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The current measles outbreak has gripped US states like Texas and New Mexico leaving people worried whether it would become a new pandemic. According to the Texas Department of State Health Services as of February 21, 90 cases were diagnosed in the last month in the South Plains area, with at least 77 of them were reported in children and teens under 17.
Measles is highly contagious and can be deadly. The outbreak, which started spreading in late January, has resulted in multiple hospitalizations, with at least nine confirmed cases and three probable cases as of early February. Health officials caution that at least one in five infected individuals will have to be hospitalized, highlighting the severity of the situation.
Misinformation surrounding vaccines and with the new Trump administration anti-vaccine campaigs, has causing parents to hesitate or refuse vaccination.
Furthermore, the country down under Australia is also witnessing a surge in measles cases as health officials in Sydney have issued an urgent alert, urging residents to watch for measles symptoms after an infected individual visited several places in Sydney over the last seven days.
Authorities report that the traveller had returned from South East Asia where there are ongoing outbreaks of measles.
Key symptoms of measles include fever, a runny nose, sore eyes, and a cough. Typically, a red, blotchy rash appears three to four days later, spreading from the head down to the body. Symptoms can manifest between 7 and 18 days after exposure.
Anyone who experiences these symptoms after potential exposure should immediately contact their doctor or emergency department. It is crucial to call ahead before visiting to avoid potentially exposing others in the waiting room. Dr. Selvey also highlighted that ongoing measles outbreaks are occurring in various parts of the world, making awareness and prompt action essential.
According to CDC everyone should get the MMR vaccine. It protects you from measles, mumps, and rubella. Getting vaccinated helps stop these diseases from spreading. There are two safe MMR vaccines available. They work the same way, so it doesn't matter which one you get. Kids can also get a shot that protects against chickenpox too, but this is only for children.
All children should get two MMR shots. The first shot should be given when they are between 12 and 15 months old. The second shot should be given when they are between 4 and 6 years old. If needed, the second shot can be given earlier, but it must be at least 28 days after the first shot.
Students going to college or other schools after high school, need two shots if they are not already immune. The shots must be at least 28 days apart.
Most adults need at least one MMR shot. Some adults need two shots, especially those who work in healthcare, travel a lot, or go to college. These people should get two shots, with 28 days between them.
Anyone traveling to other countries should make sure they are protected. Babies 6 to 11 months old should get one shot before traveling. Kids 12 months and older, teens, and adults need two shots, with 28 days between them.
People who work in healthcare should have proof that they are immune to measles, mumps, and rubella. If they are not immune, they need two MMR shots, spaced 28 days apart.
Women who might get pregnant should talk to their doctor about the MMR vaccine. It's safe to get the shot while breastfeeding.
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The Supreme Court, on Thursday, asked the Centre to form a panel to form statutory regulations against unethical practices by pharmaceutical companies. This includes gift giving, hospitality, and other incentives offered to doctors.
A bench of Justices Vikram Nath and Sandeep Mehta issued the direction while hearing a petition seeking stronger regulation of pharmaceutical marketing practices.
The court wants the committee to recommend whether, and how, the unethical interactions between pharmaceutical companies and doctors should be brought under a legally enforceable framework.
The matter will resume in court on January 29, 2027, when the Centre is expected to show compliance with the directions.
The court's order follows earlier concerns about whether the existing system is equipped to prevent unethical pharmaceutical marketing.
Justice Sandeep Mehta, reading out the order, said, “We have directed the Union of India to constitute the committee and give its recommendations in terms of our previous directives and observations.”
The committee will examine the representations received and make recommendations to the Union government on the need for statutory regulation.
The Court had reserved order after Solicitor General Tushar Mehta informed the Court that the Union government is to form a three-member committee to assess whether a statutory framework is needed to regulate unethical practices by pharmaceutical companies.
The case was filed by the Federation of Medical and Sales Representatives' Associations of India (FMRAI), which has sought accountability for alleged practices such as expensive gifts, foreign trips, hospitality and other benefits used to promote medicines to doctors.
It said, “This has led to over-prescription of drugs resulting in a serious infringement of the right to life and the right to health of the citizens.”
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Pharmaceutical companies use various marketing strategies to promote their products to healthcare professionals. These can include gifts, hospitality, sponsored travel, benefits related to conference and other promotional incentives.
The concern before the Supreme Court is not just an ordinary interaction between drug companies and doctors, but whether financial or material incentives can unethically influence drug-prescribing decisions.
India already has the Uniform Code for Pharmaceutical Marketing Practices (UCPMP), 2024, which lays down rules concerning gifts, physician samples, brand reminders, continuing medical education and other promotional activities. However, questions remain over whether the framework has adequate statutory regulation.
The Centre has previously said the UCPMP is functioning, but agreed that the question of giving pharmaceutical marketing regulation statutory backing should be examined separately.
The Centre, in its response, said, “The Department of Pharmaceuticals has issued the Uniform Code for Pharmaceutical Marketing Practices (UCPMP), which is applicable to Pharmaceutical Companies, medical representatives and agents.” The code clearly prohibits pharmaceutical companies from offering gifts, travel facilities, hospitality, cash or monetary grants to physicians or their family members, it added.
The biggest concern is that a prescribing decision could become influenced by factors other than clinical need, evidence, safety, and cost. If incentives influence prescribing, patients could potentially face:
These concerns have previously been raised before the Supreme Court in relation to alleged pharmaceutical marketing practices. The issue, therefore, goes beyond ethics for patients. The doctor-pharma relationship can directly affect what medicine a patient receives, how long they take it, and how much they pay.
