FDA Approves NovoLog(R) Labeling Update
July 15 2009 - 12:43PM
PR Newswire (US)
Increasing the Time Patients Can Use and Store NovoLog� in Their
Pumps from Two Days to Six Days PRINCETON, N.J., July 15
/PRNewswire-FirstCall/ -- Diabetes patients taking NovoLog (insulin
aspart [rDNA origin] injection) can now use the insulin in their
pump for up to six days following the U.S. Food and Drug
Administration (FDA) approval of a labeling change, diabetes care
company Novo Nordisk announced today.(1) The previous label allowed
for NovoLog to be stored in the pump reservoir for two days. This
makes NovoLog the first and only rapid-acting insulin with this
extended in-use time. An insulin pump is a small, battery powered
device designed to constantly deliver insulin into the patient's
body 24 hours a day according to a preset program. Approximately
the size of a pager, the pump system is composed of a reservoir for
the insulin, a small battery, the pump, and a thin plastic tube
with a needle on the end that passes insulin into the body, called
the infusion set. The updated NovoLog label also states that
patients using NovoLog in their pumps should change the infusion
set and the infusion set insertion site at least every three days.
The previous label stated that NovoLog in the pump reservoir,
infusion set and the infusion set insertion site be changed at
least every 48 hours. The revised label keeps the same
recommendation that NovoLog should be discarded after exposure to
temperatures that exceed 37 degrees C (98.6 degrees F). "The
ability to go longer between changes of insulin in the pump allows
people with diabetes to have more active and flexible lifestyles,
which are integral to the success of long-term diabetes
management," said Richard R. Rubin, PhD, professor, medicine and
pediatrics, The Johns Hopkins University School of Medicine. The
label change is based on the FDA's review of data from Novo Nordisk
that showed the stability of NovoLog in the pump for up to six
days. NovoLog is a rapid-acting insulin analog, meaning it works
faster and for a shorter period of time compared with regular human
insulin. NovoLog is also available in FlexPen , the world's #1
selling prefilled insulin pen. Diabetes patients who take NovoLog
can eat within 5-10 minutes of use, rather than the typical 30
minutes required with regular human insulin. NovoLog was first
approved by the FDA in 2000 and approved for use in pumps in 2001.
Prescribing information for NovoLog is available by contacting Novo
Nordisk or visiting http://www.novolog.com/. About NovoLog (insulin
aspart [rDNA origin] injection) NovoLog is a man-made insulin that
is used to control high blood sugar in adults and children with
diabetes mellitus. Important Safety Information Do not take NovoLog
if your blood sugar is too low (hypoglycemia) or if you are
allergic to anything in NovoLog . If you take too much NovoLog your
blood sugar may fall too low. NovoLog is a fast-acting insulin. You
should eat a meal within 5 to 10 minutes after using NovoLog to
avoid low blood sugar. Do not inject NovoLog if you do not plan to
eat right after using NovoLog . Check your blood sugar levels. Ask
your health care provider what your blood sugars should be and when
you should check your blood sugar levels. Alcohol, including beer
and wine, may affect your blood sugar when you take NovoLog . Do
not change the type of insulin you use unless told to do so by your
health care provider. The amount of insulin you take as well as the
best time for you to take your insulin may need to change if you
take a different type of insulin. Do not mix NovoLog with any other
insulins when used in a pump or with any insulins other than NPH
when used with injections by syringe. Tell your health care
provider about all medicines you take and all of your medical
conditions, including if you are pregnant or breastfeeding. Your
NovoLog dose may change if you take other medicines. NovoLog has
not been studied in children with type 2 diabetes or in children
with type 1 diabetes under the age of two. The most common side
effect of NovoLog is low blood sugar (hypoglycemia). Other possible
side effects include reactions at the injection site (like redness,
swelling and itching), and allergic reactions. Get medical help
right away if you experience signs of serious allergic reaction
such as body rash, trouble with your breathing, fast heartbeat, or
sweating. Ask your doctor or pharmacist for further information.
About Novo Nordisk Novo Nordisk is a healthcare company with an
86-year history of innovation and achievement in diabetes care. The
company has the broadest diabetes product portfolio in the
industry, including the most advanced products within the area of
insulin delivery systems. In addition to diabetes care, Novo
Nordisk has a leading position within areas such as hemostasis
management, growth hormone therapy, and hormone therapy for women.
Novo Nordisk's business is driven by the Triple Bottom Line: a
commitment to economic success, environmental soundness, and social
responsibility to employees and customers. With headquarters in
Denmark, Novo Nordisk employs more than 27,000 employees in 81
countries, and markets its products in 179 countries. Novo
Nordisk's B shares are listed on the stock exchanges in Copenhagen
and London. Its ADRs are listed on the New York Stock Exchange
under the symbol 'NVO'. For global information, visit
novonordisk.com; for United States information, visit
http://www.novonordisk-us.com/. (1) Revised NovoLog Prescribing
Information. "Dosage and Administration." Section 2.3. "Continuous
subcutaneous insulin infusion (CSII) by external pump." NovoLog is
a registered trademark of Novo Nordisk A/S. DATASOURCE: Novo
Nordisk CONTACT: Media: Ambre Morley, +1-609-514-8400, or
Investors: Hans Rommer, +1-609-514-8480, both for Novo Nordisk Web
Site: http://www.novonordisk-us.com/
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