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When ingested, the drug is well absorbed from the gastrointestinal tract. Absorption of the drug is not dependent on food intake.The drug begins 30 minutes after taking one tablet and lasts for 24 hours. Loratadin is metabolized in the liver with the formation of an active metabolite of descarbotoxyloratadine. Maximum concentrations of loratadine and its active metabolite in blood plasma are achieved in 1.3 - 2.5 hours after the administration of CLARIDOL. CLARIDOL does not cause drowsiness and does not affect psychomotor functions, attention, performance, mental abilities. Indications:For adults and children over 2 years of age Claridol is used to treat seasonal and allergic rhinitis, conjunctivitis, hay fever, urticaria, including chronic idiopathic urticaria, Quincke's edema, pseudo-allergic reactions, itching dermatoses, allergic reactions to insect bites. Contraindications:Hypersensitivity to any of the components of the drug. Pregnancy and lactation:You should refrain from using Claridol during pregnancy and lactation. Dosing and Administration:It is applied inside. Adults and children over 12 years of age: 10 mg Claridol (1 tablet) once a day. The daily dose is 10 mg. - 5 mg Claridol (1/2 tablet) once a day. The daily dose is 5 mg. Children with a body weight of more than 30 kg - 10 mg Claridol (1 tablet) once a day. The daily dose is 10 mg. Side effects:Possible side effects: Rarely - dry mouth, nausea, vomiting, gastritis, liver dysfunction, headache, fatigue, excitability (in children), dizziness, cough, tachycardia, allergic reactions. In some cases - alopecia. Overdose:Symptoms of overdose: drowsiness, tachycardia, headache. In case of overdose, you should consult a doctor and take measures to accelerate the removal of the drug from the gastrointestinal tract,intestinal tract and reduced absorption. Interaction:When using loratadine in therapeutic doses, its interaction with alcohol was not revealed. Erythromycin, cimetidine, ketoconazole when combined with loratadine increase the concentration of loratadine in blood plasma, without causing clinical manifestations and without affecting the ECG. Special instructions:Patients with impaired hepatic function Claridol should be administered at an initial dose of 5 mg per day due to a possible disruption in the clearance of loratadine.It is not recommended for children under 2 years old. Effect on the ability to drive transp. cf. and fur:Claridol does not cause drowsiness and does not affect psychomotor functions, attention, performance, mental abilities. Form release / dosage:Tablets 10 mg. Packaging:By 7, 8, 10, 16 tablets in the blister; 1, 2, 3, 4, 5, 10 blisters in a cardboard box or 10 tablets in a strip, 1, 2, 3, 4, 5, 10 strips in a cardboard box. Storage conditions:In a dry place, at a temperature of no higher than 30 ° C. Keep out of the reach of children. Shelf life:3 years. Do not use the drug after the expiration date indicated. Terms of leave from pharmacies:Without recipe Registration number:П N014159 / 01-2002 Date of registration:13.08.2008 Expiration Date:Unlimited The owner of the registration certificate:Shraya Life Senses Pvt. Ltd.Shraya Life Senses Pvt. Ltd. India Manufacturer: & nbspSHREYA LIFE SCIENCES, Pvt.Ltd. India Representation: & nbspSHREYA LIFE SENENSIZ Pvt.Ltd. SHREYA LIFE SENENSIZ Pvt.Ltd. India Information update date: & nbsp24.01.2018 Illustrated instructions × Illustrated instructions Instructions