The US Food and Drug Administration (FDA) has approved Ozempic to help reduce the risk of serious kidney complications in people with type 2 diabetes and chronic kidney diseases. It is a popular drug which has been previously used to treating diabetes and obesity.

Why Is Ozempic Used For Kidney Diseases?

In the US, 1 in 7 adults are experiencing some type of chronic kidney disease caused by diabetes. The new approval therefore allows doctor to prescribe Ozempic to lower the risk of kidney failure, dialysis and death from heart-related problems too.

Doctors have already been using Ozempic to manage type 2 diabetes and reduce the risk of heart diseases in patients with diabetes. Studies have also shown that those who took Ozempic, had a 24$ lower risk of kidney-related complications and could avoid dialysis and or organ transplant. Patients also showed slower rates of kidney decline.

How Does Ozempic Help?

The active ingredient is semaglutide, which is a type of glucagon-like peptide 1 receptor against (GLP-1 RA), a drug that mimics a natural hormone which helps to regulate blood sugar. GLP-1 also protects the kidney by improving blood flow, reducing inflammation and preventing damage.

As per the study led by clinical pharmacologist Hiddo L Heerspink of the University Medical Center Geoningen, in the Netherlands, it was the first time when this diabetes drug was used to treat patients with kidney damage. The study was also published in the Nature Medicine journal and presented at the annual congress of the American Society of Nephrology.

Read all about Ozempic here.

The study was conducted in four countries, including Canada, Germany, Spain and the Netherlands and found that protein in urine that indicated kidney damage had reduced by 52% for those who received a shot of semaglutide. Kidney inflammation also decreased by 30%.

This is because the drug has direct effects on inflammation parameters in the kidney and lowers fat tissue around the kidneys.

What Is Ozempic Originally Used For?

Ozempic is originally used to treat Type 2 diabetes. This drug affects the intestinal hormone GLP-1 which is responsible for proper processing of carbohydrates from food. This stimulates insulin release in pancreas and also reduces the feeling of hunger. This also causes food to move slowly from stomach to intestines. It also gives a feeling of fullness for longer, leading to weight loss.

They are also used for various other health issues, including boosting your health. As per a study based on data from the US veterans with type 2 diabetes, these drugs have shown lower rates of heart attacks, strokes and heart failure. It has also in fact shown a significant decrease in conditions like schizophrenia, suicidal thoughts, and seizures. The study further found a 12% reduction in Alzheimer's disease, especially in participants taking the drugs for 3.5 years. The drug also reduced bacterial infections, liver cancer and chronic kidney diseases, along with fever and muscle pain.

Not Ozempic, but Eli Lilly's weight-loss drug Zepabound has been previously approved by the FDA as a treatment for moderate-to-severe sleep apnea and obesity.

RFK Jr ousted all 17 experts from the vaccine advisory panel. As a counter, all the 17 experts have published a joint essay criticizing the US Health Secretary Robert F Kennedy Jr. for making abrupt and "destabilizing decisions". They said that this could jeopardize the nation's immunization strategy and increase the risk of preventable disease outbreaks.

The former panelists, ousted last week, voiced their concerns in an article published Monday in the Journal of the American Medical Association (JAMA). Their essay warns that Kennedy's actions—including disbanding the existing panel, dismissing long-serving CDC staff, and appointing controversial new members—could have serious consequences for public health.

“We are deeply concerned that these destabilizing decisions, made without clear rationale, may roll back the achievements of U.S. immunization policy, impact people’s access to lifesaving vaccines, and ultimately put U.S. families at risk of dangerous and preventable illnesses,” the authors wrote.

A Sudden Shift In Key Advisory Panel

It was only last week when Kennedy announced the "retirement" of the entire panel. This was the Advisory Committee on Immunization Practices (ACIP), the panel responsible for shaping U.S. vaccine policy. He also removed Dr. Melinda Wharton, a senior Centers for Disease Control and Prevention (CDC) official who coordinated the committee’s meetings.

Just two days after dissolving the panel, Kennedy appointed eight new members. Among them are a scientist critical of COVID-19 vaccines, a vocal opponent of pandemic lockdowns, and a member of an organization widely labeled as a key source of vaccine misinformation.

