Trade name
of Rovahol®
the International unlicensed name
Is not present
the Dosage form
of the Capsule kishechnorastvorimy
Structure
One capsule contains
active substances: α-pinene of 13.6 mg, β-pinene of 3.4 mg, left menthol of 32.0 mg. menthone of 6.0 mg, baras camphor of 5.0 mg, camphene of 5.0 mg, cineole of 2.0 mg,
excipient - olive oil,
structure of a cover of the capsule: gelatin, glycerin of 85%, sodium ethylparahydroxybenzoate (E 215), sodium propilparagidroksibenzoat (E 217), copper sodium chlorophyllin (100% water-soluble)
the Description
the Spherical, soft, gelatin, kishechnorastvorimy capsules of green color containing chartreuse solution with a strong fragrant smell
Pharmacotherapeutic group
Drugs for treatment of diseases of a liver and biliary tract. Drugs for treatment of diseases of a gall bladder. Other drugs for treatment of diseases of biliary tract.
The ATX AO5AX code
the Pharmacological
Pharmacokinetics Some Ingredients properties are well soaked up, metabolized in a liver and removed with bile and urine. Researches of bioavailability showed fast absorption at intake, for example, menthol quickly is soaked up, metabolized in a liver and removed with urine and bile in the form of glucuronides.
The pharmacodynamics
of Rovahol® is the drug which is dissolving/destroying gallstones. Ровахол® dissolves cholesteric stones and desaturirut bile concerning cholesterol. Drug is the bile-expelling means strengthening biliary secretion and eliminating bilious stagnation. Ровахол® has spasmolytic effect, weakens spastic pains. The inhibiting activity of GMG of KoA-reductase of drug weakens production of endogenous cholesterol, reducing the index of a saturation of bile, promoting, thus, to dissolution of cholesteric stones and preventing further sedimentation of stones. Ровахол® it is effective in relation to a number of gram-positive and gram-negative bacteria.
Indications
- for dissolution of X-ray negative stones in the functioning gall bladder
the Route of administration and doses
the Route of administration: inside.
The recommended dosing mode:
Adults: from 1 - 2 capsule three times a day to food. Duration of a course of treatment is established by the doctor individually depending on a course of the disease.
Side effects
At the initial stage there can be a soft taste of mint. Insignificant number of patients noted slight and passing discomfort in a stomach.
Contraindications
hypersensitivity to drug components
children's and teenage age up to 18 years
Medicinal interactions
the patients accepting the anticoagulants or drugs which are metabolized in a liver and removed through a liver need to use Drug with care.
Special instructions
the Following ingredients of the Rovahol® capsules can cause allergic reactions (perhaps, the slowed-down type): sodium ethylparahydroxybenzoate (E 215), sodium propilparagidroksibenzoat (E 217 ).
Pregnancy and the period of a lactation
the person has no data on use of drug during pregnancy. Animals have no data on teratogenecity of drug. However, at least, some of ingredients, can get through a placenta. Drug should not be used during pregnancy or feeding by a breast.
The feature of influence of medicine on ability to run the vehicle or potentially dangerous mechanisms
is not available data on influence of the Rovahol® capsules on these functions for patients.
Overdose
any case of overdose was Not registered.
In case of overdose if the drug was taken inside recently, it is necessary to carry out gastric lavage. If necessary observation should be combined with symptomatic treatment. Monitoring of warm, respiratory, renal and hepatic functions is recommended.
The form of release and packing
On 10 capsules place in blister strip packaging from a film of PVH/PVDH and aluminum foil.
On 5 or 10 packs together with the instruction for medical use in the state and Russian languages place
Storage conditions in cardboard packing
to Store at a temperature not above 25 °C, in densely closed packing.
To store out of children's reach!
Not to use a period of storage of 5 years after an expiration date.
Prescription status
Without prescription
of Rovahol®
the International unlicensed name
Is not present
the Dosage form
of the Capsule kishechnorastvorimy
Structure
One capsule contains
active substances: α-pinene of 13.6 mg, β-pinene of 3.4 mg, left menthol of 32.0 mg. menthone of 6.0 mg, baras camphor of 5.0 mg, camphene of 5.0 mg, cineole of 2.0 mg,
excipient - olive oil,
structure of a cover of the capsule: gelatin, glycerin of 85%, sodium ethylparahydroxybenzoate (E 215), sodium propilparagidroksibenzoat (E 217), copper sodium chlorophyllin (100% water-soluble)
the Description
the Spherical, soft, gelatin, kishechnorastvorimy capsules of green color containing chartreuse solution with a strong fragrant smell
Pharmacotherapeutic group
Drugs for treatment of diseases of a liver and biliary tract. Drugs for treatment of diseases of a gall bladder. Other drugs for treatment of diseases of biliary tract.
The ATX AO5AX code
the Pharmacological
Pharmacokinetics Some Ingredients properties are well soaked up, metabolized in a liver and removed with bile and urine. Researches of bioavailability showed fast absorption at intake, for example, menthol quickly is soaked up, metabolized in a liver and removed with urine and bile in the form of glucuronides.
The pharmacodynamics
of Rovahol® is the drug which is dissolving/destroying gallstones. Ровахол® dissolves cholesteric stones and desaturirut bile concerning cholesterol. Drug is the bile-expelling means strengthening biliary secretion and eliminating bilious stagnation. Ровахол® has spasmolytic effect, weakens spastic pains. The inhibiting activity of GMG of KoA-reductase of drug weakens production of endogenous cholesterol, reducing the index of a saturation of bile, promoting, thus, to dissolution of cholesteric stones and preventing further sedimentation of stones. Ровахол® it is effective in relation to a number of gram-positive and gram-negative bacteria.
Indications
- for dissolution of X-ray negative stones in the functioning gall bladder
the Route of administration and doses
the Route of administration: inside.
The recommended dosing mode:
Adults: from 1 - 2 capsule three times a day to food. Duration of a course of treatment is established by the doctor individually depending on a course of the disease.
Side effects
At the initial stage there can be a soft taste of mint. Insignificant number of patients noted slight and passing discomfort in a stomach.
Contraindications
hypersensitivity to drug components
children's and teenage age up to 18 years
Medicinal interactions
the patients accepting the anticoagulants or drugs which are metabolized in a liver and removed through a liver need to use Drug with care.
Special instructions
the Following ingredients of the Rovahol® capsules can cause allergic reactions (perhaps, the slowed-down type): sodium ethylparahydroxybenzoate (E 215), sodium propilparagidroksibenzoat (E 217 ).
Pregnancy and the period of a lactation
the person has no data on use of drug during pregnancy. Animals have no data on teratogenecity of drug. However, at least, some of ingredients, can get through a placenta. Drug should not be used during pregnancy or feeding by a breast.
The feature of influence of medicine on ability to run the vehicle or potentially dangerous mechanisms
is not available data on influence of the Rovahol® capsules on these functions for patients.
Overdose
any case of overdose was Not registered.
In case of overdose if the drug was taken inside recently, it is necessary to carry out gastric lavage. If necessary observation should be combined with symptomatic treatment. Monitoring of warm, respiratory, renal and hepatic functions is recommended.
The form of release and packing
On 10 capsules place in blister strip packaging from a film of PVH/PVDH and aluminum foil.
On 5 or 10 packs together with the instruction for medical use in the state and Russian languages place
Storage conditions in cardboard packing
to Store at a temperature not above 25 °C, in densely closed packing.
To store out of children's reach!
Not to use a period of storage of 5 years after an expiration date.
Prescription status
Without prescription
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