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Excerpts of Key Health Media Articles in Major Media

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Nick was 19 when a psychiatrist offered him the antidepressant Trintellix to treat his moderate anxiety and depression after just a few short visits. Going on the popular selective serotonin reuptake inhibitor (SSRI) ... didn't seem like a big deal at the time. But, when Nick went off the medication after six years, he immediately noticed his genitals were losing sensation. Over the course of a couple weeks, he almost entirely lost feeling in the area – and it never returned, nor did the high sex drive he once had. He would ultimately learn he suffers from Post-SSRI Sexual Dysfunction (PSSD). "I wasn't at risk of taking my own life or anything like that … I still had a hell of a lot of fun in life … I think I definitely should have [done] therapy first and foremost," he said. "Now there's just no enjoyment in anything. It's like watching a brick wall." For many, antidepressants are lifesaving treatments, but, in rare instances, they can potentially cause debilitating side effects that persist for years after stopping the drugs. SNOMED, the National Institute Of Health's official source of medical terminology for US healthcare systems, recognizes PSSD as a legitimate disorder as of last year, defining it as "persistent sexual side effects" including genital numbness and loss of libido that "can last for weeks, months, or even years after stopping" antidepressants. The rate of prescriptions for those ages 12 to 25 jumped by about two-thirds from 2016 to 2022. "The studies that were done for SSRIs to be approved by the FDA were not done on children, they were done on adults," [clinical psychologist Meg Jay] said. "But now it's much more common for tweens and teens to be prescribed medications than it used to be." In the past two years alone, [Psychopharmacologist and former professor of psychiatry David Healy] said he's known more than a dozen people, many of them young, who were so distressed by PSSD that they committed suicide.

Note: For more along these lines, read our concise summaries of news articles on Big Pharma corruption.

Antidepressants are frequently prescribed to people with dementia for symptoms like anxiety, depression, aggressiveness and sleeplessness. But a specific class of antidepressant medications - selective serotonin reuptake inhibitors (SSRIs) - actually might speed up brain decline among some dementia patients, a new Swedish study suggests. Heavier doses of certain SSRIs are tied to a higher risk for severe dementia, researchers reported in a new study ... in the journal BMC Medicine. The SSRI drug escitalopram was associated with the fastest cognitive decline, followed by citalopram and sertraline. For the study, researchers tracked the brain health of more than 18,700 patients enlisted in the Swedish Registry for Cognitive/Dementia Disorders between May 2007 and Oct. 2018. The patients' average age was 78. During an average follow-up of more than four years, about 23% of patients received a new prescription for an antidepressant, researchers said. SSRIs were the most commonly prescribed antidepressant, amounting to 65% of all those prescriptions, the study says. "Higher dispensed doses of SSRIs were associated with higher risk for severe dementia, fractures, and all-cause mortality," the researchers concluded. "These findings highlight the significance of careful and regular monitoring to assess the risks and benefits of different antidepressants use in patients with dementia."

Note: For more along these lines, read our concise summaries of news articles on Big Pharma corruption.

Pesticide company efforts to push through laws that could block litigation against them is igniting battles in several US farm states. Laws have been introduced in at least eight states so far and drafts are circulating in more than 20 states, backed by a deluge of advertising supporting the measures. The fight is particularly fierce now in Iowa, where opponents call the pesticide-backed proposed law the "Cancer Gag Act", due to high levels of cancer in Iowa that many fear are linked to the state's large agricultural use of pesticides. Iowa has the second-highest rate of new cancer cases in the United States and the fastest growing rate. The bill would bar people from suing pesticide manufacturers for failing to warn them of health risks, as long as the product labels are approved by the Environmental Protection Agency (EPA). Opponents say the legislation will rob farmers and others who use pesticides from holding companies accountable in court if their pesticide products cause disease or injury. "We're very worried. Our farmers feel that if they have injuries or illnesses due to their use of a pesticide they should have access to the courts," said [Iowa Farmers Union president] Aaron Lehman. The actions in the states come alongside a simultaneous push for changes in federal law that would in effect shield companies from lawsuits brought by people claiming they developed cancers or other diseases due to their use of pesticides.

