Myoview is a Myocardial Perfusion Imaging agent and is used around the globe. It combines diagnostic accuracy, myocardial uptake and retention, and high sensitivity and specificity for detecting angiographically significant Coronary Artery Disease. Myoview also provides for shorter study completion time with fewer re-scans due to background activity.
About Myoview
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Myoview™ (technetium Tc-99m Tetrofosmin)
In studying patients with known or suspected coronary artery disease, care should be taken to ensure continuous cardiac monitoring and the availability of emergency cardiac treatment. As with all injectable drug products, allergic reactions and anaphylaxis may occur. Pharmacologic induction of cardiovascular stress may be associated with serious adverse events such as myocardial infarction, arrhythmia, hypotension, bronchoconstriction, and cerebrovascular events. Caution should be used when pharmacologic stress is selected as an alternative to exercise; it should be used when indicated and in accordance with the pharmacologic stress agent's labeling. The most common adverse reactions reported from post-marketing experience with MYOVIEW included rash, urticaria, abnormal vision, allergic reactions, and fever. For more information and full prescribing information visit www.myoview.com.
About AdreView-NOT APPROVED IN CANADA, APPROVED IN THE U.S. and EUROPE
AdreView™ (iobenguane I 123) Injection
AdreView contains benzyl alcohol (10.3 mg/mL), which may cause serious reactions in premature or low birth-weight infants. Benzyl alcohol has been associated with a fatal "Gasping Syndrome" in premature infants and infants of low birth weight. Have anaphylactic and hypersensitivity treatment measures available prior to AdreView administration. AdreView is cleared by glomerular filtration and is not dialyzable. The radiation dose to patients with severe renal impairment may be increased due to the delayed elimination of the drug. AdreView is contraindicated in patients with known hypersensitivity to iobenguane or iobenguane sulfate. In clinical trials the most common adverse reactions seen were dizziness, rash, pruritis, flushing, or injection site hemorrhage reported in less than 1% of patients. For more information and full prescribing information visit www.adreview.com.
About GE Healthcare
GE Healthcare provides transformational medical technologies and services that are shaping a new age of patient care. Our broad expertise in medical imaging and information technologies, medical diagnostics, patient monitoring systems, drug discovery, biopharmaceutical manufacturing technologies, performance improvement and performance solutions services help our customers to deliver better care to more people around the world at a lower cost. In addition, we partner with healthcare leaders, striving to leverage the global policy change necessary to implement a successful shift to sustainable healthcare systems.
Our "healthymagination" vision for the future invites the world to join us on our journey as we continuously develop innovations focused on reducing costs, increasing access and improving quality and efficiency around the world. Headquartered in the United Kingdom, GE Healthcare is a $17 billion unit of General Electric Company (NYSE: GE). Worldwide, GE Healthcare employs more than 46,000 people committed to serving healthcare professionals and their patients in more than 100 countries. For more information about GE Healthcare, visit our website at www.gehealthcare.com.
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