The products are being advertised as more affordable alternatives to blockbuster weight-loss drugs. Here’s what doctors think ...
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 ...
Today, the U.S. Food and Drug Administration approved Miplyffa (arimoclomol), an oral medication for the treatment of Niemann-Pick disease, type C (NPC). Miplyffa, in combination with the enzyme ...
Ocrevus Zunovo with Halozyme's Enhanze drug delivery technology is used for the treatment of relapsing multiple sclerosis and ...
Solving adherence issues with prodrugs, examining whether PBMs are to blame for high drugs prices in the US, developing ...
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.
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.
Beyond MariTide, Amgen has a rich pipeline with more than 30 phase 3 programs. Some are for existing medicines seeking label expansions, such as Lumakras and Amjevita, a rheumatoid arthritis medicine.
Amber Thurman died after waiting 20 hours for medical treatment following the use of abortion pills, marking the first ...