathogens. For this reason, EUA products do not require the type of legal safety oversight that is applied in civilian contexts by the FDA.

Note: Read how the Department of Defense and the Biomedical Advanced Research and Development Authority allowed vaccine makers to bypass standard safety testing of their products. For more along these lines, see concise summaries of deeply revealing news articles on COVID vaccines from reliable major media sources.

It is against the law to use paraquat in China, Switzerland, the United Kingdom and dozens of other countries. Many countries have banned the herbicide due to its extreme toxicity, while others have expressed concerns over the possible risk for Parkinson's disease. Yet the herbicide, manufactured by a Swiss company that is owned by the Chinese state, is still widely used throughout the United States in part because it is a highly effective way to kill weeds. The company, Syngenta, says that paraquat, which it produces under the name Gramoxone, "is safe for its intended and labelled use." Clayton Tucholke, who used Gramoxone for years on his farm in LaBolt, South Dakota, and has since been diagnosed with Parkinson's disease, says otherwise. "It should have been pulled, I think, you know, so it didn't happen to somebody else," Tucholke told ABC News. The Tucholkes are among the more than 4,000 Americans who have filed lawsuits as part of a multi-district litigation against Syngenta, which currently manufactures Gramoxone, and Chevron, which distributed it in the U.S. from 1966 until 1986. Although Syngenta and Chevron told ABC News that there is no scientific evidence that supports a causal link between paraquat and Parkinson's disease, the Tucholkes and other plaintiffs allege that such a link exists, arguing that Syngenta and Chevron knew or should have known that the herbicide could "cause severe neurological injuries."

Note: Internal corporate documents reveal how global chemical giant Syngenta secretly influenced scientific research regarding links between its top-selling weedkiller and Parkinson's disease. For more along these lines, see concise summaries of deeply revealing news articles on health and food system corruption from reliable major media sources.

The Department of Defense relies on hundreds, if not thousands, of weapons and products such as uniforms, batteries, and microelectronics that contain PFAS, a family of chemicals linked to serious health conditions. Now, as regulators propose restrictions on their use or manufacturing, Pentagon officials have told Congress that eliminating the chemicals would undermine military readiness. PFAS, known as "forever chemicals" because they don't break down in the environment and can build up in the human body, have been associated with such health problems as cancer. In July, a new federal study showed a direct link between testicular cancer and PFOS, a PFAS chemical that has been found in the blood of thousands of military personnel. In a report delivered to Congress in August, Defense Department officials pushed back against health concerns raised by environmental groups and regulators. According to the report, most major weapons systems, their components, microelectronic chips, lithium-ion batteries, and other products contain PFAS chemicals. These include helicopters, airplanes, submarines, missiles, torpedoes, tanks, and assault vehicles; munitions; semiconductors and microelectronics; and metalworking, cooling, and fire suppression systems. Beyond cancer, some types of PFAS have been linked to low birth weight, developmental delays in children, thyroid dysfunction, and reduced response to immunizations.

Note: If the above link fails, you can read the article here.  PFAS are linked to serious health conditions: cancer, liver damage, hormonal disruption, reproductive issues, reduced sperm count, reduced immune response, and more. PFAS have also been found in 45% of US tap water. Read more on how war is hazardous to our health and environment in our Military-Intelligence Corruption Information Center.

Companies that make popular weight loss shots like Ozempic and Mounjaro are starting to test a version for kids as young as six years old who suffer from obesity. Pharmaceutical company Eli Lilly signaled its plans to start clinical trials with Mounjaro for kids ages 6-11, over the weekend. Novo Nordisk, the company that makes Ozempic, reported it is in phase three of testing Saxenda, a version of its drug for children ages 6-12. The rates of obesity for children in the U.S. have tripled since the 1980s, affecting close to 15 million children nationwide, according to the CDC. This is nearly one in five kids. "It's unlikely it's going to do much if you just give them the medication. You need to instill all these behavior changes, lifestyle changes, talk about the diet, nutrition consults, the exercise," said pediatrician Dr. Alison Mitzner. The concern for possible long-term impacts and side effects is one nutritionist Carrie Lupoli echoes. Both drug companies were sued earlier this year after a plaintiff said she suffered stomach paralysis. "It's scary to me that we are going down that path instead of actually working on the root cause because we know weight gain is a symptom of health and hormones," Lupoli said. CDC data shows kids may have gained weight twice as fast during the pandemic. Earlier this year, the American Academy of Pediatrics came out with new guidance that includes medication and surgery as suggestions for patients 12 and up suffering from obesity.

