The U.S. Food and Drug Administration approved Zevra Therapeutics' drug for a rare and fatal genetic disorder, making it the ...

The spray was distributed by Green Pharmaceuticals Inc., of Camarillo, Calif., and had been sold on the company’s website and ...

The snacks now have a Class I risk level, meaning there is a "reasonable probability" they could cause "serious adverse ...

Herbals LLC has issued a nationwide recall of all lots of Vail-Bon Jie Yang Wan  supplement capsules due to the presence of ...

Zevra Therapeutics has won Food and Drug Administration approval of Miplyffa for Niemann-Pick disease type C, making it the first drug cleared in the U.S. for the rare neurodegenerative disorder.

Solving adherence issues with prodrugs, examining whether PBMs are to blame for high drugs prices in the US, developing ...

Corey Lewandowski, a senior advisor to the Donald Trump campaing, shared a bombshell report about a relationship between ...

An Endodontic mode has been created within the Navident EVO system, reportedly improving the ability of the clinician to effectively detect, diagnose, and plan treatment prior to dynamic navigation.

Amber Thurman died after waiting 20 hours for medical treatment following the use of abortion pills, marking the first ...

Cooperatives and Small and Medium Enterprises Minister Teten Masduki (left) and head of the Food and Drug Supervisory ...

Pfizer Inc (NYSE: PFE) presented positive trial data for experimental drug designed for patients suffering from cancer ...

Following an investigational new drug application clearance from the FDA, a phase 1 trial plans to evaluate CD-001.