The new committee is scheduled to meet next week, though no agenda has been made public. A federal notice indicated that votes are expected on recommendations for vaccines against influenza, COVID-19, HPV, RSV, and meningococcal bacteria.

CDC Departures Raise Alarm

In addition to Wharton’s removal, several key CDC immunization staffers have either been reassigned or have resigned. Notably, Dr. Lakshmi Panagiotakopoulos left the agency earlier this month after 12 years, informing members of a COVID-19 vaccine workgroup of her decision.

Her resignation came after Kennedy revoked CDC’s recommendation for COVID-19 vaccination for healthy children and pregnant women—without consulting the advisory panel.

“My career in public health and vaccinology started with a deep-seated desire to help the most vulnerable members of our population, and that is not something I am able to continue doing in this role,” she wrote in a message viewed by the Associated Press.

The former ACIP members emphasized that the loss of experienced CDC staff would hinder the new advisers’ ability to make evidence-based recommendations swiftly and effectively.

Kennedy’s Criticisms and Questions of Credibility

A spokesperson for the U.S. Department of Health and Human Services declined to address the essay directly but referred to Kennedy’s previous comments accusing the advisory committee of being too close to vaccine manufacturers and rubber-stamping recommendations.

Kennedy, who long voiced anti-vaccine sentiments before being appointed as health secretary, has questioned the integrity of the ACIP’s review process. Though committee members are required to disclose ties to vaccine companies and recuse themselves in cases of conflict of interest, Kennedy has dismissed these safeguards as inadequate.

Founded in 1964, the ACIP provides guidance to the CDC director on how FDA-approved vaccines should be administered. Its recommendations are widely followed by medical professionals and underpin the nation’s immunization programs.

The abrupt dismissal of the entire panel, according to the former members, not only disrupts a well-established public health process but also undermines trust and efficiency at a time when evidence-based decision-making is critical.

US health officials are raising serious concerns about 'Gas Station Heroin', a substance called tianeptine. This has opioid-like-effects and the availability and accessibility is only increasing.

It is also sold as over-the-counter supplements at gas stations, smoke shops, and convenience store. The drug is also marketed as Zaza, Tianaa, Pegasus, and TD Red.

Though used as an antidepressant in some other countries, tianeptine is not approved for medical use in the United States. Experts warn that its effects can mimic those of opioids, including addiction and withdrawal symptoms, even though it is not officially classified as one.

Also Read: Lethal Fungus Is Spreading Across Many US States, Why Is It Concerning?

What Is Tianeptine?

A 2023 study published in journal Pain and Therapy, notes: "Tianeptine is an antidepressant drug approved for the treatment of major depressive disorder in countries other than the US. It is classified as an atypical tricyclic antidepressant and has shown potential benefits in addressing anxiety and irritable bowel disease. However, it is important to note that tianeptine is not approved for any use by the United States Federal Drug Administration (FDA). Despite its lack of approval by the FDA, tianeptine has been distributed online and at small retail locations."

The term “gas station drugs” refers to a wide range of substances typically available for purchase from gas stations, corner stores, bodegas, mini marts, smoke shops, and the Internet. These substances may be produced commercially by drug manufacturers or in clandestine laboratories to mimic the effects of more well-known illicit/controlled substances such as marijuana, cocaine, opioids, etc.

The study also notes that misuse of tianeptine can lead to euphoric, opioid-like highs with the potential for chronic users to develop dependence and tolerance. Overdose and use in suicide attempts have also been documented.

Its popularity stems from its ability to bind to the same brain receptors as opioids, which can create feelings of euphoria, calmness, and even pain relief. “It’s kind of this grey area of consumer products, or supplements, where the contents are not regulated or tested the way they would be with a medication,” explained Dr. Diane Calello of the New Jersey Poison Information and Education System. “You never quite know what’s in that bottle.”

Also Read: Eye Signs That Warn of Heart Disease: What Your Eyes Reveal About Heart Health

FDA Warns Against Its Easy Accessibility

In response to rising reports of adverse effects, the FDA issued a formal warning last month, calling tianeptine "a dangerous and growing health trend." The agency urged retailers to stop selling these products and asked consumers to avoid purchasing or using them altogether.

