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NSF - Nephrogenic Systemic Fibrosis
MRI Contrast Dye - Nephrogenic Systemic Fibrosis (NSF) 

MRI Gadolinium Contrast Dye Side Effects - NSF & NFD

Recently MRI contrast dye has been found to cause a rare fibrosing disease called Nephrogenic Systemic Fibrosis (NSF) and Nephrogenic Fibrosing Dermopathy (NFD). Both are a rare and serious syndromes that involves fibrosis of red skin, joint pain, muscle pain, yellow spots on eyes and renal & kidney failure. The cause of NFD and NSF are not fully understood, but it seems to be associated with exposure to gadolinium used in MRIs and MRAs with contrast dyes. Many of these patients suffer from serious skin and joint problems along with severe kidney failure, renal insufficiency and some have even required liver transplants.

NOTE: While many believe that the MRI dye recall should be ordered by the FDA, patients are still receiving MRI's & MRA's with gadolinium contrast dye, except that new warnings are now given to patients needing MRIs and MRAs with gadolinium contrast dye. As of Jan 2008, no MRI Dye Recall has been ordered by the FDA.

As stated above some, MRI dye side effects include Nephrogenic Systemic Fibrosis (NSF). Patients with NSF often develop large areas of hardened skin with fibrotic nodules and plaques, reddened skin, muscle tightening, muscle weakness, joint pain and burning in joints along with itchy, thick areas of skin, usually on one's limbs.

Flexion contractures can also occur with an accompanying limitation of range of motion.Many doctors and patients mistake Nephrogenic Systemic Fibrosis (NSF) for scleromyxedema, because it shows has a proliferation of dermal fibroblasts and dendritic cells, thickened collagen bundles and an increase of elastic fibers. Nephrogenic Systemic Fibrosis (NSF) by definition occurs with some renal failure, however many have never undergone dialysis and others have received only peritoneal dialysis. Recently, it also appears many patients may not have any renal failure or kidney, liver failure, but the disease it confined to the skin, muscle and joints. MRI Side Effects causing NSF can be deadly.

MRI Contrast Dyes with Gadolinum

According to the FDA, Four of the five approved Gadolinium contrast agents (dyes) have been principally implicated in Nephrogenic Systemic Fibrosis (NSF), including Omniscan, Multihance, Magnevist, and OptiMARK.

MRI Dye Lawsuits - NSF & NFD Legal Actions

If you had a MRI/MRA and a Gadolinium-based contrast dye was used to enhance the MRI image, then your health may be at risk. If you developed Nephrogenic Systemic Fibrosis (NSF), Nephrogenic Fibrosing Dermopathy (NFD), skin problems, skin tightening, severe joint problems, kidney failure, or renal failure, then you may be eligible to file a MRI Gadolinium Lawsuit for your injuries. It is important that you get tested for NSF and NFD. Call us to discuss your symptoms and conditions. Call and talk to a law firm that understand the symptoms and side effects of Gadolinium contrast dyes. Do Not Wait.

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NSF from MRI Gadolinium Contrast Dye in Kidney Failure, Dialysis Patients & Renal Failure  The FDA has reported a possible link between NSF/NFD, kidney failure and renal failure and the exposure to MRI dye / contrast called gadolinium. Patients with kidney disease, kidney failure, kidney or renal insufficeincy and kidney patients on kidney dialysis, may have contracted a horrible fibrosing skin disease from the gadolinium based contrast dyes used in MRIs. These MRI dyes have serious side effects which includes a rare skin, muscle & joint disorder called Nephrogenic Systemic Fibrosis (NSF). Patients with NSF often develop large areas of hardened skin with fibrotic nodules and plaques, reddened skin, muscle tightening, muscle weakness, joint pain and burning in joints along with itchy, thick areas of skin, usually on one's limbs. Click here for more information about Nephrogenic Systemic Fibrosis (NSF)  Recent reports link fractured femurs to the use of Fosamax. If you have fractured your leg or femur and have taken fosamx get a free case evaluation at www.fosamax-femur-fractures.com Fosamax Femur Fracture Lawsuits Fosamax Lawsuits Recent RFDA Depakote alert warns of Depakote use during pregnancy. Depakote may cause harm to the fetus resulting in spinal bifida, neural tube defects, growth retardation and other birth defects. For more information see depakote spina bifida  FDA warning Reglan may cause Tardive Dyskinesia (TD) a rare side effect of long time Reglan usage. Reglan has been linked to Tardive Dyskinesia. Tardive Dyskinesia is a central nervous system disorder characterized by involuntary movements of the limbs as well as twitching of the face and tongue similar to Parkinson's disease. See Metoclopramide and Tardive Dyskinesia TD for more information about reglan side effects. See Reglan Tardive Dyskinesia (TD) side effects lawsuits. Dilantin can cause SJS Stevens Johnson Syndrome and TENS. Get more info about Dilantin SJS Stevens Johnson Syndrome Lawsuit  Dilantin also can cause TEN (Toxic Epidermal Necrolysis) are more severe than others. Erythema multiforme minor is the milder form of SJS and not as serious as Erythema multiforme majoris. However, full blown Stevens-Johnson syndrone. If you or a loved one have taken Dilantin (phenytoin),Tegretol (carbamazepine), Lamictal (lamotrigue) or Levaquin (levofloxacin) and have been diagnosed with SJS or TENS or a loved one has died for complications of SJS Syndrome or TEN, Stevens-Johnson Syndrome (SJS) is a life-threatening condition affecting the skin in which cell death causes the epidermis (the outer layers of skin) separating from the dermis (inner layers of skin). See information about Stevens-Johnson Syndrome (SJS) Dilantin Lawsuit.Talk to a Dilantin SJS Dilantin Stevens Johnson Syndrome SJS Dilantin TEN lawyer about Dilantin TEN Toxic Epidermal Necrolysis Diagosis and your legal rights to a Dilantin lawsuit .Byetta Pancreatitis Lawsuits Toyota Gas Pedal Recall News

 

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