Stylage® S Bi-Soft with Lidocaine

General Information

STYLAGE® S BI-SOFT® with Lidocaine is a sterile, injectable hyaluronic acid dermal filler manufactured by Laboratoires VIVACY in France. It is formulated to correct fine lines and superficial to medium-depth wrinkles, particularly in delicate facial areas where early signs of ageing become visible.

The formulation contains 16 mg/g of cross-linked hyaluronic acid, 9 mg/mL of mannitol and 3 mg/mL of lidocaine hydrochloride (0.3%). Hyaluronic acid helps fill skin depressions and smooth wrinkles. Mannitol acts as an antioxidant, while lidocaine is a local anaesthetic included to help reduce discomfort during injection.

The Bi-SOFT® syringe system is designed to provide practitioners with improved grip, handling and injection control.

Indications for STYLAGE® S BI-SOFT® with Lidocaine

STYLAGE® S BI-SOFT® with Lidocaine is intended for the correction of fine lines and superficial facial wrinkles. Depending on the approved instructions for use and the practitioner’s assessment, treatment areas may include:

• Crow’s feet around the eyes
• Fine forehead lines
• Glabellar lines between the eyebrows
• Perioral wrinkles around the lips
• Selected superficial facial lines and skin depressions

The product is intended for injection into the appropriate dermal layer by a qualified medical professional. Lidocaine helps make the injection procedure more comfortable.

Contraindications and Precautions

STYLAGE® S BI-SOFT® with Lidocaine should not be used in individuals with known hypersensitivity to hyaluronic acid, mannitol, lidocaine or other amide-type local anaesthetics. It should not be injected into areas affected by active skin infections or inflammation.

Medical assessment is particularly important for individuals with a history of severe allergies, porphyria, autoimmune conditions, bleeding disorders or hypertrophic scarring. Treatment during pregnancy or breastfeeding and in minors should be avoided unless specifically permitted by the applicable product instructions and medical guidance.

The product must not be injected into blood vessels. It should only be administered by appropriately trained healthcare professionals.

Potential Side Effects

Common temporary reactions may include redness, swelling, bruising, tenderness, itching, pain and small lumps at the injection site. These effects generally resolve over time.

Rare but serious complications include infection, vascular occlusion, tissue damage, skin necrosis and visual disturbances, including blindness. Severe or unusual pain, skin colour changes or vision symptoms after treatment require immediate medical attention.

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