Sanofi Diabetes
Print | Adjust Font Size Decrease font size Increase font size   Search:
Prescribing information
LANTUS® 10th Anniversary

Choosing an Insulin: Frequently Asked Questions

What is LANTUS®?

What are the benefits of LANTUS® long-acting basal insulin?

What are some of the possible risks or adverse reactions of insulin therapy, including LANTUS®?

Is my patient ready for LANTUS®?

How does LANTUS® work?

What is the long-term safety of LANTUS®?

Can LANTUS® be mixed with other insulin?

What is LANTUS®?

LANTUS®, or insulin glargine, is a once-daily long-acting basal insulin for patients with diabetes mellitus. It is indicated to improve glycemic control in adults and children (6 years and older) with type 1 diabetes and in adults with type 2 diabetes. LANTUS® should be administered once a day at the same time each day. LANTUS® is not recommended for the treatment of diabetic ketoacidosis. Use intravenous short-acting insulin instead.

A recombinant human insulin analog, LANTUS® provides 24-hour basal coverage with no pronounced peak, mimicking the steady basal secretion of insulin provided by a normal pancreas.3

Link to reference Link to reference The mechanics of sustained release

Adapted from LANTUS® Prescribing Information3 and McKeage.4

LANTUS® is engineered to begin microprecipitation upon subcutaneous injection, slowly releasing small amounts of basal insulin for the next 24 hours. This profile allows LANTUS® to be dosed once a day as a patient's basal insulin.

The time course of action of insulin, including LANTUS®, may vary between individuals and within the same individual.

Back to Top  

What are the benefits of LANTUS® long-acting basal insulin?

Long-acting basal insulins like LANTUS® mimic normal physiologic insulin secretion.15

Link to reference LANTUS® + rapid-acting insulin

Adapted from Leahy.17

As this chart demonstrates, to closely mimic normal physiologic insulin secretion, a constant supply of basal insulin (glargine) and a mealtime dosing of prandial insulin is essential.17

Long acting LANTUS® insulin:3

  • Is relatively continuous over 24 hours
  • Suppresses blood glucose production between meals and overnight
  • Should contribute approximately 50% of daily insulin needs
  • Has no pronounced peak19

Back to Top  

What are some of the possible risks or adverse reactions of insulin therapy, including LANTUS®?

Hypoglycemia is the most common adverse reaction of insulin therapy, including LANTUS®, which may be serious. Some of the other common adverse reactions associated with LANTUS® include:3

  • Allergic reactions
    • Severe, life-threatening, generalized allergy, including anaphylaxis, can occur
  • Rash, lipodystrophy, pruritus
  • Weight gain

In order to limit the risk of hypoglycemia, it’s important for physicians to ensure that patients are taking their insulin as directed. Patients should be made aware of the activities that might alter blood glucose such as exercise, which stimulates glucose removal from the blood.15

These are some of the side effects for insulins such as LANTUS®. See the full Prescribing Information for full details.

Useful tools for your LANTUS® patients

Back to Top  

Is my patient ready for LANTUS®?

LANTUS® is indicated to improve glycemic control in adults and children (6 years and older) with type 1 diabetes, and adults with type 2 diabetes. After lifestyle management and OADs alone have failed to yield target glycemic goals, the addition of insulin, such as LANTUS®, should be considered in patients with type 2 diabetes. This stepwise approach to treatment reflects the progressive nature of the disease.5

Link to reference Stepwise approach for continuity of therapy

Adapted from Raccah.5

As type 2 diabetes progresses, pancreatic function declines, requiring intensification of therapy. When diet, exercise, and oral therapies are no longer enough to achieve the desired glycemic goal, it may be time to consider the addition of a basal insulin. The option exists to further intensify insulin coverage to achieve glycemic goals by progressively adding rapid-acting prandial insulin to select meals beginning with the largest meal, and then ultimately full basal-bolus therapy for all meals if necessary.5

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

Back to Top  

How does LANTUS® work?

Long-acting LANTUS® is a recombinant human insulin analog that works as a parenteral blood-glucose-lowering agent.

LANTUS® is produced by using a non-pathogenic laboratory strain of Escherichia coli (K12) as the production organism. Specific amino acids are then added or replaced, shifting the isoelectric point and producing a solution that is completely soluble at pH of approximately 4.3

When injected into the neutral pH environment of the subcutaneous tissue, the acidic solution microprecipitates, slowly releasing insulin. This accounts for the lack of a pronounced peak, which allows LANTUS® to be dosed once daily at the same time each day.3

LANTUS® is metabolized at the injection site and in the systemic circulation to two main active metabolites, designated M1 and M2. M1 and M2 are very close in structure and function to human insulin, but have slightly weaker interactions with the insulin and IGF-1 receptors than human insulin. Both LANTUS® and its active metabolites have been detected in systemic circulation.3

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.

Back to Top  

What is the long-term safety of LANTUS®?

Diabetes mellitus increases the lifetime risk of both cancer and retinopathy, and it is important to establish that diabetes therapies do not increase that risk. In a large, 5-year study of patients with type 2 diabetes, the risk of cancer or retinopathy was no greater with LANTUS® than with human insulin.

Back to Top  

Can LANTUS® be mixed with other insulin?

LANTUS® cannot be diluted or mixed with any other solution, including insulin. Diluting or mixing LANTUS® may produce a cloudy solution, and pharmacokinetic/ pharmacodynamic profiles may be altered in an unpredictable manner.3

If your patients' A1C goals are not being reached by a basal insulin alone, consider timely intensification of insulin therapy to a basal-prandial regimen.5 If your patients are on a basal-prandial regimen, know that LANTUS® may be taken in conjunction with a rapid-acting insulin such as APIDRA®.

Hypoglycemia is the most common adverse reaction of insulin, including LANTUS®. The risk of hypoglycemia increases with intensive glycemic control. Patients must be educated to recognize and manage hypoglycemia.

Back to Top  

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.

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.

Mobile Optimized site

Request Samples

Access product
samples, like the
LANTUS® SoloSTAR®
pen, for your patients.*
Request Samples Now » *Must register to request samples. Certain restrictions may apply.
LANTUS® Formulary Tool
See how LANTUS® is covered on your patients' insurance plans.

Visit Formulary
Tool >