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Quademic 2025: Hospitals in the United States are dealing with a surge in patients admission, the reason is the quademic it is dealing with at this moment. This has led to an influx of patients. It is all caused by seasonal infections, including common flu, Covid-19, and respiratory syncytial virus (RSV) that dominate the winter season in the US. This year, norovirus also joined the list, which has further increased the load on the healthcare.
The healthcare company founded in academics M Health Fairview, confirmed that their hospitals are overflowing due to the quademic.
The hospitals of M Health Fairview's volume is up by 30% and as a results, patients are being treated in the hallways and in alternative care areas. There is also a longer wait time and shortages for resources that are required to treat these emergencies. This has also impacted other life-threatening emergencies like heart attacks and strokes, as the healthcare resources and caregivers are occupied with the surge in seasonal cases.
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Common cold and flu: The common cold and influenza (flu) are perhaps the most well-known illnesses that peak during the fall. As temperatures drop and humidity levels fluctuate, viruses that cause colds and the flu become more active. The flu, in particular, can be more severe than a common cold, leading to complications such as pneumonia, especially in vulnerable populations like the elderly and those with pre-existing health conditions. Symptoms include a runny nose, sore throat, coughing, fever, and body aches.
Covid-19: As per the World Health Organization, Coronavirus disease or COVID-19 is an infectious disease caused by the SARS-CoV-2 virus. Most people infected with this virus will experience mild to moderate respiratory illness and recover without requiring special treatment, However, there could be some cases of seriously ill patients who may require medical attention. It is also because of the other existing medical conditions like cardiovascular diseases, diabetes, chronic respiratory diseases, cancers, or older age.
The best way to protect against this virus is by following social isolation form those who are infected, using mask to prevent droplets from infecting others when you cough or sneeze and to wash your hands for 20 seconds frequently.
RSV or Respiratory Syncytial Virus: As per the Centers of Diseases Control and Prevention (CDC), RSV is a common respiratory virus that infects nose, throat and lungs. Though symptoms are similar to the viruses like flu or COVID-19, the disease in itself is different. It also peaks during the winter season, especially between December and January.
However, the main difference between RSV and other respiratory illness, above mentioned is that RSV can cause pneumonia or bronchiolitis, especially for those who are over the age of 50 or with an existing heart or lung disease.
Norovirus: It is a number 1 cause of foodborne illness in the US and this happens when virus gets into the food and then it accidentally enters your mouth. These particles are from faeces or vomit from infected people, or can be transmitted via contaminated food and water. It could also spread by touching unclean surfaces like door handles or cutlery.
For most people, having norovirus is unpleasant, but mild and recovery could be made in 1 to 2 days. However, it could be more serious for babies, older people and anyone with any existing health condition.
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The potential benefits of Ivermectin and Mebendazole, two anti-parasitic drugs, for cancer treatment have sparked a debate.
A recent real-world study stated that an astonishing 84.4% clinical benefit rate was reported among cancer patients who took these two drugs together. But the number does not mean that 84% of the patients improved with the help of thesedrugs. The findings come with significant limitations.
Published in Anticancer Research in June 2026, the study followed 197 cancer patients who had been prescribed ivermectin and mebendazole off-label through a US telemedicine platform.
The patients received compounded capsules containing 25 mg of ivermectin and 250 mg of mebendazole. But only 122 patients, or 61.9%, completed the six-month follow-up.
Among those who completed follow-up, 48.4% of the patients had no tumour regression or no sign of the disease. Another 36.1% showed no change, while in 15.6% of the patients, the disease had progressed. This generated the study's 84.4% Clinical Benefit Ratio.
So, the number should not be interpreted as 84% of patients had their cancer tumours shrink or the disease disappeared.
The researchers also reported that 25.4% of participants faced side effects, most of which were mild and mainly gastrointestinal.
It is also important to note that patients were also receiving other treatments, including chemotherapy, radiation, and surgery, while nearly half reported using supplements. Many also made changes to their diets.
Also read: Daraxonrasib: New Drug Approved For Pancreatic Cancer Shows Promise In Lung Cancer Treatment
This was a prospective observational study, not a randomised controlled clinical trial. There was no comparison group receiving standard treatment or a placebo.
The cancer results were also self-reported through digital surveys rather than independently verified as part of the study.
That makes it impossible to determine whether ivermectin and mebendazole caused the reported improvements.
Patients were also receiving other cancer treatments and making changes to their diets or taking supplements. These factors could have influenced the outcomes.
PubMed currently carries an 'Expression of Concern' for the paper, dated June 9, 2026. The study's own authors describe their findings as “hypothesis-generating” and say randomized controlled trials are needed.
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Researchers are also exploring whether ivermectin can be delivered to brain tumours through the nose.
In a study in rats with glioma, ivermectin packed inside tiny nanocapsules and given through the nose reduced tumour size after 10 days.
The nano-formulation performed better than regular ivermectin, while another silica-based formulation did not have the same effect on the rats.
The idea is to use the nose as a possible route to help drugs reach the brain, where the blood-brain barrier can make drug delivery difficult.
However, this was an animal study. The results therefore show a potential research direction, not definite evidence that nasal ivermectin can treat brain cancer in humans.
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A 2025 case series described three people with advanced breast, prostate and melanoma cancers who self-administered fenbendazole alongside other treatments. The report described complete or near-complete remissions.