Note: The pharmaceutical companies behind these weight loss drugs are raking it in despite significant efficacy and safety concerns. Sales of Ozempic generated revenue of $3.2 billion in the second quarter (up from $2.1 billion during the same period in 2022) and Mounjaro generated $980 million in sales for the company during the second quarter (a 72% increase compared to the first quarter). For more along these lines, see concise summaries of deeply revealing news articles on Big Pharma corruption from reliable major media sources.

Braven Environmental [is] a company that says it can recycle nearly 90 percent of plastic waste through a form of chemical recycling called pyrolysis. Traditional recycling is able to process only about 8.7 percent of America's plastic waste; pyrolysis uses high temperatures and low-oxygen conditions to break down the remaining plastics, like films and Styrofoam, ideally turning them into feedstock oil for new plastic production. The American Chemistry Council, the country's leading petrochemical industry trade group, claims that chemical recycling will create a "circular economy" for the bulk of the world's plastic, diverting it from oceans and landfills. Plastic giants have gone so far as to dub the process "advanced recycling," but environmentalists say this is a misnomer because the majority of the plastic processed at such facilities is not recycled at all. In fact, researchers have found that the process uses more energy and has a worse overall environmental impact than virgin plastic production. Despite these challenges, lawmakers nationwide are now embracing the technology, thanks to a massive lobbying push from ... petrochemical groups. One list of warnings in a Braven air permit application reads like a toxicologist's worst nightmare: The pyrolysis oil may cause cancer and genetic defects, as well as damage to organs, fertility, and unborn children. Other hazards included being "extremely flammable" and "very toxic to aquatic life" with "long lasting effects."

Note: For more along these lines, see concise summaries of deeply revealing news articles on corporate corruption from reliable major media sources.

Fort Ord was one of 800 U.S. military bases, large and small, that were shuttered between 1988 and 2005. The cities of Seaside and Marina, Calif., where Fort Ord had been critical to the local economy, were left with a ghost town of clapboard barracks and decrepit, World War II-era concrete structures that neither of the cities could afford to tear down. Also left behind were poisonous stockpiles of unexploded ordnance, lead fragments, industrial solvents and explosives residue, a toxic legacy that in some areas of the base remains largely where the Army left it. Across the country, communities were promised that closed bases would be restored, cleaned up and turned over for civilian use. But the cleanup has proceeded at a snail's pace at many of the facilities, where future remediation work could extend until 2084 and local governments are struggling with the cost of making the land suitable for development. At more than 1,000 sites within the closed bases, the land is so badly contaminated that no one will ever be allowed to live on it. Sites that were supposed to be clean were later found full of asbestos, radioactivity and other health threats. Military base cleanups are often full of surprises, but Hunters Point is in a league of its own. Two former supervisors at an environmental firm, Tetra Tech EC, which the Navy hired to help clean up the base, were convicted in 2018 of fraudulently submitting clean dirt to a laboratory in place of the contaminated dirt at the shipyard.

Note: For more along these lines, see concise summaries of deeply revealing news articles on military corruption from reliable major media sources.

Nearly three months into taking Ozempic for diabetes, Jenny Kent had already lost 12 pounds, and her blood sugar numbers were looking better than they had in a while. Ozempic, the injectable drug approved for Type 2 diabetes, has taken the world by storm. Despite not being approved by the Food and Drug Administration for weight loss, Ozempic has prompted people on TikTok and Instagram to speculate about which stars have used it to shed pounds seemingly overnight. But for Kent something else changed after she started taking Ozempic. "I was just constantly in a state of being overwhelmed," says Kent. "So my response to that was just I was just crying all the time. Sobbing, crying ... I still didn't put it together, so I kept ... taking my injections." She's one of many people taking Ozempic and related drugs who describe mental health problems. But that side effect isn't mentioned in Ozempic's instructions for use, or drug label. In July, the European Medicines Agency said that it was looking into the risk of thoughts of self-harm and suicidal thoughts with the use of Ozempic and similar drugs. The FDA hasn't taken that step. NPR analyzed the FDA's adverse event reporting system, or FAERS, and learned that the agency has received 489 reports of patients experiencing anxiety, depression or suicidal thoughts while taking semaglutide drugs, including Ozempic, Wegovy and Rybelsus. In 96 of those reports, the patient had suicidal thoughts. Five of them died.

