enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Area under the curve (pharmacokinetics) - Wikipedia

    en.wikipedia.org/wiki/Area_under_the_curve...

    Absolute bioavailability refers to the bioavailability of a drug when administered via an extravascular dosage form (i.e. oral tablet, suppository, subcutaneous, etc.) compared with the bioavailability of the same drug administered intravenously (IV). This is done by comparing the AUC of the non-intravenous dosage form with the AUC for the drug ...

  3. Bioavailability - Wikipedia

    en.wikipedia.org/wiki/Bioavailability

    To ensure that the drug taker who has poor absorption is dosed appropriately, the bottom value of the deviation range is employed to represent real bioavailability and to calculate the drug dose needed for the drug taker to achieve systemic concentrations similar to the intravenous formulation. [4] To dose without knowing the drug taker's ...

  4. Pharmacokinetics - Wikipedia

    en.wikipedia.org/wiki/Pharmacokinetics

    Once a drug's bioavailability has been established it is possible to calculate the changes that need to be made to its dosage in order to reach the required blood plasma levels. Bioavailability is, therefore, a mathematical factor for each individual drug that influences the administered dose.

  5. Volume of distribution - Wikipedia

    en.wikipedia.org/wiki/Volume_of_distribution

    A V D greater than the total volume of body water (approximately 42 liters in humans [5]) is possible, and would indicate that the drug is highly distributed into tissue. In other words, the volume of distribution is smaller in the drug staying in the plasma than that of a drug that is widely distributed in tissues. [6]

  6. Elimination rate constant - Wikipedia

    en.wikipedia.org/wiki/Elimination_rate_constant

    In first-order (linear) kinetics, the plasma concentration of a drug at a given time t after single dose administration via IV bolus injection is given by; = / where: C 0 is the initial concentration (at t=0)

  7. Cmax (pharmacology) - Wikipedia

    en.wikipedia.org/wiki/Cmax_(pharmacology)

    After an intravenous administration, C max and t max are closely dependent on the experimental protocol, since the concentrations are always decreasing after the dose. But after oral administration, C max and t max are dependent on the extent, and the rate of drug absorption and the disposition profile of the drug. They could be used to ...

  8. AOL Mail

    mail.aol.com

    Get AOL Mail for FREE! Manage your email like never before with travel, photo & document views. Personalize your inbox with themes & tabs. You've Got Mail!

  9. Intravenous therapy - Wikipedia

    en.wikipedia.org/wiki/Intravenous_therapy

    Intravenous therapy (abbreviated as IV therapy) is a medical technique that administers fluids, medications and nutrients directly into a person's vein.The intravenous route of administration is commonly used for rehydration or to provide nutrients for those who cannot, or will not—due to reduced mental states or otherwise—consume food or water by mouth.