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  2. Equianalgesic - Wikipedia

    en.wikipedia.org/wiki/Equianalgesic

    An equianalgesic chart is a conversion chart that lists equivalent doses of analgesics (drugs used to relieve pain). Equianalgesic charts are used for calculation of an equivalent dose (a dose which would offer an equal amount of analgesia) between different analgesics. [1]

  3. List of adverse effects of valproate - Wikipedia

    en.wikipedia.org/wiki/List_of_adverse_effects_of...

    Liver failure; Pancreatitis (these two usually occur in first 6 months and can be fatal); Leukopenia (low white blood cell count); Neutropenia (low neutrophil count); Pure red cell aplasia

  4. Valproate - Wikipedia

    en.wikipedia.org/wiki/Valproate

    Valproic acid was first synthesized in 1882 by Beverly S. Burton as an analogue of valeric acid, found naturally in valerian. [69] Valproic acid is a carboxylic acid, a clear liquid at room temperature. For many decades, its only use was in laboratories as a "metabolically inert" solvent for organic compounds.

  5. Valpromide - Wikipedia

    en.wikipedia.org/wiki/Valpromide

    Valpromide is no safer during pregnancy than valproic acid. Valpromide is formed through the reaction of valproic acid and ammonia via an intermediate acid chloride. In pure form, valpromide is a white crystalline powder and has a melting point 125–126 °C. It is soluble only in hot water. It is available on the market in some European countries.

  6. GABA transaminase inhibitor - Wikipedia

    en.wikipedia.org/wiki/GABA_transaminase_inhibitor

    Examples include valproic acid, [2] vigabatrin, [3] [4] phenylethylidenehydrazine (and drugs that metabolize to it, such as phenelzine [5]), ethanolamine-O-sulfate (EOS), and L-cycloserine. [ 6 ] Certain members of this class are used as anticonvulsants .

  7. Route of administration - Wikipedia

    en.wikipedia.org/wiki/Route_of_administration

    The term injection encompasses intravenous (IV), intramuscular (IM), subcutaneous (SC) and intradermal (ID) administration. [35] Parenteral administration generally acts more rapidly than topical or enteral administration, with onset of action often occurring in 15–30 seconds for IV, 10–20 minutes for IM and 15–30 minutes for SC. [36]

  8. Pharmacokinetics - Wikipedia

    en.wikipedia.org/wiki/Pharmacokinetics

    The use of these models allows an understanding of the characteristics of a molecule, as well as how a particular drug will behave given information regarding some of its basic characteristics such as its acid dissociation constant (pKa), bioavailability and solubility, absorption capacity and distribution in the organism.

  9. Fetal valproate spectrum disorder - Wikipedia

    en.wikipedia.org/wiki/Fetal_Valproate_Spectrum...

    Minor limb malformations seen after valproate exposure. Fetal valproate spectrum disorder (FVSD), previously known as fetal valproate syndrome (FVS), is a rare disease caused by prenatal exposure to valproic acid (VPA), a medication commonly used to treat epilepsy, bipolar disorder, and migraines.

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