Note: A deeper investigation explores the concerning scope of health issues related to weight-loss drug side effects. For more along these lines, see concise summaries of deeply revealing news articles on Big Pharma corruption from reliable major media sources.

France's radiation watchdog has banned sales of Apple's iPhone 12 after tests that it said showed the smartphone breached European radiation exposure limits. The Agence Nationale des Frequences (ANFR) said on Tuesday the model's Specific Absorption Rate (SAR) - a measure of the rate of radiofrequency energy absorbed by the body from a piece of equipment - was higher than legally allowed. Jean-Noel Barrot, France's junior minister for the digital economy, told newspaper Le Parisien a software update could fix the problem. If Apple does not resolve the issue, the ANFR said it would order a recall of the device across France. "Specific Absorption Rate" refers to the dose of energy that the body absorbs from any source of radiation. It is expressed as watts per kilogram of body weight. The radiation from mobile phones is a result of the way they work, by transmitting radiofrequency waves, creating electromagnetic fields. The ANFR said it recently carried out random tests on 141 phones, including iPhone 12, bought from shops. In independent laboratory tests, two iPhone 12s did not comply with EU standards, the office of the Digital Minister told Reuters. Smartphone radiation tests have so far led to 42 imposed sale stops in the country, it said. The ANFR said accredited labs had found an SAR of 5.74 watts per kilogram during tests of the iPhone 12 being held in the hand or kept in a trouser pocket. The EU standard is 4.0 watts per kilogram.

Note: Explore an excellent investigation into how the FCC shields cell phone companies from valid safety concerns. This Wired article quotes the result of a mega-study that reveals there is "significant evidence linking cellular phone use to increased tumor risk." Unlike the U.S., many countries have regulations in place to protect people from cell phone radiation exposure. Check out this comprehensive list of countries with official recommendations and policies on cell phone radiation exposure. For more along these lines, see concise summaries of news articles on wireless technology risks from reliable major media sources.

Less than 2% of the deaths reported by the Centers for Disease Control and Prevention last week were caused by the coronavirus, new data shows. According to the CDC's COVID-19 dashboard, just 324 deaths logged in the week ending Aug. 19 – 1.7% of all fatalities nationwide – were attributed to the virus. This is a staggering difference from the peak of the pandemic in 2021, when one in three deaths had COVID-19 cited as the main cause. In New York, 2.1% of the deaths last week were tied to the virus. Florida and Maryland have the highest COVID-19 death rates at 3.4%, followed by Washington with 2.4%, while Tennessee and North Carolina each reported 2% – behind New York, but above the national average. The primary cause of death is defined as the condition, injury, disease, situation or event that initiated the chain of events resulting in a person's death. Weekly COVID-19 deaths are at their lowest numbers since March 2020, according to CDC data. But coronavirus cases recently jumped nationwide – with New York reporting a 55% increase at the beginning of August. The spike came as a new variant – dubbed EG.5, or Eris – emerged as the dominant strain, causing about 17% of COVID cases nationwide.

Note: For more along these lines, see concise summaries of deeply revealing news articles on the coronavirus from reliable major media sources.

In May, the World Health Organization issued an alarming report that declared widely used non-sugar sweeteners like aspartame are likely ineffective for weight loss, and long term consumption may increase the risk of diabetes, cardiovascular diseases and mortality in adults. A few months later, WHO declared aspartame, a key ingredient in Diet Coke, to be a "possible carcinogen", then quickly issued a third report that seemed to contradict its previous findings – people could continue consuming the product at levels determined to be safe decades ago. That contradiction stems from beverage industry corruption of the review process by consultants tied to an alleged Coca-Cola front group, the public health advocacy group US Right to Know said in a recent report. It uncovered eight WHO panelists involved with assessing safe levels of aspartame consumption who are beverage industry consultants who currently or previously worked with the alleged Coke front group, International Life Sciences Institute (Ilsi). Aspartame was first approved for use in the US in the early 1980s over the objection of some researchers who warned of potential health risks. In recent years, as evidence of health threats has mounted, industry has ramped up a PR campaign to downplay the issues. Ilsi representatives have sought to shape food policy worldwide. [Gary Ruskin, US Right to Know's executive director], characterized the aspartame controversy as a "masterpiece in how Ilsi worms its way into these regulatory processes".

Note: Explore a comprehensive overview of key scientific studies on aspartame harms, and how they were covered up by the sugar industry. For more along these lines, see concise summaries of deeply revealing news articles on corruption in the food system and in the corporate world from reliable major media sources.

