Glucagon Information
Help patients learn to recognize and treat severe hypoglycemia.
Hypoglycemia
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Hypoglycemia is one of the most common adverse events associated with taking insulin. The most common causes of hypoglycemia include: The level of glucose that produces symptoms of hypoglycemia varies from patient to patient and for the same patient under different circumstances. In general, hypoglycemia is identified as having a blood glucose level of 70 mg/dL or less. Patients should be educated on the warning signs of hypoglycemia and how to treat the condition right away. To help your patients learn more about hypoglycemia and how to treat severe lows with glucagon, please see the Low Blood Sugar section on the patient website.

Mild Hypoglycemia
Typical warning signs Treatment
  • Rapid heartbeat
  • Perspiration
  • Shakiness
  • Anxiety
  • Tiredness
  • Hunger
  • Blurry vision
Eat approximately 15 grams of carbohydrate, such as:
  • 3 glucose tablets (5 g each)
  • ½ cup fruit juice or regular soda (not sugar-free or diet)
  • 6 or 7 hard candies (not sugar-free)
  • 1 tablespoon honey or sugar
   

After eating or drinking something, patients should: Important tips for patients Education to help prevent hypoglycemia
When you start a patient on insulin, there are tips you can give him or her to help them lower their risk of hypoglycemia. These tips include: Hypoglycemia requiring emergency treatment
If your patients do not take action quickly, blood glucose can drop dangerously low. This may result in the following: You can help protect your patients from the effects of a severe hypoglycemic event with a prescription for Lilly Glucagon [glucagon by injection (rDNA origin)]. Glucagon quickly eases the symptoms of hypoglycemia by releasing a burst of glucose into the blood. Each kit includes easy-to-follow administration graphics, so it's simple for patients' friends and family to also use in an emergency. You can also refer your patients to the Lilly Glucagon Tutorial on the patient website.

For important safety information and other prescribing considerations, please see Lilly Glucagon Information for the Physician.

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Important Safety Information
Humalog insulins are contraindicated during episodes of hypoglycemia and in patients sensitive to Humalog or one of its excipients. The safety and effectiveness of Humalog in patients less than 3 years of age have not been established. Safety and effectiveness of Humalog Mix75/25 and Humalog Mix50/50 in patients less than 18 years of age have not been established. There are no adequate and well-controlled clinical studies of the use of Humalog in pregnant or nursing mothers.

Potential side effects associated with the use of all insulins include hypoglycemia, weight gain, hypokalemia, lipodystrophy, and hypersensitivity. Because of the difference in action of Humalog, care should be taken in patients in whom these conditions may be clinically relevant (e.g., those who are fasting, have autonomic neuropathy or renal impairment, are using potassium-lowering drugs, or taking drugs sensitive to serum potassium level). Patients should be advised not to mix Humalog Mix75/25 or Humalog Mix50/50 with another insulin. Starting or changing insulin therapy should be done cautiously and only under medical supervision.

When used in an external insulin pump, Humalog should not be diluted or mixed with any other insulin. Humalog Mix75/25 and Humalog Mix50/50 are not indicated for use in external insulin pumps.

Humalog differs from regular human insulin by its rapid onset of action, as well as a shorter duration of activity. Therefore, Humalog and Humalog Mixtures should be given within 15 minutes before a meal. Humalog can also be given immediately after a meal. The short duration of action of Humalog means that patients such as those with type 1 diabetes, whose basal insulin levels are inadequate, will also require a longer-acting insulin to give optimal glucose control (except when using an insulin pump).

Clinical studies comparing Humalog Mix75/25 with human insulin mixtures did not show a difference in the overall rate of hypoglycemia between the two treatments. The overall rate of hypoglycemia did not differ between type 1 and type 2 patients treated with Humalog, as compared with regular human insulin. The lower rate of hypoglycemia with Humalog may be related to higher nocturnal blood glucose levels, as reflected by a small increase in the mean fasting blood glucose levels.

The clinical significance of improvement in postmeal hyperglycemia has not been established. In 12-month clinical studies, A1C did not differ between patients treated with regular human insulin and those treated with Humalog.

Humalog, Humalog Mix75/25, and Humalog Mix50/50 are available by prescription only.

For other important safety information and prescribing considerations, please see Humalog, Humalog Mix75/25, and Humalog Mix50/50 Prescribing Information.

Humalog is a registered trademark of Eli Lilly and Company. Humalog Mix75/25 and Humalog Mix50/50 are trademarks of Eli Lilly and Company.

Humalog Prescribing Information | Humalog Mix75/25 Prescribing Information | Humalog Mix50/50 Prescribing Information | Important Safety Information