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87 Cards in this Set

  • Front
  • Back
absolute refractory period
early phase of cardiac repolzrization in which the heart muscle annoy be stimulated to depolarize
absorption
process by which the molecules of a substance are moved from the site of entry to admin to systemic circulation
acetycholinesterase
enzyme that breaks down acetylcholine
active metabolite
medication that has undergone biotransformation and is able to alter a cellular process or body function
Active Transport
process of molecules binding with carrier proteins when energy is used to move the molecules against a concentration gradient
affinity
ability of a medication to bind with a particular receptor site
agonist medications
group of meds that initiates or alters a cellular activity by attaching to receptor sites
- promotes cellular response
anaphylaxis
an extreme systemic form of an allergic reaction involving two or more body systems
antagonist medications
group of medication that prevent endogenous or exogenous agonist chemical from reaching cell receptor sites an initiating or altering a particular cellular activity
antibiotics
meds used to fight infection by killing the microorganisms or preventing their multiplication to allow the body's immune system to overcome them
antifungals
meds used to treat fungal infections
antimicrobials
medications used to kill or suppress the growth of microorganisms
automaticity
state in which cardiac cellos are at rest, waiting for the generation of a spontaneous impulse from within
bioavailability
percentage of the unchanged medication that reaches systemic circulation
biotranformation
process with 4 possible effects of a medication absorbed into the body
1. inactive substance becomes active, capable of producing desired or unwanted clinical effects
2. active med can be changed into another active med
3. active med becomes partially or completely inactive
4. meds is transformed into a substance that is eaters to eliminate from body
chelating agents
meds that bind with heavy metals in the body and create a compound that can be eliminated
- ingestion or poisonings
cholinergic
term to describe the fibers in the parasympathetic NS that real seas a chemical acetylcholine
competitive antagonist
meds that temporarily bind with cellular receptors sites, displacing agonist chemicals
competitive depolarizing
term used to describe paralytic agent that act at the neuromuscular junction by binding with nicotinic receptors on muscles, causing fasiciulations and preventing additional activation by ACh.
cross-tolerance
process in which repeated exposure to ames within a particular class causes a tolerance that may be "transferred" to other meds in the same class
cumulative action
several smaller doses of a particular med capable of producing the same clinical effects as a single larger does of that same med
cytochrome P-450 system
hemoprotein involved in the detoxification of many drugs
dependence
physical, behavioral, or emotional need for a med or chemical in order to maintain "normal" physiologic function
depolarizaiton
process of discharging resting cardiac muscle fibers by an electric impulse that causes them to contract
depressant
chemical or med that decreases the performance of the CNS or sympathetic NS
distribution
movement and transport of a med throughout the bloodstream to tissues and cells, and ultimate mate its target receptor
diuretic
chemical that increase urinary output
dose-response curve
graphic illustration of the response of a drug according to the dose admin
dosing
specific amount of a med to be given at a specific interval
down-regualtion
process in which a mechanism reducing available cell receptors for a particular med results in tolerance
duration of effect
time a medication concentration can be expected to remain about the min level needed to provide the intended action
dystonic
pertaining to voluntary muscle movements that are distorted or impaired because of abnormal muscle tone
ectopic foci
sites of generation of electrical impulses other than normal pacemaker cells
efficacy
pharmacologic context: ability of a med to produce the desired effect
elimination
pharmacologic context: removal of a med or its by-products from the body
endogenous
originating from within the organism
exogenous
originating outside the organism
extravasation
seepage of blood and med into the tissue surrounding blood vessel
facilitated diffusion
process of med molecules binding with carrier proteins when no energy is expended
fasciculation
brief, uncoordinated, visible twitching of small muscle groups; may be caused by the admin of depolarizing neuromuscular blocking agent
- succs
filtration
use of hydrostatic pressure to force water or dissolved particles through a semipermeable membrane
first-order elimination
process in which the rate of elimination is directly influenced by plasma levels of a substance
