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levonorgestrel studies |
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levonorgestrel studies Generic Name: Lidocaine HCl and Epinephrine Iontophoretic Patch Date of Approval: May 10, 2004 Company: Vyteris, Inc. Treatment for: Localized Pain Treatment The United States Food and Drug Administration (FDA) has approved LidoSite TopicalSystem. The system has been approved for use on normal intact skin to provide a localanalgesia that numbs the skin prior to the administration of superficial dermatologicalprocedures such as venipuncture (drawing blood with a needle from a vein usuallyin the forearm), intravenous cannulation (administration of fluids and/or medications),and laser ablation (high power laser pulses) of superficial skin lesions levonorgestrel studies. Theproduct is approved for use on patients five-years-of-age and older levonorgestrel studies. LidoSite uses an active transdermal delivery technology known as iontophoresis,which administers medications through the skin via a mild electric current levonorgestrel studies. The LidoSite system administers lidocaine and epinepherine using a patentedelectrotransport technology that enables the controlled delivery of medicationover a predetermined period of time, from minutes to days levonorgestrel studies. Topical anestheticcreams and patches can take up to an hour to numb the skin, while LidoSite worksin 10 minutes levonorgestrel studies. This product has successfully completed clinical trials and hasbeen found to significantly decrease pain from needle injections and similarprocedures in both adults and children levonorgestrel studies. Lidosite is intended to also addressa strong need in adult applications levonorgestrel studies. Its major impact is expected to be in thepediatric population, where pain associated with needlesticks, blood-draw proceduresand immunizations is a major issue for the clinician, child and parent. Studies Demonstrate Safety and Efficacy |
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