Bifidumbacterin forte powder vn.pr. 50mln.koe / 5doz 0.85g pack. 30 pc

$9.60

Bifidumbacterin forte powder vn.pr. 50mln.koe / 5doz 0.85g pack. 30 pc

Quantity:

Description

Composition
Active substance:
1 sachet contains: bifidobacteria adsorbed on activated carbon particles – no less than 50 million colony forming units.
Excipients:
Lactose monohydrate – 0.85 g
Description:
Powder from light gray to dark gray with carbon black particles and possible splashes of beige color with a faint smell of fermented milk.
Product form:
Bifidumbacterin forte® powder for oral administration, 50 million cfu bifidobacteria in batch adsorbed multilayer metal-polymer material. 10 or 30 packages with instructions for use in a stack of cardboard. In one package 5 doses.
Contraindications
Congenital lactase deficiency. Malabsorption of glucose-galactose.
Indications
Intestinal dysbacterioses of various etiology (including caused by the intake of antibiotics, antimicrobials, glucocorticoid hormones, drugs that have ulcerogenic action on the gastrointestinal tract); acute intestinal established infection (shigellosis, salmonellosis, staphylococcal enterocolitis, rotavirus infection) and of unknown etiology; foodborne diseases.
In the combined therapy of diseases involving intestinal dysbiosis: chronic disease with lesions of the gastrointestinal tract (stomach and duodenal ulcer, pancreatitis, cholecystitis, liver and biliary tract, chronic constipation, malabsorption syndrome); allergic diseases; pneumonia, acute and chronic bronchitis; acute respiratory viral infections; Infectious mononucleosis; inflammatory diseases of the urogenital tract; in surgical patients in the preoperative period and after operations on the intestine, liver, pancreas, intestine microbiocenosis for correction and prevention of inflammatory diseases.
The drug is used to prevent: nosocomial infections in hospitals and clinics; disbacterioses ARI in sickly children and adults.
Interaction with other drugs
In simultaneous reception Bifidumbacterin forte® with vitamins (especially B) effect of the drug is enhanced. When antibiotics recommended interval between the reception and the antibiotic drug Bifidumbacterin forte® is 3 – 4 hr.
Overdose
Cases of overdose were observed.
pharmachologic effect
Pharmacological group:
MIP – probiotic.
Pharmacological properties:
The action of the drug due to high concentration of particles adsorbed on activated charcoal bifidobacteria (Bifidobacterium bifidum), which are antagonists of a wide spectrum of pathogens (shigella, salmonella, Staphylococcus aureus and others.) And conditionally pathogenic microorganisms (proteus, klebsiella and others.). Microcolonies sorbed bifidobacteria provide rapid restoration of the normal microflora, which, being naturally biosorbents, accumulates in a large amount falling outside or generated in an organism toxic substances. Sorbed bifidobacteria activates the regenerative processes in the mucosal membrane digestion, the synthesis of vitamins and amino acids, strengthens the immune defense of the body.
Pregnancy and breast-feeding
The drug is approved for use in women during pregnancy and breastfeeding. Special reception conditions there.
Conditions of supply of pharmacies
Available without prescription.
side effects
Not installed.
special instructions
The drug does not affect the ability to drive vehicles, machinery.
Storage conditions
Store at a temperature not higher than 10 ° C. The lower limit of the temperature is not limited.
KEEP OUT OF THE REACH OF CHILDREN.
Dosing and Administration
The drug is used for children from birth (including premature), adults of all ages.
Depending on the severity of diseases Bifidumbacterin forte® used in ordinary or increased doses.
Bifidumbacterin forte® for therapeutic purposes in normal doses: children up to 1 year to 1 packet 2-3 times a day for children from 1 year of age or older on 1 packet 3-4 times a day, adults 2 pack 2-3 times a day .
treatment of acute intestinal infections and food poisoning 5-7 days in other diseases 15-21 days (depends on the nature and severity of the disease). If necessary, treatment can be repeated 2-3 times, each course is one month after the end of the previous course of treatment.
Patients with surgical pathology – for 3-5 days before surgery and for 10-15 days after surgery: children up to 1 year to 1 package 3 times a day; children from 1 year of age or older on 1 packet 3-4 times a day; 2 for adults packet 3 times a day.
Bifidumbacterin forte® for therapeutic purposes in increased doses administered to children from 1 year and adults.
In acute intestinal infection and acute respiratory viral infections since the early days of the disease: children 5 packages 6 times a day; adult to 10 packages 3 times a day.
Course of treatment 1-3 days, depending on the severity of the condition.
In infectious mononucleosis: children up to 3 years to 3 Pack 3 times a day, the course of 5 days; then 3 packet once in the evening, the course of 5 days, for children from 3 to 7 years to 4 packet 3 times a day, the course of 5 days; then packet 4 once in the evening, the course of 5 days, children 7 to 10 years old packet 3 to 6 times a day, 5 days a course; then a 6 pack single night, the course of 5 days. children over 10 years 7-8 packets 3 times a day, the course of 5 days; then 7-8 packets single night, the course of 5 days.
In chronic diseases of the gastrointestinal tract: the children of 5 packs 1-3 times a day; adult to 10 packets 1-3 times a day. The course of treatment 10-14 days.
Patients with diabetes should be aware that in 5 batches of the drug contained 0.35 XE.
With prophylactic purposes for children up to 1 year, 1 package 1 time per day, the rest of the package 1-2 1-2 times a day. Preventive course spend 10-15 days, 2-3 times a year.
Bifidumbacterin forte® taken with a meal, if necessary, regardless of the meal. The drug is mixed before the use with liquid food, preferably dairy products, or a small amount of boiled water at room temperature to obtain a slurry with particles of a black color of the sorbent. The resulting slurry (suspension) should be drunk without achieving complete dissolution. Newborns and children the drug can be mixed with breast milk or a mixture of artificial feeding.
Information
Appearance may differ from that depicted in the picture. There are contraindications. You need to read the manual or consult with a specialist

Additional information

Weight0.100 kg
Manufacturer

PARTNER

There are no reviews yet.

Add your review