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Prescribing information
LANTUS® 10th Anniversary

Managing a Patient on LANTUS®: Frequently Asked Questions

When it comes to taking insulin, what are the benefits of the LANTUS® SoloSTAR® pen?

How can I switch my inpatients from IV-RHI to LANTUS®?

Does the LANTUS® SoloSTAR® pen have good insurance coverage?

How can I reduce the risk of hypoglycemia when managing patients?

How do the pharmacodynamic profiles of LANTUS® and NPH compare?

How does basal-bolus insulin therapy compare with sliding-scale insulin delivery in hospitalized patients with diabetes?

When it comes to taking insulin, what are the benefits of the LANTUS® SoloSTAR® pen?

One of the reasons certain patients are hesitant about starting insulin therapy is that insulin therapy regimens can be confusing.74

In a survey of 456 patients using an insulin pen, 77% reported finding it easier to comply with their insulin regimen.74

The LANTUS® SoloSTAR® pen is designed for ease of use and has optimized dose and injection features. It’s easy to teach, as it can be used in 5 straightforward steps. The LANTUS® SoloSTAR® pen is also easy to use, allowing doses between 1 and 80 units with just one injection.

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How can I switch my inpatients from IV-RHI to SC LANTUS®?

LANTUS® should be administered once a day at the same time each day. The dose of LANTUS® should be individualized based on clinical response. Blood glucose monitoring is essential to all patients receiving insulin therapy.

If an inpatient on an IV drip of regular human insulin (RHI) is being switched to LANTUS®, begin the patient on LANTUS® 2 hours before stopping the RHI drip. For patients receiving a very-low-calorie intake, there are two options for initial dosage: the first is to estimate the 24-hour insulin use based on the IV drip rate during the last 6 or 8 hours, then multiply that number by 80%. The second option is to multiply the mean overnight drip rate (units per hour) by 20 hours. Adjust as needed.

For patients with normal oral intake, or who are receiving an IV of dextrose or enteral feedings, the LANTUS® dose should match the patient’s 24-hour combined basal and nutritional requirements.

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Does the LANTUS® SoloSTAR® pen have good insurance coverage?

The LANTUS® SoloSTAR® pen is available for the same copay as the LANTUS® vial for most managed care plans. This may translate to patients receiving 50% more LANTUS® units per prescription for the same copay as the vial. One prescription for the LANTUS® SoloSTAR® pen provides a box with 5 pens, each one containing 300 units of LANTUS® insulin for a total of 1500 units. One prescription for a vial of LANTUS® insulin is only 1000 units. For the same copay, many of your patients could save on the cost of LANTUS® insulin with the LANTUS® SoloSTAR® pen.

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How can I reduce the risk of hypoglycemia when managing patients?15

In order to limit the risk of hypoglycemia, it’s important for physicians to ensure that patients are taking their insulin as prescribed. Make patients aware of the common causes of hypoglycemia, such as too much insulin, too little food or missed meals, and too much exercise or activity. Early warning signs of hypoglycemia may be different, less noticeable or not noticeable at all in some people. That is why it is important for patients to check their blood sugar. Patients should be informed that the ability to concentrate and react may be impaired as a result of hypoglycemia. This may present a risk in situations where these abilities are especially important, such as driving or operating other machinery.

A Low Rate of Severe Hypoglycemia in Patients Taking Once-Daily LANTUS®36

Link to reference Rates of hypoglycemia in the INSIGHT study

a Hypoglycemic events were classified as severe if patients required assistance and either promptly responded to therapy with oral carbohydrate, intravenous glucose, or parenteral glucagon, or had a documented capillary glucose ≤36 mg/dL. Data were based on numbers of patients experiencing specified adverse events. From Gerstein and data on file.36

b(P=NS)

If you are managing inpatients, hypoglycemia is a common obstacle to improving diabetes care. Detailed planning is required when discharging inpatients with diabetes to ensure the patient is educated about the risks of hypo- and hyperglycemia:

Reemphasize to the patient his or her diabetes diagnosis. Give clear recommendations for short- and long-term glycemic management. Finally, connect the patient with a Certified Diabetes Educator, or CDE, and schedule a follow-up visit to educate the patient about diabetes management.

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How do the pharmacodynamic profiles of basal insulins compare?

