Bobotik drops for oral administration 66.66mg/ml 30ml №1

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Bobotik drops for oral administration 66.66 mg/ml in vial. 30ml No. 1
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Thick, opaque liquid of white or almost white color with a fruity odor. The main active ingredient Simethicone Release form Drops Dosage 66.66 mg / ml in a vial. Indications for use For the symptomatic treatment of disorders of the gastrointestinal tract caused by increased gas formation, for example, flatulence, colic in infants (three-month colic). In preparation for endoscopic, ultrasound or radiological examinations of the gastrointestinal area. Dosage and administration Inside. Before use, the vial must be vigorously shaken until a homogeneous liquid is obtained. For accurate dosing of the drug during the counting of drops, the vial should be held vertically. Increased gas formation and accumulation of gases in the gastrointestinal tract: Bobotik is usually used after meals three times a day and at bedtime: children from infancy to 3 years old, 8 drops (20 mg of simethicone) 4 times a day, children from 3 to 6 years old, 14 drops (35 mg simethicone) 4 times a day children over 6 years old and adults 16 drops (40 mg simethicone) 4 times a day food, or non-carbonated liquid. Continue treatment until the ailments disappear. Preparation for diagnostic procedures: X-ray examination of the gastrointestinal tract One day before the examination, a dose should be taken in the morning and evening: children from infancy to 3 years, 10 drops (25 mg of simethicone) 2 times a day, children from 3 to 6 years, 16 drops (40 mg of simethicone) 2 times a day, children over 6 years old and adults, 20 drops (50 mg of simethicone) 2 times a day in preparation for radiographic examination. Repeat the dose three hours before the start of the study. An open vial should be used within 2 months. Use during pregnancy and lactation Use during pregnancy and lactation is possible if, in the opinion of the doctor, the benefit to the mother outweighs the potential risk to the fetus and child. The ability to influence the reaction rate when driving vehicles or working with other mechanisms Does not affect. Precautions When using the drug Bobotik should not drink carbonated liquid. The medicinal product contains methyl parahydroxybenzoate and propyl parahydroxybenzoate, which may cause allergic reactions (delayed type reactions are possible). Interaction with other drugs Some reports suggest that simethicone may interfere with the absorption of oral anticoagulants. The use of simethicone can give false positive results in diagnostic tests using guaiac resin, but does not affect the results of a rapid urease test (diagnosis of Helicobacter pylori). Contraindications Hypersensitivity to simethicone or to any excipient Intestinal obstruction Obstructive diseases of the gastrointestinal tract Children under 28 days Composition Active ingredient: simethicone (dimethicone activated with silicon dioxide) 66.66 mg / ml Excipients: sodium saccharinate (E 954), methyl parahydroxybenzoate (E 218), propyl parahydroxybenzoate (E 216), sodium carmellose, citric acid monohydrate (E 330), raspberry flavor, purified water. Overdose The drug is chemically inert and is not absorbed from the gastrointestinal tract, so far there is no information about an overdose of Bobotik. Side effects No adverse effects associated with the use of Bobotik have been reported in studies. The appearance of all side (unusual) effects, including those not listed in the package insert, must be reported to the attending physician. Storage conditions Store in the original packaging at temperatures between 15 and 25 °C. The drug should be stored out of the reach of children. Buy Bobotik drops for oral administration 66.66mg/ml 30ml No. 1 Price for Bobotik drops for oral administration 66.66mg/ml 30ml No. 1