Gadolinium Toxicity

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Report your Gadolinium-related problems to the FDA.

Medwatch_thumb.gifIf you suspect that your unexplained symptoms were caused by the contrast agent you received for your MRI or MRA, you need to file a MedWatch Adverse Event report with the FDA.  You don’t have to be able to prove anything – you only need to suspect that your health problems were caused by the Gadolinium-based Contrast Agent that you received. (more…)

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