LANTUS® is the only 24-hour insulin approved exclusively for use once a day, and has been shown to exhibit a longer duration at a dose of 0.3 Units/kg over a 24-hour period.19

Link to reference Link to reference Profile of LANTUS® vs NPH in Patients with Type 1 Diabetes

a Glucose utilization rate in mg/kg/min, determined as the amount of glucose infused to maintain constant plasma glucose levels (hourly mean values); indicative of insulin activity.

Adapted from Lepore.19

The graph shows results from a study in patients with type 1 diabetes. The median time between injection and the end of the pharmacological effect was 14.5 hours for neutral protamine Hagedorn, or NPH, insulin and 24 hours for LANTUS®. Comparing the profile of NPH to LANTUS® after subcutaneous injection in type 1 patients, LANTUS® shows no peak over 24 hours.19

The longer duration of action of LANTUS® is directly related to its slower rate of absorption and supports once daily subcutaneous administration. LANTUS® should be administered at the same time each day. The time course of insulins, including LANTUS®, may vary between individuals and within the same individual.

This is the action profile of LANTUS® compared to detemir in patients with type 1 diabetes.

Profile of LANTUS® vs Detemir

d Glucose infusion rate (mg/kg/min).

Adapted from Porcellati.30

Twenty-four subjects with type 1 diabetes naïve to glargine and detemir were studied twice in a randomized, double-blind crossover study. Plasma glucose was clamped at 100 mg/dL for 24 hours after subcutaneous injection of 0.35 Units/kg of either glargine or detemir. At 0.35 Units/kg, this study showed that LANTUS® had no pronounced peak and lasted a full 24 hours, and the mean action profile of detemir tapered off around hour 16.30

In this single-center, double-blind study, 12 subjects with type 1 diabetes were randomized to a specific treatment sequence encompassing 5 dose levels of insulin detemir. The subjects were kept isoglycemic, defined as 130 mg/dL, and C-peptide–negative, defined as levels less then 0.03 nmol/L.31

Link to reference Profile of detemir vs NPH

d Glucose infusion rate (mg/kg/min).

Adapted from Plank.31

When we look at detemir, we see the duration of action is dose-dependent.30,31

Detemir can be administered once or twice daily. The mean duration of action of detemir ranged from 5.7 hours at the lowest dose to 23.2 hours at the highest dose (sampling period of 24 hours).

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How does basal-bolus insulin therapy compare with sliding-scale insulin delivery in hospitalized patients with diabetes?

Sliding-scale insulin monotherapy may lead to wide fluctuations in blood glucose levels.55

Link to reference SSI

Adapted from Clement.55

A review of 52 studies published over a 37 year period suggests that sliding scale insulin alone is suboptimal. Sliding-scale insulin monotherapy, or SSI, has many limitations.55 Many regimens include the practice of insulin initiation when glucose levels exceed 200 mg/dL.59 With SSI, dosing is reactive, based on inadequacy of previous doses, rather than proactive.55

Treatment with a basal-bolus insulin regimen achieved better glycemic control than SSI delivery in noncritically ill hospitalized patients and nonsurgical patients with type 2 diabetes.59

With the blood glucose target of <140 mg/dL, 66% in the basal-bolus group reached the target, while only 38% in the SSI group met this goal. There were no differences between the groups in the rate of hypoglycemia.59

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Useful tools for your LANTUS® patients >

Important Safety Information for Lantus®

CONTRAINDICATIONS

Lantus® is contraindicated in patients hypersensitive to insulin glargine or one of its excipients.

WARNINGS AND PRECAUTIONS

Monitor blood glucose in all patients treated with insulin. Insulin regimens should be modified cautiously and only under medical supervision. Changes in insulin strength, manufacturer, type, or method of administration may result in the need for a change in insulin dose or an adjustment in concomitant oral antidiabetic treatment.

Do not dilute or mix Lantus® with any other insulin or solution. If mixed or diluted, the solution may become cloudy, and the onset of action/time to peak effect may be altered in an unpredictable manner. Do not administer Lantus® via an insulin pump or intravenously because severe hypoglycemia can occur. Insulin devices and needles must not be shared between patients.

Hypoglycemia is the most common adverse reaction of insulin therapy, including Lantus®, and may be life-threatening.

Severe life-threatening, generalized allergy, including anaphylaxis, can occur.

A reduction in the Lantus® dose may be required in patients with renal or hepatic impairment.