A number of hospitals have been sued for refusing to allow patients dying of COVID to receive treatment with ivermectin. If the hospital lost, it appealed the decision, even if the patient did receive ivermectin and recover, according to attorney Andrew Schlafly in the summer issue of the Journal of American Physicians and Surgeons. "Hospitals wanted to establish precedents for their side, so that next time they could deny treatment by pointing to appellate decisions in their favor," Schlafly writes. They adopted a "strategy of seeking to establish precedents that increased their authority, and to remove any precedents against unlimited power for them." Ivermectin is a long-established safe drug that is widely used to treat parasitic infections. It has also been shown to have antiviral activity. Many physicians have reported successful use in COVID patients, and many though not all studies have shown safety and benefit. Many state appellate courts cite the Food and Drug Administration's (FDA's) disparagement of ivermectin as a legal basis for hospitals to deny access by dying patients to this drug, long approved by the FDA as safe. Schlafly writes that the FDA has "been able to evade judicial review for too long. The more the FDA avoids submitting to discovery procedures that are commonplace for every other defendant, the bigger the mushrooms can grow in the dark at this federal agency."

Note: Explore a comprehensive look into the benefits and uses of ivermectin, despite establishment media's concerted effort to discredit its efficacy and safety. For more along these lines, see concise summaries of deeply revealing news articles on corporate corruption and the coronavirus from reliable major media sources.

On Feb. 3, a train of about 150 freight cars – many carrying several loads of hazardous materials – crashed and exploded in the town of East Palestine, Ohio. The tangled knot of boxcars operated by Norfolk Southern Railway shot out flames reaching 100 feet and sent a massive plume of coal-black smog. Five days later, crews ignited a controlled burn of the toxic chemicals in order to prevent a much bigger explosion, but the situation appears to be worsening. Residents and local news agencies have posted viral videos of streams and creeks cluttered with dead fish and frogs. Reports have also surfaced that fumes sickened and even killed pets. Many are drawing comparisons to the 1986 Chernobyl nuclear disaster, which turned Pripyat, a city of roughly 50,000 people, into a ghost town. "We basically nuked a town with chemicals so we could get a railroad open," Sil Caggiano, a hazardous materials specialist, told WKBN. On Feb. 8, state officials told residents that they could "safely" return home. "If it's safe and habitable, then why does it hurt?" Nathen Velez, a resident of East Palestine, said to CNN. "Why does it hurt me to breathe?" As more details emerge, the gravity of the situation only seems to worsen. In a letter sent to Norfolk Southern Railway on Feb. 11, the Environmental Protection Agency (EPA) said that in addition to vinyl chloride, four additional toxic chemicals were on board the train: ethylene glycol monobutyl ether, ethylhexyl acrylate, butyl acrylate and isobutylene.

Note: An on-the-ground report discusses this tragic issue beyond the official narrative: how corporate greed is the underlying cause of the crash, local media outlets owned by private equity firms who have significant stakes in Norfolk Southern, and potential long-term impacts. For more along these lines, see concise summaries of deeply revealing news articles on corporate corruption from reliable major media sources.

Since the rollout of mRNA COVID-19 vaccines, experts and academics from around the world have been raising numerous short-term and long-term safety concerns. One of these deals with the spike protein that the human cell is instructed to generate as a result of the shot, and how it differs from the spike protein that's generated from a natural infection. A "pseudouridine" molecule has been added to the mRNA to give it a longer half-life than normal mRNA. Therefore, the production of spike protein within the cell, of those who have been vaccinated, is not being turned off. This is concerning because multiple studies have shown that the vaccine induced spike protein can leak outside of the cell and enter into the blood- stream. This is one possible mechanism of action in which vaccine injuries are occurring. During an autopsy of a vaccinated person who had died after mRNA vaccination, it was found that the vaccine disperses rapidly from the injection site and can be found in nearly all parts of the body. Looking into these concerns is important to figure out why so many COVID vaccine injuries around the world have been reported compared to previous vaccines. Approximately 50 percent of vaccine injuries reported to the Vaccine Adverse Events Reporting System (VAERS) in the last 30 years have all been from COVID products. Concerning autopsy results have also been published. It's quite clear something very serious about these shots is and has been ignored.

