Drug Guide
Liraglutide
Classification
Therapeutic: Antidiabetic agent / Weight management agent
Pharmacological: GLP-1 receptor agonist
FDA Approved Indications
- Type 2 diabetes mellitus (Victoza)
- Chronic weight management in adults with obesity or overweight with comorbidities (Saxenda)
Mechanism of Action
Liraglutide is a glucagon-like peptide-1 (GLP-1) receptor agonist that enhances glucose-dependent insulin secretion, suppresses glucagon secretion, delays gastric emptying, and promotes satiety, leading to reduced blood glucose levels and weight loss.
Dosage and Administration
Adult: Victoza: 0.6 mg daily, can be increased to 1.2 mg or 1.8 mg based on response; Saxenda: 0.6 mg daily, titrated up to 3.0 mg daily.
Pediatric: Not approved for pediatric use.
Geriatric: Use with caution; no specific dosing adjustments, monitor renal and hepatic function.
Renal Impairment: Use with caution; no specific dose adjustment recommended but monitor renal function.
Hepatic Impairment: Use with caution; limited data available.
Pharmacokinetics
Absorption: Slowly absorbed after subcutaneous injection.
Distribution: Wide distribution; bound minimally to plasma proteins (~50%).
Metabolism: Metabolized via proteolytic degradation to small peptides and amino acids.
Excretion: Excreted primarily via urine as metabolites.
Half Life: Approx. 13 hours, allowing once-daily dosing.
Contraindications
- Personal or family history of medullary thyroid carcinoma
- Multiple endocrine neoplasia syndrome type 2
Precautions
- History of pancreatitis
- Renal impairment
- Hepatic impairment
- Pregnancy and lactation (use only if clearly needed)
Adverse Reactions - Common
- Nausea (Common)
- Diarrhea (Common)
- Vomiting (Common)
- Upper respiratory infection (Common)
Adverse Reactions - Serious
- Pancreatitis (Serious, rare)
- Thyroid C-cell tumors (Serious, animal studies; human relevance unknown)
- Hypoglycemia (with concomitant insulin or secretagogues) (Serious)
Drug-Drug Interactions
- Insulin, sulfonylureas (risk of hypoglycemia)
- Other medications affecting gastrointestinal motility
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor blood glucose levels, renal function, and signs of pancreatitis.
Diagnoses:
- Risk for hypoglycemia
- Risk for pancreatitis
- Impaired gastrointestinal motility
Implementation: Administer once daily, optionally titrate based on tolerance and effectiveness.
Evaluation: Assess blood glucose control, weight loss, tolerance, and adverse effects.
Patient/Family Teaching
- Take medication exactly as prescribed, preferably at the same time each day.
- Report symptoms of pancreatitis (severe abdominal pain, nausea, vomiting).
- Be aware of the possible gastrointestinal side effects when initiating therapy.
- Use contraception if applicable, as safety in pregnancy is not established.
- Maintain a healthy diet and exercise program.
Special Considerations
Black Box Warnings:
- Thyroid C-cell tumors observed in rodents; human risk unknown.
Genetic Factors: Limited data; no established genetic considerations.
Lab Test Interference: No known interference.
Overdose Management
Signs/Symptoms: Severe nausea, vomiting, hypoglycemia, or pancreatitis symptoms.
Treatment: Supportive care; monitor vital signs and laboratory parameters; symptomatic management.
Storage and Handling
Storage: Store in a refrigerator (36°F to 46°F / 2°C to 8°C); do not freeze.
Stability: Stable for 21 days at room temperature (up to 86°F / 30°C).