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The Latest Breaking News from the Food and Drug Administration

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

From analysis to the latest developments in health,
read the most diverse news in one place.

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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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…

Tribune News Service

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…

The Conversation

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.

Inverse

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.

Roll Call

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.

Chicago Sun-Times

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

Daily Mirror

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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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WEKU

FDA warns stores to stop selling Elf Bar, the top disposable e-cigarette in the U.S.

The warning from the Food and Drug Administration is the latest attempt by regulators to crack down on illegal disposable vapes that have poured into U.S. stores in recent years.

WEKU

Are masks for the birds? We field reader queries about this new stage of the pandemic

The official emergency is over but COVID is still here. And that means ... lots of questions. We asked our readers what's on their mind and then called on experts for advice.

WEKU

FDA advisers back updated COVID shots for fall vaccinations

A panel of advisers to the Food and Drug Administration has recommended revising the current COVID-19 vaccine so that it specifically targets omicron.

WEKU

FDA advisers endorse new RSV antibody drug for babies

A panel of experts to the Food and Drug Administration has recommended the agency approve a long-acting antibody drug that can protect infants from the seasonal virus, RSV.

Chicago Tribune

Commentary: By avoiding funding Alzheimer’s research, the government is cutting seniors’ life spans

Millions of patients and their caregivers breathed a collective sigh of relief when drugmaker Eli Lilly recently announced its new experimental Alzheimer’s medication appears to slow cognitive decline by 35%. The Food and Drug Administration could approve the new treatment, donanemab, as soon as this year.

Tribune News Service

The FDA approved a new drug for hot flashes. Here's why it shows 'a lot of promise'

The Food and Drug Administration last Friday approved fezolinetant, or Veozah, to treat hot flashes for women in menopause. The non-hormonal drug treatment is the first of its class and represents an option for women who cannot take hormones.

WEKU

FDA advisers support approval of RSV vaccine to protect infants

At least 58,000 childern younger than 5 years old are hospitalized each year with RSV infections. A Pfizer vaccine given to pregnant people could help protect their infants from severe RSV illness.

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