Note: VAERS only captures a portion of vaccine injuries and deaths. Vaccine adverse event numbers are made publically available, and currently show 2,579,111 COVID vaccine injury reports and 37,100 COVID Vaccine Reported Deaths (out of 47,290 Total Reported Deaths from all vaccines). Read our in-depth report about this concerning trend, and how the VAERS system presents an incomplete picture of vaccine injuries. For more along these lines, see concise summaries of deeply revealing news articles on COVID vaccines from reliable major media sources.

After ProPublica and the New Yorker published an exposé of hospice fraud, members of Congress have called on the Department of Health and Human Services to "immediately investigate this situation." The ... investigation described how the lucrative design of the Medicare benefit incentivizes many profit-seeking hospices to cut corners on care and target patients who are not actually dying. It chronicled the lack of regulation and the frustrated efforts of whistleblowers to hold end-of-life care conglomerates accountable. And it drew on state and federal data to reveal how, in the absence of oversight, the number of for-profit hospice providers in California, Texas, Arizona and Nevada has lately exploded. Hospice began more than 60 years ago as a countercultural charity movement to help patients die with comfort, support and as little pain as possible. After the 1980s, when President Ronald Reagan authorized Medicare to cover the service, dying became a big business. In 2000, less than a third of all hospices were for-profit. Today, more than 70% are. Between 2011 and 2019, the number of hospices owned by private equity firms tripled. For profit-seeking providers, hospice is lucrative: Medicare pays a fixed rate per patient a day, regardless of how much help is offered. The aggregate Medicare margins of for-profit providers hover around 20% compared with just 5% for nonprofits. For-profit hospices are more likely than their nonprofit counterparts to have less skilled staff ... and fewer home visits.

Note: For more along these lines, see concise summaries of deeply revealing news articles on corporate corruption and health from reliable major media sources.

Timothy York knows what works to treat his decades-long opioid addiction: Suboxone, a medication that effectively quiets cravings. In 2019, he was relieved to learn that the federal Bureau of Prisons was starting a program to expand access to Suboxone. He's still waiting. In the meantime, he's been punished for using Suboxone without a prescription. Last year, after York, 46, was caught with the medication, he spent a month in solitary confinement and had his visitor privileges revoked for a year. York is not alone. The Marshall Project spoke to more than 20 people struggling with addictions in federal prison, and they described the dire consequences of being unable to safely access a treatment that Congress has instructed prisons to provide. Some have overdosed. The lack of Suboxone treatment comes amid a rise in drug-related deaths behind bars. A variety of substances are routinely smuggled into prisons and jails through mail, drone drops, visitors or corrections officers and other staff. In the last two decades, federal data shows that fatal overdoses increased by more than 600% inside prisons and more than 200% inside jails. Forty-seven incarcerated people died of overdoses in federal prison from 2019 through 2021. The data does not specify how many of these overdose deaths were caused by opioids and could have been prevented by medications like Suboxone. During the same period, correctional staff administered Narcan – a drug that reverses opioid overdoses – almost 600 times.

Note: For more along these lines, see concise summaries of deeply revealing news articles on prison system corruption from reliable major media sources.

There has been a steady increase in the number of children who are seen in emergency rooms for suicidal thoughts, according to a new study. The study, published ... in the journal Pediatrics, used data from hospitals in Illinois. The researchers looked at the number of children ages 5 to 19 who sought help for suicide in emergency departments between January 2016 and June 2021. In that period, there were 81,051 emergency department visits by young people that were coded for suicidal ideation. About a quarter of those visits turned into hospital stays. The study found that visits to the ER with suicidal thoughts increased 59% from 2016-17 to 2019-21. There was a corresponding increase in cases in which suicidal ideation was the principal diagnosis, which rose from 34.6% to 44.3%. Hospitalizations for suicidal thoughts increased 57% between fall 2019 and fall 2020. "It just really highlights how mental health concerns were really a problem before the pandemic. I mean, we saw this huge increase in [emergency department] visits for kids of all ages, honestly, in 2019, and it's very concerning," said study co-author Dr. Audrey Brewer. Dr. Nicholas Holmes ... at Rady Children's Hospital in San Diego, said the increase in the number of kids seeking help in his health care system has been "profound." "Over the last nine years, where we would see about anywhere from one to two patients a day that were having a behavioral health crisis, now we're seeing 20-plus a day," said Holmes.

Note: For more along these lines, see concise summaries of deeply revealing news articles on health from reliable major media sources.