habituation
unusual tolerance to the therapeutic and adverse clinical effects of a me or chemical
half-life
time needed in an average person for metabolism or elimination of 50% of a substance in the plasma
hematrocrit
percentage of RBC's in a blood sample
hemolysis
destruction of RBC's by disruption of the cell membrane
hydrophilic
attracted to water molecules
idiosyncratic
pharmacologic context: abnormal susceptibility of a med, possibly due to genetic traits or dysfunction of a metabolic enzyme, that is peculiar to an individual PT
inactive metabolite
med that has undergone biotransformation and now is no longer able to alter a cell process or body function
ions
charged particles
interference
one med or chemical taken by a PT that undermine the effectiveness of another med taken by or admin to a PT
lipophilic
attracted to fats or lipids
median effective does (ED50)
weight-based does of a med that was effective in 50% of the humans and animals tested
median lethal does (LD50)
weight-based does of a med that caused death in 50% of the animals tested
median toxic does (TD50)
weight-based dose of a med that demonstrated toxicity in 50% of the animals tested
medication monograph
document that give detailed information about drugs, such as the indication and uses, dosing information, precautions, contraindications, and adverse effects
medication sensitivity
mile to severe reaction after the first exposure to a med or other substance, often with may of the same signs and symptoms as an immune-mediated reaction
noncompetitive antagonist
meds that permanently bind with receptor sites and prevent activation by agonist chemicals
nondepolarizing
term used to describe drugs that produce muscle realization by interfering with impulses between the nerve ending and muscle receptor.
nonionic
uncharged
onset
time needed for the concentration of the med at the target tissue to reach the min effective level
osmosis
movement of a solvent from an area of low solute concentration to one of high concentration through a selectively permeable membrane to equalize concentrations of a solute on both sides of the membrane
osmotic
characterized by the movement of a solvent across a semipermeable membrane from an area of lower to higher concentration of solute molecules
paradoxical
opposite from expected
partial agonist
chemical that binds to the receptor site but does not initiate as much cellular activity or change as other agonists do; lowers the efficacy of other agonist chemicals presents at the cell
peak
pharmacology context: point of max effect of a drug
pharmacodynamics
biochemical and physiologic effects and MoA in the body
pharmacokinetics
fate of meds in the body, such as distribution and elimination
pharmacology
scientific study of how various substances interact with or alter the function of living organisms
pinocytosis
process by which cells ingest the extracellular fluid and its contents
placebo effect
pharmacologic context: positive and negative effects of an inactive med on a person that are related to the person's expect ions and other factors
plasma protein binding
process in which med molecules temporarily attach to proteins in the blood plasma, significantly altering med distribution in the body
potency
relationship between the desired response of a med and the does required to achieve the response
receptor
specialized area in tissues that initiates certain actions after specific stimulations
relative refractory period
period in the cell-firing cycle at which it is possible but difficult to restimulate the cell to fire another impulse
Stevens-Johnson syndrome
severe, possibly fatal reaction that mimics a burn, may be due to medication
stimulant
med or chemical that temporarily enhances CNS and sympathetic NS functioning
sympathomimetics
meds admin to stimulate the sympathetic NS
tachyphylaxis
condition in which repeated doses of med within a short period rapidly cause tolerance, making the med virtually ineffective
therapeutic index
relationship between the median effective does and the median legal dose or median toxic dose; also known as the therapeutic ratio
threshold level
pharmacologic context: concentration of medication at which initiation or alternation of cellular activity begins
tolerance
condition that develops following related use by a PT of med that results in decreed efficacy or potency
untoward effect
clinical change caused by a med that causes harm or discomfort to a PT; adverse effect
Vaughan-Williams
classification scheme based on the MoA rather than a specific medication group
volume of distribution
extent to which a med spread within the body
water-soluble
property that indicates a material can be dissolved in water
zero-order elimination
process in which a fixed amount of a substance is removed during a certain period, regardless of the total amount in the body