Generic
Insulin Glulisine
2 brands available in the market
At a glance
Insulin Glulisine is a rapid-acting human insulin analog used to improve glycemic control in adults and pediatric patients with diabetes mellitus.
Description
Insulin Glulisine is a rapid-acting human insulin analog produced by recombinant DNA technology using a non-pathogenic laboratory strain of Escherichia coli (K12). It binds to insulin receptors to regulate glucose metabolism, facilitating glucose uptake in muscle and fat cells and inhibiting glucose output from the liver. It has a more rapid onset and shorter duration of action compared with human insulin after subcutaneous administration.
Indications
- Improvement of glycemic control in adults and pediatric patients with diabetes mellitus
Therapeutic class
Rapid Acting Insulin
Pharmacological class
Rapid-acting Insulin Analog
Pharmacology
Regulation of glucose metabolism is the primary activity of insulins and insulin analogs, including insulin glulisine. Insulins lower blood glucose by stimulating peripheral glucose uptake by skeletal muscle and fat, and by inhibiting hepatic glucose production. Insulins inhibit lipolysis and proteolysis and enhance protein synthesis.
Mechanism of action
Lowers blood glucose by binding to insulin receptors, facilitating glucose uptake in muscle and fat cells, and inhibiting glucose output from the liver.
Dosage
Adult Dose (Subcutaneous):
- Diabetes Mellitus: 0.5-1 unit/kg/day (individualized)
- Inject within 15 minutes before a meal or within 20 minutes after starting a meal
- Should generally be used in regimens with intermediate or long-acting insulin
- Hepatic impairment: Dose reduction may be needed
Child Dose (Type 1, 4-17 years): 0.8-1.2 units/kg/day during growth spurts; otherwise adult dosing (0.5-1 unit/kg/day)
Administration
Administer within 15 minutes before a meal or within 20 minutes after starting a meal as subcutaneous injection into abdomen, thigh, or upper arm; rotate injection sites within same region to reduce risk of lipodystrophy; IV administration only under medical supervision.
Missed dose
If you miss a dose, check your blood sugar and take the next dose accordingly; consult your doctor.
Side effects
Side Effects:
- Hypoglycemia
- Allergic reactions
- Injection site reactions
- Lipodystrophy
- Pruritus
- Rash
- Weight gain
Precautions & warnings
Precautions:
- Your ability to drive may be affected if blood sugar is too low or too high
- Hypoglycemia may be life-threatening; increase frequency of glucose monitoring with changes to insulin dosage, coadministered glucose lowering medications, meal pattern, physical activity
- Caution in patients with renal impairment or hepatic impairment or hypoglycemia unawareness
- Hypoglycemia due to medication errors: Check insulin labels before injection
- Hypokalemia: Monitor potassium levels in patients at risk
- Fluid retention and heart failure can occur with concomitant use of TZDs
Contraindications
Contraindications:
- Hypoglycemia
- Hypersensitivity to insulin glulisine or any excipients
Drug interactions
Drug Interactions:
- Oral antidiabetic agents, ACE inhibitors, disopyramide, fibrates, fluoxetine, MAOIs, propoxyphene, salicylates, somatostatin analog, sulfonamide antibiotics increase effect
- Corticosteroids, niacin, danazol, diuretics, sympathomimetic agents, isoniazid, phenothiazine derivatives, somatropin, thyroid hormones, oral contraceptives, lithium decrease effect
- Beta-blockers, clonidine, guanethidine, reserpine may blunt signs/symptoms of hypoglycemia
Food interactions
Food Interactions: It is unsafe to consume alcohol with Insulin Glulisine.
Use in pregnancy
Use in Pregnancy: Category C; animal studies have shown adverse effect on fetus; no adequate human studies; potential benefits may warrant use despite potential risks.
Pregnancy Category: C — always consult a doctor before taking during pregnancy.
Use in lactation
Use in Lactation: Unknown whether insulin glulisine is excreted in human milk; caution due to many drugs excreted in human milk; lactating women may require adjustments of insulin doses.
Pediatric use
Safety and effectiveness established in pediatric patients (4-17 years) with type 1 diabetes; not studied in patients <4 years with type 1 diabetes or in patients with type 2 diabetes.
Geriatric use
In clinical trials, HbA1c values and hypoglycemia frequencies did not differ by age; however caution should be exercised in geriatric patients.
Renal / hepatic impairment
Renal Impairment: Dose reduction may be needed; regular blood glucose monitoring recommended.
Hepatic Impairment: Dose reduction may be needed; regular blood glucose monitoring recommended.
Overdose effects
Overdose: Excess insulin may cause hypoglycemia and, particularly when given intravenously, hypokalemia; mild episodes treated with oral glucose; severe episodes (coma, seizure, neurologic impairment) treated with IM/SC glucagon or IV glucose; hypokalemia must be corrected appropriately.
Storage conditions
Unopened vials and cartridge systems: Store in refrigerator 2°C-8°C; protect from light; do not freeze; opened vials must be used within 28 days.
Chemical structure
Insulin Glulisine