logo
Influenza rates are 'very high' in Indiana. How to protect yourself

Influenza rates are 'very high' in Indiana. How to protect yourself

Yahoo12-02-2025

Indiana is seeing "very high" rates of influenza activity in emergency rooms and primary care offices across the state, as national cases of influenza hit a 15-year high.
Influenza rates in Indiana jumped from high to very high Tuesday, according to Indiana Department of Health data. Indiana's influenza uptick is in line with activity in other states as flu season hits its seasonal peak, said state epidemiologist Eric Hawkins.At the same time, other respiratory viruses — like respiratory syncytial virus (RSV), the common cold and coronavirus —are also circulating.
Most pharmacies have at-home tests available to test for the flu and coronavirus. However, other respiratory illnesses, such as RSV, require testing at a primary or urgent care office.
But this week has been one of the highest influenza peaks since the coronavirus pandemic.
Elderly patients and infants are among the most vulnerable patients. Indiana has recorded 57 influenza-related deaths this season as of Tuesday, with people over the age of 65 accounting for 41 of the deaths.
No Indiana infants under the age of four have died from influenza this year, according to IDOH.
In the past week, 13% of children under four years old visiting the emergency room presented signs of influenza, based on state data collected from 119 hospital emergency rooms and 23 urgent care centers.
"Right now, the important thing is it's respiratory season, so we have lots of things circulating, and the reason we have this information out there is to make people aware that there are things that they can do to prevent illness and respiratory illnesses," Hawkins said.
Influenza or flu typically presents with a high fever (over 100 degrees) accompanied by a cold or sore throat. Influenza spreads through person-to-person interactions, usually when a sick person coughs, sneezes or talks.
Vaccines can prevent severe infections and medical complications from the flu, said Dr. John Christenson, associate medical director of pediatric infection prevention at Riley Hospital for Children.
It's not too late for patients to receive the flu vaccine from a pharmacy or primary care provider, Christenson said. The vaccine takes up to 10 days to take effect.
"We hope that [parents] consider that influenza is still here and get this flu vaccine, so they can protect their family," Christenson said. "The vaccine is not a perfect vaccine. We've known that for decades. It may not prevent infection, but one thing we are pretty certain of is that the vaccine prevents death and hospitalizations."
Those who are elderly, immunocompromised or under the age of four can develop severe complications with influenza. If parents notice children having difficulty breathing or not taking enough food or fluids, they should seek additional medical care, Christenson said.
Even those vaccinated can still catch influenza. People can protect themselves and others with the "three C's," Hawkins said: cleaning hands and surfaces regularly; covering one's mouth when coughing; and containing the virus by staying home if ill.
"It does fluctuate and go up and down, but the take home message here with influenza always around is, what are the things you could do to prevent illness? And I think that's one thing that we can help with," Hawkins said.
Flu season runs from October to May, with peaks varying year to year. Doctors expect flu activity to start to decrease in March.
Flu rates reached unusual lows in the 2020-21 winter season due to widespread masking. However, in the last three years, flu rates in the colder months have ticked back up.
More: Flu has officially hit a second high in the US: Know the symptoms
The flu and COVID-19 have several symptoms in common. Here's how to tell the difference between the two viruses:
Alysa Guffey covers business and development for IndyStar. Have a story or tip? Contact her at amguffey@gannett.com.
This article originally appeared on Indianapolis Star: Flu rates are 'very high' in Indiana. How to prevent catching irus

Orange background

Try Our AI Features

Explore what Daily8 AI can do for you:

Comments

No comments yet...

Related Articles

EMA Accepts GSK's Filing for Expanded Use of RSV Vaccine Arexvy
EMA Accepts GSK's Filing for Expanded Use of RSV Vaccine Arexvy

