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FDA, Covid-19 and vaccine

FDA requires Covid vaccine makers to expand warning about risk of rare heart inflammation

The US Food and Drug Administration will now require Covid-19 vaccines from Pfizer/BioNTech and Moderna to use expanded warning labels with more information about the risk of a rare heart condition after vaccination.

CBS News on MSN · 16h

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

The Food and Drug Administration says it has decided to continue approving COVID-19 vaccine updates for seniors and others at higher risk of severe disease, but will require vaccine makers to conduct major new clinical trials before approving them for wider use.

STAT · 14h

Five burning questions on the FDA’s new Covid-19 vaccine framework

But the framework has perhaps created as much confusion as clarity. Broadly, the FDA said it will limit approval of Covid-19 vaccines to people 65 and older and to those at risk for severe Covid outcomes, and will require vaccine makers to conduct clinical trials investigating whether the shots benefit healthy adults and children.

FDA announces cucumber recall

AOL · 8h

FDA Warns Consumers "Do Not Eat" Recalled Cucumbers in These 15 States

Bedner Growers and Fresh Start Produce Sales Inc. have issued a recall on their cucumbers due to the presence of Salmonella, which has hospitalized nine so far.

NBC New York · 1d

FDA recalls cucumbers due to multistate Salmonella outbreak sickening over 20 people

The U.S. Food and Drug Administration said the cucumbers were distributed in 15 states, including Florida and New York.

WSLS 10 · 14h

FDA recalls whole cucumbers linked to Salmonella outbreak

The U.S. Food and Drug Administration has announced a recall of whole cucumbers linked to a multistate outbreak of Salmonella infections.

FDA Clears 1st Blood Test to Diagnose Alzheimer’s Disease

People on MSN · 13h

FDA Clears First Blood Test to Diagnose Alzheimer’s Disease

The blood test is nearly 92% as accurate as a PET scan or spinal tap in detecting patients with Alzheimer’s The FDA greenlit marketing for the first blood test to help diagnose Alzheimer’s disease The test measures two proteins,

NPR · 12h

First FDA-cleared Alzheimer's blood test could make diagnoses faster, more accurate

The first Alzheimer's blood test cleared by the Food And Drug Administration is poised to change the way doctors diagnose and treat the disease.

scmp.com · 1d

First blood test to diagnose Alzheimer’s disease to be available in US starting late June

The test will initially be available at about 50 American research institutes and hospitals that specialise in Alzheimer’s disease, said the head of Fujirebio Holdings.

13hon MSN

FDA issues warning about popular allergy medications

The FDA warns that longtime users of popular allergy medications may experience "severe itching" after stopping use.

13h

Trump FDA Reveals Canada Will Play Major Role In Bringing Drug Prices Down

The Food and Drug Administration (FDA) announced Wednesday plans to help states and Indian tribes import cheaper prescription ...

FDA Commissioner Makary Cites Real Clear Journal Article At Panel On Talc In The American Food Supply

"Expert Panels with the FDA" are a series of roundtable discussions to provide an open public discourse on the latest medical and scientific information on several important topics. At this roundtable ...

1don MSN

Food and Drug Administration lays out new requirements for annual COVID-19 vaccines

Under a new policy announced Tuesday by the Trump administration, only people age 65 and older and children or young adults ...

STAT1d

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 ...

The FDA Is Replacing Synthetic Food Dyes, and These 3 Just Got the Green Light

The FDA is embracing natural colorants, with three approvals meant to replace synthetic dyes. Galdieria extract, butterfly ...

3dOpinion

Lisa Jarvis: FDA appointee is a drug critic with a lot to prove

The gravity of these decisions calls for a degree of humility on the part of an FDA leader. And that’s the rub with Vinay ...

Pharmaceutical Technology on MSN6d

FDA awards cancer drug approvals to AbbVie and MSD

The FDA has approved MSD’s Welireg for rare adrenal tumours, and AbbVie’s Emrelis for treating c-Met+ lung cancer patients.

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