The U.S. Food and Drug Administration on Friday approved Mekinist for use with another drug, Tafinlar, to treat advanced melanoma that is spreading or cannot be removed by surgery. Melanoma is the most deadly form of skin cancer, ...
The U.S. Food and Drug Administration today approved the first gel sealant for use in stopping fluid from leaking through the incision in a patient's cornea after cataract surgery with intraocular lens placement in adults. Prior to today's ...
Tags: Gel for Sealing Corneal Incision, First Gel After Cataract Surgery
The drugs Mekinist and Tafinlar were approved for combination treatment of advanced melanoma skin cancer, the U.S. Food and Drug Administration announced Friday. The two medicines "are the first drugs approved for combination treatment of ...
Tags: FDA, 2-Drug Combo Treatment, Combo Treatment for Advanced Melanoma
A sealant gel to prevent fluid leakage after cataract surgery has been approved by the U.S. Food and Drug Administration. While gels such as ReSure have been approved to seal small incisions in other parts of the body, this is the first ...
Tags: Sealant Gel, Eye Surgery
Farxiga (dapaglifozin) has been approved by the U.S. Food and Drug Administration to treat adults with type 2 diabetes, the agency said Wednesday in a news release. The drug, to be used for blood sugar control along with proper diet and ...
Tags: Farxiga, Type 2 Diabetes, Medicine News
The US Food and Drug Administration (FDA) has approved GlaxoSmithKline's (GSK) use of Mekinist (trametinib) in combination with Tafinlar (dabrafenib) for the treatment of patients with unresectable melanoma or metastatic melanoma with BRAF ...
Tags: FDA, Combination Drug
Cardica, a medical device company, has received 510(k) approval from the US Food and Drug Administration (FDA) for its MicroCutter Xchange 30 device and blue staple cartridge for medium thickness tissue. The company has designed the ...
Tags: Cardica, medical device
Radius Medical has announced the US Food and Drug Administration (FDA) approval and product introduction of its new Prodigy support catheter. The company has designed the Prodigy support catheter for providing back up support to the ...
Tags: Radius Medical, Medicine
Officials at the U.S. Food and Drug Administration say they want to hear from people if they think a tobacco product is defective or causes a health issue. The Department of Health and Human Services' Safety Reporting Portal was revised ...
A new kind of implant may offer people suffering from sleep apnea an alternative to wearing an air mask while they snooze, researchers report. With the implant, a pacemaker delivers electrical impulses to a nerve that controls the tongue ...
The liquid form of the flu drug Tamiflu is in short supply because of early strong demand.But the shortage is expected to be brief, lasting only through mid-January, according to its manufacturer, Genentech. Doctors typically give the ...
Tags: Tamiflu, Tamiflu Shortage, Health News
Merck (NYSE:MRK), known as MSD outside the United States and Canada, announced today that the U.S. Food and Drug Administration (FDA) recently approved ISENTRESS® for oral suspension, a new pediatric formulation of Merck's integrase ...
Tags: Merck, ISENTRESS®, oral suspension, pediatric formulation
Mylan Inc. (Nasdaq: MYL) today announced that its U.S.-based subsidiary Mylan Pharmaceuticals Inc. has launched Mycophenolic Acid Delayed-release Tablets, 180 mg and 360 mg. This product is the generic version of Novartis' Myfortic® ...
Members of the Safe Food Coalition and the Worker Health and Safety Coalition wrote to members of Congress this week, asking them not to reduce the budget for the U.S. Department of Agriculture's Food Safety Inspection Service and to remove ...
Tags: HIMP, Budget Negotiations, USDA, FDA
A GE Healthcare voluntary recall of an anesthesia devices part has received a Class I classification from the FDA, which means the fault might cause serious health problems or death. The part involved is the GE Healthcare Multi Absorber ...
Tags: Anesthesia, Ge Anesthesia Devices, FDA