cetirizine hydrochloride: prescribing and clinical use
Focused clinical detail for use alongside current product information, local policy and patient-specific assessment.
cetirizine hydrochloride: clinical details
Prescribing considerations
- Assess renal function because cetirizine is predominantly eliminated renally and product-specific adjustment may be necessary.
- Check the formulation's licensed age and excipients, particularly for children or people with carbohydrate intolerances.
- Use caution with urinary-retention risk factors, epilepsy or susceptibility to convulsions.
- Advise about possible somnolence, alcohol and safety-critical activities.
- Antihistamines suppress allergy skin-test responses; coordinate any interruption with the testing service.
- Long-term dry mouth may increase caries risk; reinforce oral hygiene.
Contraindications and cautions
- Hypersensitivity to cetirizine, hydroxyzine, piperazine derivatives or product excipients.
- End-stage or severe renal impairment as defined by the individual product SmPC; wording varies between products.
- Some liquids are unsuitable in specific inherited sugar-intolerance disorders because of excipients such as sorbitol or maltose. Tablets containing lactose are unsuitable in specified galactose or glucose-galactose disorders.
Monitoring
- Renal function where impairment is known or suspected.
- Somnolence, dizziness and impaired performance.
- Urinary retention in susceptible patients.
- Seizure control in people with epilepsy or increased convulsion risk.
- Dry mouth and dental health during prolonged use.
- Breastfed infants for drowsiness, irritability, poor feeding and weight gain.
Clinical pharmacology
Cetirizine is a selective peripheral H1-receptor antagonist and a human metabolite of hydroxyzine. It undergoes little first-pass metabolism, is highly protein-bound and is largely excreted unchanged in urine; renal impairment therefore prolongs exposure.
Formulation and product differences
- Products include film-coated tablets and oral liquids or syrups; minimum licensed ages differ.
- The selected tablet formulation contains lactose.
- Liquids vary in excipients and may contain sorbitol, propylene glycol, parabens, maltose, flavourings or a very small quantity of ethanol.
- Measure liquids with the supplied calibrated device.
cetirizine hydrochloride preparations and strengths
Oral solution
Route: Oral
Strengths: 5 mg/5 mL
Tablet
Route: Oral
Strengths: 10 mg
cetirizine hydrochloride interactions
Cetirizine has relatively few clinically important medicine interactions, but additive adverse effects can occur.
Alcohol
Alcohol can increase sleepiness and reduce alertness, so avoid it if cetirizine affects you.
Sedatives and other central nervous system depressants
Combined use may further impair alertness or performance in sensitive people.
Medicines causing drowsiness, dry mouth or urinary difficulty
Cetirizine may make these effects more likely or troublesome.
Sources
These sources were used to prepare and review this medicine page.
Prepared and reviewed by the iatroX editorial team.