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  2. 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 ]

  3. Lidocaine - Wikipedia

    en.wikipedia.org/wiki/Lidocaine

    The volume of distribution is 1.1 L/kg to 2.1 L/kg, but congestive heart failure can decrease it. About 60% to 80% circulates bound to the protein alpha 1 acid glycoprotein. The oral bioavailability is 35% and the topical bioavailability is 3%. Lidocaine efficacy may be reduced in tissues that are inflamed, due to competing inflammatory ...

  4. Orthopedic cast - Wikipedia

    en.wikipedia.org/wiki/Orthopedic_cast

    2 (CaSO 4 ·½ H 2 O) + 3 H 2 O → 2 (CaSO 4.2H 2 O) + Heat [4] The setting of unmodified plaster starts about 10 minutes after mixing and is complete in about 45 minutes; however, the cast is not fully dry for 72 hours. [5]

  5. Dental anesthesia - Wikipedia

    en.wikipedia.org/wiki/Dental_anesthesia

    Lidocaine's half-life in the body is about 1.52 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.

  6. Local anesthetic - Wikipedia

    en.wikipedia.org/wiki/Local_anesthetic

    Many local anesthetics fall into two general chemical classes, amino esters (top) and amino amides (bottom). A local anesthetic (LA) is a medication that causes absence of all sensation (including pain) in a specific body part without loss of consciousness, [1] providing local anesthesia, as opposed to a general anesthetic, which eliminates all sensation in the entire body and causes ...

  7. Ringer's lactate solution - Wikipedia

    en.wikipedia.org/wiki/Ringer's_lactate_solution

    Ringer's lactate has an osmolarity of 273 mOsm L −1 [14] and a pH of 6.5. [10] The lactate is metabolized into bicarbonate by the liver, which can help correct metabolic acidosis. Ringer's lactate solution alkalinizes via its consumption in the citric acid cycle , the generation of a molecule of carbon dioxide which is then excreted by the lungs.