DRUG INTERACTIONS

Certain drugs may affect glucose metabolism, requiring insulin dose adjustment and close monitoring of blood glucose. The signs of hypoglycemia may be reduced in patients taking anti-adrenergic drugs (e.g., beta-blockers, clonidine, guanethidine, and reserpine).

ADVERSE REACTIONS

Other adverse reactions commonly associated with Lantus® are injection site reaction, lipodystrophy, pruritus, and rash.

In clinical studies in adult patients there was a higher incidence of treatment-emergent injection-site pain (2.7% Lantus® vs. 0.7% NPH). The reports of pain at the injection site were usually mild and did not result in discontinuation of therapy.

Important Safety Information for Lantus® SoloSTAR®

Lantus® SoloSTAR® is a disposable prefilled insulin pen. To help ensure an accurate dose each time, patients should follow all steps in the Instruction Leaflet accompanying the pen; otherwise they may not get the correct amount of insulin, which may affect their blood glucose.

Indications and Usage for Lantus®

Lantus® is a long-acting insulin analog indicated to improve glycemic control in adults and children (6 years and older) with type 1 diabetes mellitus and in adults with type 2 diabetes mellitus. Lantus® should be administered once a day at the same time every day.

Important Limitations of Use: Lantus® is not recommended for the treatment of diabetic ketoacidosis. Use intravenous short-acting insulin instead.

Lantus® SoloSTAR® is a disposable prefilled insulin pen.

Please click here for full prescribing information.


Important Safety Information for
Apidra® (insulin glulisine [rDNA origin] injection)

CONTRAINDICATIONS

Apidra® is contraindicated during episodes of hypoglycemia and in patients hypersensitive to Apidra® or any of its excipients.

WARNINGS AND PRECAUTIONS

Closely monitor blood glucose in all patients treated with insulin. Change insulin regimens cautiously and only under medical supervision. Changes in insulin strength, manufacturer, type, or method of administration may result in the need for a change in insulin dose or an adjustment in concomitant oral antidiabetic treatment. As with all insulin preparations, the time course of Apidra® action may vary by individual or at different times in the same individual and is dependent on many conditions, including the site of injection, local blood supply, or local temperature.

Hypoglycemia is the most common adverse reaction of insulin therapy, including Apidra®, which may be serious.

Severe life-threatening, generalized allergy, including anaphylaxis, can occur. All insulins, including Apidra®, can cause hypokalemia, which if untreated, may be serious.

A reduction in the Apidra® dose may be required in patients with renal or hepatic impairment.

Apidra® for subcutaneous injection should not be mixed with insulins other than NPH. Do not mix Apidra® with any insulin when used in the pump or for intravenous administration. Insulin devices and needles must not be shared between patients.

DRUG INTERACTIONS

Certain drugs may affect glucose metabolism, requiring insulin dose adjustment and close monitoring of blood glucose. The signs of hypoglycemia may be reduced in patients taking anti-adrenergic drugs (e.g., beta-blockers, clonidine, guanethidine, and reserpine).

ADVERSE REACTIONS

Other adverse reactions commonly associated with Apidra® include injection site reactions, lipodystrophy, pruritus, and rash.

Indications and Usage for Apidra®

Apidra® is a rapid-acting insulin analog indicated to improve glycemic control in adults with type 2 diabetes or adults and children (4 years and older) with type 1 diabetes.

When used as a mealtime insulin, the dose of Apidra® should be given within 15 minutes before or within 20 minutes after starting a meal. Apidra® given by subcutaneous injection should normally be used in regimens that include a longer-acting insulin.

Please click here for full prescribing information for Apidra®


Click herefor information on Sharps Medical Waste Disposal.

Lantus® is a long-acting insulin analog indicated to improve glycemic control in adults and children (6 years and older) with type 1 diabetes mellitus and in adults with type 2 diabetes mellitus. Lantus® should be administered once a day at the same time every day.

Important Limitations of Use: Lantus® is not recommended for the treatment of diabetic ketoacidosis. Use intravenous short-acting insulin instead.

Important Safety Information for Lantus®

Contraindications

Lantus® is contraindicated in patients hypersensitive to insulin glargine or one of its excipients.

Warnings and Precautions

Monitor blood glucose in all patients treated with insulin. Insulin regimens should be modified cautiously and only under medical supervision. Changes in insulin strength, manufacturer, type, or method of administration may result in the need for a change in insulin dose or an adjustment in concomitant oral antidiabetic treatment.

Please click here for additional Important Safety Information.

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