However, that paper was subsequently retracted in January 2026. PubMed now lists the retraction, making the original case series unsuitable as reliable evidence that fenbendazole treats cancer.
The study provides possible cancer treatment options that can be investigated treatment as they are not proven yet.
A 2025 review highlighted several possible anticancer mechanisms for ivermectin, including effects on YAP1, Wnt/TCF and AKT/mTOR signalling, oxidative stress and apoptosis.
But the review also noted that the human cases it examined were not designed to test ivermectin as a cancer treatment. So as of now, there is no robust clinical evidence that says ivermectin, mebendazole or fenbendazole as effective cancer treatments.
For cancer patients, these drugs should not be substituted for established treatment on the basis of these studies alone.
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A cancer drug that was approved in the US just last week for pancreatic cancer is also showing promise in lung cancer treatment.
The drug, daraxonrasib (Rasonque), showed encouraging results in patients with previously treated RAS-mutant non-small cell lung cancer (NSCLC) in a Phase 1/2 clinical trial led by researchers at The University of Texas MD Anderson Cancer Center. The results were published in the New England Journal of Medicine on September 2.
Rasonque is not approved for lung cancer yet. The new findings are early-stage evidence, and a larger Phase 3 trial is now underway.
Pancreatic cancer is considered one of the most RAS-driven cancers, with more than 90% of patients carrying tumours driven by RAS protein mutations.
RAS mutations are found in about 30% of non-small cell lung cancers, making them among the most common cancer-driving alterations in the disease. Yet, apart from treatments targeting the specific KRAS G12C mutation, patients with other RAS mutations have had few treatment options.
Also read: Daraxonrasib: US FDA Approves Once-Daily Pill for Metastatic Pancreatic Cancer
The most relevant results came from 38 patients with NSCLC who received doses of 160 to 220 mg. These patients had already been treated with chemotherapy and immunotherapy but had not received docetaxel.
The tumours shrank in about 42% of patients. The duration of response was 11.5 months, while progression-free survival was 8.3 months and overall survival was 16 months.
For comparison, earlier studies of docetaxel in this treatment setting have reported response rates of around 9% to 14%, with progression-free survival of roughly 3 to 4.5 months.
As these results come from a small, early-stage study and are not a comparison with docetaxel, they need to be interpreted further cautiously.
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David Hong, M.D., deputy chair of Investigational Cancer Therapeutics at MD Anderson and the study's lead investigator, said, “Immunotherapy has improved outcomes for many patients with non-small cell lung cancer, but the majority of these cancers eventually progress.”
“At that point, the few treatment options available to these patients often have modest clinical benefit and substantial toxicities, so these early results are encouraging.”
The drug did cause side effects. At the Phase 3-selected dose, 51% of patients experienced a grade 3 or higher adverse event, while 71% required dose modifications and 10% discontinued treatment. Rash was particularly common, affecting 90% of patients, while diarrhoea, nausea and vomiting were also reported.
Hong noted that “the toxicities are largely manageable compared to the alternatives available.”
The interesting development comes shortly after the US FDA approved Rasonque on August 26, 2026. It is first targeted therapy in this new class for metastatic pancreatic adenocarcinoma.
In a 500-patient pancreatic cancer trial, median overall survival was 13.2 months with daraxonrasib versus 6.7 months with standard chemotherapy. Similar RAS-targeting drugs are now being developed by other companies for pancreatic, lung and colon cancers.
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The Pentagon has implemented a new policy requiring US service members aged 30 and older to undergo annual testosterone screening. The hormone is often associated with ageing, muscle and sexual health.
The policy, announced by US Defense Secretary Pete Hegseth in July, is meant to identify testosterone deficiency and assess whether it could affect the health and performance of service members. The latest Pentagon guidance means the screening is now set to begin immediately.
But being over 30 automatically does not mean you need to get your testosterone levels checked. Medical guidelines generally distinguish between simply having a low testosterone reading and having clinically significant testosterone deficiency.
Testosterone levels naturally change with age, but a lower reading does not automatically mean a person has a hormone disorder.
The Endocrine Society recommends diagnosing hypogonadism only when a man has symptoms or signs consistent with testosterone deficiency as well as consistently low testosterone levels. It also recommends confirming a low result with a repeat morning fasting testosterone test.
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Possible symptoms of low testosterone include:
Poor sleep, obesity, stress, medications and other medical conditions can also contribute to fatigue, low libido or changes in physical performance. That is why a blood test alone should not be used to diagnose the condition.
This is where the Pentagon's approach differs from conventional clinical practice. The Endocrine Society's guideline recommends against routine screening of men in the general population for hypogonadism. Instead, testing is generally considered when symptoms and clinical circumstances suggest testosterone deficiency.
That distinction has sparked questions from doctors about the evidence behind universal screening of military personnel aged 30 and above.
According to Reuters, four of six doctors consulted questioned whether there was strong evidence that testing every service member in this age group would improve combat readiness.
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The Endocrine Society also recommends evaluating the underlying cause of low testosterone before treatment. That is important because testosterone levels can sometimes be affected by an underlying illness or other reversible factors.
The symptoms, repeated hormone measurements and the reason behind the low level of testosterone play a key role in deciding whether someone actually has testosterone deficiency and needs treatment.
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