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FDA approves 1st flu and COVID-19 combo home test

FDA authorizes 1st over-the-counter combo flu and COVID test outside of emergency use

The FDA has authorized the first over-the-counter combination COVID-19 and flu test outside of emergency use, which delivers results at home in about 15 minutes.

MarketWatch · 19h

FDA Authorizes Marketing of First Home Flu and COVID-19 Combination Test Outside of Emergency Use Authorities

Today, the U.S. Food and Drug Administration granted marketing authorization for the Healgen Rapid Check COVID-19/Flu A&B Antigen Test. The test, authorized for use without a prescription, is for use by individuals experiencing respiratory symptoms and uses a nasal swab sample to deliver at-home results in approximately 15 minutes for COVID-19 and influenza (flu).

Yahoo · 14h

FDA approves first flu and COVID-19 combo home test

The authorization allows individuals to purchase the test over the counter without a prescription. The home test, which checks for the flu and the COVID-19 virus, uses a swab to collect a sample from the nose and gives results in about 15 minutes.

FDA is warning of serious health effects, possibly death

YAHOO!News · 2h

The FDA is warning of serious health effects, possibly death, from a Wisconsin farm's eggs

A recall of eggs from a Wisconsin farm has been upgraded to "Class 1 status," meaning consumers may be at risk of serious health consequences and possibly death, according to the Food and Drug Administration.

USA TODAY on MSN · 11h

FDA upgrades recall of eggs linked to salmonella to 'serious' health risks or 'death'

FOX News on MSN · 17h

Consumers asked to throw away millions of eggs as FDA upgrades recall status to most serious category

The FDA announced that the recall of "Milo’s Poultry Farms" and "Tony’s Fresh Market" has been upgraded to Class I, meaning the eggs may cause serious health issues or death.

Lilly, FDA

FiercePharma · 3h

Compounders sue FDA for removing Eli Lilly's tirzepatide from shortage list

With an estimated 2 million people in the United States taking copycat vers | A compounding industry group has sued the FDA, claiming its action to remove Eli Lilly’s Mounjaro and Zepbound from its drug shortage list is a “reckless and arbitrary decision—lacking any semblance of lawful process.

Hosted on MSN · 21h

Compounding group sues FDA for removing Lilly's weight loss drug from shortage list

A drug compounding industry group on Monday sued the U.S. Food and Drug Administration over its decision to take Eli Lilly’s blockbuster weight loss and diabetes drugs off its list of medicines in short supply last week.

Bloomberg L.P. · 18h

Lilly Weight-Loss Drug Copycat Makers Sue FDA Over Shortage End

A group representing companies that made copycat versions of Eli Lilly & Co.’s weight-loss drugs sued the US Food and Drug Administration over the agency’s decision to remove Lilly’s medications from its shortage list.

Were FDA's 'Black Box' Warnings on Antidepressants a Mistake? Youth Suicides Rose Afterwards

The FDA required that a Black Box warning be placed on antidepressants in 2005, notifying doctors of this possible effect in ...

STAT4h

Pharmalittle: We’re reading about compounders suing the FDA, Biogen turning to telehealth, and more

A trade group representing large compounding pharmacies sued the FDA over its removal of a widely prescribed Lilly diabetes ...

21hon MSN

FDA antidepressant warnings of suicide risk among kids may have the opposite effect, study finds

FDA black box warnings that antidepressants may be linked with suicidality among youth may have unintended, yet harmful, ...

4hon MSN

Brownie Recall Update As FDA Sets Highest Risk Level

The brownies were found to contain an undeclared allergen, which can pose a serious risk to allergy sufferers.

Modern Healthcare9h

Upcoming FDA draft on pulse oximetry's racial bias draws questions

The FDA's upcoming guidelines aim to eliminate pulse oximetry’s racial bias, but clinicians and scientists are unsure what to ...

ABC714h

FDA approves 1st at-home nasal spray flu vaccine, paving the way for other medicines

The FDA has approved a new flu vaccine nasal spray for at-home use. While this self-administered version won't be available ...

1don MSN

Vegetable Recall Update: Warning for State As FDA Sets Highest Risk Level

The vegetable products were recalled due to a possible contamination with the bacteria Listeria monocytogenes.

1don MSN

FDA announces recall of dipping sauce due to 'potential mold growth contamination'

Lunds & Byerlys Lone Star Dip products are being recalled over "potential mold growth contamination," according to the FDA.

12h

Zealand, Boehringer win FDA breakthrough status to treat fatty liver

Denmark's Zealand Pharma and German partner Boehringer Ingelheim have won the U.S. Food and Drug Administration's ...

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