Active ingredients
- Not indicated. See instructions
Pharmacological action
- Not indicated. See instructions
- Description of the pharmacological action of Alflutop
- Composition of Alflutop
- Indications for use of the drug Alflutop
- Release form of the drug Alflutop
- Contraindications to the use of the drug Alflutop
- Side effects of the drug Alflutop
- Method of administration and dosage of the drug Alflutop
- Overdose of Alflutop
- Interactions of Alflutop with other drugs
- Special instructions when taking Alflutop
- Storage conditions for the drug Alflutop
Description of pharmacological action
Pharmacodynamics. The drug regulates metabolism in cartilage tissue. It has a chondroprotective effect by normalizing the biosynthesis of hyaluronic acid and type II collagen, as well as inhibiting the activity of hyaluronidase and other enzymes that take part in the destruction of the intercellular matrix. These effects determine the activation of the processes of restoration of the structure of cartilage and prevent the destruction of the macromolecular structures of cartilage tissue. By restoring homeostasis in the joint, the drug inhibits the biosynthesis of inflammatory mediators, including cytokines. As a result, the drug has a pronounced anti-inflammatory and analgesic effect, which manifests itself on the 8–10th day of treatment. Proteoglycans, which are part of the drug, have a trophic effect and have a replacement effect, significantly increasing MRI indicators of hydrophilicity, cartilage height and bone tissue homogeneity. Pharmacokinetics. The effect of an extract of marine organisms is the combined effect of its active components, so the study of pharmacokinetic characteristics is impossible.
Description and composition of Alflutop
It is impossible to name just one active substance of Alflutop - this is a whole list of biologically active components obtained from small sea fish, including sprat, bellyfish, anchovy and whiting. The main value of the composition lies in the content of mucopolysaccharides, amino acids and peptides, as well as a large number of minerals: calcium, potassium, copper, magnesium, zinc, sodium and iron.
Therapy with Alflutop helps prevent the destruction of the structure of healthy tissues, and also triggers the processes of cell division from which cartilage is formed. In addition, the therapeutic effect is enhanced by the natural synthesis of hyaluronic acid. Both processes complement each other and restore cartilage that has lost its functions. This explains the drug's ability to relieve pain.
Side effects
In rare cases, dermatitis, skin hyperemia and a burning sensation at the injection site, and short-term myalgia may occur. In some cases, with intra-articular administration, a transient increase in the severity of pain is possible (with intra-articular administration due to activation of metabolism and intensification of blood circulation). Isolated cases of allergic reactions were also observed, including skin rash, itching, urticaria, swelling of the neck, difficulty breathing, agitation, fear of death, palpitations, general weakness, anaphylactic shock, rash and itching at the injection site, swelling of the lower extremities.
Alflutop instructions and frequently asked questions
INSTRUCTIONS
for medical purposes
ALFLUTOP
(ALFLUTOP®)
Stock:
dyucha speech
: 1 ml mixed with 0.1 ml of bioactive concentrate from sea fish (dry resin: chondroitin sulfate, amino acids, sucrose, myoinositol, salts Na, K, Ca, Mg, Cu, Fe, Mn, Zn; semi-glycero group phospholipids, to the main These products, including nitrogen and alcohol, include glycerin and phosphorus);
additional speeches:
phenol, water for injection.
Medicine form.
Order for injections.
Main physical and chemical authorities:
prozory rozchin without suspended particles.
Pharmacotherapeutic group.
What to do with pathology of the musculoskeletal system. Code ATX M09A X.
Pharmacological power.
Pharmacodynamics.
The drug regulates the metabolism of cartilage tissue.
To repair Chondroprotectornu by the Normaliza byosynthesis gilauronic acid і Kolagen II TO TAP Actively GIALURURENIDASI TO ONISH, YAKI BRERUT Participated by Ruinanni Mzhklitin Matrix. These effects are due to the activation of the processes of renewal of the structure of cartilage and the destruction of the macromolecular structures of normal cartilage tissue.
By restoring homeostasis in the sorrel, the drug inhibits the biosynthesis of inflammatory mediators, including proinflammatory cytokines. The inheritance of this drug has a pronounced anti-inflammatory and analgesic effect, which manifests itself on the 8-10th day of treatment.
Proteoglycans, which are included in the preparation, have a trophic effect and a replacement effect, significantly increasing MRI indicators of hydrophilicity, cartilage height and homogeneity of bone tissue.
Pharmacokinetics.
The action of the extract of marine organisms is the combined action of its active components, so it is impossible to change the pharmacokinetic characteristics.
Clinical characteristics.
Showing.
Degenerative-rheumatic illness of the joints:
— osteoarthrosis of various localizations (coxarthrosis, gonarthrosis, arthrosis of the joints);
- spondylosis.
The extended period after injuries and surgical interventions on the sides.
Contraindicated.
Contraindications for hypersensitivity to any component of the drug.
Interactions with other medicinal drugs and other types of interactions.
When taking the drug Alflutop for one hour with local anesthetic drugs, immediately before the release of para-aminobenzoic acid (novocaine), remember about the side effects of the rest.
Features of stagnation.
The drug should be administered with care under the full supervision of a doctor, especially in cases of autoimmune diseases (rheumatoid polyarthritis, ankylopoetic spondylitis, worm's eye disease, scleroderma). The drug may cause anaphylactic reactions. Use caution in persons with a significant history of allergies.
Suspension during pregnancy or breastfeeding.
Do not treat with vaginal or breastfeeding period.
This is due to the fluidity of the reaction during treatment with vehicles or other mechanisms.
The drug does not affect the vehicle or folding mechanisms.
Method of congestion and dosage.
Let's take the drug when we grow up.
Alflutop is administered deeply internally. Prescribe 1 ml 1 time per dose, the course of treatment is 20 days.
In case of inflammation of the great globules, the drug is administered internally at a dose of 1-2 ml at an interval of 3 days between injections. Treatment course - 5 injections for the skin.
If medically indicated, the course of treatment should be repeated after 3-6 months.
Children.
Do not prescribe the drug to children based on the availability of clinical data that confirm the safety and effectiveness of its treatment in this group.
Overdose.
Some patients may experience allergic reactions.
Adverse reactions.
Rarely: changes at the injection site, including the liver at the injection site, darkening of the skin.
In single episodes: immediate intensification of pain syndrome (with intraglobular injection, subsequent activation of metabolism and intensification of blood circulation), short-term myalgia. Also watch out for episodes of hypersensitivity reactions, including rash, dermatitis, urticaria, itching, angioedema, anaphylactic shock.
Term of attribution.
3 rocks.
Save your mind.
Store at a temperature not exceeding 25 ° C in the original packaging for light protection.
Nonsense.
There is daily information about the inconsistency of Alflutop with other drugs, so Alflutop should not be mixed with any other drugs in one syringe.
Package.
1 ml dose in ampoules; 5 ampoules per contour package; 2 contour packages at a time with instructions for medical storage in a cardboard box.
1 ml dose in ampoules; 5 ampoules per contour package with foil; 2 contour packages at a time with instructions for medical storage in a cardboard box.
Release category.
For the recipe.
Virobnik.
"Biotechnos" AT.
The location of the distributor and the address of the place of promotion of activity.
Vul. Gorunului, 3-5, m. Otopeni-Ilfov, index 075100, Rumunia / Str. Gorunului nr. 3-5, Oras Otopeni, Jud. Ilfov, code 075100, Romania.
Special instructions for use
The drug must be used with caution and under strict medical supervision, especially in the case of autoimmune diseases (rheumatoid polyarthritis, ankylosing spondylitis, systemic lupus erythematosus, scleroderma). The drug may cause anaphylactic reactions. Prescribe with caution to patients with a history of allergic reactions. Use during pregnancy and lactation. Not prescribed during pregnancy and breastfeeding. Children. The drug is not prescribed to children and adolescents due to the lack of clinical data confirming the safety and effectiveness of its use in these age groups. The ability to influence reaction speed when driving vehicles or working with other mechanisms. Does not affect.
Contraindications, negative side effects
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The drug should not be used in children under 18 years of age. Other contraindications:
- increased sensitivity to the composition and tendency to allergic reactions;
- pregnancy;
- breastfeeding period.
There are currently no data on drug interactions. However, if it is necessary to use Alflutop together with other medications, it is important to notify your doctor.
In old age, it is necessary to undergo treatment with Alflutop only under the supervision of a doctor and with reduced risks.
Possible negative manifestations in patients using Alflutop:
- allergic reaction;
- short-term or persistent myalgia;
- increased pain (in some cases, has a short-term effect);
- dermatitis, skin itching.
The occurrence of pronounced side effects does not require adjustment of therapy or discontinuation of the drug. If an allergy occurs, you should consult a doctor as soon as possible and stop taking it.
Storage conditions
In a place protected from light at a temperature not exceeding 25° C.
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The description of vitamin Alflutop is intended for informational purposes only. Before starting to use any drug, it is recommended to consult a doctor and read the instructions for use. For more complete information, please refer to the manufacturer's instructions. Do not self-medicate; EUROLAB is not responsible for the consequences caused by the use of information posted on the portal. Any information on the project does not replace consultation with a specialist and cannot be a guarantee of the positive effect of the drug you use. The opinions of EUROLAB portal users may not coincide with the opinions of the site Administration.
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