Bellafill

Should only be used by trained and experienced healthcare practitioners. Must administer the Bellafill skin test for a 4-week period and evaluate prior to inj. Patients with positive skin test or 2 equivocal skin tests, or abnormal baseline anti-bovine collagen serum IgG level results: do not consider for treatment. Obtain patient's complete medical history prior to initiation. Avoid intravascular inj; discontinue immediately if changes in vision, signs of stroke, blanching of skin or unusual pain during or shortly after procedure occurs. Risk of infection. Defer if active inflammatory process or infection is present at specific sites. Possible risk of an inflammatory reaction at implant site if laser treatment, chemical peeling, or any other procedure based on active dermal response is considered after Bellafill treatment or if product is given before skin has healed completely after such a procedure. Advise patients to avoid excessive sun, UV-lamp exposure, extreme cold weather. Use in non-dermal spaces, thin or flaccid skin, or for ice pick or sinus tract scars: not studied. Non-distensible atrophic acne scars, connective tissue disorder: not established. Patients (<21yrs), pregnancy, nursing mothers: not established.