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FDA Adds Contrast Agent Label Warning

Cheryl Clark, for HealthLeaders Media, September 13, 2010

The FDA advised providers to record the specific GBCA and the dosage given to each patient.

 

 

 

  • Do not exceed recommended dose and prior to re-administration, allow sufficient time for elimination from body, respecting half life.
  • For patients who are receiving hemodialysis, consider promptly initiating hemodialysis following GBCA administration.
  • Present patients with a list of symptoms.
  • Report adverse events with GBCAs to Fed's MedWatch program.
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    Cheryl Clark is senior quality editor and California correspondent for HealthLeaders Media. She is a member of the Association of Health Care Journalists.
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