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US FDA approves new nasal spray for depression treatment

Hosted on MSN · 12h

FDA approves Johnson & Johnson’s ketamine-derived nasal spray for depression as standalone treatment

The announcement was welcome news for those with major depressive disorder, affecting an estimated 8.3% of the adult population.

CNN on MSN · 1d

FDA approves standalone use of J&J’s ketamine-derived depression treatment

The U.S. Food and Drug Administration expanded approval for Johnson & Johnson’s nasal spray, Spravato, to allow it to be used as a standalone treatment for patients with severe depression, the company said on Tuesday.

Popular Science · 22h

FDA approves first-of-its-kind nasal spray for severe depression

Johnson & Johnson has announced the FDA’s approval of a first-of-its-kind, esketamine nasal spray called Spravato for the standalone treatment of major depressive disorder (MDD), PTSD, and similar psychiatric conditions.

the FDA is banning red dye No. 3

Orange County Register · 20h

What the FDA ban on Red Dye No. 3 means for consumers

For consumers, the ban on Red No. 3 represents a small victory for public health and safety. It shows that the FDA is actively engaged in protecting the American food supply from harmful additives. As more studies emerge and consumer advocacy grows, we may see additional changes in how artificial dyes are used.

The Conversation · 1h

FDA bans Red 3 dye from food and drugs – a scientist explains the artificial color’s health risks and long history

Over 35 years after the first study linking Red 3 to thyroid cancer in rats was published, the US is beginning to wean it out of foods and drugs.

The Washington Post · 15h

Why the FDA is banning red dye No. 3

The FDA said the food color additive must be removed from food by 2027. The Post's Rachel Roubein explains the reasons behind the decision and its potential impact.

17h

Federal regulations paused, halting FDA's proposed ban on formaldehyde in hair products

Over the years, an increasing number of studies have linked formaldehyde to cancers that are especially prevalent among Black ...

1don MSN

FDA proposes mandatory front-of-package nutrition labels to combat spike in chronic diseases

The U.S. Food and Drug Administration (FDA) is demanding increased, in-your-face food transparency when it comes to nutrition ...

Hosted on MSN15h

FDA Approves Treosulfan as Part of AML/MDS Conditioning Regimen

The FDA approved treosulfan (Grafapex) with fludarabine as a preparative regimen for allogeneic hematopoietic stem cell ...

Three former FDA officials: Here’s what Trump and his nominees need to know

The FDA is the leading science-based consumer protection agency in the world. Three former senior officials write about what ...

20hon MSN

Why is the FDA slow to ban food additives?

Red Dye No. 3 is a "color additive made from petroleum," which "could previously be used in foods in small amounts as ...

The American Journal of Managed Care16h

FDA Warns of Severe Allergic Reactions With Certain Multiple Sclerosis Drugs

Today, the FDA issued a warning about the risk of anaphylaxis, a rare but life-threatening allergic reaction, linked to ...

1d

FDA makes key decision on Zyn nicotine pouches

In a statement, the FDA said it has authorized the marketing and sale of Philip Morris International’s Zyn nicotine pouches.

39mon MSN

Amneal gains FDA approval for dementia and oncology drugs

BRIDGEWATER, N.J. - Amneal Pharmaceuticals, Inc. (NASDAQ:AMRX), a pharmaceutical company with a market capitalization of ...

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