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Result : Searchterm 'mra' found in 2 terms [] and 57 definitions []
| previous 56 - 59 (of 59) Result Pages : [1] [2 3 4 5 6 7 8 9 10 11 12] | | | | Searchterm 'mra' was also found in the following services: | | | | |
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From Toshiba America Medical Systems Inc.;
the Ultra™ system was developed to help healthcare providers be more competitive by delivering greater patient comfort and a broad range of clinical capabilities, says Anita Bowler, product manager, MRI Business Unit, Toshiba America Medical Systems Inc With its unique, powerful gradient technology, the Ultra™ performs advanced clinical studies and consistently provides high-resolution images that are typically associated with high field MRI systems. At the same time, the Ultra™ offers a truly open feeling that makes patients more relaxed, especially those with claustrophobic tendencies.
Device Information and Specification CLINICAL APPLICATION Whole Body Quadrature, solenoid and multi-channel configurations SE, FE, IR, FastSE, FastIR, FastFLAIR, Fast STIR, FastFE, FASE, Hybrid EPI, Multi Shot EPI, Single shot EPI diffusion, True SSFP, SuperFASE; Angiography: 2D(gate/non-gate)/3D TOF, SORS-STC, Black Blood MRA POWER REQUIREMENTS 380/400/415/440/480 V COOLING SYSTEM TYPE Cryogenless | | | | | |
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Vasovist™ is an albumin-targeted intravascular contrast agent. It is indicated for contrast enhanced MR angiography (CE- MRA) for the visualization of abdominal or limb vessels in patients with suspected or known vascular disease. After IV injection, Vasovist™ binds reversibly to human albumin in plasma, which results in long-lasting increased relaxivity. Imaging from 5 to 50 min is possible. A small unbound portion is, by glomerular filtration, eliminated by the kidneys.
AngioMARK® was the formerly trade name and MS-325 the research name. Currently the phase III clinical trials are completed to determine its efficacy for peripheral vascular disease and coronary artery disease.
In the U.S., EPIX received an approvable letter from the U.S. Food and Drug Administration (FDA) for Vasovist™ in January 2005. In 2009, Epix Pharmaceuticals has sold the U.S., Canadian and Australian rights for its blood pool agent (now named ABLAVAR™), to Lantheus Medical Imaging, Inc..
WARNING: NEPHROGENIC SYSTEMIC FIBROSIS
Gadolinium-based contrast agents increase the risk for nephrogenic systemic fibrosis (NSF) in patients with acute or chronic severe renal insufficiency (glomerular filtration rate less than 30 mL/min/1.73m 2), or acute renal insufficiency of any severity due to the hepato-renal syndrome or the liver transplantation period.
See also MRI Safety.
Drug Information and Specification NAME OF COMPOUND Diphenylcyclohexyl phosphodiester-Gd-DTPA, gadofosveset trisodium, MS-325 T1, predominantly positive enhancement 20-45 mmol-1sec-1, Bo=0,47T PHARMACOKINETIC Intravascular, short elimination half life CONCENTRATION 244 mg/mL, 0.25mmol/mL DOSAGE 0.12 mL/kg, 0.03 mmol/kg DEVELOPMENT STAGE approved DO NOT RELY ON THE INFORMATION PROVIDED HERE, THEY ARE NOT A SUBSTITUTE FOR THE ACCOMPANYING PACKAGE INSERT!
Distribution Information TERRITORY TRADE NAME DEVELOPMENT STAGE DISTRIBUTOR North America, Australia for sale | | | | • View the DATABASE results for 'Vasovist™' (7).
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Quick Overview
DESCRIPTION
Loss of signal of flowing blood
Image Guidance
| | | | • View the DATABASE results for 'Venetian Blind Artifact' (3).
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