| Subject: | FDA Issues Update on Gadolinium-containing Contrast Agents for Magnetic Resonance Imaging (MRI) |
| Category: | Food and Drug Administration (FDA)
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| Published: | Fri, 29 Dec 2006 - 12:00 am |
| The FDA has issued a Public Health Advisory to notify healthcare professionals that it has received additional information about a new disease, known as Nephrogenic Systemic Fibrosis or Nephrogenic Fibrosing Dermopathy (NSF/NFD), which may occur in patients with moderate to end-stage kidney disease after they have had a Magnetic Resonance Imaging (MRI) or Magnetic Resonance Angiography (MRA) scan with a gadolinium-based contrast agent. The FDA has received reports of 90 patients with moderate... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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