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The Latest Breaking News from the Food and Drug Administration

FDA skeptical of experimental ALS treatment pushed by patient advocates

The Food and Drug Administration meets this week to consider a much-debated treatment for Lou Gehrig’s disease

The Independent UK

Joe Biden sends message to Americans on Covid booster shots: ‘Stay up-to-date on vaccines’

US president’s message comes after CDC and FDA decide to recommend Covid booster shots amid rising cases

The Independent UK

US health agency recommends updated COVID boosters, President Biden calls it "important" milestone

he US health agency Centers for Disease Control and Prevention (CDC) on Tuesday authorized, approved, and recommended everyone 6 months and older get an updated COVID-19 booster.

Dynamite News

From analysis to the latest developments in health,
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Advisers to the Food and Drug Administration voted unanimously on Tuesday against the effectiveness of the key drug phenylephrine found in popular versions of Sudafed, Dayquil and other medications stocked on store shelves.

Chicago Sun-Times

Kentuckians can access FDA, CDC approved new COVID vaccine targeting Omicron subvariants in coming d

As new variants of COVID are making the rounds, the Food and Drug Administration and Centers for Disease Control and Prevention have approved a new round of COVID-19 vaccines.

WEKU

New COVID vaccines get FDA approval

Vaccines for a fall immunization drive against COVID-19 just got the green light from the Food and Drug Administration. The agency says the vaccines can protect people, as hospitalizations tick up.

WEKU

Sleeping pill could reduce levels of Alzheimer’s proteins

The sleeping pill, known as suvorexant, which has been approved by the Food and Drug Administration (FDA) is used to aid insomnia - now researchers are seeing if it can help slow down Alzheimer’s proteins

The Independent UK

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Court revives doctors' lawsuit saying FDA overstepped its authority with anti-ivermectin campaign

A federal appeals court in New Orleans has revived a lawsuit by three doctors who say the Food and Drug Administration overstepped its authority in a campaign against the use of a drug that is not approved to treat COVID-19

The Independent UK

FDA's greenlighting of maternal RSV vaccine represents a major step forward in protecting young babies against the virus

With the Food and Drug Administration’s Aug. 21, 2023, approval of the first vaccine against respiratory syncytial virus, or RSV, for use during late pregnancy, the U.S. will soon have a major new tool at its disposal to protect infants against the highly contagious virus.

The Conversation

Pfizer's RSV vaccine to protect babies gets greenlight from FDA

The Food and Drug Administration has approved the first vaccine for expectant mothers to shield their babies from RSV.

WEKU

Is the FDA failing to protect us?

A slew of public health alarms raise concerns about what's going on at the Food and Drug Administration

Salon

The FDA approves the first pill specifically intended to treat postpartum depression

The Food and Drug Administration granted approval of the drug, Zurzuvae, for adults experiencing severe depression related to childbirth or pregnancy. The pill is taken once a day for 14 days.

WEKU

Karl Rove brings whiteboard to Fox News to explain that RFK Jr is a ‘nut’

Veteran GOP operative says it would be ‘nutty’ to put RFK Jr in charge of health agencies

The Independent UK

Ilhan Omar supports woman jailed for taking abortion pill and burning foetus: ‘A violation of autonomy’

Prosecutors said Celeste Burgess used abortion pills well beyond the 10-week limit approved by the Food and Drug Administration

The Independent UK

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Tribune News Service

Drug to prevent RSV in babies approved: What you need to know

The Food and Drug Administration (FDA) approved a drug to help protect infants from respiratory syncytial virus (RSV). The medication, given as a single-dose injection prior to or during RSV season, is a monoclonal antibody. It is intended for babies born during or entering their first RSV season and for…

The Conversation

How does the new over-the-counter birth control pill, Opill, work to prevent pregnancy? 5 questions answered

The Food and Drug Administration’s July 13, 2023, approval of the first over-the-counter birth control pill, called Opill, broadens the options for people seeking to prevent pregnancy. When Opill becomes available, presumably in the first quarter of 2024, it will be sold in grocery and convenience stores, in pharmacies and…

Inverse

The WHO Says Aspartame is “Possibly Carcinogenic” — But This Public Health Organization Disagrees

The World Health Organization's cancer research arm deemed aspartame as possibly carcinogenic to humans, but the Food and Drug Administration doesn't agree.

Inverse

The FDA Just Approved OTC Hormonal Birth Control — Here’s When It Will Be Available

Opill becomes the first hormonal birth control pill in the United States to be approved for over-the-counter sale by the Food and Drug Administration.

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Roll Call

FDA approves first OTC birth control pill - Roll Call

The Food and Drug Administration on Thursday approved Opill, making it the nation’s first over-the-counter birth control pill.

Chicago Sun-Times

The FDA is being asked to look into Logan Paul’s energy drink, which has the caffeine of 6 Coke cans

The influencer-backed energy drink Prime is popular among children but lawmakers and health experts are concerned over its potentially dangerous levels of caffeine.

Daily Mirror

Miracle new Alzheimer's drug which slows cognitive decline of disease to be rolled out

The Food and Drug Administration (FDA) has approved the much awaited drug Leqembi which has been shown to slow the cognitive decline caused by Alzheimer’s, the most common type of dementia

WEKU

Alzheimer's drug Leqembi gets full FDA approval. Medicare coverage will likely follow

The first drug found to slow the progression of Alzheimer's disease has been granted full approval by the Food and Drug Administration.

The Independent UK

5 takeaways from the AP's report on Chinese disposable e-cigarettes flooding the US market

The Associated Press has found that the Food and Drug Administration can't keep up with a flood of illegal disposable e-cigarettes from China

Zenger

Moderna Stock Rises After FDA Application For Updated Vaccine

Moderna's potential beyond COVID-19 is underappreciated, says analyst Eliana Merle, who upgraded the stock to Buy

WEKU

An Alzheimer's drug is on the way, but getting it may still be tough. Here's why

The Food and Drug Administration is expected to grant full approval to the Alzheimer's drug lecanemab by July 6. But access to the drug may still be limited.

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