Note: Thousands of farmers and everyday people have filed lawsuits against major corporations for failing to warn consumers about the health risks associated with these chemicals. For more along these lines, read our concise summaries of news articles on toxic chemicals and food system corruption.

Is President Trump pushing gender-confused kids to commit suicide? This shocking claim hit mainstream and social media within minutes of the president's Jan. 28 executive order banning federal funding for child sex-change treatments. The way the argument goes, if kids can't get puberty blockers, cross-sex hormones and surgeries, their mental health will deteriorate to the point of no return. But as I've seen while working with more than 1,000 such kids, there are deeper reasons why they're so unhappy – and giving them powerful experimental drugs and irreversible surgeries is more likely to worsen their condition. From 2018 to 2022, I worked as a case manager for the Washington University Transgender Center at St. Louis Children's Hospital. As kids kept coming back for follow-up check-ins and treatment – almost every kid who begins puberty blockers goes on to receive cross-sex hormones – I realized something was very wrong. When my colleagues and I asked about their mental health, they usually reported that it was the same or better. But as soon as we dug deeper, it became clear that the real answer was no – that their mental anguish was worsening. We ignored or explained away co-morbidities like autism, depression and bipolar disorder while using every new development or difficulty in a kid's life to justify continuing down the sex-change road. In my experience, kids typically find the "treatment brings happiness" mantra of their doctors, nurses and case managers hard to see through. Some literally couldn't look themselves in the mirror, even if they physically looked the part of a boy-turned-girl or vice-versa. While activists insist that kids simply "know who they are," reality is more complicated.

Note: This article was written by Jamie Reed, a queer woman married to a trans man. Many transgender medical care experiences can indeed be life-changing and even life-saving, yet not all experiences align with the mainstream narratives. Reed isn't the only whistleblower who's worked in the field of youth transgender medicine. Even advocates who publicly promote gender medicine for kids question its ethics behind closed doors. Watch our nuanced 25-minute Mindful News Brief on the controversy surrounding youth gender medicine. For more along these lines, read our concise summaries of news articles on transgender medicine.

Alzheimer's ... afflicts nearly seven million Americans, about one in every nine people over the age of 65, making it a leading cause of death among older adults. Up to 420,000 adults in the prime of life – including people as young as 30 – suffer from early-onset Alzheimer's. The annual number of new cases of dementia is expected to double by 2050. Yet despite decades of research, no treatment has been created that arrests Alzheimer's cognitive deterioration, let alone reverses it. Over the past 25 years, Alzheimer's research has suffered a litany of ostensible fraud and other misconduct by world-famous researchers and obscure scientists alike. These deceptions have warped the trajectory of Alzheimer's research and drug development, prompting critical concerns about how bad actors, groupthink and perverse research incentives have undermined the pursuit of treatments and cures. This may have jeopardized the well-being of patients. I asked a team of brain and scientific imaging experts to help me analyze suspicious studies by 46 leading Alzheimer's researchers. Collectively, the experts identified nearly 600 dubious papers from the group that have distorted the field – papers having been cited some 80,000 times. Many of the most respected Alzheimer's scholars – whose work steers the scientific discourse – repeatedly referred to those tainted studies to support their own ideas. This has compromised the field's established base of knowledge.

Note: Top leaders in the field of medicine and science have spoken out about the rampant corruption and conflicts of interest in those industries. For more along these lines, read our concise summaries of news articles on corruption in science.

