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Sunday, feb 16
News
Covid-
19: FDA Advisory Panel Votes To Recommend Moderna Booster For Certain Groups Of People
A US Food and Drug Administration (FDA) advisory panel has endorsed emergency authorization for Moderna’s half-dose COVID-19 vaccine booster shot for certain groups of people. The latest guidance from the feds calls for Moderna booster shots to be administered at least six months following the completion of the two-dose vaccination process for certain groups. Currently, the booster is recommended for people 65 and older and Americans between the ages of 18 and 64 who are immunocompromised and at a greater occupational risk of exposure or severe side effects from the virus. Related story …
News
Covid-
19: Pfizer Asks FDA To Approve Vaccine For Children Ages 5 To 11
Pfizer has officially asked the US Food and Drug Administration (FDA) for emergency use authorization for its COVID-19 vaccine to be administered to children between the ages of 5 and 11. With parents and politicians alike agreeing that keeping children learning in the classroom after a lost year in 2020, Pfizer is pushing to allow its vaccine to be administered among younger Americans. Pfizer tweeted this week that the company had submitted their formal request for Emergency Use Authorization of the vaccine to the FDA. "With new cases in children in the U.S. continuing to be at a high lev…
News
Covid-
19: Don't Use Certain Hand Sanitizers That May Contain Cancer-Causing Chemicals, FDA Says
The US Food and Drug Administration (FDA) is cautioning some Americans against using a certain hand sanitizer that could potentially contain high levels of potentially cancer-causing chemicals. An alert was issued by the FDA this week advising that it found unacceptable levels of benzene, acetaldehyde, and acetal contaminants in certain artnaturals brand scent-free hand sanitizer labeled with “DIST. by artnaturals Gardena, CA 90248.” According to the FDA, consumers should not use any artnaturals hand sanitizer products, saying the company has not replied to the FDA to help identif…
News
Covid-
19: Johnson & Johnson To Seek Authorization For Booster Shot
Johnson & Johnson is seeking federal approval for its COVID-19 booster shots, which could make it the latest to be authorized by the US Food and Drug Administration (FDA). On Monday, Oct. 4, a spokesperson for the pharmaceutical company announced that they were looking to gain approval to begin administering booster shots for its one-dose vaccine. Last month, regulators authorized a booster shot for some recipients of the Pfizer vaccine and are considering authorization this month for recipients of the Moderna vaccine. In total, according to reports, more than 15 million Am…
News
Covid-
19: Drugmaker To Seek Emergency Approval For Pill To Treat Virus
A new pharmaceutical company is throwing its hat in the ring as the country continues its fight against COVID-19. Merck and Ridgeback Biotherapeutics announced on Friday, Oct. 1 that it is planning to apply for federal emergency approval of a pill that can reportedly help prevent hospitalizations and deaths in COVID-19 patients. According to the company, trials have found that the pill - dubbed molnupiravir - could potentially reduce the risk of hospitalization or death in patients with mild to moderate COVID-19 by approximately 50 percent. The results of the late-stage trial have bee…
News
Covid-
19: FDA Likely To Approve Brand-New Time Frame For Booster Shot
The timeline for COVID-19 booster shots may be accelerated as the US Food and Drug Administration (FDA) is expected to approve booster shots for all Americans after six months, not eight, as previously announced. According to reports, as more data is examined by federal health officials, it is more likely that booster shots will be required sooner than later for the Pfizer and Moderna vaccines. Before they can go into arms, the FDA must authorize booster shots for each vaccine. A spokesperson for the agency said that under its general policy it "cannot comment on or confirm the existence" o…
News
Covid-
19: FDA Grants Full Approval For Pfizer Vaccines, With More Mandates Now Expected
The US Food and Drug Administration (FDA) has granted full approval to the Pfizer/BioNTech COVID-19 vaccine for anyone 16 and older. On Monday, Aug. 23, the FDA announced that the Pfizer vaccine has been granted full approval, which is expected to potentially open the door for more COVID-19 vaccine mandates. The Pentagon will mandate vaccines for its 1.4 million active-duty service members, following the FDA approval Monday. United Airlines recently said its employees will be required to show proof of vaccination within five weeks of regulatory approval. Pfizer is the first COVID-1…
Schools
Covid-
19: Increase In Cases Among Children Could Be 'Just The Beginning,' Experts Say
With new COVID-19 infections and hospitalizations threatening to overwhelm hospitals in some parts of the country, officials are cautioning that the rise in cases among children “is just the beginning.” As the new academic year approaches, top US health experts are cautioning that the rise in new COVID-19 cases among children who are still ineligible to get vaccinated is likely to get worse when classes resume. According to the American Academy of Pediatrics (AAP), more than 121,000 new COVID-19 cases were reported in the US among children last week, more than 14 times the weekly number as…
News
Covid-
19: CDC Announces Starting Date For Booster Shots
Federal health officials have set a date for when they plan to begin rolling out COVID-19 booster shots to help curtail the spread of new variants of the virus. Citing new data that showed Pfizer and Moderna vaccines’ effectiveness wanes over time, President Joe Biden’s administration announced that beginning the week of Monday, Sept. 20, booster shots would be made available for many Americans. Earlier story - COVID-19: US Expected To Announce Time Frame For All Americans To Get Booster Shots The Centers for Disease Control and Prevention (CDC) and US Food and Drug Administration (FDA) sa…
News
Hostess Recalls Hot Dog, Hamburger Buns Due To Possible Salmonella, Listeria Contamination
Hostess Brands is recalling certain hamburger and hot dog bun products because they might be contaminated with Salmonella and Listeria monocytogenes. The company said it was made aware of this issue through its co-manufacturer Best Harvest Bakeries' environmental monitoring program, according to an announcement on the US Food and Drug Administration's website on Monday, Aug. 16. Salmonella and Listeria monocytogenes can both cause serious infections among children, senior citizens and those with weakened immune systems. Hostess said the products were sold to distributors, conveni…
News
Covid-
19: US Expected To Announce Time Frame For All Americans To Get Booster Shots
Federal health officials have outlined their plans for when most Americans should get COVID-19 booster shots after becoming fully vaccinated. Pending authorization from the US Food and Drug Administration (FDA), a plan still being developed would advise Americans to get a COVID-19 booster shot eight months after becoming fully vaccinated to help stave off variants of the virus. Both Pfizer and Moderna, two of the three shots currently being administered in the US, have already submitted initial data to the FDA regarding their booster doses of their COVID-19 vaccines and are awaiting appro…
News
Covid-
19: FDA Expected To Authorize Booster Shots For Immunocompromised People
The US Food and Drug Administration is expected to move forward quickly with authorization of COVID-19 booster shots for some Americans who are immunocompromised, according to reports. Health officials said that the third shot of the current two-dose Pfizer and Moderna vaccine could be authorized within the next 48 hours, though no official timetable has been set as variants of the virus and COVID-19 mutations continue to cause a surge in new cases. Before a vaccine can be used in new ways outside existing authorization it requires new approval from the FDA. Currently, the Moderna, Pfizer…
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