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Recent related articles ( fda approves knee injury device humans spiritindia):

Final FDA approval for generic version of antiretroviral Zerit capsules
Mylan Inc. has announced that Matrix Laboratories Limited, its India-based subsidiary in which it holds a 71.5% controlling interest, received final approval from the U.S. Food and Drug Administration (FDA) on December 29, for its Abbreviated New Drug Application (ANDA) for Stavudine Capsules USP, 15 mg, 20
Final FDA approval for generic version of antiretroviral Zerit capsules...

Successful abo-incompatible heart transplantation in a child despite blood-group sensitization after ventricular assist device support
Urschel S, Dalla Pozza R, Loeff M, Schmitz C, Sodian R, Schmoeckel M, Kowalski C, Netz H. Successful ABO-incompatible heart transplantation in a child despite blood-group sensitization after ventricular assist device support.Pediatr Transplantation 2008. © 2008 Wiley Periodicals, Inc.Abstract: In the first two yr of life blood-group incompatible
Successful abo-incompatible heart transplantation in a child despite blood-group sensitization after ventricular assist device support...

New Evidence That Humans Make Aspirin's Active Principle -- Salicylic Acid
Scientists are reporting evidence that humans can make their own salicylic acid -- the material formed when aspirin breaks down in the body. Salicylic acid, which is responsible for aspirin's renowned effects in relieving pain and inflammation, may be the first in a new class of bioregulators, according
New Evidence That Humans Make Aspirin's Active Principle -- Salicylic Acid...

FDA Approves Gadofosveset for Vascular Imaging
Epix Pharmaceuticals on Monday announced the U.S. approval of gadofosveset trisodium as a contrast agent for use in adults undergoing magnetic resonance angiography (MRA) for the assessment of aortoiliac occlusive disease.
FDA Approves Gadofosveset for Vascular Imaging...

FDA Panel Debates Merits of Next-Generation Opioid Formulations
An FDA advisory panel on November 13–14 examined clinical evidence for a pair of extended-release, abuse-resistant opioid drug products while trying to weigh the needs of patients against the threat of misuse by others. Remoxy XRT, an oxycodone product, and Embeda, a morphine–naltrexone formulation, were designed to deter abusers
FDA Panel Debates Merits of Next-Generation Opioid Formulations...

Lipid-Control Drug Approved by FDA
FDA this week approved a new fibrate drug designed to reduce serum levels of triglycerides and low-density lipoprotein cholesterol while raising high-density lipoproteins. Abbott Laboratories received marketing approval for fenofibric acid, which will be marketed as TriLipix, according to the Illinois pharmaceutical company. The drug can be used alone
Lipid-Control Drug Approved by FDA...

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