KODATEF is not approved for use in the U.S. Demand for ARAKODA has been steadily growing in recent months as awareness and ...

The FDA announced a very serious recall. A product sold in New York can cause serious, life threatening, or fatal respiratory ...

More than 90% of Omvoh-treated patients who were in clinical remission at one year sustained it with two years of continuous treatment Omvoh works to reduce inflammation within the gastrointestinal ...

In this week’s “Psychedelic,” The Fly’s recurring series focused on psychedelic stock news, The Fly looks back on an acquisition, study results ...

The fireside chat will be webcasted and available under “Events & Presentations” in the Investor Relations section of the Company’s website at www.rhythmtx.com. A replay of the webcast will be ...

Alvogen has issued a nationwide recall of one lot of Fentanyl Transdermal System 25 patches because the patches may stick ...

Alvogen, Inc. is voluntarily recalling one lot of Fentanyl Transdermal System 25 mcg/h transdermal patches to the consumer level. The reason for the recall is that there is a potential that patches ...

An injectable blood pressure drug has been recalled after the FDA has warned it could cause side effects, such as stroke or death.

Devon and Cornwall Police said officers were called to a serious assault on Wednesday evening Police in Plymouth say they are searching for a suspect following a "serious assault" in the West Hoe ...

We have been issued a Form 483 with one observation and the Company will address the said observation within stipulated timelines," Laurus Labs said in a regulatory filing. The inspection focused on ...