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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.

Yahoo · 17h

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.

MarketWatch · 22h

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).

FDA Updates Egg Recall

YAHOO!News · 5h

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.

American Military News · 1h

FDA recalls millions of eggs, issues major warning amid bacteria outbreak

The FDA has upgraded a recall on millions of eggs, warning consumers that the eggs could cause "serious adverse health consequences or death."

FOX News on MSN · 20h

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.

FDA, Lilly

The Hill · 1h

Trade group sues FDA over ending Mounjaro/Zepbound shortage

A trade organization representing compounding pharmacies that make unbranded versions of the weight loss drugs Mounjaro and Zepbound has filed a lawsuit against the Food and Drug Administration

FiercePharma · 6h

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.

U.S. News & World Report · 1d

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 from its shortage list last week,

10h

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 ...

STAT7h

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 ...

7hon 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.

1don MSN

FDA's promised guidelines on pulse oximeters unlikely to end decades of racial bias

For decades, widely used pulse oximeters have underestimated the oxygen needs of darker-skinned patients. Will the FDA's new ...

1don 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, ...

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.

20hon MSN

US FDA approves Elanco's treatment for parasitic infections in dogs

The U.S. Food and Drug Administration has approved Elanco Animal Health's oral drug to protect dogs against six parasitic ...

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