Adant Dispo 1 pack X 10 pcs, 2,5 mg each.

$299 $249

Product Description

Maker: Meiji Seika Pharma

Form : Solution for intra-articular injection in a syringe . 1 syringe contains 2, 5 mg of sodium hyaluronate .

Excipients: sodium chloride, sodium phosphate dodecahydrate , hydrochloric acid concentrated , sodium hydroxide , water for injections .


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Indications for use

Osteoarthritis of the knee and Steynbrokera syndrome .
Osteoarthritis trapezoid – carpal joint I, II and III .
Pain and limited mobility due to degenerative and traumatic changes of the cartilage and synovial fluid of other joints.

Hypersensitivity , allergic to the drug , pregnancy, lactation , infancy .

Side effects of the drug

Possible: Pain, redness , swelling , burning sensation of fullness and at the injection site . In rare cases, the allergic reaction can occur . In such cases, use of the drug should be discontinued immediately . Occasionally reported anaphylactic shock . In the case of its occurrence must discontinue use , carefully examine the patient and provide appropriate treatment.

mode of application

Adults are encouraged to intraarticular injection of the drug 1 time per week for 5 weeks. Agent should be administered in interarticular interval knee , shoulder joint ( glenohumeral joint interarticular interval , pidakromialnu bag , long flexor tendon sheath ) , trapezoid – carpal joint or the affected synovial joint .
In the case of administration to a trapezoidal – carpal joint two recommended route of administration depending on the degree of osteoarthritis : lateral external path ( I rizoartroz power ) and the introduction of fingers in between the first commissure ( rizoartroz II and III ) . The decision to use a particular method adopted in each case . In this regard, the introduction easier to carry under the endoscope . In all cases, the dose should be adjusted according to the severity of symptoms of the disease .
At intraarticular injection drug should meet the following requirements : As introduced in adanta interarticular space operation should be performed only in a sterile environment . If there are no signs of improvement during the first 5 weeks of treatment , treatment should be discontinued . In the presence of even a minor reduction of synovial fluid should make joint puncture . Be taken to avoid injection into the blood vessels. Avoid contact with eyes . Given vyazkoelastichnist drug is recommended to use the needles 22-23 G.
If the preparation is frozen before use to give it to warm to room temperature. Means used only once and immediately after opening. Unused drug residues should be disposed of . Avoid exposure to disinfectants , such as ammonium salts ( including , benzalkonium chloride or chlorhexidine ) , may be formed as a precipitate.

Not determined the influence of the drug on the ability to drive vehicles and other classes of potentially hazardous activities that require high concentration and speed of psychomotor reactions.

Interaction with other drugs

Data on the interaction with other drugs is not available.

Additional Information

Weight 1 kg


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