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Cresemba (isavuconazonium sulfate) has been approved by the U.S. Food and Drug Administration to treat invasive aspergillosis and invasive mucormycosis

FDA Approves Cresemba for Serious Fungal Infections

New drug targets cell walls of the fungi; available in oral and intravenous formulations
A new cardiopulmonary resuscitation system designed to increase the chance of survival in people experiencing cardiac arrest has been approved by the U.S. Food and Drug Administration.

FDA Approves New CPR Devices

Used together, they up the amount of oxygenated blood circulating through the body during CPR
The U.S. Food and Drug Administration has approved the first device to treat dialysis-related amyloidosis (DRA)

FDA: Device Authorized for Use in Dialysis-Related Amyloidosis

Lixelle Beta 2-microglobulin Apheresis Column authorized for use in DRA
The U.S. Food and Drug Administration has approved Zarxio (filgrastim-sndz)

FDA Approves First Biosimilar Drug in U.S.

Zarxio is highly similar to long-sanctioned cancer drug
U.S. Food and Drug Administration approval of Opdivo (nivolumab) has been expanded to include advanced non-small-cell lung cancer

FDA: Opdivo Approval Expanded to Include Lung Cancer

FDA approves drug for NSCLC patients who have been treated with platinum-based chemotherapy
The combination antibiotic Avycaz (ceftazidime-avibactam) has been approved by the U.S. Food and Drug Administration to treat adults with complicated infections of the intra-abdominal area or urinary tract

FDA Approves New Combination Antibiotic Avycaz

Combination drug sanctioned for abdominal, urinary tract infections
Farydak (panobinostat) has been approved by the U.S. Food and Drug Administration to treat multiple myeloma. Farydak inhibits the activity of histone deacetylases

FDA Approves Farydak for Multiple Myeloma

Drug is sanctioned for people who have received at least two prior standard therapies
A huge recall of products that contain cumin spice possibly contaminated with peanut has been ongoing in the United States since December

FDA: People With Peanut Allergy Should Avoid Cumin Products

Huge recall of products that contain cumin spice possibly contaminated with peanut
The VenaSeal closure system has been approved by the U.S. Food and Drug Administration to treat superficial varicose veins of the legs that cause symptoms.

FDA: New Device Treats Superficial Varicose Veins

Seals the affected superficial veins using an adhesive agent
The U.S. Food and Drug Administration has allowed marketing of the Eclipse System for the treatment of fecal incontinence in adult women aged 18 to 75

FDA Permits Marketing of Device for Female Fecal Incontinence

Use of Eclipse System led to 50 percent decrease in episodes