Restylane was first introduced in Europe by Swedish manufacturer Q-Med in 1996. December 2003 Medicis received FDA approval for the dermal filler Restylane. This is first biodegradable non-animal stabilized hyaluronic acid developed to provide fullness to skin. Restylane is a clear jell that once injected attracts and binds to water molecules to provide volume for 4-9 months. A recent study found by topping up the treatment approximately 4 months later extended the length of the results by up to 18 months. The body gradually absorbs Restylane over time.

Restylane is used to temporarily plump the dermal to eliminate the appearance of wrinkles. Since 1996 in over 60 countries outside of the USA doctors used Restylane was used over 9 million times to temporarily enhance lips, plump the back of the hands, under eye area and other body parts.

Since Hyaluronic acid is a substance naturally found in the body Restylane is well tolerated with no allergy testing required. The most common side effect is redness and swelling at injection site. You should take a few precautions before being treated with Restylane. A week prior to treatment avoid using St. John's Wort, high doses of Vitamin E, blood thinners, aspirin, and other non-steroidal anti-inflammatory medications, such as ibuprofen. These agents may increase bruising and bleeding at the injection site.

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