The Environmental Protection Agency said last week that it needed more time to study the health impacts of paraquat, a powerful herbicide that has drawn scrutiny for its possible links to Parkinson's disease, a move that would allow it to remain on the market. Several advocacy groups had sued the EPA over an interim registration decision it issued in 2021 ... on the grounds that it was not protective enough. In a statement, the EPA said additional data was necessary to resolve uncertainty around the risks of inhaling the herbicide. For as long as David Jilbert could remember, he wanted to be a farmer. For five years, Jilbert personally mixed, loaded and sprayed paraquat to control weeds in his vineyard. Then he began having difficulty tying his shoes and buttoning his shirts. He started to walk with a slow, shuffling gait around the winery. He was soon diagnosed with Parkinson's disease, a degenerative neurological disorder that affects motor functions and causes cognitive impairment, despite having no family history or genetic predisposition to the disease. He and his doctors blame paraquat. Jilbert is among the nearly 6,000 Americans who have filed lawsuits against Syngenta and Chevron, which distributed paraquat products in the United States until 1986. The suits allege that the companies failed to warn consumers about paraquat's substantial health risks. Paraquat ... is among the most widely used pesticides in the United States.

Note: Read our latest Substack article on how the US government turns a blind eye to the corporate cartels fueling America's health crisis. For more along these lines, read our concise summaries of news articles on government corruption and toxic chemicals.

Colon cancer rates are rocketing among athletic young people in their 20s, 30s, and 40s, and survival rates are dropping. The most convenient explanations for the rise in young colon cancer are diet and weight. We know diet can influence colorectal cancer risk, and it's something people can fix, to a degree. Plus, our diets have changed. These days we all consume more sugar, more ultra-processed foods, more oil and butter, while moving less. Still, doctors say the trend we're seeing now defies neat categories of genetics or lifestyle, and it's baffling. Other factors are clearly messing with our digestive systems, but they're tough to pinpoint. Pollution, microplastics, and artificial light – all are pervasive in society, yet very tricky to study. Something shifted in the 1960s. Everyone born after 1960 has a higher colon cancer risk than previous generations. In the US, young colon cancer rates have been rising about 3% every year since the early 1990s, according to National Cancer Institute data. It's hard to dismiss the role our changing food landscape has played. We are undoubtedly eating worse than our grandparents did 100 years ago. Take fiber, for example. Found in abundance in whole plant foods like beans, it is a nutrient clearly associated with lower risk of cancer. Some of the most popular foods in US supermarkets ... have fiber stripped out during processing, and extra salt, sugar, and oils added in to make them more palatable and shelf-stable.

Note: Read our latest Substack article on how the US government turns a blind eye to the corporate cartels fueling America's health crisis. For more along these lines, read our concise summaries of news articles on health and toxic chemicals.

The Food and Drug Administration said Wednesday it's banning the use of Red No. 3, a synthetic dye that gives food and drinks their bright red cherry color but has been linked to cancer in animals. The dye is still used in thousands of foods, including candy, cereals, cherries in fruit cocktails and strawberry-flavored milkshakes, according to the Center for Science in the Public Interest, a food safety advocacy group that petitioned the agency in 2022 to end its use. More than 9,200 food items contain the dye, including hundreds of products made by large food companies. The FDA is not prohibiting other artificial dyes, including Red No. 40, which has been linked to behavioral issues in children. The FDA's decision is a victory for consumer advocacy groups and some U.S. lawmakers who have long urged it to revoke Red No. 3's approval, citing ample evidence that its use in beverages, dietary supplements, cereals and candies may cause cancer as well as affect children's behavior. "At long last, the FDA is ending the regulatory paradox of Red 3 being illegal for use in lipstick, but perfectly legal to feed to children in the form of candy," said Dr. Peter Lurie, president of the CSPI. The agency banned the additive in cosmetics in 1990 under the Delaney Clause, a federal law that requires the FDA to ban food additives that are found to cause or induce cancer in humans or animals. Food manufacturers will have until Jan. 15, 2027, to reformulate their products.

Note: For more along these lines, read our concise summaries of news articles on food system corruption.