Poison control centers have seen a sharp rise in tianeptine-related incidents. The FDA noted that many of these cases involve young people, and the symptoms often require emergency medical attention. Reported side effects include seizures, low blood pressure, rapid heartbeat, and mental distress. In a review of 20 recent cases, more than half of the patients had to be admitted to intensive care units.

The Alabama Case Study

The state of Alabama serves as a stark example of the risks associated with tianeptine. Between 2018 and 2021, poison control calls related to the drug spiked by over 1,400%. However, after the state imposed strict regulations and bans, the number of such incidents saw a notable decline. This indicates that legal restrictions can play a significant role in curbing misuse.

Health professionals are urging federal and state authorities to take faster and stronger action before tianeptine use becomes a full-blown public health crisis. Some compare the current trajectory of the drug to the early days of the opioid epidemic, which caught the country off guard and led to long-term consequences.

A dangerous airborne fungus that has the potential to rot human tissue from the inside is spreading at a considerably increasing rate across the United States. It has prompted concerns among the medical professionals and public health authorities. Aspergillus fumigatus. This is said to be the culprit behind this surge and poses a risk to especially those whose immune system had been compromised. The cases are becoming harder to treat due to widespread drug resistance and climate-linked proliferation.

The World Health Organization (WHO) has classified Aspergillus fumigatus as a “critical priority” due to its high mortality rate and growing resistance to existing treatments.

Silent Invader

It is called a silent invader for a reason. Once you inhale, the fungus can cause aspergillosis. This is a serious lung infection. The spores are microscopic, which mean hat people can breathe them in unknowingly. For patients who are already vulnerable medically, for instance, those battling cancer, asthma, HIV or recovering from organ transplants, the infection can lead to chronic lung disease, systemic organ failure, or even death. If invasive, it can also spread to your brain, hear, and kidneys.

Despite its potentially fatal consequences, aspergillosis is not classified as a reportable disease in the United States. This means infections are not systematically tracked, leaving health officials with limited data and making it harder to trace or contain outbreaks.

Infections On The Rise

Between 2000 to 2013, hospitalizations have increased in the case of invasive aspergillosis in the US. The rate is reported by a 3% increased, annually. In 2014, the infection led to 15,000 hospital stays, with a cost up to $1.2 billion.

As the US News notes, postmortem examinations in intensive care units suggest that aspergillosis is among the top four infections most likely to be fatal.

While about 400,000 Americans may be living with chronic pulmonary aspergillosis — the long-term form of the disease — invasive cases, though less frequent, are significantly deadlier. Survival rates drop sharply: just 59% of organ transplant patients and only 25% of stem cell transplant patients live beyond a year after infection.

What Is Causing Its Spread?

The fungus thrives in hot, damp, and humid environment. They can also endure up to 120 degree Fahrenheit. This is especially true in compost or agricultural waste. States like Florida, Texas, Georgia, Louisiana, and California — with their humid climates and farming activity — are seeing some of the highest exposure levels. Cities such as New York, Houston, and Los Angeles are also at risk due to overcrowding, aging buildings, and limited ventilation.

According to a University of Manchester study, if fossil fuel use continues at current levels, Aspergillus fumigatus could expand its range by over 75% by 2100 — putting millions more at risk across the southern US.

What is making it even more difficult to control is the increasing drug resistance. Azole drugs — commonly used to treat human fungal infections — are also applied to protect crops. This dual-use, experts say, may be fueling cross-environmental resistance, with drug-resistant spores jumping from soil to humans.

A study published in Applied and Environmental Microbiology found resistant fungal strains in agricultural soil across at least seven US states. Some strains are resistant to multiple standard antifungals, making treatment increasingly difficult.

WHO has also urged pharmaceutical companies to invest in new antifungals, including children in drug trials, and enhance diagnostic and treatment protocols globally.

Preventive Measures

As of now, doctors recommend to avoid contact with soil, mold, and gardening. It is important to wear protective masks when in dusty areas, and ensure good air filtration at home.