Artrakam since. d / inv. solution for oral administration 1.5 g Pak. # 20
Category
Bone metabolism
Scope of the drug
Musculoskeletal system
Release form
Powder
Manufacturer country
Russia
Package quantity, pcs
twenty
Amount in a package
twenty
Dosage form
oral solution
Manufacturer
PharmVILAR FPK, Russia
Structure
1 sachet of powder for oral solution contains:
active substance: glucosamine sulfate sodium chloride in terms of 100% substance 1.884 g, including glucosamine sulfate - 1.5 g,
excipients: sorbitol, citric acid to obtain the mass of the contents of one sachet 2.2 g.
pharmachologic effect
Glucosamine sulfate has anti-inflammatory and analgesic effects, replenishes endogenous glucosamine deficiency, stimulates the synthesis of proteoglycans and hyaluronic acid in synovial fluid.
Increases the permeability of the joint capsule, restores enzymatic processes in the cells of the synovial membrane and articular cartilage.
Promotes sulfur fixation during the synthesis of chondroitinsulfuric acid, inhibits the development of degenerative processes in the joints, restores their function, reduces joint pain.
Pharmacokinetics
Absorption in the gastrointestinal tract 90%, bioavailability 26%, half-life 70 hours.
Indications
Osteoarthritis of the peripheral joints and joints of the spine, osteochondrosis.
Contraindications
Individual hypersensitivity to glucosamine sulfate and other components of the drug Artrakam.
Severe chronic renal failure,
pregnancy,
lactation period.
It is not recommended to prescribe the drug in childhood (up to 12 years) due to the lack of clinical data in this category of patients.
With caution: with intolerance to seafood (shrimp, shellfish), the likelihood of developing allergic reactions to the drug increases.
Bronchial asthma, diabetes mellitus.
Side effects
The drug is well tolerated, in some cases it is possible:
gastralgia,
flatulence,
diarrhea,
constipation,
allergic reactions - urticaria, itching.
Interaction
Compatible with non-steroidal anti-inflammatory drugs, paracetamol and glucocorticosteroids.
Increases the absorption of tetracyclines, reduces - semi-synthetic penicillins, chloramphenicol.
Information about the possible effect of the medicinal product for medical use on the ability to drive vehicles, mechanisms:
Influence on the ability to drive vehicles, mechanisms is not registered.
How to take, course of administration and dosage
Inside.
The content of one sachet Artrakam is dissolved in 200 ml of water, taken orally 1 time per day for 6 weeks.
According to the doctor's prescription, the course of treatment can be repeated at intervals of 2 months.
Overdose
Overdose cases are unknown.
Treatment: gastric lavage, symptomatic therapy.
Release form
powder for oral solution
Storage conditions
In a dark place at a temperature not exceeding 25 ° C.
Keep out of the reach of children.
Shelf life
2 years.
Active substance
Chondroitin sulfate
Terms of dispensing from pharmacies
On prescription
Name ENG
ARTRACAM
Clinical and pharmacological group
A drug that affects the metabolism in cartilage tissue.
Proteoglycan biosynthesis stimulator
ATX code
Glucosamine
Dosage
1.5g x 2.2g
Structure
1 sachet of powder for preparation of oral solution contains: active substance: glucosamine sulfate sodium chloride in terms of 100% substance 1.884 g, including glucosamine sulfate - 1.5 g.
excipients: sorbitol, citric acid to obtain the mass of the contents of one sachet 2.2 g.
Indications
Osteoarthritis of the peripheral joints and joints of the spine, osteochondrosis.
INN / Active ingredient
Chondroitin sulfate
Storage conditions and periods
In a dark place at a temperature not exceeding 25 degrees.
Expiration date: 3 years
Contraindications
Individual hypersensitivity to glucosamine sulfate and other components of the drug Artrakam. Severe chronic renal failure, pregnancy, lactation.
It is not recommended to prescribe the drug in childhood (up to 12 years) due to the lack of clinical data in this category of patients.
With caution: with intolerance to seafood (shrimp, shellfish), the likelihood of developing allergic reactions to the drug increases.
Bronchial asthma, diabetes mellitus.
Specifications
Category
Bone metabolism
Scope of the drug
Musculoskeletal system
Release form
Powder
Manufacturer country
Russia
Package quantity, pcs
twenty
Way of introduction
Through the mouth
Vacation conditions
Without recipe
Brand name
PharmVILAR
The amount of the dosage form in the primary package
2.2 g
Primary packaging type
Package
Type of consumer packaging
Pack of cardboard
Pharmaco-therapeutic group
Tissue repair stimulant
Anatomical and therapeutic characteristics
M01AX05 Glucosamine
Dosage form
Powder for preparation of oral solution
Expiration date in days
1095
The target audience
Adult
Package weight, g
85
Mode of application
:
Inside. < br> Contents of one sachet Artrakam is dissolved in 200 ml of water, taken orally 1 time per day for 6 weeks. < br> According to the doctor's prescription, the course of treatment can be repeated at intervals of 2 months.
Dosage (volume) of the substance in the preparation
:
glucosamine sulfate sodium chloride in terms of 100% substance 1.884 g, including glucosamine sulfate - 1.5 g
Information on technical characteristics, delivery set, country of manufacture