The payment scheme for people injured by vaccines has cost taxpayers more to run than it has paid out to victims, official figures suggest, fuelling calls for "urgent reform". The Government has spent more than Ł25 million since Nov 1 2021 on medically assessing thousands of claims that vaccinations have left people seriously disabled. It is more than the total Ł23.6 million that since that date has been paid out to 197 victims, with each claim worth Ł120,000. The Vaccine Damage Payment Scheme (VDPS) was established in 1979 and pays tax-free cash to those deemed to have suffered life-changing injuries as a result of certain vaccinations – including those against Covid-19. It awards a one-off Ł120,000 tax-free payment to people who have been severely injured, or to the families of those who have died, as a result of a vaccination. The scheme has been heavily criticised for being too slow to assess cases. Victims also claim that the payouts are insufficient and that the threshold claimants must meet to qualify for a payout is too harsh a measure. Kate Scott, whose husband was left with permanent brain damage after taking the AstraZeneca vaccine against Covid-19, criticised the imbalance between the money the scheme costs to run and the sums paid out. Public hearings for the fourth module of the Covid-19 inquiry started in London on Tuesday. It will hear issues around vaccine safety from families of those who suffered side effects from Covid jabs.

Note: The Vaccine Adverse Event Reporting System (VAERS) is a voluntary government reporting system that only captures a portion of the actual injuries. Vaccine adverse event numbers are made publicly available, and currently show 38,264 COVID Vaccine Reported Deaths and 1,658,330 COVID Vaccine Adverse Event Reports. Our Substack dives into the complex world of COVID vaccines with nuance and uncensored investigation.

For decades, a little-known company now owned by a Goldman Sachs fund has been making millions of dollars from the unlikely dregs of American life: sewage sludge. Synagro, sells farmers treated [sewage] sludge from factories and homes to use as fertilizer. But that fertilizer, also known as biosolids, can contain harmful "forever chemicals" known as PFAS linked to serious health problems including cancer and birth defects. Farmers are starting to find the chemicals contaminating their land, water, crops and livestock. Just this year, two common types of PFAS were declared hazardous substances by the Environmental Protection Agency under the Superfund law. Now, Synagro is part of a major effort to lobby Congress to limit the ability of farmers and others to sue to clean up fields polluted by the sludge fertilizer. In a letter to the Senate Committee on Environment and Public Works in March, sludge-industry lobbyists argued that they shouldn't be held liable because the chemicals were already in the sludge before they received it and made it into fertilizer. [Synagro's] earnings hit $100 million to $120 million last year. An investment fund run by Goldman Sachs ... acquired Synagro in 2020 in a deal reported to be worth at least $600 million. As concerns over PFAS risks have grown, Synagro has stepped up its lobbying. Chemical giants 3M and DuPont, the original manufacturers of PFAS, for decades hid evidence of the chemicals' dangers. The chemicals are now so ubiquitous ... that nearly all Americans carry PFAS in their bloodstream. As many as 200 million Americans are exposed to PFAS through tap water.

Note: Remember when Goldman Sachs once asked in a biotech research report: "Is curing patients a sustainable business model?" For more along these lines, read our concise summaries of news articles on toxic chemicals and food system corruption.

When Megan Rothbauer suffered a heart attack at work in Wisconsin, she was rushed to hospital in an ambulance. The nearest hospital was "not in network", which left Ms Rothbauer with a $52,531.92 bill for her care. Had the ambulance driven a further three blocks to Meriter Hospital in Madison, the bill would have been a more modest $1,500. The incident laid bare the expensive complexity of the American healthcare system with patients finding that they are uncovered, despite paying hefty premiums, because of their policy's small print. In many cases the grounds for refusal hinge on whether the insurer accepts that the treatment is necessary and that decision is increasingly being made by artificial intelligence rather than a physician. It is leading to coverage being denied on an industrial scale. Much of the work is outsourced, with the biggest operator being EviCore, which ... uses AI to review – and in many cases turn down – doctors' requests for prior authorisation, guaranteeing to pay for treatment. The controversy over coverage denials was brought into sharp focus by the gunning down of UnitedHealthcare's chief executive Brian Thompson in Manhattan. The [words written on the] casings [of] the ammunition – "deny", "defend" and "depose" – are thought to refer to the tactics the insurance industry is accused of using to avoid paying out. UnitedHealthcare rejected one in three claims last year, about twice the industry average.

Note: For more along these lines, read our concise summaries of news articles on AI and corporate corruption.

