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  2. Lidocaine - Wikipedia

    en.wikipedia.org/wiki/Lidocaine

    Lidocaine is an antiarrhythmic medication of the class Ib type. [8] This means it works by blocking sodium channels thus decreasing the rate of contractions of the heart. [11] [8] When injected near nerves, the nerves cannot conduct signals to or from the brain. [9] Lidocaine was discovered in 1946 and went on sale in 1948. [12]

  3. Dental anesthesia - Wikipedia

    en.wikipedia.org/wiki/Dental_anesthesia

    Lidocaine's half-life in the body is about 1.5–2 hours. [2] The time it takes for the anesthetic medication to prevent pain in the area (speed of onset) and length of time that the area does not have painful sensations are considerations when choosing an appropriate approach to dental treatment.

  4. GI cocktail - Wikipedia

    en.wikipedia.org/wiki/GI_cocktail

    The GI cocktail is a mixture of a viscous anesthetic, an antacid, and an anticholinergic. [1] [2] Common viscous anesthetics use are viscous lidocaine or xylocaine.Common antacids used are magnesium hydroxide, aluminum hydroxide, or simethicone (more commonly known as Mylanta or Maalox). [3]

  5. Procaine - Wikipedia

    en.wikipedia.org/wiki/Procaine

    Aside from its use as a dental anesthetic, procaine is used less frequently today, since more effective (and hypoallergenic) alternatives such as lidocaine (Xylocaine) exist. Like other local anesthetics (such as mepivacaine , and prilocaine ), procaine is a vasodilator, thus is often coadministered with epinephrine for the purpose of ...

  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. Dyclonine - Wikipedia

    en.wikipedia.org/wiki/Dyclonine

    The product Sucrets was introduced in Baltimore, Maryland, by Sharp & Dohme in 1932. [3]In 1966 the Federal Trade Commission ordered Merck and Company to discontinue the false claims of germ-killing and pain-relieving properties for its Sucrets and Children's Sucrets throat lozenges. [4]

  8. Chloroprocaine - Wikipedia

    en.wikipedia.org/wiki/Chloroprocaine

    It has a significantly shorter duration of action than lidocaine and is significantly less toxic. Chloroprocaine has a motor block lasting for 40 minutes, a rapid onset time of 3–5 minutes (9.6 min ± 7.3 min at 40 mg dose; 7.9 min ± 6.0 min at 50 mg dose) and a time to ambulation of 90 minutes without complications, especially lacking ...

  9. Pramocaine - Wikipedia

    en.wikipedia.org/wiki/Pramocaine

    Pramocaine (INN and BAN, also known as pramoxine or pramoxine HCl) is a topical anesthetic discovered at Abbott Laboratories in 1953 [1] and used as an antipruritic. During research and development, pramocaine hydrochloride stood out among a series of alkoxy aryl alkamine ethers as an especially good topical local anesthetic agent. [ 1 ]

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