Yahoo

timea day ago

  • Yahoo

EMA Accepts GSK's Filing for Expanded Use of RSV Vaccine Arexvy

GSK plc GSK announced that the European Medicines Agency (EMA) has accepted the regulatory application seeking approval to expand the use of its adjuvanted recombinant respiratory syncytial virus (RSV) vaccine, Arexvy, for use in adults aged 18 years and above. With the EMA accepting the application for review, a final decision from the regulatory body in Europe is expected in the first half of 2026. Arexvy is currently approved for the prevention of lower respiratory tract disease ('LRTD') caused by RSV in all individuals aged 60 years and above, as well as for high-risk individuals aged 50-59 years. GSK is currently seeking approval for the expanded use of Arexvy in adults aged 18 years and above in the United States and Japan. Year to date, shares of GSK have risen 20.8% against the industry's decline of 0.6%. Image Source: Zacks Investment Research Arexvy was the first RSV vaccine for older adults to be approved anywhere in the world. However, sales of the vaccine have been lukewarm, mainly due to the revised recommendations for RSV vaccinations issued by the Advisory Committee on Immunization Practices ('ACIP') in June 2024. In June, the ACIP recommended the use of Arexvy for all adults aged 75 years and above. However, for adults aged 60-74 years, the ACIP recommended the vaccine only for those who are at increased risk of severe RSV disease. Arexvy generated sales worth £78 million in the first quarter of 2025, down 57% year over year due to lower demand in the United States. Pfizer's PFE Abrysvo is approved for the prevention of RSV-associated LRTD in all individuals aged 60 years and above, as well as in infants, through maternal immunization. PFE's Abrysvo is also approved for use in high-risk adults aged 18-59 years in the United States and Europe. Earlier this year, the ACIP recommended the expanded use of Arexvy and Abrysvo for use in adults aged 50-59 years who are at high risk for severe RSV disease. The updated ACIP recommendation lowers the recommended age for RSV vaccination from 60 years to 50 years for high-risk adults. The ACIP's recommendation is pending final approval by the director of the U.S. Centers for Disease Control and Prevention ('CDC') and the Department of Health and Human Services. Moderna's MRNA RSV vaccine, mResvia, was approved last year by the FDA and the European Commission to prevent RSV-LRTD in older adults aged 60 years and above. Last week, the FDA approved MRNA's mResvia for use in high-risk adults aged 18-59 years. Moderna is also working on expanding the vaccine's use in pediatric populations. We note that RSV vaccine sales have been weak across the industry for the 2024-2025 vaccination season due to the restrictive recommendation issued by the U.S. CDC last year for individuals in the 60-74 age bracket. mResvia generated sales worth $2 million during the first quarter of 2025, while sales of Pfizer's RSV vaccine, Abrysvo, fell 9% year over year to $131 million. GSK currently carries a Zacks Rank #2 (Buy). You can see the complete list of today's Zacks #1 Rank (Strong Buy) stocks here. Want the latest recommendations from Zacks Investment Research? Today, you can download 7 Best Stocks for the Next 30 Days. Click to get this free report GSK PLC Sponsored ADR (GSK) : Free Stock Analysis Report Pfizer Inc. (PFE) : Free Stock Analysis Report Moderna, Inc. (MRNA) : Free Stock Analysis Report This article originally published on Zacks Investment Research ( Zacks Investment Research Error in retrieving data Sign in to access your portfolio Error in retrieving data Error in retrieving data Error in retrieving data Error in retrieving data

New CDC advisers will skip some expected topics and explore a target of antivaccine activists

time2 days ago

New CDC advisers will skip some expected topics and explore a target of antivaccine activists

