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  2. Pharmacokinetics - Wikipedia

    en.wikipedia.org/wiki/Pharmacokinetics

    Clinical pharmacokinetics (arising from the clinical use of population pharmacokinetics) is the direct application to a therapeutic situation of knowledge regarding a drug's pharmacokinetics and the characteristics of a population that a patient belongs to (or can be ascribed to).

  3. Clinical Pharmacokinetics - Wikipedia

    en.wikipedia.org/wiki/Clinical_Pharmacokinetics

    Clinical Pharmacokinetics is a peer-reviewed medical journal published by Adis International (Springer Nature) that covers topics related to pharmacokinetics.According to the Journal Citation Reports, the journal has a 2023 Impact Factor™ of 4.6 ranked 77 of 277 journals in the Pharmacology & Pharmacy category [Clarivate Analytics]; 2023 CiteScore™ of 8.8 ranked 81 of 272 journals in the ...

  4. Absorption rate constant - Wikipedia

    en.wikipedia.org/wiki/Absorption_rate_constant

    The absorption rate constant K a is a value used in pharmacokinetics to describe the rate at which a drug enters into the system. It is expressed in units of time −1. [1] The K a is related to the absorption half-life (t 1/2a) per the following equation: K a = ln(2) / t 1/2a. [1] K a values can typically only be found in research articles. [2]

  5. Area under the curve (pharmacokinetics) - Wikipedia

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

    The use of trapezoidal rule in AUC calculation was known in literature by no later than 1975, in J.G. Wagner's Fundamentals of Clinical Pharmacokinetics. A 1977 article compares the "classical" trapezoidal method to a number of methods that take into account the typical shape of the concentration plot, caused by first-order kinetics. [8]

  6. Malcolm Rowland - Wikipedia

    en.wikipedia.org/wiki/Malcolm_Rowland

    Rowland became a member of the joint Pharmacy-Medicine NIGMS funded program in Clinical Pharmacology, and moved his research from a prevailing descriptive approach to a more mechanistic, physiologically-based one, [6] including the clearance concept [7] [8] that helped lay the foundations of modern pharmacokinetics.

  7. Physiologically based pharmacokinetic modelling - Wikipedia

    en.wikipedia.org/wiki/Physiologically_based...

    Species: e.g., transpositions from rodents to human, prior to giving a drug for the first time to subjects of a clinical trial, or when experiments on humans are deemed unethical, such as when the compound is toxic without therapeutic benefit; Individuals: e.g., from males to females, from adults to children, from non-pregnant women to pregnant

  8. PK/PD model - Wikipedia

    en.wikipedia.org/wiki/PK/PD_model

    This page was last edited on 26 November 2024, at 01:38 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  9. Maintenance dose - Wikipedia

    en.wikipedia.org/wiki/Maintenance_dose

    In pharmacokinetics, a maintenance dose is the maintenance rate [mg/h] of drug administration equal to the rate of elimination at steady state. This is not to be confused with dose regimen, which is a type of drug therapy in which the dose [mg] of a drug is given at a regular dosing interval on a repetitive basis.