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Gadolinium MRI/MRA Contrast Dye
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Gadolinium Side Effects Could Result In Kidney Failure Lawsuits

Gadolinium | Lawsuits, Lawyers | Side Effects: Kidney Failure, Renal Failure, Nephrogenic Systemic Fibrosis (NSF), Tissue Fibrosis

Recent News

Dying for an MRI - 7 News Investigation (WSVN 7 Fox News Miami/Fort Lauderdale)

Parker Waichman LLP Files Suit Against Bayer-Schering on Behalf of Woman Who Developed Nephrogenic Systemic Fibrosis (NSF) from Contrast Agent Magnevist

Drug Safety Update Volume 1 Issue 1 August 2007.pdf

EMEA Report.pdf

Court Filed Complaint.pdf

FDA Gadolinium Warning 5/23/07

In May 2007, the FDA requested that the manufacturers of the five gadolinium based contrast agents used in MRIs include a boxed warning – the FDA’s strongest possible safety warning – on product labels highlighting the risk they posed to patients with kidney problems. The FDA warned that patients who are at risk for NSF should be monitored by their doctors, and told to report any symptoms associated with the condition immediately. The FDA has also set up a reporting program so that healthcare providers can report instances of NFS caused by Gadolinium based contrast agents.

FDA News

Questions and Answers

FDA Information for Healthcare Professionals PDF

FDA Gadolinium Warning 12/22/06 In December of 2006, the FDA issued its second public health advisory regarding gadolinium based contrast dyes. At that time, the FDA said it had received 90 reports of patients with moderate to end-stage kidney disease who developed NSF after being exposed to gadolinium based contrast agents. At the time of this alert, the FDA said about 215 patients worldwide were known to have NSF. Of those whose medical history were known, all had been exposed to gadolinium contrast agents prior to diagnosis.

Public Health Advisory

Questions and Answers

Information for Healthcare Professionals

FDA Gadolinium Warning 6/08/06

In June 2006, the Food & Drug Administration (FDA) issued what would be the first of three warnings on gadolinium contrast dyes. Following the publication of the Dutch NSF study in 2006, the FDA issued an alert to healthcare providers that gadolinium based agents had been tied to multiple cases of NSF. Although these cases were not limited to one gadolinium based contrast agent, three were most often associated with the onset of NSF. Those three were Ominiscan, Magnevist and OptiMark. At that time the FDA warned physicians to screen patients for kidney problems prior to using gadolinium based contrast agents during MRIs.

Public Health Advisory

Questions and Answers

Information for Healthcare Professionals

FDA Information for Healthcare Professionals PDF

Gadolinium MRI Side Effects

Gadolinium side effects have been know to cause Nephrogenic Systemic Fibrosis (NSF) a disorder characterized by widespread tissue fibrosis.  The controversy surrounding the use of gadolinium contrast dye in magnetic resonance imaging (MRI) continues to swirl, yet many people don’t know what gadolinium is or why they should be concerned. However, the data which continues to be reported about gadolinium and its uses suggests that everyone should have a strong interest in learning more about gadolinium.

Our Dedicated Lawyers and Attorneys Have Years of Experience Handling Defective Drug Lawsuits Such as Gadolinium Which is Associated With Diseases That Cause Kidney and Renal Failure Such as NSF and NFD

Gadolinium Contrast Agent MRA Side Effects

Magnetic Resonance Angiography (MRA) is a type of MRI that is used to provide pictures of blood vessels inside the body.  Often gadolinium based MRI contrast agents are used to enhance these images. The use of gadolinium based MRI contrast agents for MRAs is an off-label use that has never been approved by the Food & Drug Administration (FDA). However, the use of gadolinium based MRI contrast agents in MRAs is a growing practice that is putting  kidney patients at an even greater risk of developing Nephrogenic Systemic Fibrosis/ Nephrogenic Fibrosing Dermopathy (NSF/NFD)  because these procedures use far more gadolinium than a typical MRI.

For gadolinium based MRI contrast agents to be effective in an MRA, they must be administered at three times the approved dose. If a person’s kidneys are not functioning properly, it is extremely unlikely that so much gadolinium will be eliminated from the body.  This makes it far more likely that a patient with pre-existing kidney disease will develop NSF/NSD if exposed to gadolinium based MRI contrast agents. In fact, some of the first reports of NSF/NSD actually occurred in patients who were exposed to gadolinium based MRI contrast agents during MRAs.

Gadolinium Side Effects Linked to NSF & NFD

The FDA says that people who get an MRI with gadolinium based contrast agents are at risk for NSF.   Because NSF is debilitating and may cause death, the FDA urges that anyone who develops the disease undergo immediate dialysis.  The FDA says there are 215 patients with NSF in the world. About 75 of those people had gotten a gadolinium-based contrast agent for an MRI or MRA. The FDA adds that it has identified gadolinium in skin biopsies of patients with NSF. The agency says they are unsure why those with moderate to end-stage kidney disease who receive a gadolinium based contrast agent develop NSF. As of December 21, 2006, 90 patients with moderate to end-stage kidney disease are known to have developed the new disease, called nephrogenic systemic fibrosis or nephrogenic fibrosing dermopathy (NSF/NFD), after they had an MRI or MRA with a gadolinium-based contrast agent.

