Боботик®

General characteristics. Structure:

Active ingredient: 66,66 mg/ml of a simetikon (in the form of 30% of an emulsion — 222,2 mg/ml).

Excipients: sodium saccharinate, methylparahydroxybenzoate, пропилпарагидроксибензоат, a karmelloza of sodium, citric acid monohydrate, fragrance crimson, the water purified.

Pharmacological properties:

Pharmacodynamics. Simetikon (activated диметикон) represents a combination of the metilirovanny linear siloxane polymers stabilized by trimetilsiloksilovy groups from silicon dioxide. Reducing surface intention on limit of the section of phases, complicates education and promotes destruction of gas bubbles in contents of intestines and slime of the digestive tract (DT). The gases released at the same time can be absorbed by walls of intestines or be removed thanks to a peristaltics. It prevents formation of the big gas and mucous conglomerates causing painful abdominal distention.

At sleepy and a X-ray analysis prevents appearance of defects of the image; promotes the best irrigation of a mucous membrane of a large intestine contrast agents, interfering with a rupture of a contrast film.

Owing to chemical inertness does not influence the microorganisms and enzymes which are present at a GIT. Does not reduce absorption of food, does not change reaction and volume of a gastric juice.

Pharmacokinetics. Simetikon after peroral introduction is not soaked up from a GIT and brought through intestines in not changed look.

Indications to use:

- The strengthened gas generation and accumulation of gases in a GIT (gripes, feeling of filling in an abdominal cavity, a meteorism, including in the postoperative period, Remgeld's syndrome, an aerophagia);
- preparation for diagnostic testings of abdominal organs and a small pelvis (a X-ray analysis, a sonografiya, gastroscopy and a duodenoskopiya - prevention of foaming).

Route of administration and doses:

Inside, after food. Before use to shake up before receiving a homogeneous emulsion. For an exact dosage of drug, during an instillation, the bottle should be held vertically.

The strengthened gas generation and accumulation of gases in a GIT:
• children from 28 in the afternoon lives up to 2 years on 8 drops (20 mg of a simetikon) 4 times a day;
• children from 2 to 6 years on 14 drops (35 mg of a simetikon) 4 times a day;
• children are more senior than 6 years and adults on 16 drops (40 mg of a simetikon) 4 times a day.
 
For more convenient administration of drug, in particular to small children, it is possible to mix it previously with a small amount of cold boiled water, baby food or not gassy liquid. After disappearance of symptoms administration of drug should be stopped.

Preparation for diagnostic procedures. Radiographic research GIT. In one day prior to a research drug is accepted by 2 times a day (in the morning and in the evening):

• children from 28 in the afternoon lives up to 2 years - 10 drops (25 mg)
• children from 2 to 6 years - 16 drops (40 mg)
• children are more senior than 6 years and adults - 20 drops (50 mg)
 
Sonografichesky research GIT. In one day prior to a research drug is accepted by 2 times a day (in the morning and in the evening) in the dosages recommended by preparation for a radiographic research. In three hours prior to the research the dose should be repeated.

Features of use:

Drug does not contain sugar, use by patients with a diabetes mellitus and with digestion disturbances is possible.

During treatment reception of carbonated drinks is not recommended.

Administration of drug can distort results of some diagnostic tests, for example the test with use of guaiac pitch.

Driving of vehicles and service of the working mechanical devices. Drug does not exert impact on driving of vehicles and service of mechanical devices.
 
Use at pregnancy and in the period of a lactation. During pregnancy use of drug is possible only when the estimated advantage for mother exceeds potential risk for a fruit. There are no data on safety of use of drug for the feeding women. During feeding by the child's breast drug has to be used only in case of unconditional need.

Side effects:

Development of allergic reactions is possible.

Interaction with other medicines:

Simetikon can cause disturbance of absorption of peroral anticoagulants.

Contraindications:

- hypersensitivity to a simetikon and/or other components of drug;
- intestinal impassability;
- obstructive gastrointestinal diseases;
- newborn children till 28 in the afternoon lives.

Overdose:

Messages on overdose are absent. Simetikon is not soaked up from a GIT and the overdose does not pose a threat for life and health.

Storage conditions:

In the place protected from light, at a temperature from 15 °C to 25 °C. To store in the place, unavailable to children. Not to use after the expiry date specified on packaging. A period of validity - 2 years.

Issue conditions:

Without recipe

Packaging:

Drops for intake, 66,66 mg/ml. On 30 ml in bottles of dark glass with a polyethylene stopper dropper and the screwing-up polyethylene cover. 1 bottle together with the application instruction in a cardboard pack.