Product Liability: Gadolinium | MRI Contrast Agent | MRA Contrast Agent

Gadolinium MRI Contrast Agent


Nephrogenic Systemic Fibrosis (NSF) | Nephrogenic Fibrosing Dermopathy (NFD)

Gadolinium is an FDA-approved contrast agent for magnetic resonance imaging (MRI). Gadolinium is also called gadolinium-DPTA and gadodiamide, and it goes by various brand names. Gadolinium is non-radioactive and resembles plain water.

FDA REPORTS

FDA reports have identified a possible link between Nephrogenic Systemic Fibrosis (NSF) and/or Nephrogenic Fibrosing Dermopathy (NFD) and exposure to gadolinium containing contrast agents used at high doses for a procedure called Magnetic Resonance Angiography (MRA).

In particular, the FDA black box warning - updated on 5/23/2007 - reports that patients with severe kidney insufficiency who receive gadolinium-based agents are at risk for developing a debilitating, and a potentially fatal disease known as nephrogenic systemic fibrosis (NSF).

For more on gadolinium contrast agent cases, please follow this link.


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