Published:
Covidien Submits Label Change for Optimark Contrast Agent
ST. LOUIS - (BUSINESS WIRE) - Covidien (NYSE:COV), a leading global provider of healthcare products,
today announced that it will voluntarily contraindicate the use of its
Optimark gadoversetamide injection, a gadolinium-based contrast agent
(GBCA), in magnetic resonance imaging (MRI) procedures involving
patients with severe renal impairment. The Company is modifying the
product's label to reflect a contraindication for this small patient
population, which constitutes less than 0.5 percent of the U.S.
population.
Mallinckrodt Inc., a Covidien company, has submitted this label change
to the U.S. Food and Drug Administration (FDA) and is implementing the
new label in the U.S. effective immediately. The revised label
contraindicates the product's use in patients with acute or chronic
severe renal insufficiency (glomerular filtration rate of less than 30
mL/min/1.73m2) or acute renal insufficiency of any severity
due to hepato-renal syndrome or in the perioperative liver transplant
period.
The Company is implementing this label change in all other countries
where Optimark contrast agent has been approved for sale, in accordance
with local regulatory requirements. Covidien also will update its
educational materials to help physicians make informed decisions
regarding the appropriate use of this product.
GBCAs are important tools to aid physicians seeking to diagnose and
treat patients. In 2008, more than 9.5 million patients in the U.S. were
given GBCAs to help improve the diagnostic quality of MRI scans.
When used as directed in appropriately-screened patients, GBCAs have a
favorable safety profile, with the majority of any adverse reactions in
this class being mild and usually transitory. A possible relationship,
however, has been asserted between the use of GBCAs and nephrogenic
systemic fibrosis (NSF) among patients with severe renal impairment.
This subset of patients can be easily identified by obtaining patient
history and/or laboratory tests.
"We have concluded that Optimark contrast agent should be reserved for
the vast majority of the population - more than 99 percent - where the
risk/benefit profile is well established," said Dr. Herbert Neuman, Vice
President, Medical Affairs and Chief Medical Officer, Pharmaceuticals,
Covidien. "For the small percentage of the U.S. population - less than
0.5 percent - with severe renal impairment, we believe it is prudent to
act now, rather than wait for a causal link between GBCAs and NSF to be
established. Although the label already advises caution when using GBCAs
with these patients, we are voluntarily taking this next step to help
ensure this small, at-risk population does not receive administration of
a contrast agent that could pose a risk of NSF."
In 2007, the FDA recommended that use of all GBCAs should be avoided in
patients with severe renal impairment unless the diagnostic information
is essential and only available with a contrast-enhanced MRI procedure,
resulting in a boxed warning for each GBCA. In addition, the FDA will
hold a joint Advisory Committees Meeting on December 8 to discuss
whether other steps are necessary to ensure the safe use of all GBCAs.
"At Covidien, patient safety is our highest priority," Dr. Neuman said.
"The extensive efforts of the FDA, industry, clinician organizations and
thought leaders since 2006 have increased awareness of NSF and its
apparent relationship to GBCAs in patients with severely impaired renal
function. This increased awareness has had a noticeable impact on the
practice of medicine and contributed to a significant reduction in the
incidence of the disease. We look forward to additional dialog with the
FDA and the joint Advisory Committees on this important topic."
About Covidien
Covidien is a leading global healthcare products company that creates
innovative medical solutions for better patient outcomes and delivers
value through clinical leadership and excellence. Covidien manufactures,
distributes and services a diverse range of industry-leading product
lines in three segments: Medical Devices, Pharmaceuticals and Medical
Supplies. With 2008 revenue of $10 billion, Covidien has more than
41,000 employees worldwide in 59 countries, and its products are sold in
over 140 countries. Please visit www.covidien.com
to learn more about our business.
Forward-Looking Statements
Any statements contained in this communication that do not describe
historical facts may constitute forward-looking statements as that term
is defined in the Private Securities Litigation Reform Act of 1995. Any
forward-looking statements contained herein are based on our
management's current beliefs and expectations, but are subject to a
number of risks, uncertainties and changes in circumstances, which may
cause actual results or Company actions to differ materially from what
is expressed or implied by these statements. The factors that could
cause actual future results to differ materially from current
expectations include, but are not limited to, our ability to effectively
introduce and market new products or keep pace with advances in
technology, the reimbursement practices of a small number of large
public and private insurers, cost-containment efforts of customers,
purchasing groups, third-party payers and governmental organizations,
intellectual property rights disputes, complex and costly regulation,
including healthcare fraud and abuse regulations, manufacturing or
supply chain problems or disruptions, rising commodity costs, recalls or
safety alerts and negative publicity relating to Covidien or its
products, product liability losses and other litigation liability,
including legacy Tyco-related litigation, divestitures of some of our
businesses or product lines, our ability to execute strategic
acquisitions of, investments in or alliances with other companies and
businesses, competition, risks associated with doing business outside of
the United States, foreign currency exchange rates, issues related to
our existing material weakness in accounting for income taxes or
potential environmental liabilities. These and other factors are
identified and described in more detail in our filings with the SEC. We
disclaim any obligation to update these forward-looking statements other
than as required by law.
Covidien
Erica Abbett, 314-654-3247
Manager, Media Relations
Vice President
Pharmaceuticals
erica.abbett@covidien.com
or
Coleman
Lannum, CFA, 508-452-4343
Investor Relations
cole.lannum@covidien.com
or
Bruce
Farmer, 508-452-4372
Vice President
Public Relations
bruce.farmer@covidien.com
or
Brian
Nameth, 508-452-4363
Director
Investor Relations
brian.nameth@covidien.com
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