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Artificial intelligence (AI) is moving deeper into biological research, with Meta, Google DeepMind, the US government and other partners backing a $1.8 billion effort to build AI-ready biological datasets and predictive models of life that could help scientists better understand, predict and treat diseases.
Mark Zuckerberg and Priscilla Chan-backed nonprofit Biohub first announced the Virtual Biology Initiative in April 2026 with a $500 million commitment.
The five-year effort aims to generate large-scale, multimodal biological data that could help scientists develop AI models capable of predicting how cells respond to different interventions — potentially accelerating disease research, drug discovery and the development of new treatments.
The initiative has now expanded through partnerships involving the US Department of Energy, National Institutes of Health, Meta, Google DeepMind and Isomorphic Labs, bringing the total commitment to $1.8 billion.
“An accurate predictive model of biology could dramatically accelerate scientific discovery by enabling scientists to perform experiments digitally. The insights that come from this could unlock a far greater understanding of disease and open up completely new paths for cures,” said Biohub Head of Science Alex Rives.
“Because of this potential, the creation of a virtual cell is one of the most important challenges for the next era of science. It will require coordinated data generation efforts at a national and international scale, which is why these partners are coming together. We invite the worldwide scientific community to join us in this project,” he added.
Also read: Anthropic, OpenEvidence Expand Clinical AI Globally: WHO Warns of Ethics Risks
The Virtual Biology Initiative aims to coordinate biological data generation across institutions and scientific disciplines, creating open, AI-ready datasets that can support predictive models of life.
The broader goal is to build increasingly accurate models of the complex workings of cells, allowing scientists to investigate biological mechanisms and understand how diseases develop. Such models could allow researchers to ask and test questions digitally at a scale and speed that would be difficult to achieve through laboratory experiments alone.
If successful, the approach could help accelerate scientific discovery, identify potential biological targets and support the development of therapies for complex diseases.
Of that commitment, $400 million supports technologies designed to expand what scientists can measure, including cryo-electron tomography to resolve near-atomic details inside cells, microscopy capable of imaging millions to billions of cells in living tissue, and engineering tools to build and perturb biology at molecular, cellular, tissue and whole-organism levels. A further $100 million supports research outside Biohub.
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France is reporting a rise in COVID-19 cases as the government prepares to launch its autumn COVID and flu vaccination campaign on October 13. The increase comes as neighboring UK is also reporting higher COVID activity and hospitalizations.
Data from the Réseau Sentinelles and other networks monitored by Santé publique France showed an increase in COVID-19 infections during the week of September 21-27, The Connexion reported.
The estimated number of people with COVID-19 who consulted GPs for acute respiratory infections rose to 13 per 100,000, up from nine the previous week. This translates to around 8,806 new cases, compared with about 6,000 the previous week.
The figures cover only people who consulted a GP, so the actual number of infections could be higher.
Overall, acute respiratory infections reported by GPs rose from 103 to 151 cases per 100,000 people. Rhinoviruses were more common, detected in 40% of samples, compared with 10% for COVID.
Emergency visits for suspected COVID among people aged 15 and older also increased by 22%, or 114 visits. However, hospital admissions following emergency visits remained stable and overall COVID activity remained at a low level.
"As always, it's not the patient's interest that counts, but that of the system," said Jérôme Marty, a GP in southern France, according to Franceinfo. Marty said he had been seeing a steady stream of COVID patients in recent weeks.
Also read:‘American Covid’ Strain Drives 50% Surge in UK Hospital Admissions: XFG Symptoms to Know
The French government has rejected demands from a doctors’ union to bring forward the vaccination campaign.
Marty, who is also president of the UFML doctors’ union, said he was “dismayed” by the decision to start the campaign on October 13.
"There is no public health campaign; people are not reminded to wear a mask when they have symptoms... We are lagging!" he said.
The office of Health Minister Stéphanie Rist said that “indicators do not show a situation justifying the early launch of the campaign.”
Meanwhile, pharmacy groups have raised concerns about vaccine administration supplies. In an open letter to the minister, they warned that multi-dose vaccine vials require suitable syringes and needles, which pharmacists must now purchase themselves.
The groups called for sufficient supplies and financial coverage and urged greater use of pre-filled syringes in future campaigns.
Read More: COVID-19 May Raise Risk of 6 Allergic Conditions, Study Finds
For autumn 2026, France will use the monovalent Comirnaty XFG vaccine.
COVID vaccination is particularly recommended for people at higher risk of severe disease, including those aged 65 and over, pregnant women, people with weakened immune systems and those with certain chronic conditions.
The 30-microgram dose is for people aged 12 and older, while the 10-microgram dose is for children aged 6 months to 11 years.
In England, COVID activity increased in the week to September 20. Hospital PCR positivity rose from 5.9% to 7.0%, while hospital admissions increased from 0.81 to 1.20 per 100,000 people. Overall activity remained low.
In the US, CDC data from September 29 showed cases rising in some states while falling or remaining stable in others.
XFG is a recombinant SARS-CoV-2 variant formed from Omicron subvariants LF.7 and LP.8.1.2. The WHO records the earliest documented XFG sample on January 27, 2025, and designated it a variant under monitoring in June 2025.
The variant has since been detected in multiple countries and remains among the SARS-CoV-2 variants being monitored by WHO.
What Are the Symptoms of XFG?
COVID symptoms can vary between individuals. Reported symptoms associated with the current circulation of XFG include:
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