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