Covid-19 vaccine mandates did "more harm than good", a House of Representatives report has claimed. A 525-page report from the coronavirus pandemic select committee argued that Joe Biden's policy had cost thousands of people their jobs, harmed public confidence in health professionals and damaged military readiness. The report said that "the vaccine ... did not stop transmission and therefore making the jabs mandatory was ineffective at stopping the spread of Covid. The report also suggested that the "more likely" origin of the coronavirus pandemic was a lab leak. "Since the Select Subcommittee commenced its work ... more and more senior intelligence officials, politicians, science editors, and scientists increasingly have endorsed the hypothesis that Covid-19 emerged as the result of a laboratory or research related accident," it said. Mr Biden's administration introduced several vaccine mandates from 2021 for members of the armed forces, federal workers, healthcare workers, and businesses with more than 100 employees. Many state and local governments, along with private employers, followed suit. Some 8,000 members of the armed services were discharged as a result of the vaccine mandate. Only 43 rejoined when this was rescinded. The report argued that vaccine mandates appeared to "fly in the face of decades of scientific research", by not making an exception for those who had acquired immunity by having previously been infected.

Note: For more along these lines, read our concise summaries of news articles on COVID vaccines and government corruption.

The House Select Subcommittee on the Coronavirus Pandemic has released its final report, summarizing two years of investigations into the origins and handling of COVID-19. The 520-page report, published Monday, concludes that the virus most likely originated from a laboratory in Wuhan, China. The Republican-led committee cited biological characteristics of the virus and reports of illnesses among researchers at the Wuhan Institute of Virology in late 2019 as key evidence for its findings. The report also scrutinized the World Health Organization (WHO), accusing it of prioritizing the Chinese Communist Party's interests over its global mission to protect public health. The subcommittee criticized U.S. health officials and the Biden administration for what it described as overselling the effectiveness of vaccines in preventing transmission and infection. However, the report praised the early travel restrictions implemented by the Trump administration as a significant step in mitigating the pandemic's spread. This conclusion contrasts with other research pointing to the Huanan Seafood Market in Wuhan as the most likely origin of the virus. The WHO and many scientists have stated that the exact origins of the pandemic remain uncertain. The release of the report highlights the ongoing debate over the pandemic's beginnings and the global response, underscoring the complexities of managing an unprecedented public health crisis.

Note: Watch our Mindful News Brief on the strong evidence that bioweapons research created COVID-19. For more along these lines, read our concise summaries of news articles on COVID corruption and COVID vaccines.

A spritz of perfume may feel like such a minor chemical exposure compared to the pollutants elsewhere in our environment – microplastics, air pollution, PFAS. But scientists and clinicians are increasingly raising alarm over a group of chemicals used in many personal care products: phthalates. Phthalates – found in popular perfumes, nail polishes and hair care products – have been linked to numerous adverse health outcomes: insulin resistance, cardiovascular disease and impaired neurodevelopment. A study published in JAMA Network Open found that higher urinary concentrations of phthalates from personal care products was linked to a 25 percent increased risk of hyperactivity problems among adolescents. Another study of the same cohort found that increased phthalate exposure was also associated with poorer performance in math. The concerns about childhood exposure to phthalates are high enough that in the United States, certain types of the chemical are banned in children's toys and items such as pacifiers and baby bottles. For Andrea Gore, a professor of pharmacology and toxicology at the University of Texas at Austin ... the harms are clear enough that she advises everyone to try to reduce their exposure, especially parents starting a family and those with young children. "I recommend avoiding added fragrances altogether – in perfumes, scented lotions and shampoos, even scented detergents and antiperspirants," she said.

Note: For more along these lines, read our concise summaries of news articles on health and toxic chemicals.

