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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

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

allergy/drugs/cetirizine.txt · Last modified: by andrew2393cns