Name:
Loratadin tablets 10mg cont cell pack No. 10×1
Description:
Tablets of white or white color with a yellowish tint, flat-cylindrical, with a chamfer, with a risk on one side. The main active substance Loratadine Form of release tablets Dosage 10 mg Indications for use For the symptomatic treatment of allergic rhinitis and chronic idiopathic urticaria. Dosage and administration Adults and children over 12 years old – 1 tablet (10 mg) 1 time per day. Children 5-12 years old weighing more than 30 kg – 1 tablet (10 mg) 1 time per day. Children 5-12 years old weighing less than 30 kg – according to? tablets (5 mg) 1 time per day. For children aged 2-5 years, the drug (5 mg) is prescribed in the form of a syrup. The “tablet” dosage form is not recommended for children under six years of age. The efficacy and safety of the drug in children under the age of 2 years has not been established. In adults with impaired liver and kidney function (creatinine clearance less than 30 ml / min), the initial dose should be 1 tablet (10 mg) every other day. In children aged 2-5 years with impaired liver and kidney function, the initial dose is 5 ml (as syrup) every other day. Use during pregnancy and lactation The safety of using loratadine in pregnant women has not been established, so the drug should be prescribed only if the expected benefit to the mother outweighs the potential risk to the fetus. Loratadine is excreted in breast milk, so the use of the drug during breastfeeding is not recommended. Precautions In adults with impaired liver and kidney function (creatinine clearance less than 30 ml / min), the initial dose should be 1 tablet (10 mg) every other day. In children aged 2-5 years with impaired liver and kidney function, the initial dose is 5 ml (as syrup) every other day. The “tablet” dosage form is not recommended for children under six years of age. It is recommended to stop treatment at least 1 week before skin testing for allergens. The medicinal product contains lactose and is therefore not recommended in patients with rare hereditary problems of galactose intolerance, the Lapp lactase deficiency or glucose-galactase malabsorption. Interaction with other drugs With the simultaneous use of the drug with ketoconazole, erythromycin, cimetidine, an increase in the concentration of loratadine in the blood plasma is noted, but without any clinical manifestations. Lowers the level of erythromycin in plasma by 15%. Does not potentiate the effect of alcohol on the central nervous system. Contraindications Hypersensitivity to the drug. Active ingredient: loratadine – 10 mg Excipients: microcrystalline cellulose, sodium starch glycolate, magnesium stearate, sodium lauryl sulfate, lactose monohydrate. Overdose In case of overdose, drowsiness, tachycardia, and headache may develop. In this case, it is necessary to wash the stomach and prescribe activated charcoal. Side effects From the nervous system: headache, drowsiness, fatigue, in 2% or less – dizziness, nervousness, insomnia, anxiety, excitability (in children), fainting, depression, pain in the ears and eyes, tinnitus. Very rarely – convulsions. From the digestive tract: dry mouth, nausea, vomiting, dyspepsia, gastritis, constipation or diarrhea, taste disturbance. From the respiratory system: nasal congestion, sneezing, sinusitis, dry nose, cough, bronchitis, upper respiratory tract infections. From the genitourinary system: discoloration of urine, dysmenorrhea, vaginitis, weakening of libido, impotence, very rarely – edema. Allergic reactions: hyperemia, urticaria, rash, itching. From the side of the cardiovascular system: hypertension or hypotension, palpitations, tachycardia. Other: thirst, asthenia, malaise, chills, excessive sweating, weight gain. Storage conditionsIn a place protected from moisture and light at a temperature not exceeding +25°C. Buy Loratadine Pharmland tablets 10mg №10×1
INN | LORATADIN |
---|---|
The code | 76 621 |
Barcode | 4 810 368 008 879 |
Dosage | 10mg |
Active substance | Loratadine |
Manufacturer | Pharmland SP LLC, Belarus |
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