U.S. government researchers have found that a widely prescribed asthma drug originally sold by Merck & Co, may be linked to serious mental health problems for some patients, according to a scientific presentation reviewed by Reuters. The researchers found that the drug, sold under the brand name Singulair and generically as montelukast, attaches to multiple brain receptors critical to psychiatric functioning. By 2019, thousands of reports of neuropsychiatric episodes, including dozens of suicides, in patients prescribed the drug had piled up on internet forums and in the U.S. Food and Drug Administration's tracking system. Such "adverse event" reports do not prove a causal link between a medicine and a side effect, but are used by the FDA to determine whether more study of a drug's risks are warranted. The reports and new scientific research led the FDA in 2020 to add a "black box" warning to the montelukast prescribing label, flagging serious mental health risks like suicidal thinking or actions. The behavior of montelukast appears similar to other drugs known to have neuropsychiatric effects, such as the antipsychotic risperidone. When the FDA added the black box, it cited research from Julia Marschallinger and Ludwig Aigner. The two scientists told Reuters ... the new data showed significant quantities of montelukast present in the brain. The receptors involved play a role in governing mood, impulse control, cognition and sleep, among other functions, they said.

Note: Reuters reported that the FDA received more than 80 reports of suicides in people taking the medicine. Learn more about how US courts protected Merck from lawsuits regarding Singulair. For more along these lines, explore concise summaries of news articles on mental health and Big Pharma profiteering from reliable major media sources.

A health department in Idaho has voted to halt its COVID-19 vaccination program, joining the growing number of regional governments pushing back against federal vaccination recommendations. Board members at Southwest District Health, outside of Boise, questioned the vaccine's safety during their Oct. 22 meeting and narrowly voted to stop providing the shot in the six counties they serve. Health departments in Texas, Florida and Michigan ... have also pushed back against the COVID-19 vaccine. Last year, Texas policymakers banned health departments and other organizations funded by the state government from using funds to promote their vaccination efforts. The Florida Department of Health issued guidance in September warning Floridians not to get mRNA COVID-19 shots. In Michigan, commissioners in Ottawa County turned down a $900,000 grant for their health department in September. Joe Moss, chair of the commission, said at the time he was "opposed to accepting any COVID grants." The [Idaho] board's physician representative, Dr. John Tribble, questioned the vaccine's safety and cited COVID-19's "diminishing risk" as a reason for the agency's decision to discontinue the shot. "We weighed the risks versus the benefits for all individuals considering the shots," Tribble wrote. "We could not, in good faith, continue to offer a pharmaceutical product that does more harm than good."

Note: The Vaccine Adverse Event Reporting System (VAERS) is a voluntary government reporting system that only captures a portion of the actual injuries. Vaccine adverse event numbers are made publicly available, and currently show 38,068 COVID Vaccine Reported Deaths and 1,652,230 COVID Vaccine Adverse Event Reports. Our Substack dives into the complex world of COVID vaccines with nuance and uncensored investigation.

A former director at the tobacco giant Philip Morris International (PMI) was handed a role on an influential expert committee advising the UK government on cancer risks. Ruth Dempsey, the ex-director of scientific and regulatory affairs, spent 28 years at PMI before being appointed to the UK Committee on Carcinogenicity of Chemicals in Food, Consumer Products and the Environment (CoC). The committee's role is to provide ministers with independent advice. Yet since taking up the position in February 2020, Dempsey has continued to be paid by PMI for work including authoring a sponsored paper about regulatory strategies for heated tobacco products. She also owns shares in the tobacco giant ... and receives a PMI pension. But her appointment, unreported until now, raises questions about the potential for undue influence and possible access to inside information on policy and regulatory matters that may be valuable to the tobacco industry. PMI has a long history of lobbying and influence campaigns, including pushing against planned crackdowns on vaping. It has also invested heavily in promoting heated tobacco as an alternative to smoking and expects to ship around 140bn heated tobacco units in 2024, a 134% increase on its 59.7bn sales in 2019. Sophie Braznell, who monitors heated tobacco products as part of the University of Bath's Tobacco Control Research Group, said Dempsey's position on the committee risked undermining its work. "In permitting a former senior tobacco employee and consultant for the world's largest tobacco company to join this advisory committee, we jeopardise its objectivity and integrity."

