The composition may be subject to variations, so we advise you to always check the list on the purchased product.
Composition:
Crosslinked Hyaluronic Acid ....................................... 25 mg
Lidocaine Hydrochloride ... ....................................... 3 mg
Phosphate buffer pH 7.3 ... ................................. qs 1 ml
TEOSYAL® PureSense Global Action should not be used:
- for the correction of superficial wrinkles,
- for injections other than intradermal,
- for injections in the eyelids,
- if the patient suffers from skin conditions, inflammation or in the area to be treated or in the vicinity of this area,
- in the case of patients with known hypersensitivity to hyaluronic acid, with a history of severe allergies or anaphylactic shock,
- in case of hypersensitivity known to lidocaine and / or amide-type local anesthetics,
- in combination with a peel, a laser or ultrasound treatment,
- in the case of patients suffering from autoimmune diseases,
- in the case of patients suffering from cardiac diseases and / or undergoing treatment for heart diseases (beta-blockers),
- in the case of patients with hepatocellular deficiencies and / or undergoing treatment for liver disease,
- for patients with persons with epilepsy, or with porphyria,
- interactions with other filling implants not studied, it is inadvisable to inject TEOSYAL® PureSense Global Action into areas with other filling implants, -z pregnant woman, breastfeeding, or in children.
Athletes should be alerted to the fact that this product contains an active component that can induce a positive reaction of anti-doping tests.
Do not inject into the blood vessels.
Side effects
The practitioner must inform the patient that there are potential side effects related to the implantation of this device that may occur immediately after the injection or delayed. Among these (non-exhaustive list):
- Local manifestations: inflammatory reactions (erythema, edema, pain at the injection site), hematomas, itching, temporary loss of sensitivity around the injected area, dyschromia, abscesses, indurations, nodules (may be granulomas).
- General manifestations: immediate hypersensitivity up to anaphylactic shock, migration of the implant.
Rare but serious adverse reactions associated with intravascular injection of facial fillers have been reported and include vision problems including temporary or permanent blindness, cutaneous necrosis and stroke.
The patient should also inform the practitioner of any side effects other than those described above or any lasting effects beyond a week. The practitioner will inform the dealer of the product as soon as possible.
Precautions for use
The practitioner must take into account the presence of lidocaine in this filling product. Check the expiry date and integrity of the package before use. Do not use if the expiry date has passed or if the packaging is damaged. Patients should not be advised to take high-dose vitamin E, aspirin, anti-inflammatory drugs or anticoagulants the week before the injection. Recommend to the patient not to wear makeup during the twelve hours following the injection and not to expose oneself to extreme temperatures (intense cold, sauna, hammam ...) during the week following the treatment. At the end of the treatment session, it is imperative to discard any remaining unused product. This device is intended for a single use. In case of reuse,
Discard used needles in collectors
Store between 2 ° C and 25 ° C away from direct sunlight.
The list of ingredients may be subject to variations, we advise you to always check the list on the purchased product.
