Food and Drug Administration
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Genentech, Biogen get FDA request on Rituxan...lymphocytic leukemia. It is the most common adult leukemia in the U.S. Genentech and Biogen said they will continue final label discussions with the FDA. Shares of Biogen, which is based in Cambridge, Mass., closed up 11 cents at... In this article: Food and Drug Administration, Genentech, Biogen, Rituxan, Leukemia, Cancer, Rheumatoid arthritis, Cambridge, and NEW YORK |
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www.usatoday.com
China recalls tainted leukemia drugs - USATODAY.com
Chinese authorities ordered the recall of tainted leukemia drugs blamed for leg pains and other problems, state media ... Food and Drug Administration and ...
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www.leukemia-web.org
New Drug Helps Children Fight Leukemia
For the first time in more than a decade, there's a new drug to help children fight leukemia, Local 2 reported Tuesday. The Food and Drug Administration recently ...
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www.rxlist.com
FDA Approves New Leukemia Drug - on RxList
The U.S. Food and Drug Administration today approved Arzerra (ofatumumab) for patients with chronic lymphocytic leukemia (CLL), a slowly progressing cancer of the ...
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www.leukemia-lymphoma.org
The Leukemia & Lymphoma Society : LLS - News from Press Releases
Fighting leukemia, lymphoma, Hodgkin's disease ... U.S. Food and Drug Administration Approves ... U.S Food and Drug Administration. National Cancer ...
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www.cancer.gov
Imatinib mesylate (Gleevec®) - National Cancer Institute
... leukemia (CML) responded well to the molecularly targeted drug imatinib ... 05/10/2001) - The U.S. Food and Drug Administration (FDA) announced today its ...
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Dasatinib - National Cancer Institute
... about dasatinib and a collection of links to more information about the use of this drug, related research results, ... Food and Drug Administration (FDA) ...
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goliath.ecnext.com
16-JUL-07 | China's SFDA Recalls Leukemia Drug
Price: $4.95 | China's State Food and Drug Administration has suspended sales of methotrexate, an injectable drug for leukemia and rheumatoid arthritis, after reports...
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www.fda.gov
FOOD AND DRUG ADMINISTRATION
Accordingly, the Food and Drug Administration make no ... leukemia induction and stem cell fitness. What is not necessarily a disadvantage is that ...
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www.medscape.com
Voreloxin Granted Orphan Drug Status for Acute Myeloid Leukemia
: The US Food and Drug Administration has granted orphan drug designation for voreloxin in the treatment of acute myeloid leukemia.
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Description from Wikipedia:
The Food and Drug Administration (FDA) is an agency of the United States Department of Health and Human Services and is responsible for the safety regulation of most types of foods, dietary supplements, drugs, vaccines, biological medical products, blood products, medical devices, radiation-emitting devices, veterinary products, and cosmetics. The FDA also enforces section 361 of the Public Health Service Act and the associated regulations, including sanitation requirements on interstate travel as well as specific rules for control of disease on products ranging from pet turtles to semen donations for assisted reproductive medicine techniques.
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