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US FDA approves new nasal spray for depression treatment

Hosted on MSN · 11h

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 · 20h

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

The Week US on MSN · 19h

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 approved by the FDA on a per-case basis," said Forbes. It was banned in cosmetics after being linked to cancer in rats.

Orange County Register · 18h

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.

FDA Bans Red Dye No. 3: These Beloved Foods Will Be Affected

Discover which popular foods will be affected by the FDA's new ban on Red No. 3, the synthetic dye that adds a vibrant pop of color to candies, cakes, and some foods you wouldn't even expect.

20hon MSN

FDA warns of serious allergic reactions with some multiple sclerosis drugs

The U.S. Food and Drug Administration on Wednesday warned about the risk of a rare but serious allergic reaction with the use ...

16h

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 ...

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 ...

The American Journal of Managed Care14h

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 ...

21hon MSN

FDA Changes Food Safety Protocol for Fresh and Frozen Berries

The FDA just announced changes to help make berries sold in the U.S. safer to eat, lowering the odds you’ll get norovirus or ...

31mon MSN

Face moisturiser recalled: FDA issues advisory on First Aid Beauty Ultra Repair Cream

FDA issues advisory on First Aid Beauty Ultra Repair Cream - The First Aid Beauty ‘Ultra Repair Intense Hydration’ cream is ...

Vanzacaftor, tezacaftor, deutivacaftor safe in children with cystic fibrosis

Patients aged 6 to 11 years with cystic fibrosis receiving 24-week once-daily vanzacaftor/tezacaftor/deutivacaftor generally ...

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