Schedule A Consultation
Bellafill® is an FDA approved dermal filler for the correction of facial wrinkles known as nasolabial folds or smile lines. It is a unique, injectable collagen filler with microspheres that can instantly smooth facial wrinkles for beautiful, natural-looking results that last.
Bellafill® replaces lost volume in the skin below the wrinkle for results that are immediate and lasting. The injectable gel is comprised of 80% purified collagen and 20% PMMA (polymethylmethacrylate) microspheres (add Lemperle reference).
Treatment with Bellafill® is very similar to treatment with conventional injectable fillers. The main difference is that Bellafill® requires a skin test in the United States to identify those patients who may have an allergy to bovine collagen or lidocaine. Lidocaine is provided to minimize discomfort during injection.
First Appointment: Your skin test. A small amount of purified bovine collagen gel is injected in the forearm to ensure you have no adverse reactions to bovine collagen and/or lidocaine.
Second appointment: Four weeks later, if there have been no adverse reactions to the initial test, you are ready for treatment. Upon injection, you will usually see immediate improvement to lines and wrinkles. The amount of Bellafill® required will depend on the severity of the lines/wrinkles being addressed.
Third appointment: A follow-up is suggested at 4-6 weeks. This also allows you to decide if you would like to further enhance or correct the area.
If you’re looking to add volume with Bellafill® performed by a physician in and around Peabody and Boston, request a consultation online, or contact us at (978) 854-5035 to schedule your appointment.
Important Safety Information
Bellafill® is indicated for the correction of nasolabial folds and moderate to severe, atrophic, distensible facial acne scars on the cheek in patients over the age of 21 years. Patients who have had a positive reaction to the Bellafill® Skin Test, have a history of severe allergies, have known bovine collagen allergies, are allergic to lidocaine, have bleeding disorders or are prone to thick scar formation and/or excessive scarring should not receive Bellafill®. The safety of Bellafill® for use during pregnancy, breastfeeding, or in patients under 21 has not been established. You may experience temporary swelling, redness, pain, bruising, lumps/bumps, itching, and discoloration at the treatment site. These side effects are usually transient and typically resolve within 1–7 days. You may experience lumps/bumps/papules that may occur more than one month after injection and that may persist. Less common side effects include rash and itching more than 48 hours after treatment, persistent swelling or redness, lumps/bumps, acne, and increased sensitivity at treatment sites. Infrequently, granulomas may occur and may be treated by your licensed physician provider. Be sure to call your licensed provider immediately if you notice any unusual skin reactions around the treatment area. Based on the 5-year Post-Approval Study on nasolabial folds with 1,008 patients, long-term safety of Bellafill® for up to 5 years has been established.