Loratadine Dosing Recommendations
For adults with no significant medical history, the standard dose of loratadine is 10 mg once daily, which should not be exceeded within 24 hours. 1
Standard Adult Dosing
- Adults and children 6 years and older should take 10 mg (2 teaspoonfuls of 5 mg/5 mL solution or one 10 mg tablet) once daily 1
- The maximum dose is 10 mg in any 24-hour period 1
- Loratadine reaches peak plasma concentration in 1-2 hours with onset of action within 1 hour and duration of at least 24 hours 2
Pediatric Dosing
- Children 2 to under 6 years of age: 5 mg (1 teaspoonful) once daily; do not exceed 5 mg in 24 hours 1
- Children under 2 years of age: consult a physician before use 1
- Children 6 years and older follow adult dosing of 10 mg once daily 1
Dosing in Hepatic or Renal Impairment
Patients with liver or kidney disease should consult a physician before using loratadine, as dose adjustment may be necessary. 1 This is particularly important because:
- Loratadine undergoes hepatic metabolism to its active metabolite descarbethoxyloratadine, which is four times more active than the parent drug 2
- The elimination half-life of loratadine is approximately 10 hours, while its active metabolite has a half-life of 20 hours 2
- Impaired hepatic or renal function may lead to drug accumulation 1
The FDA label specifically flags hepatic and renal disease as conditions requiring medical consultation before initiating therapy, though it does not provide specific dose reduction guidelines 1. In clinical practice, a conservative approach would be to start with 10 mg every other day or 5 mg daily in patients with significant hepatic or renal impairment, though this should be done under physician guidance.
Geriatric Considerations
- No specific dose reduction is mandated for geriatric patients based solely on age 1
- However, elderly patients with concurrent renal or hepatic impairment should follow the guidance for organ dysfunction 1
- Loratadine demonstrates a favorable safety profile with minimal sedation (3% incidence) compared to older antihistamines 3
Clinical Efficacy and Safety Profile
- Loratadine is significantly superior to placebo and comparable to other second-generation antihistamines including terfenadine, cetirizine, and astemizole for allergic rhinitis and chronic urticaria 4, 5
- The overall incidence of side effects is low (14%), with minimal sedation (3%) and dry mouth (4%) 3
- Serious ventricular arrhythmias have not been observed with loratadine, unlike some other second-generation antihistamines 4
- Tachyphylaxis has not been noted in humans, and there is minimal potential for drug interactions 2
Key Clinical Advantages
- Once-daily dosing improves compliance 5, 6
- Faster onset of action (within 1 hour) compared to astemizole which requires several days 2
- Minimal CNS penetration with threefold greater affinity for peripheral versus central H1-receptors 2
- Efficacy is maintained throughout prolonged treatment courses (28+ days) 3