Usage
- Human insulin/soluble insulin is prescribed for the treatment of type 1 and type 2 diabetes mellitus. It is also used to manage hyperglycemia (high blood sugar) and diabetic ketoacidosis (DKA). In some cases, it’s used during surgical procedures or in intensive care settings.
- Pharmacological Classification: Rapid-acting insulin, antidiabetic agent.
- Mechanism of Action: Mimics the action of endogenous insulin, facilitating glucose uptake by cells in muscle, liver, and adipose tissue, thereby lowering blood glucose levels.
Alternate Names
- Regular insulin, neutral insulin, soluble insulin
- Brand Names: Actrapid, Humulin R, Novolin R, others.
How It Works
- Pharmacodynamics: Lowers blood glucose by promoting glucose uptake into cells and inhibiting hepatic glucose production. It also affects fat and protein metabolism.
- Pharmacokinetics:
- Absorption: Rapidly absorbed following subcutaneous injection, with peak action within 1-3 hours. Intravenous administration results in immediate action.
- Metabolism: Primarily metabolized in the liver and kidneys.
- Elimination: Excreted primarily through the kidneys.
- Mode of Action: Binds to insulin receptors on cell surfaces, triggering a cascade of intracellular events leading to increased glucose transport into cells via GLUT4 transporters.
- Receptor Binding: Binds to insulin receptors.
- Elimination Pathways: Primarily renal excretion.
Dosage
Standard Dosage
Adults:
- Type 1 Diabetes: 0.5-1 unit/kg/day subcutaneously, divided into multiple doses.
- Type 2 Diabetes: Starting dose: 0.1-0.2 unit/kg/day or 10 units/day subcutaneously, usually given in the evening or divided twice daily. Titrate upwards based on blood glucose levels.
Children:
- Dose is individualized based on the child’s weight, age, and metabolic needs, typically starting at 0.2-0.4 units/kg/day, divided into multiple doses. Pediatric endocrinologist consultation recommended.
Special Cases:
- Elderly Patients: May require lower doses due to age-related decline in renal function and insulin sensitivity.
- Patients with Renal Impairment: Dose reduction may be necessary depending on the degree of renal impairment.
- Patients with Hepatic Dysfunction: Dose adjustments may be necessary.
- Patients with Comorbid Conditions: Dosage adjustments may be necessary based on other medical conditions.
Clinical Use Cases:
- Intubation/Surgical Procedures/Mechanical Ventilation/ICU Use: Continuous IV infusion at 0.1 unit/kg/hour is commonly used, titrated to maintain desired blood glucose levels.
- Emergency Situations (e.g., DKA): 0.1 unit/kg IV bolus followed by 0.1 unit/kg/hour continuous IV infusion. Alternatively, 0.14 unit/kg/hour IV infusion without bolus can be administered. Blood glucose levels must be closely monitored, and dose adjusted accordingly. When blood glucose is <250 mg/dL, switch to glucose-containing fluids orally and reduce insulin to 0.05 unit/kg subcutaneously.
Dosage Adjustments:
- Renal/hepatic dysfunction: Reduce dose based on individual patient’s clearance.
- Metabolic disorders: Adjust dose based on specific metabolic needs.
Side Effects
Common Side Effects:
- Hypoglycemia (low blood sugar), weight gain, injection site reactions (redness, swelling, itching).
Rare but Serious Side Effects:
- Severe hypoglycemia (loss of consciousness, seizures), allergic reactions (rash, hives, difficulty breathing).
Long-Term Effects:
- Lipodystrophy (changes in fat tissue at injection site) with repeated injections at the same site.
Adverse Drug Reactions (ADR):
- Anaphylaxis (severe allergic reaction).
Contraindications
- Hypoglycemia.
- Hypersensitivity to insulin or any component of the formulation.
Drug Interactions
- Medications that can affect blood sugar levels (e.g., corticosteroids, beta-blockers, thiazide diuretics).
- Alcohol can increase the risk of hypoglycemia.
- Beta-blockers can mask the symptoms of hypoglycemia.
Pregnancy and Breastfeeding
- Pregnancy Safety Category: Generally considered safe during pregnancy. Blood glucose monitoring is crucial. Insulin requirements may change during pregnancy.
- Breastfeeding: Insulin is not likely to be excreted in breast milk in significant amounts. Dosage adjustments may be necessary during breastfeeding.
Drug Profile Summary
- Mechanism of Action: Facilitates glucose uptake by cells, lowering blood glucose.
- Side Effects: Hypoglycemia, weight gain, injection site reactions.
- Contraindications: Hypoglycemia, hypersensitivity.
- Drug Interactions: Corticosteroids, beta-blockers, thiazide diuretics, alcohol.
- Pregnancy & Breastfeeding: Generally safe, monitor blood glucose, may require dosage adjustments.
- Dosage: Individualized, starting at 0.2-0.4 unit/kg/day for type 1 diabetes, 0.1-0.2 unit/kg/day for type 2 diabetes.
- Monitoring Parameters: Blood glucose levels, HbA1c.
Popular Combinations
- Often combined with intermediate- or long-acting insulins (e.g., NPH insulin, glargine) to provide both basal and bolus insulin coverage.
Precautions
- General Precautions: Monitor blood glucose regularly. Rotate injection sites.
- Specific Populations: Dosage adjustments as needed for pregnant/breastfeeding women, children, and the elderly.
- Lifestyle Considerations: Diet and exercise play a significant role in managing diabetes.
FAQs (Frequently Asked Questions)
Q1: What is the recommended dosage for Human Insulin/Soluble Insulin?
A: Highly individualized, but generally 0.5-1 unit/kg/day for type 1 and 0.1-0.2 unit/kg/day or 10 units/day for type 2, divided into multiple doses.
Q2: How should Human Insulin be administered?
A: Subcutaneously, usually before meals. Can be given intravenously in hospital settings.
Q3: What are the signs and symptoms of hypoglycemia?
A: Sweating, trembling, dizziness, confusion, hunger, headache, and in severe cases, loss of consciousness and seizures.
Q4: What should a patient do if they experience hypoglycemia?
A: Consume a fast-acting carbohydrate (e.g., glucose tablets, juice, candy) and recheck blood sugar after 15 minutes. If symptoms persist, seek medical attention.
Q5: Can Human Insulin be used during pregnancy?
A: Yes, it is generally considered safe, but close blood glucose monitoring and dosage adjustments may be necessary.
Q6: What are the long-term complications of poorly controlled diabetes?
A: Cardiovascular disease, nephropathy, neuropathy, retinopathy, and foot problems.
Q7: How often should a patient on Human Insulin monitor their blood glucose?
A: Frequency depends on individual needs and diabetes management plan, but usually multiple times per day.
Q8: What are the potential drug interactions with Human Insulin?
A: Corticosteroids, beta-blockers, thiazide diuretics, and alcohol.
Q9: What is the role of diet and exercise in managing diabetes with Human Insulin?
A: Diet and exercise are essential components of diabetes management, along with insulin therapy, to maintain optimal blood glucose control and overall health.
Q10: What are the storage requirements for Human Insulin?
A: Unopened vials should be refrigerated. In-use vials can be stored at room temperature for up to 28 days. Do not freeze.