U.S. Health Secretary Robert F. Kennedy Jr.'s new vaccine advisers meet next week, but their agenda suggests they'll skip some expected topics — including a vote on COVID-19 shots — while taking up a longtime target of anti-vaccine groups. The Advisory Committee on Immunization Practices makes recommendations on how to use the nation's vaccines, setting a schedule for children's vaccines as well as advice for adult shots. Last week, Kennedy abruptly dismissed the existing 17-member expert panel and handpicked eight replacements, including several anti-vaccine voices. The agenda for the new committee's first meeting, posted Wednesday, shows it will be shorter than expected. Discussion of COVID-19 shots will open the session, but the agenda lists no vote on that. Instead, the committee will vote on fall flu vaccinations, on RSV vaccinations for pregnant women and children and on the use of a preservative named thimerosal that's in a subset of flu shots. It's not clear who wrote the agenda. No committee chairperson has been named and the U.S. Department of Health and Human Services did not comment. Missing from the agenda are some heavily researched vaccine policy proposals the advisers were supposed to consider this month, including shots against HPV and meningococcal bacteria, said Dr. Susan Kressly, president of the American Academy of Pediatrics. Instead, the committee is talking about subjects 'which are settled science,' she said. 'Every American should be asking themselves how and why did we get here, where leaders are promoting their own agenda instead of protecting our people and our communities,' she said. She worried it's "part of a purposeful agenda to insert dangerous and harmful and unnecessary fear regarding vaccines into the process.' The committee makes recommendations on how vaccines that have been approved by the Food and Drug Administration should be used. The recommendations traditionally go to the Centers for Disease Control and Prevention director. Historically, nearly all are accepted and then used by insurance companies in deciding what vaccines to cover. But the CDC has no director and the committee's recommendations have been going to Kennedy. Thimerosal was added to certain vaccines in the early 20th century to make them safer and more accessible by preventing bacterial contamination in multi-dose vials. It's a tiny amount, but because it's a form of mercury, it began raising questions in the 1990s. Kennedy — a leading voice in an antivaccine movement before he became President Donald Trump's health secretary — has long held there was a tie between thimerosal and autism, and also accused the government of hiding the danger. Study after study has found no evidence that thimerosal causes autism. But since 2001, all vaccines manufactured for the U.S. market and routinely recommended for children 6 years or younger have contained no thimerosal or only trace amounts, with the exception of inactivated influenza vaccine. Thimerosal now only appears in multidose flu shot vials, not the single-shot packaging of most of today's flu shots. Targeting thimerosal would likely force manufacturers to switch to single-dose vials, which would make the shots 'more expensive, less available and more feared,' said Paul Offit, a vaccine expert at Children's Hospital of Philadelphia. Last week, 30 organizations called on insurers to continue paying for COVID-19 vaccines for pregnant women after Kennedy said the shots would no longer be routinely recommended for that group. Doctors' groups also opposed Kennedy's changes to the vaccine committee. The new members he picked include a scientist who researched mRNA vaccine technology and became a conservative darling for his criticisms of COVID-19 vaccines, a top critic of pandemic-era lockdowns and a leader of a group that has been widely considered to be a source of vaccine misinformation. The American Academy of Pediatrics has long put out its own immunization recommendations. In recent decades it has matched what the government recommended. But asked if they might soon diverge, depending on potential changes in the government's vaccination recommendations, Kressly said; 'Nothing's off the table.' 'We will do whatever is necessary to make sure that every child in every community gets the vaccines that they deserve to stay healthy and safe,' she said. ___ The Associated Press Health and Science Department receives support from the Howard Hughes Medical Institute's Department of Science Education and the Robert Wood Johnson Foundation. The AP is solely responsible for all content.

Expert Warns of Health Crisis After CDC Resignation
Expert Warns of Health Crisis After CDC Resignation

Buzz Feed

time2 days ago

  • Buzz Feed

Expert Warns of Health Crisis After CDC Resignation

If the policies of Health Secretary Robert F. Kennedy Jr. aren't reversed, 'a lot of Americans are going to die as a result of vaccine-preventable diseases.' Unfortunately, that quote is not attributable to Chicken Little. Instead, it's the opinion of Dr. Fiona Havers, formerly a top scientist at the Centers for Disease Control and Prevention, who resigned from the agency Monday. In her first interview after leaving, Havers told the New York Times that Kennedy's attacks on science and how science is conducted will have dire consequences. 'It's a very transparent, rigorous process, and they have just taken a sledgehammer to it in the last several weeks,' she said. 'CDC processes are being corrupted in a way that I haven't seen before.' At the CDC, Havers oversaw the team that collects data on COVID-19 and RSV hospitalizations and helped craft national vaccine policy. In a goodbye email to her colleagues that was seen by Reuters, Havers said she no longer had confidence that her team's output would 'be used objectively or evaluated with appropriate scientific rigor to make evidence-based vaccine policy decisions.' Kennedy's attacks on vaccination, coupled with the shocking firing of all 17 members of the Advisory Committee for Immunization Practices earlier this month, helped persuade her to go. The health secretary has since named eight replacements to the influential panel. Among them are a scientist who criticized COVID-19 vaccines, a critic of pandemic-era lockdowns and another person the Associated Press described as 'widely considered to be a leading source of vaccine misinformation.' 'I could not be party to legitimizing this new committee,' Havers told the Times. 'I have utmost respect for my colleagues at CDC who stay and continue to try and limit the damage from the inside,' she added. 'What happened last week was the last straw for me.' Asked to respond to the concerns Havers raised in her resignation email, a Department of Health and Human Services spokesperson told CBS that 'under Secretary Kennedy's leadership, HHS is committed to following the gold standard of scientific integrity. Vaccine policy decisions will be based on objective data, transparent analysis, and evidence – not conflicts of interest or industry influence.' HuffPost.

DOWNLOAD THE APP

Get Started Now: Download the App

Ready to dive into a world of global content with local flavor? Download Daily8 app today from your preferred app store and start exploring.
app-storeplay-store