Symptoms of NSF/NSD may appear within two days or even as long as 18 months after exposure to the contrast agent. The dosage associated with NSF/NSD can vary as well.  Some patients have developed the disease after receiving only one dose of the contrast agent, while others patients who received a higher dosage also developed NSF/NSD.

Experts have warned that gadolinium based MRI scans be avoided in patients with advanced kidney disease until more is known about the true causal link between gadolinium and Nephrogenic Systemic Fibrosis (NSF).

Warning signs that a patient may have NSF or NFD are: burning, itching, swelling, hardening and tightening of the skin; red or dark patches on the skin; yellow spots on the whites of the eyes; stiffness in joints with trouble moving or straightening the arms, hands, legs, or feet; pain deep in the hip bones or ribs; and muscle weakness.

What is Gadolinium?

Gadolinium, a chemical element in the periodic table, is used in an MRI/MRA in order to better observe lesions with abnormal vascularity (or those thought to cause abnormalities in the blood-brain barrier) in the brain (intracranial lesions), spine, and associated tissues. Gadolinium, which is pronounced gad•o•lin•i•um, has been shown to improve the high-temperature characteristics of iron, chromium, and related alloys, and is most notably used with magnetic resonance imaging.

Gadolinium was endorsed for use in MRI scans in 1988 and has been used in millions of studies since. The element is the preferred contrast agent for folks with chronic kidney disease, however recent finding are causing many to reconsider this preference. Gadolinium gained favor because the use of iodine-containing contrast agents is still a common cause of hospital-acquired acute renal failure and is associated with increased death & morbidity.

Gadolinium Contrast Dye Brand Names

  • Omniscan™ by GE Healthcare
  • OptiMARK by Mallinckrodt/Tyco Healthcare
  • Magnevist by Bayer/Schering AG/Berlex
  • ProHance by Bracco Diagnostics,
  • MultiHance by Bracco Diagnostics

Legal Help For Victims Of Gadolinium MRI MRA Contrast Agent

If you or a loved developed NSF as a result of Gadolinium MRI Contrast Dye you have valuable legal rights. Please fill out the form at the right for a free case evaluation or call 1-800-YOURLAWYER (1-800-968-7529).


GadoliniumRSS Feed

FDA Investigating Risk of Brain Deposits with Gadolinium-Based MRI Contrast Agents

Jul 29, 2015
The Food and Drug Administration (FDA) is investigating the risk of brain deposits following repeated use of gadolinium-based contrast agents (GBCAs) for magnetic resonance imaging (MRI). Recent publications in the medical literature have reported that deposits of GBCAs remain in the brains of some patients who undergo four or more contrast MRI scans, long after the last administration. The FDA says it is not known whether gadolinium deposits are harmful or can lead to adverse health...

Fewer Kidney Patients Received Gadolinium Agents Following 2006 NSF Alert

Nov 4, 2010 | Parker Waichman LLP
MR Studies Since The (FDA) First Issued Warnings About Their Association With NSF Fewer kidney patients have received gadolinium contrast dyes during MR studies since the US Food & Drug Administration (FDA) first issued warnings about their association with nephrogenic systemic fibrosis (NSF) in 2006. NSF is a condition involving the formation of excess fibrous connective tissue in the skin, joints, eyes, and internal organs that can be fatal. Evidence suggests that NSF is most...

FDA Stregnthens Warnings on Gadolinium MRI Dyes

Sep 9, 2010 | Parker Waichman LLP
New Warnings on their labels regarding their association with NSF, according to the FDA Gadolinium-based contrast dyes will now bear new warnings on their labels regarding their association with nephrogenic systemic fibrosis (NSF), according to the Food & Drug Administration (FDA). Gadolinium-based contrast dyes are intravenous drugs approved by the FDA for use with magnetic resonance imaging (MRI) or magnetic resonance angiography (MRA) to help detect abnormalities of body organs,...

Omniscan, Magnevist and OptiMARK Associated with Most NSF Cases

Jun 24, 2010 | Parker Waichman LLP
GE Healthcare, Magnevist by Bayer Healthcare Pharmaceuticals and Covidien’s OptiMARK Omniscan by GE Healthcare, Magnevist by Bayer Healthcare Pharmaceuticals and Covidien’s OptiMARK are linked to the highest number of nephrogenic systemic fibrosis (NSF) cases, according the American College of Radiology. The group has advised radiologists to avoid using these three gadolinium contrast agents when administering MRIs to patients with chronic or acute kidney disease. According to...

Dutch Regulators Fault GE for Failing to Report Omniscan NSF Case

Jun 18, 2010 | Parker Waichman LLP
The Danish Medicines Agency has charged that GE Healthcare violated Dutch Law The Danish Medicines Agency has charged that GE Healthcare violated Dutch law when it failed to promptly and completely inform regulators about a patient who died after developing nephrogenic systemic fibrosis (NSF) following exposure to Omniscan contrast dye. According to a report on ProPublica’s Web site, because the statute of limitations had expired, the agency said it would not pursue further action...

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