Generic
Insulin Human [rDNA]
27 brands available in the market
At a glance
Insulin Human (rDNA) is used for treatment of type 1 diabetes, type 2 diabetes (not adequately controlled by diet and oral hypoglycemic agents), diabetic ketoacidosis, hyperosmolar non-ketotic syndrome, and gestational diabetes.
Description
Insulin Human (rDNA) is a sterile, clear, colorless solution produced by recombinant DNA technology. It is a fast-acting insulin with a relatively short duration of action compared with other insulins. It lowers blood glucose by binding to insulin receptors, facilitating glucose uptake in muscle and fat cells, and inhibiting glucose output from the liver.
Indications
- Type 1 diabetes mellitus
- Type 2 diabetes mellitus (not adequately controlled by diet and/or oral hypoglycemic agents)
- Diabetic ketoacidosis
- Hyperosmolar non-ketotic syndrome
- Gestational diabetes
Therapeutic class
Long Acting Insulin
Pharmacological class
Rapid-acting Insulin (Human Insulin)
Pharmacology
The blood glucose lowering effect of insulin is due to the facilitated uptake of glucose following binding of insulin to receptors on muscle and fat cells and to the simultaneous inhibition of glucose output from the liver. Insulin has a half-life of a few minutes in the blood stream. After subcutaneous injection: Onset of action within 30 minutes, peak plasma levels between 1-3 hours, duration of action approximately 4-6 hours.
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):
- Type 1 Diabetes: 0.5-1.0 units/kg/day; prepubertal children: 0.7-1.0 units/kg/day
- Type 2 Diabetes: 0.3-0.6 units/kg/day (initial)
- Higher doses may be required in insulin-resistant patients (puberty or obesity)
- Meal or snack containing carbohydrates should follow within 30 minutes of injection
Renal and Hepatic Impairment: Insulin requirements may be reduced
Administration
Usually administered subcutaneously in the abdominal wall; thigh, gluteal region or deltoid region may also be used; abdominal wall injection ensures faster absorption; rotate injection sites to avoid lipodystrophy; IM administration possible (under physician guidance); IV administration only by physician.
Missed dose
If you miss a dose, please consult your doctor.
Side effects
Side Effects:
- Hypoglycemia
- Lipodystrophy (due to failure to rotate injection sites)
- Generalized hypersensitivity (skin rash, itching, sweating, gastrointestinal upset, angioneurotic edema, breathing difficulties, palpitation, reduced blood pressure) - potentially life-threatening
- Edema (upon initiation of insulin therapy, usually transient)
Precautions & warnings
Precautions:
- Inadequate dosing or discontinuation of treatment (especially type 1) may lead to hyperglycemia; untreated hyperglycemia may lead to diabetic ketoacidosis (potentially lethal)
- Hypoglycemia may occur if insulin dose is too high in relation to insulin requirement
- Transferring to another type or brand of insulin should be done under strict medical supervision
- Changes in strength, brand, type, species and/or method of manufacture may result in need for dosage change
- Consult doctor before traveling between different time zones
Contraindications
Contraindications:
- Hypoglycemia
- Hypersensitivity to human insulin or any excipients
Drug interactions
Drug Interactions:
- Oral hypoglycemic agents (OHA), MAOIs, nonselective beta-blockers, ACE inhibitors, salicylates, alcohol reduce insulin requirements
- Thiazides, glucocorticoids, thyroid hormones, beta-sympathomimetics, growth hormone, danazol increase insulin requirements
- Beta-blockers may mask symptoms of hypoglycemia and delay recovery
- Octreotide/lanreotide may both increase and decrease insulin requirement
- Alcohol may intensify and prolong hypoglycemic effect of insulin
Food interactions
No food interaction found/established.
Use in pregnancy
Use in Pregnancy: Insulin does not cross placental barrier; insulin requirements fall in 1st trimester, increase in 2nd and 3rd; return to pre-pregnancy values after delivery; both hypoglycemia and hyperglycemia increase risk of fetal malformations and death.
Use in lactation
Use in Lactation: Insulin treatment of nursing mother involves no risk to baby; however insulin dosage, diet or both may need adjustment.
Pediatric use
Prepubertal children: 0.7-1.0 units/kg/day; limited data for type 2 diabetes in children.
Geriatric use
No specific data for elderly; however caution advised.
Renal / hepatic impairment
Renal Impairment: Renal impairment may reduce insulin requirements; dose adjustment may be needed.
Hepatic Impairment: Hepatic impairment may reduce insulin requirements; dose adjustment may be needed.
Overdose effects
Overdose: No specific overdose definition for insulin; hypoglycemia may develop; mild episodes treated with oral glucose or sugary products; severe episodes with glucagon (0.5-1 mg) IM/SC or IV glucose; oral carbohydrate recommended after regaining consciousness.
Storage conditions
Store between 2°C-8°C in refrigerator; do not freeze; protect from light; during use may be stored below 25°C for 6 weeks or below 30°C for 4 weeks.
Chemical structure
Insulin Human (rDNA)