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  2. Lidocaine - Wikipedia

    en.wikipedia.org/wiki/Lidocaine

    Lidocaine is an antiarrhythmic medication of the class Ib type. [7] This means it works by blocking sodium channels thus decreasing the rate of contractions of the heart. [10] [7] When injected near nerves, the nerves cannot conduct signals to or from the brain. [8] Lidocaine was discovered in 1946 and went on sale in 1948. [11]

  3. Topical anesthetic - Wikipedia

    en.wikipedia.org/wiki/Topical_anesthetic

    A topical anesthetic is a local anesthetic that is used to numb the surface of a body part. They can be used to numb any area of the skin as well as the front of the eyeball, the inside of the nose, ear or throat, the anus and the genital area. [1]

  4. Dental anesthesia - Wikipedia

    en.wikipedia.org/wiki/Dental_anesthesia

    Maximum dose (mg/kg) Articaine with adrenaline Bartinest Septanest 4 7 Bupivacaine Marcain 0.25 2.5 Lidocaine 1 3 2 Lidocaine with adrenaline Utilycaine Lignospan Special Xylocaine 1 7 2 Mepivacaine Scandonest 2 1.36 (3 mg per pound), less than 400 mg in adults 3 Prilocaine with Felypressin Citanest 0.5 7 1 Prilocaine Plain Citanest Plain 1 6

  5. Prilocaine - Wikipedia

    en.wikipedia.org/wiki/Prilocaine

    It is used as a eutectic mixture with lidocaine, 50% w/w, as lidocaine/prilocaine. The mixture is an oil with a melting point of 18 °C (64 °F). A 5% emulsion preparation, containing 2.5% each of lidocaine/prilocaine, is marketed by APP Pharmaceuticals under the trade name EMLA (an abbreviation for eutectic mixture of local anesthetics). [3]

  6. Lidocaine/prilocaine - Wikipedia

    en.wikipedia.org/wiki/Lidocaine/prilocaine

    Lidocaine/prilocaine is a eutectic mixture of equal quantities (by weight) of lidocaine and prilocaine. A 5% emulsion preparation, containing 2.5% each of lidocaine/prilocaine, is marketed by APP Pharmaceuticals under the trade name EMLA (an abbreviation for Eutectic Mixture of Local Anesthetics ). [ 5 ]

  7. Stephen L. Hammerman - Pay Pals - The Huffington Post

    data.huffingtonpost.com/paypals/stephen-l-hammerman

    From January 2008 to May 2008, if you bought shares in companies when Stephen L. Hammerman joined the board, and sold them when he left, you would have a -32.7 percent return on your investment, compared to a -4.0 percent return from the S&P 500.