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OPTIMARK (gadoversetamide injection) – Association with Nephrogenic Systemic Fibrosis (NSF) in Patients with Renal Impairment – For the Public
- Starting date:
- January 12, 2010
- Posting date:
- January 12, 2010
- Type of communication:
- Public Communication
- Source of recall:
- Health Canada
- Important Safety Information
- General Public
- Identification number:
This is duplicated text of a letter from Tyco Healthcare (Covidien).
Contact the company for a copy of any references, attachments or enclosures.
Public Communication – Health Canada Endorsed Important Safety Information on OPTIMARK
January 12, 2010
Subject: Association of OPTIMARK® (gadoversetamide injection) with Nephrogenic Systemic Fibrosis (NSF)
Tyco Healthcare/Covidien in consultation with Health Canada, wishes to highlight important safety information pertaining to gadoversetamide (Optimark®), a gadolinium-based contrast agent used during magnetic resonance imaging (MRI). MRI is a test that uses a magnetic field and pulses of radio wave energy to make pictures of organs in order to detect the presence of disease.
Tyco Healthcare/Covidien continues to receive post-market reports of NSF associated with Optimark®. NSF is a rare condition that has been observed so far only in patients with kidney disease. From August 15, 2006 to October 15, 2009, a total of 93 reports of NSF have been reported as associated with the use of Optimark® worldwide. There are no cases of NSF reported with Optimark® in Canada at this time.
Optimark® will now be contraindicated in patients with 1) severe short-term or long-term kidney problems or 2) a short-term kidney problem of any severity due to the hepato-renal (liver-kidney) syndrome or in the time period around liver transplantation.
Optimark® is not recommended for use in children below the age of two years because the safety and efficacy of Optimark®, as well as impact of use in patients with an immature kidney function have not been studied.
This advisory and letters issued to health care professionals can be accessed on Health Canada's Web site. Tyco Healthcare/Covidien has provided this information to relevant health care professionals across Canada.
For more information about Optimark®, patients should consult their health care professional or refer to the Canadian Product Monograph that provides current full prescribing information for Optimark®. A copy of the most up-to-date Canadian Product Monograph for Optimark® can be found on the Health Canada Web site.
Managing marketed health product-related adverse reactions depends on health care professionals and consumers reporting them. Any case of serious Nephrogenic Systemic Fibrosis (NSF) or other serious or unexpected adverse reactions in patients receiving Optimark should be reported to Tyco Healthcare/Covidien or Health Canada at the following addresses:
Tyco Healthcare (Covidien)
Any suspected adverse reaction can also be reported to:
Canada Vigilance Program
Marketed Health Products Directorate
Address Locator: 0701D
Ottawa, Ontario, K1A 0K9
Telephone: 613-957-0337 or Fax: 613-957-0335
To report an Adverse Reaction, consumers and health professionals may call toll free:
For other inquiries related to this communication, please contact Health Canada at:
Marketed Health Products Directorate (MHPD)
original signed by
Joseph Di Marzo
Director, Regulatory Affairs and Quality Assurance
- Date modified: