Alflutop, 2 ml 5 pcs.
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Pharmacotherapeutic group: tissue repair stimulator of natural origin
ATX code: M09AX
Alflutop is a chondroprotector, the active component of which is bioactive concentrate of small marine fish. The concentrate contains mucopolysaccharides (chondroitin sulfate), amino acids, peptides, ions of sodium, potassium, calcium, magnesium, iron, copper and zinc.
Alflutop prevents destruction of the macromolecular structures of normal tissues, stimulates repair processes in the interstitial tissue and articular cartilage tissue, which explains its analgesic effect.
The anti-inflammatory action and tissue regeneration are based on inhibition of hyaluronidase activity and normalization of hyaluronic acid biosynthesis.
These two effects are synergistic and have the effect of activating tissue repair processes (in particular the restoration of cartilage structure).
Arthritis, Osteoarthritis, Osteochondrosis, Arthritis, Pain in the joints (arthralgia) Alflutop is used in adults with primary and secondary osteoarthritis of various localizations (coxarthrosis, gonarthrosis, arthrosis of small joints), osteochondrosis and spondylosis.
Composition of the drug per 1 ml:
The active ingredient:
Bioactive concentrate of small marine fish 0.1 ml;
phenol not more than 0.005 g,
water for injection up to 1 ml.
How to take, the dosage
In polyosteoarthritis and osteochondrosis the drug is administered deeply intramuscularly:
– 1 ml per day, the course of treatment is 20 injections (1 injection per day for 20 days)
– 2 ml every other day, the course of treatment is 10 injections (1 injection every other day for 20 days).
If large joints are affected predominantly, the drug is injected intraarticularly 1 to 2 ml into each joint at intervals of 3 to 4 days. A total of 5 to 6 injections into each joint for the course.
A combination of intraarticular and intramuscular methods of administration is possible.
The course of treatment is recommended to be repeated in 6 months after physician’s consultation.
In case of individual intolerance of seafood (sea fish) the risk of allergic reactions increases.
Impact on driving and operating machinery
The use of the drug does not affect the ability to perform potentially hazardous activities requiring increased concentration and speed of psychomotor reactions (driving vehicles, operating moving mechanisms, work of dispatcher and operator).
Colorless or slightly brownish-yellow, or slightly yellow, transparent liquid.
Hypersensitivity to the components of the drug.
Pregnancy and breast-feeding.
Children under 18 years of age (due to lack of clinical data in this category of patients).
The side effects are grouped according to the WHO classification of the incidence of adverse reactions: very frequently (≥1/10), frequently (≥1/100 to <1/10), infrequently (≥1/1000 to <1/100), rarely (≥1/10000 to <1/1000), very rarely (<1/10000), frequency is unknown (frequency cannot be determined based on available data).
Rare: itchy dermatitis, reddening of the skin and burning sensation at the site of drug administration, transient myalgia. Very rare: development of anaphylactic reactions. Frequency unknown: with intra-articular injections a transient increase in pain syndrome is possible.
In overdose, dose-dependent adverse drug reactions increase.
The drug is contraindicated in pregnancy and during breast-feeding.
3 years. Do not use the drug with an expired shelf life.
|Conditions of storage|
In the dark place at the temperature from 15 ° C to 25 ° C. Store out of the reach of children.
S.C.Zentiva S.A., Romania
solution for injection
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