Pharm 2 Flashcards
Pharmacokinetics
Action of body on the drug via movement of the drug in and out of the body.
Pharmacodynamics
Action of drug within the body via a drug-receptor action
Absorption
Dependent on bioavailability, route of administration, first pass effect
Distribution
Dependent on tissues penetration, volume of distribution, fat/water solubility
Distribution phase: time between administration of dose and its equilibration between central and peripheral compartments
Metabolism
Biotransformation within the body
Excretion
The removal of a drug or its metabolites from the body, primarily by the kidneys and urination.
Loading dose
Given to rapidly establish a therapeutic plasma drug concentration. Can be calculated by multiplying the volume of distribution by the desired plasma drug concentration.
Maintenance dose
Given to establish or maintain the desired steady-state plasma drug concentration.
Volume of distribution (Vd)
Amount of volume necessary to fill the internal and external compartments of the body
Clearance
Clearance (Cl) is the most fundamental expression of drug elimination. It is defined as the volume of body fluid (blood) from which a drug is removed per unit of time.
Elimination half-life (t½)
Is the time required to reduce the plasma drug concentration by 50%.
ED50 (or ED99)
Median effective dose (ED50), which is the dose that produces 50% of the maximal response.
TD50
The median toxic dose (TD50) of a drug or toxin is the dose at which toxicity occurs in 50% of cases.
LD50
Lethal dose (LD50) is the amount of an ingested substance that kills 50 percent of a test sample.
Tmax
The time needed to reach the maximum