An off-label clot-busting drug appears to work slightly better in treating stroke patients than an approved medication, a new review finds. FDA approves first once-weekly drug treatment regimen ...
Data released by Food and Drugs Administration (FDA ... The rise had been steady and uniform over the period with the steepest jump registered between March 25 and March 26 when it had increased ...
Orphan drug status, a status designated by the Food and Drug Administration (FDA), gives companies researching cures for rare diseases a seven-year window of exclusive marketing rights post ...
On October 29, 1959, the pharmaceutical company G.D. Searle filed an application with the U.S. Food and Drug Administration (FDA) to license their drug Enovid for use as an oral contraceptive.
BERLIN--(BUSINESS WIRE)--Bayer today announced that the U.S. Food and Drug Administration (FDA) has accepted the company’s New Drug Application (NDA) for the investigational compound ...
A top U.S. commercial bakery is pushing back on a Food and Drug Administration warning to ... The company said it creates “nationally uniform labels” that prevent people from inadvertently ...
Australians have been urged to look before they cook and read the safety advice on food labels. The Food Safety Information Council (FSIC) issued the call ahead of Australian Food Safety week from ...
His background includes 10 years overseeing food safety research at the U.S. Food and Drug Administration, which sets the guidelines by which most U.S. health departments conduct inspections.
The Food and Drug Administration approved a drug produced by AbbVie for the treatment of late stage Parkinsons disease the company announced Thursday. The regulator approved Vyalev, also known as ...
The Food and Drug Administration approved Mifeprex (mifepristone ... them on the list of Schedule IV drugs under the state’s Uniform Controlled Dangerous Substances Law. This could open the ...
For a time, a medication approved by the Food and Drug Administration called Belviq seemed helpful, but it was pulled from the market in 2020 after it was linked to an increased cancer risk.
The Food and Drug Administration approved use of a naloxone nasal spray without a prescription last year, a move the agency said was designed to make the medication readily available in drugstores ...