Gadolinium Toxicity

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Revised GBCA Product Labeling with Medication Guide is now available for all agents

As of April 26, 2018, the revised Product Labeling with the Medication Guide for all gadolinium-based contrast agents (GBCAs) were posted on the FDA’s website.  The FDA announced on December 15, 2017, that it was requiring GBCA manufacturers to revise product labeling and create a Medication Guide for each GBCA.  The purpose of the Medication Guide is to provide patients with information about gadolinium retention in the body so that they can make an informed decision before agreeing to have an MRI with contrast – an MRI with a gadolinium-based contrast agent.  Gadolinium (Gd) is a toxic metal and any amount that remains in the brain and other parts of the body has the potential to have a harmful effect.  While the linear GBCAs are the least stable, macrocyclic agents have been found to leave residual gadolinium in patients’ bodies as well.  The long-term effects of gadolinium deposition are still unknown; however, research is ongoing.

The Medication Guide for each agent mentions “many doses of gadolinium medicines” as a possible risk factor.  Gadolinium-based contrast agents are intravenously administered prescribed drugs that can have a toxic effect even after one dose of contrast.  Currently, no one knows why some patients become symptomatic after having one or more MRIs with a GBCA, while others do not.  However, it appears that everyone retains an unknown amount of gadolinium from each dose of a gadolinium-based contrast agent they receive.

Links to the new Product Labeling for each agent are provided below. (more…)

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