Sculptra: Difference between revisions
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[[File:Doctor injecting PLLA compound.jpg|alt=Doctor injecting Sculptra|thumb|Doctor injecting Sculptra]] |
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'''Sculptra''', {{zh|c=舒顏萃}}, is a proprietary formulation of [[polylactic acid|poly-<small>L</small>-lactic acid]] (PLLA) that is an [[Food and Drug Administration|FDA]]-approved [[dermal]] filler manufactured by Dermik Laboratories, which conducts the North American business of Aventis Dermatology, the global dermatology unit of [[Aventis]] (of [[Sanofi-Aventis]]). |
'''Sculptra''', {{zh|c=舒顏萃}}, is a proprietary formulation of [[polylactic acid|poly-<small>L</small>-lactic acid]] (PLLA) that is an [[Food and Drug Administration|FDA]]-approved [[dermal]] filler manufactured by Dermik Laboratories, which conducts the North American business of Aventis Dermatology, the global dermatology unit of [[Aventis]] (of [[Sanofi-Aventis]]). |
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Revision as of 23:32, 8 May 2022
Sculptra, Chinese: 舒顏萃, is a proprietary formulation of poly-L-lactic acid (PLLA) that is an FDA-approved dermal filler manufactured by Dermik Laboratories, which conducts the North American business of Aventis Dermatology, the global dermatology unit of Aventis (of Sanofi-Aventis).
PLLA was approved by the FDA on August 3, 2004, for the treatment of facial fat loss (also called facial lipoatrophy). According to documents from the US Food and Drug Administration, the FDA initially approved the drug on the basis of small studies conducted on HIV patients, specifically “for restoration and/or correction of the signs of facial fat loss (lipoatrophy) in people with human immunodeficiency virus (HIV).[1][2] Facial lipoatrophy is a condition in which people lose fat in their faces, especially in their cheeks and around their eyes and temples. People with HIV who take anti-HIV drugs may develop lipoatrophy. Sculptra was subsequently approved by the FDA for use with non-HIV patients with wrinkles, despite substantial complications reported to the FDA.[3]
After the injection, it will take around 1 to 1.5 months to grow natural collagen. Bruising and swelling may occur post injection, which will go down within a week. After the injection, patients are directed to massage the treatment area in order to maintain smooth, level and evenly distributed results and prevent granuloma formation.
References
- ^ US FDA. "Sculptra Aesthetic Label" (PDF). www.accessdata.fda.gov.
- ^ US FDA. "Medical Device User Fee and Modernization Act (MDUFMA) 2005". Retrieved 12 August 2013.
- ^ US FDA. "Sculptra Aesthetic Modified Label" (PDF). Retrieved 12 August 2013.