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FDA, COVID

FDA tightens requirements for COVID vaccine, adding trials for healthy adults

The U.S. Food and Drug Administration on Tuesday said it plans to require new clinical trials for approval of annual COVID-19 boosters for healthy Americans under age 65, effectively limiting them to older adults and those at risk of developing severe illness.

USA TODAY on MSN · 5h

FDA sets new COVID booster guidelines for healthy adults under 65

The FDA plans to require new clinical trials for approval of annual COVID-19 boosters for healthy Americans under 65.

The Associated Press on MSN · 14h

FDA sets new requirements for COVID vaccines in healthy adults and children

Federal health officials will no longer routinely approve annual COVID-19 shots for younger adults and children who are healthy

FDA, cucumber and salmonella

UPI on MSN · 12h

FDA says Florida cucumbers linked to salmonella outbreak in 15 states

FDA officials have warned the American public to not eat, sell or serve cucumbers grown and distributed by two Florida companies after a salmonella outbreak in more than a dozen states.

NBC News · 15h

Cucumbers recalled after more than 20 people are sickened in Salmonella outbreak

The Food and Drug Administration announced a recall of cucumbers grown by Bedner Growers and distributed by Fresh Start Produce Sales because of a multistate Salmonella outbreak that has sickened more than 20 people.

Yahoo · 9h

Cucumbers Recalled Due to Salmonella Outbreak in 15 States, FDA Warns

Common symptoms of salmonella infection include fever, diarrhea, nausea, vomiting, and abdominal pain. If you have cucumbers in your refrigerator, it is advised that you dispose of them immediately. The U.

1st Blood Test to Diagnose Alzheimer’s Cleared by FDA

Richmond · 1d

FDA OKs first blood test that can help diagnose Alzheimer's disease

The test can aid doctors in determining whether a patient's memory problems are due to Alzheimer's or a number of other medical conditions that can cause cognitive difficulties.

MarketWatch · 9h

Global Alzheimer's Platform Foundation Applauds FDA Authorization of the First Blood-Based Diagnostic Test for Assessing Alzheimer's Disease

Hermes-001, played a principal role in the dataset used to support Fujirebio's FDA application for clearance of the first groundbreaking blood based IVD available for the diagnosis of Alzheimer's Disease (AD).

ABC7 San Francisco · 1d

FDA clears 1st blood test to help diagnose Alzheimer's disease

The test is for those aged 55 and older who are already exhibiting signs and symptoms of the disease, the FDA says.

13hon MSN

Who can get updated COVID vaccines this fall? FDA will OK for high-risk groups, calls for new clinical trials

"The FDA will approve vaccines for high-risk persons and, at the same time, demand robust, gold-standard data on persons at ...

14hon MSN

FDA to limit future Covid-19 shots to older people and those at risk of serious infection

The US Food and Drug Administration is changing the way it approves Covid-19 vaccines for Americans — a move that will limit ...

STAT12h

FDA will limit Covid vaccines to people over 65 or at high risk of serious illness, leaders say

The FDA announced it will limit access to Covid-19 vaccines going forward to people 65 and older and others at high risk of ...

15hon MSN

FDA to limit covid shot approval to elderly, those with medical conditions

The agency will narrow its approval for updated coronavirus vaccines, marking a significant shift in the agency’s approach to ...

12hon MSN

US FDA advisers to consider if new COVID shots should target LP.8.1 subvariant

Advisers to the U.S. Food and Drug Administration will discuss recommendations for updated COVID-19 vaccines ahead of the ...

1don MSN

Baked bean recall update as FDA sets highest risk level

Nearly 4,500 cases were pulled from shelves in 23 states after it was found that the affected cans had been mislabeled.

STAT17h

Pharmalittle: We’re reading about FDA eyeing PDUFA changes, compounded weight loss drugs, and more

Online weight loss company Noom has begun offering smaller doses of compounded versions of Novo Nordisk's Wegovy ...

FDA Launches Postmarket Chemical Review Program to Ensure Food Safety

By Stephanie Brown HealthDay ReporterMONDAY, May 19, 2025 (HealthDay News) -- Last week, the U.S. Food and Drug ...

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FDA, COVID

FDA, cucumber and salmonella

1st Blood Test to Diagnose Alzheimer’s Cleared by FDA

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