ADVERSE REACTIONS
Patients must be informed of the potential risks and adverse events related to the injection procedure and to the use of this product. A slight bleeding may occur during the injection, and it disappears spontaneously as soon as the injection is finished. In occasional cases one or more of the following may occur either immediately or as a delayed reaction (list not exhaustive) Reactions usually associated with injections such as redness, erythema, oedema or pain sometimes accompanied by itching in the treated area. These reactions may last for a week. Hematomas in the treated area, Swelling in the treated area, Indurations or nodules in the treated area, Coloration or discoloration in the treated area, Allergy to one of the product’s components, especially to sodium hyaluronate. Cases of necrosis, abscesses and granulomas after sodium hyaluronate injections have been reported in the literature.
These rare potential risks must nevertheless be considered. Patients should be instructed to report any side effects which last for more than one week to his/her practitioner.
The practitioner may then prescribe the patient appropriate treatment.
Any other undesirable side effects associated with injection of the product must be reported to the distributor and/or to the manufacturer.
MODEL | Fine 1ml/2ml |
HA CONCENTRATION | 23mg/ml |
INGREDIENT | Cross-Linked Hyaluronic Acid |
PARTICLE SIZE | 0.1-0.15mm |
DURATION | 12-18 months |
NEEDLE SIZE | 30GX2 |
Indications: | Upper part of dermis |
Shallow wrinkle remove, removing wrinkles around eyes, E.g Crow's feet ,Corrects scars,Frown. |