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The drug is prescribed orally, regardless of food intake.
Adults (including elderly patients) and adolescents over the age of 12 are recommended to take Claritin at a dose of 10 mg (1 tab. or 2 teaspoons / 10 ml / syrup) 1 time / day.
For children aged 2 to 12 years, the dose of Claritin is recommended to be prescribed depending on body weight: with a body weight of less than 30 kg – 5 mg (1/2 tab. or 1 teaspoon / 5 ml / syrup) 1 time / day, with a body weight of 30 kg or more – 10 mg (1 tab. or 2 teaspoons / 10 ml / syrup) 1 time / day.
For adults and children with a body weight of more than 30 kg with severe liver dysfunction, the initial dose is 10 mg (1 tab. or 2 teaspoons / 10 ml / syrup) every other day, with a body weight of 30 kg or less – 5 mg (1 teaspoon / 5 ml / syrup) every other day.
In elderly patients and in patients with chronic renal insufficiency, dose adjustment is not required.
In clinical studies
In clinical studies involving children aged 2 to 12 years who took Claritin®, headache (2.7%), nervousness (2.3%), fatigue (1%) were observed more often than in the placebo group.
From the nervous system: in children aged 2-12 years – headache (2.7%), nervousness (2.3%), fatigue (1%); in adults – headache (0.6%), drowsiness (1.2%), insomnia (0.1%).
From the digestive system: in adults – increased appetite (0.5%).
In the post-marketing period
From the nervous system: very rarely (< 1/10 000) – dizziness, fatigue.
From the digestive system: very rarely (< 1/10 000) – dry mouth, gastrointestinal disorders (nausea, gastritis), liver dysfunction.
Allergic reactions: very rarely (< 1/10 000) – rash, anaphylaxis.
From the cardiovascular system: very rarely (< 1/10 000) – palpitations, tachycardia.
From the skin: very rarely (< 1/10 000) – alopecia.
Contraindications to use
age up to 2 years (for syrup);age up to 3 years (for tablets);lactation (breastfeeding); rare hereditary diseases (galactose tolerance disorders, lapp lactase deficiency or glucose-galactose malabsorption) – due to the presence of lactose, which is part of the tablets; sucrose/isomaltase deficiency, fructose intolerance, glucose-galactose malabsorption – due to the presence of sucrose, which is part of the syrup; hypersensitivity to the components of the drug.
With caution, the drug should be prescribed to patients with severe liver dysfunction, during pregnancy.
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