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How is America allowed to feed us certain products that are harmful and banned in other countries? What some people may dismiss as a fixation of "granola moms" is actually a legitimate concern, says Melanie Benesh, the vice president of government affairs at the Environmental Working Group. The impact many of these chemicals have is chronic: They accumulate over time, after a lot of tiny exposures. For example, the whitening agent titanium dioxide in soups and dairy products can build up in the body and even damage DNA. European countries take a much more precautionary approach to additives in their food, Benesh says. "If there are doubts about whether a chemical is safe or if there's no data to back up safety, the EU is much more likely to put a restriction on that chemical." California banned four chemicals in 2023: brominated vegetable oil, Red Dye No. 3, propylparaben, and potassium bromate. This year, lawmakers in about a dozen states have introduced legislation banning those same chemicals and, in some states, additional chemicals as well. But federal oversight has been limited. When Congress wrote the food chemical law, they included an exception for things that are generally recognized as safe, or GRAS. This was intended to be a narrow loophole, an exception for ... things like spices or vinegar or flour or table salt. An analysis in 2022 ... found that 99 percent of new food chemicals were exploiting this GRAS loophole.

Note: Read more about the growing list of chemicals banned in the EU but not the US. For more along these lines, explore concise summaries of revealing news articles on food system corruption.

Pfizer Inc. failed to warn patients that its injectable contraceptive drug Depo-Provera can increase the risk of developing brain tumors, a new lawsuit alleged. "For several decades the manufacturers and sellers of Depo-Provera and its authorized generic and generic analogues" had a responsibility to investigate whether the medication could contribute to the growth of brain tumors, according to the complaint filed Monday in the US District Court for the Central District of California. Plaintiff Taylor Devorak alleged that researchers have found Depo-Provera and similar progesterone medications have been linked to a greater incidence of brain tumors called intracranial meningioma. She's seeking damages on her failure-to-warn, defective design, negligence, misrepresentation, and breach of warranty claims against the pharmaceutical giant. Devorak's complaint comes in the wake of a handful of substantially similar lawsuits filed in other federal courts in California and Indiana in recent weeks. The American label for Depo-Provera "still makes no mention of the increased risk to patients of developing intracranial meningiomas," even though the EU and UK now list meningioma under the medication's warning section, Devorak's complaint said. Devorak cited a 2024 study published in the British Medical Journal that said prolonged use of medroxyprogesterone acetate medications like Depo-Provera were found to significantly increase the risk of developing intracranial meningioma.

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

The food system is inextricably linked to an economic system that, for decades, has been fundamentally biased against the kinds of changes we need. Economic policies almost everywhere have systematically promoted ever-larger scale and monocultural production. Those policies include: Massive subsidies for globally traded commodities, direct and hidden subsidies for global transport infrastructures and fossil fuels, ‘free trade' policies that open up food markets in virtually every country to global agribusinesses, [and] health and safety regulations [that] destroy smaller producers and marketers and are not enforced for giant monopolies. Monocultures rely heavily on chemical inputs–fertilizers, herbicides, fungicides, and pesticides–which pollute the immediate environment, put wildlife at risk, and–through nutrient runoff–create "dead zones" in waters ... thousands of miles away. More than half of the world's food varieties have been lost over the past century; in countries like the U.S., the loss is more than 90 percent. Agribusiness has gone to great lengths to convince the public that large-scale industrial food production is the only way to feed the world. But the global food economy is massively inefficient. More than one-third of the global food supply is wasted or lost; for the U.S., the figure is closer to one-half. The solution to these problems ... requires a commitment to local food economies. [Several towns in the state of Maine] declared "food sovereignty" by passing ordinances that give their citizens the right "to produce, process, sell, purchase, and consume local foods of their choosing." In 2013, the government of Ontario, Canada, passed a Local Food Act to increase access to local food, improve local food literacy, and provide tax credits for farmers who donate a portion of their produce to nearby food banks.

Note: Read the full article for a comprehensive explanation of why local food and economies are far better for human health and environment. For more along these lines, explore concise summaries of news articles on food system corruption.

Important Note: Explore our full index to key excerpts of revealing 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.