Every day, farms across the country use a potentially cancer-causing chemical that is in the world's most common weedkillers. And data shows that it's most used in the Midwest and parts of the South. Glyphosate, the active ingredient in many herbicides, has been in use for nearly 50 years. The World Health Organization's International Agency for Research on Cancer concluded in a 2015 report that the chemical "is probably carcinogenic to humans." Glyphosate's main use is in agriculture. Weedkillers containing it are used on nearly half of all planted acres of corn and soybeans in the U.S. They're also used on acres of farmland where wheat, oats, fruits and cotton are grown. Pesticide residue testing from the FDA found glyphosate residues on a wide variety of crops, including oats, soybeans, cranberries, grapes, raisins, oranges, apples, cherries and beans. A 2020 Department of Health and Human Services report notes that the greatest potential exposure is among farm workers and gardeners that use glyphosate-based herbicides and those who live near farms, manufacturing plants ... and hazardous waste disposal sites. For the general public, the report notes that exposure to glyphosate typically comes by touching or eating food or water containing residues. Some studies have found a link between increased cancer rates and higher levels of exposure. Several peer-reviewed studies have also suggested that herbicides containing glyphosate may disrupt hormones and alter the gut microbiome. 

Note: Don't miss the interactive map of glyphosate usage available at the link above. For more along these lines, see concise summaries of deeply revealing news articles on food system corruption and health from reliable major media sources.

We urgently need a national debate about guns. But we also urgently need a national debate about the epidemic of mood-altering drugs being prescribed to young Americans. Mass shooters in the United States tend to be young, obsessive, male loners and many have been prescribed psychoactive drugs. For example, Eric Harris, one of the two shooters at Columbine High School in Columbine, Colorado, in 1999–which ushered in the current spate of mass shootings–was on the psychotropic drug Luvox. Prescribing information for the antidepressant says, "Close supervision of patients and in particular those at high risk should accompany drug therapy." Jeff Weise, who fatally shot his grandfather, his grandfather's girlfriend, and then seven others at the Red Lake Senior High School in Minnesota in 2005, was on the well-known antidepressant Prozac. Two years later, Cho Seung-Hui, who perpetrated the Virginia Tech mass shooting, also was found to be on psychoactive antidepressants. Jeanne Stolzer, associate professor of child and adolescent development at the University of Nebraska-Kearney, observes that "despite the multitude of international drug regulatory warnings on all classifications of psychiatric medications citing adverse reactions such as suicidal ideation, homicidal ideation, violence, and psychosis, not one local, state, or federal commission has investigated the correlation between the mass shootings in America and the use of psychiatric medications."

Note: Although Epoch Times is often deemed as a controversial media platform, this article raises legitimate questions on an important topic seldom discussed. Read a revealing article that investigates the alarming adverse events associated with common mood-altering medications prescribed for those struggling with mental illness. For more on this concerning trend, consider exploring an in-depth article written by an anonymous doctor who reveals the decades of evidence showing how adverse reactions from psychiatric drugs can manifest as both suicides and homicides.

Over the past decades, regulatory agencies have seen large proportions of their budgets funded by the industry they are sworn to regulate. In 1992, the US Congress passed the Prescription Drug User Fee Act (PDUFA), allowing industry to fund the US Food and Drug Administration (FDA) directly through "user fees." The FDA moved from a fully taxpayer funded entity to one supplemented by industry money. Net PDUFA fees collected have increased 30 fold–from around $29m in 1993 to $884m in 2016. In Europe, industry fees funded 20% of ... the European Medicines Agency (EMA), in 1995. By 2010 that had risen to 75%; today it is 89%. Australia had the highest proportion of budget from industry fees (96%) and in 2020-2021 approved more than nine of every 10 drug company applications. But for decades academics have raised questions about the influence funding has on regulatory decisions, especially in the wake of a string of drug and device scandals–including opioids, Alzheimer's drugs, influenza antivirals, pelvic mesh, joint prostheses, breast and contraceptive implants, cardiac stents, and pacemakers. An analysis of three decades of PDUFA in the US has shown how a reliance on industry fees is contributing to a decline in evidentiary standards, ultimately harming patients. A BMJ investigation last year found several expert advisers for covid-19 vaccine advisory committees in the UK and US had financial ties with vaccine manufacturers–ties the regulators judged as acceptable.

Note: For more on this massive legal corruption, see this article. For more along these lines, see concise summaries of deeply revealing news articles on corruption in government and in Big Pharma from reliable major media sources.

Important Note: Explore our full index to revealing excerpts of key major media news articles on several dozen engaging topics. And don't miss amazing excerpts from 20 of the most revealing news articles ever published.