allergy:drugs:cetirizine
Cetirizine
Classification
- Second-Generation H1 Antihistamine
- Peripheral H1 receptor inverse agonist
- Active metabolite of hydroxyzine
Parent class: Histamine & Antihistamines
Mechanism of Action
Cetirizine selectively blocks peripheral H1 receptors.
Effects:
- ↓ Histamine-mediated vasodilation
- ↓ Capillary permeability
- ↓ Pruritus
- ↓ Sneezing and rhinorrhea
Compared to first-generation antihistamines:
- Minimal anticholinergic activity
- Limited blood-brain barrier penetration
- Low but not zero sedation
Pharmacokinetics
- Oral administration
- Rapid onset (~1 hour)
- Duration: ~24 hours
- Primarily renally eliminated
- Minimal hepatic metabolism
Dose adjustment required in renal impairment.
Indications
- Chronic idiopathic urticaria
- Seasonal allergies
- Pruritus
Effective for:
- Sneezing
- Itching
- Rhinorrhea
Less effective for:
- Nasal congestion (intranasal steroids superior)
Dosing (Adult)
- 10 mg PO once daily
- Consider 5 mg daily in renal impairment
Pediatric dosing based on age.
Adverse Effects
Generally well tolerated.
Possible:
- Mild drowsiness (more than loratadine)
- Fatigue
- Dry mouth (rare)
Sedation risk:
- Higher than loratadine
- Lower than diphenhydramine
Contraindications / Cautions
- Severe renal impairment (dose adjust)
- Hypersensitivity
Use caution:
- Elderly
- Concomitant CNS depressants
Drug Interactions
- Minimal CYP interaction
- Additive sedation with alcohol or CNS depressants
Clinical Pearls
- Slightly more effective for urticaria than loratadine.
- Slightly more sedating than loratadine.
- Good balance of potency and tolerability.
- Renal clearance makes it safer in hepatic disease.
Comparison Within Class
| Drug | Sedation Risk | Elimination | Notes |
|---|---|---|---|
| Loratadine | Very low | Hepatic (CYP3A4) | Active metabolite = desloratadine |
| Cetirizine | Low | Renal | Active metabolite of hydroxyzine |
| Fexofenadine | Minimal | Renal | Least sedating |
Related Pages
allergy/drugs/cetirizine.txt · Last modified: by andrew2393cns
