Byetta Label Revised
Zacks.com - 53 minutes agoAmylin and Eli Lilly have announced that the U.S. Food and Drug Administration has implemented label changes for Byetta which is indicated for the treatment of type II diabetes.
4920 Stories, most recent news story added 3 minutes ago
Amylin and Eli Lilly have announced that the U.S. Food and Drug Administration has implemented label changes for Byetta which is indicated for the treatment of type II diabetes.
Hundreds have undergone brain surgery for problems like depression, anxiety, even obesity.
Experimental operations to treat disorders like O.C.D. have been encouraging. But with hope comes risk, since doctors do not know much about the circuits they are tampering with.
Caldolor , the first injectable product available in the U.S.reduced fever in burn patients over the first 24 hours of treatment.
SOUTH SAN FRANCISCO, CA--(Marketwire - November 27, 2009) - Theravance, Inc. ( NASDAQ : THRX ) announced today that it received a Complete Response letter from the U.S. Food and Drug Administration (FDA) related to the telavancin New Drug Application (NDA) for the treatment of nosocomial pneumonia (NP). Telavancin is a bactericidal, once-daily injectable investigational antibiotic for the ...
After an accelerated approval, the positive effects of a full approval are minimal.
It's Black Friday, after all.
Timco Worldwide Inc. is recalling a limited number of its Large Seedless Watermelons because the watermelons have the potential to be contaminated with the dangerous, sometimes deadly, Salmonella pathogen. According to the U.S. Food and Drug Administration (FDA), no illnesses have been reported, to date, in connection with this occurrence. Salmonella is an organism that can [...]
Here's a strange twist: you can find a child safety cap on a bottle of Listerine mouthwash, but not on Lysol, Pine Sol or Mr. Clean.Go figure.
("Teva Files 2nd Citizen's Petition To Block Generic Copaxone" published at 3: 44 p.m. EST Wednesday misstated the year when a generic Copaxone could enter the market in the 10th paragraph. The correct version follows.)
Protests from lawmakers in states along the Gulf of Mexico prompted the government to back away Nov. 13 from the ban. The Food and Drug Administration cited about 15 deaths a year from bacteria in the shellfish that cause kidney failure and intense pain.
A recent study shows that herbal supplements appeared to cause an increase in blood levels of lead among women.Dr.
Dozens of Dallas-area clinics that offer mammograms are largely ignoring new guidelines that could drastically reduce the amount of breast-cancer screening in the U.S.
The West Aurora High School Distinguished Alumni Hall of Honor recognizes graduates who gain recognition for outstanding accomplishments in their fields of endeavor.The induction ceremony is sponsored by the A+ Foundation of West Aurora Schools and will be held April 17 at the Aurora Country Club. For dinner information, call Randi Ochsenschlager at 630-897-6785.This year's inductees will be ...
SACRAMENTO – the Board of Equalization (BOE) has announced that it has notified wholesalers and distributors that it is illegal to sell flavored cigarettes or roll-your-own (RYO) under the federal U.S. Food and Drug Administration (FDA) provision of the Family Smoking Prevention and Tobacco Control Act.
BANGALORE -(Dow Jones)- Ranbaxy Laboratories Ltd. (500359.BY) Friday said it has launched a generic version of GlaxoSmithKline's (GSK.LN) anti-herpes medicine Valtrex in the U.S., a development expected to significantly boost its financial results.