Obolenskoe FP Neobutin tablets 100mg # 10
Category
Preparations for the gastrointestinal tract
Scope of the drug
Gastrointestinal tract
Release form
Tablet
Manufacturer country
Russia
Package quantity, pcs
ten
Structure
1 tablet contains:
active substance: trimebutine maleate 100 mg
excipients: lactose monohydrate 81.6 mg, corn starch 32 mg, colloidal silicon dioxide (aerosil) 3.2 mg, magnesium stearate 3.2 mg.
pharmachologic effect
Antispasmodic
Indications
- irritable bowel syndrome
- postoperative paralytic intestinal obstruction.
Contraindications
- children's age up to 3 years (for this dosage form)
- pregnancy
- lactose intolerance, lactase deficiency, glucose-galactose malabsorption
- hypersensitivity to trimebutin maleate and other components that make up the drug.
Side effects
From the digestive system: dry mouth, unpleasant taste, diarrhea, dyspepsia, nausea, constipation.
From the nervous system: drowsiness, fatigue, dizziness, headache, anxiety, feeling of heat or cold.
Allergic reactions: skin rash.
Others: menstrual irregularities, painful enlargement of the mammary glands, urinary retention.
Interaction
Drug interaction of the drug Neobutin is not described.
How to take, course of administration and dosage
The drug is taken orally, before meals.
Adults and children over 12 years of age are prescribed 100-200 mg 3 times / day.
To prevent recurrence of irritable bowel syndrome after the course of treatment during the period of remission, it is recommended to continue taking the drug at a dose of 300 mg / day for 12 weeks.
Children aged 5-12 years are prescribed 50 mg 3 times / day, children aged 3-5 years - 25 mg 3 times / day.
Overdose
To date, no cases of trimebutine overdose have been reported.
Special instructions
The course of treatment of irritable bowel syndrome in the acute period at a dose of 600 mg / day for 4 weeks and the continuation of treatment after the course of the course at a dose of 300 mg / day for 12 weeks avoids the recurrence of the disease.
Influence on the ability to drive vehicles and use mechanisms
The drug does not have a sedative effect, does not affect the speed of psychomotor reactions and can be used in people of various professions, incl.
requiring increased attention and coordination of movements.
However, given the possible side effects that can affect these abilities (dizziness and others), care should be taken when driving and engaging in other potentially hazardous activities.
Active substance
Trimebutin
Name ENG
NEOBUTIN
Clinical and pharmacological group
A drug that regulates the motor function of the gastrointestinal tract
ATX code
Trimebutine
Dosage
100mg
Structure
1 tablet contains: active ingredient: trimebutine maleate 100 mg excipients: lactose monohydrate 81.6 mg, corn starch 32 mg, colloidal silicon dioxide (aerosil) 3.2 mg, magnesium stearate 3.2 mg.
Indications
Irritable bowel syndrome postoperative paralytic ileus
Contraindications
children under 3 years of age (for this dosage form)
pregnancy
lactose intolerance, lactase deficiency, glucose-galactose malabsorption
hypersensitivity to trimebutin maleate and other components that make up the drug.
INN / Active ingredient
Trimebutin
Storage conditions and periods
At a temperature not higher than 25 degrees.
Expiration date: 3 years
Specifications
Category
Preparations for the gastrointestinal tract
Scope of the drug
Gastrointestinal tract
Release form
Tablet
Manufacturer country
Russia
Package quantity, pcs
ten
Scope of application
Gastroenterology
Minimum age from
3 years old
Way of introduction
Through the mouth
Vacation conditions
Without recipe
Brand name
Obolenskoe FP
The amount of the dosage form in the primary package
10 pieces.
Primary packaging type
Blister
Type of consumer packaging
Pack of cardboard
Pharmaco-therapeutic group
Antispasmodic
Anatomical and therapeutic characteristics
A03AA05 Trimebutin
Dosage form
Pills
Expiration date in days
1095
Dosage (volume) of the substance in the preparation
1 tablet contains: trimebutin maleate 100 mg
The target audience
Adult
Package weight, g
twenty
Mode of application
:
The drug is taken orally, before meals. < br> Adults and children over 12 years of age are prescribed 100-200 mg 3 times / day. < br> To prevent recurrence of irritable bowel syndrome after the course of treatment during the period of remission, it is recommended to continue taking the drug in the dose 300 mg / day for 12 weeks. < br> Children aged 5-12 years are prescribed 50 mg 3 times / day, children aged 3-5 years - 25 mg 3 times / day. < br>