Drug Guide
Levocetirizine Dihydrochloride
Classification
Therapeutic: Antihistamine, allergic rhinitis and urticaria treatment
Pharmacological: Selective peripheral H1-antihistamine
FDA Approved Indications
- Relief of symptoms associated with allergic rhinitis (seasonal and perennial)
- Relief of symptoms of uncomplicated chronic idiopathic urticaria
Mechanism of Action
Levocetirizine is a selective antagonist of peripheral H1 receptors, which prevents the effects of histamine released during allergic reactions, thereby reducing allergy symptoms.
Dosage and Administration
Adult: 5 mg once daily, with or without food.
Pediatric: 2.5 mg once daily for children 2-6 years; 5 mg for children 6 years and older.
Geriatric: Typically 5 mg once daily; adjust based on renal function.
Renal Impairment: Reduce dose in patients with renal impairment; dosage varies based on creatinine clearance.
Hepatic Impairment: No specific dose adjustments recommended.
Pharmacokinetics
Absorption: Rapidly absorbed, peak plasma levels in approximately 1 hour.
Distribution: Crosses the blood-brain barrier minimally, low penetration into the CNS.
Metabolism: Metabolized minimally by the liver; primarily excreted unchanged.
Excretion: Excreted mainly via the kidneys (about 85%), with some in feces.
Half Life: Approximately 22 hours.
Contraindications
- Known hypersensitivity to levocetirizine or other piperazine derivatives.
Precautions
- Use with caution in patients with renal impairment; dose adjustment required.
- Potential for somnolence; caution when performing activities requiring mental alertness.
Adverse Reactions - Common
- Headache (Common)
- Somnolence (Common)
- Pharyngitis (Common)
- Fatigue (Common)
Adverse Reactions - Serious
- Anaphylaxis (Rare)
- Severe skin reactions such as Stevens-Johnson syndrome (Rare)
- Drowsiness that impairs ability to perform tasks (Uncommon)
Drug-Drug Interactions
- CNS depressants (enhanced sedative effect)
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor for effectiveness in symptom relief; assess for excessive somnolence.
Diagnoses:
- Ineffective airway clearance due to sedation
Implementation: Administer as prescribed; instruct patient to avoid activities requiring alertness until response is known.
Evaluation: Assess reduction in allergy symptoms and adverse effects.
Patient/Family Teaching
- Take medication as directed, with or without food.
- Do not exceed recommended dose.
- Be cautious when engaging in activities requiring alertness.
- Report any signs of allergic reactions or severe side effects.
Special Considerations
Black Box Warnings: N/A
Genetic Factors: None specified.
Lab Test Interference: None noted.
Overdose Management
Signs/Symptoms: Sedation, drowsiness, and dizziness; in severe cases, agitation or hallucinations.
Treatment: Supportive care; activated charcoal if ingestion was recent; dialysis may be considered in severe cases, especially in renal impairment.
Storage and Handling
Storage: Store at room temperature, away from moisture and light.
Stability: Stable under recommended storage conditions.