Attorneys in Drug Product Liability

FREE CASE REVIEW

If you or someone you love is suffering, speak with an attorney who has experience with NSF and NDF patients.
Name:
Home # *
 
* required fields
Cell #
Zipcode:
Email:
1. Have you had a MRI where contrast was used?YesNo
2. Have you been diagnosed with
NSF or NDF? Yes No
3. Have you had a liver transplant or liver disease? Yes No
4. Did you have a prior kidney condition? Yes No
5. Have you been diagnosed
with Diabetes?Yes No
6. Do you have any of the following:
Hardening of the skin
Darkened patches on the skin
Burning sensations on the skin
Red areas on the skin
Headaches, nausea and dizziness
Bone pain in the hips or ribs
Muscle weakness
Yellow in the whites of the eyes
Joint stiffness, making it hard to straighten the limbs, hands or feet
Provide any additional information:
 Click to review terms

What is Gadolinium?

Kedneys with Gadolinium contractGadolinium is a paramagnetic metal ion which moves differently within a magnetic field. This trait makes gadolinium a useful contrast agent during an MRI. Gadolinium is used during an MRI because it allows the physician to see the exact size and location of the area that needs to be treated. After the Gadolinium is injected into the bloodstream is exposed to the MRI, and becomes very bright, highlighting any deposits of the fluid which indicates abnormal tissue growth. Contrast agents that use Gadolinium provide the physician with greater clarity and makes the smaller tumors very bright and easy to see.

Once administered, the solution is rapidly removed from the body by the kidneys. The most common side effects associated with the use of Gadolinium based contrast agents are headache, nausea, and a localized burning sensation. Some individuals have been found to be allergic to Gadolinium, experiencing hives, eye irritation, and shortness of breath.

There are currently five FDA-approved gadolinium-based contrast agents, Magnevist, MultiHance, Omniscan, OptiMARK, and ProHance. These agents are approved for use during an MRI scan, but not for MRA. The FDA is asking health care professionals and patients to report possible cases of NSF/NFD through FDA’s MedWatch program.