Drug Guide
Insulin Aspart Protamine Recombinant & Insulin Aspart Recombinant
Classification
Therapeutic: Antidiabetic agent
Pharmacological: Insulin, insulin analog
FDA Approved Indications
- Management of blood glucose levels in patients with diabetes mellitus type 1 and type 2
Mechanism of Action
Insulin Aspart is a rapid-acting insulin analog that facilitates cellular glucose uptake, inhibits hepatic glucose production, and promotes storage of glucose as glycogen. The protamine component prolongs the action of insulin Aspart, creating an intermediate-duration insulin.
Dosage and Administration
Adult: Dosing individualized based on patient needs; typical starting dose varies
Pediatric: Dosing individualized; initiated based on blood glucose monitoring
Geriatric: Careful dosing adjustments recommended, considering renal and hepatic function
Renal Impairment: Use with caution; may require dose adjustments
Hepatic Impairment: Use with caution; monitor closely and adjust doses accordingly
Pharmacokinetics
Absorption: Rapid after subcutaneous injection
Distribution: Widely distributed throughout body water compartments
Metabolism: Metabolized primarily in the liver and kidneys
Excretion: Metabolites excreted via renal pathways
Half Life: Approximately 1 hour for insulin Aspart; duration influenced by formulation and site of injection
Contraindications
- Hypersensitivity to insulin Aspart or any excipients
Precautions
- Risk of hypoglycemia, especially in those with renal or hepatic impairment, during concurrent illness, or when changing insulin types
Adverse Reactions - Common
- Hypoglycemia (Common)
- Injection site reactions (Less common)
Adverse Reactions - Serious
- Severe hypoglycemia (Rare)
- Allergic reactions including anaphylaxis (Rare)
Drug-Drug Interactions
- Use with other hypoglycemic agents (e.g., sulfonylureas) may increase hypoglycemia risk
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor blood glucose and adjust doses accordingly; assess for signs of hypoglycemia and hyperglycemia
Diagnoses:
- Risk for unstable blood glucose levels
- Risk for hypoglycemia or hyperglycemia
Implementation: Administer subcutaneously as prescribed; rotate injection sites; instruct on proper storage and handling
Evaluation: Effectiveness assessed by blood glucose control and patient reporting
Patient/Family Teaching
- Instruct on proper injection technique, site rotation, and storage
- Recognize signs of hypoglycemia and hyperglycemia and how to respond
- Importance of regular blood glucose monitoring
Special Considerations
Black Box Warnings:
- Potential for severe hypoglycemia
Genetic Factors: None specific
Lab Test Interference: May alter some laboratory glucose tests
Overdose Management
Signs/Symptoms: Severe hypoglycemia: sweating, trembling, confusion, seizures, unconsciousness
Treatment: Administer oral glucose if alert; in severe cases, provide IV glucose or glucagon, and seek emergency care
Storage and Handling
Storage: Store unopened vials/cartridges in the refrigerator; opened vials may be kept at room temperature for up to 28 days
Stability: Stable at room temperature up to 28 days once opened