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158 Cards in this Set
- Front
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synergistic effect
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a drug interaction that results from combined drug effects that are greater than those that could have been achieved if the drug were gived alone
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substrate
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a substance on which an eczyme acts
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steady state
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the physiologic state in which the amount of drug removed via elimination is equal to the amount of drug absorbed with each dose
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side effect
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any undesirable effect of a medication that is expected or anticipated to occur in a predictable percentage of pt who recieve a given med
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receptor
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a molecular structure within or on the outer surface of cells receptors are characterized by the binding of specific substances
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prodrug
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an inactive drug dosage form that is converted to an active metabolite by various biochemical chemical reactions once inside the body
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pharmacogenetics
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the study of genetic factors and their influence on drug response
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parent drug
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the chemical form of a drug that is administered to the body before it is metabolized by the bodys biochemical reactions into its active or inactive metabolites
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3 primary protiens that bind to and carry drugs
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albumin, alpha-acid glycoprotein, corticosteroid-binding globulin
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3 routes of administration
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enteral, patenteral, topical
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bioequivalent
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two meds have the same bioavailability
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pharmacodynamic phase
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drug receptor interaction
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pharmacokinetics
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absorption, distribution,metabolism,excretion
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pharmaceutical phase
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disintegration of dosage form dissolution of drug
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pharmaceutics,pharmacokinectics,pharmacodynamics describe what
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the relationship between the dose of a drug give to a pt and the effectiveness of the drug in treating the pt's disease
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metabolites
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a chemical form of a drug that is the product of one or more biochemical metabolic reactions involving the parent drug.
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med use process
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the administration dispensing monitoring and prescribing of meds
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medication misadventure
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the broadest term for any undesirable medication related event in patient care that is usually iatrogenic in nature
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incompatibility
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reaction that occurs when two parenteral drugs or solutions are mixed together resulting in chemical deterioration of at least one of the drugs
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idiosyncratic reaction
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an abnormal and unexpected susceptibility to a medication other that an allergic reaction that is peculiar to an individual pt
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latrogenic hazard
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any potential or actual pt harm that is caused by errant actions of health care staff members
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cytochrome p-450
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general term for a wide variety of tissue enzymes that play a significant role in drug metabolism
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contraindication
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any condition including any current or recent drug therapy especially related to disease states or other pt characteristics that renders a particular form of treatment improper or undesirable
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duration of action
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the length of time that a drug concentration in the blood or tissues is suffecient to elicit a therapeutic response
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toxicology
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the study of poisions and unwanted responses to therapeutic agents
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latrogenic response
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unintentional adverse effects that are treatment induced
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therapeutic index
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the ratio between a drug's therapeutic benefit and it's toxic effects
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pharmacotherapeutics types of therapy
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acute,maintenance,supplemental,palliative,supportive,prophylactic,empiric
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3 mechanisms of action in pharmacodynamics
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receptor interactions,enzyme interactions,nonspecific interactions
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once a drug is at the site of action what does it do
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it can modify the rate at which the cells or tissues function
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drug effect
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the physiologic reaction of the body to the drug
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drug action
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the cellular processes involved in the drug and cell interaction
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duration
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the time a drug concentration is sufficient to elicit a therapeutic response
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peak
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time it takes for a drug to reach its maximum therapeutic response
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onset
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time it takes for the drug to elicit a therapeutic response
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half life
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the time it takes for one half of the original amount of a drug in the body to be removed
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stimulating drug metabolism causes
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diminished pharmocologic effects
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delayed drug metabolism results in
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accumulation of drugs prolonged action of the drug
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factors that increase metabolism
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fastacetylator,barbiturate,
rifampin therapy |
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metabolism is the biologic transformation of a drug into
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an inactive metabolite,a more soluable compound, a more potent metabolite
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drug metabolism or biotransformation
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the biologic transformation of a drug into an inactive metabolite , a more soluable compound or a more potent metabolite
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areas of rapid distribution
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heart,liver,kidneys,brain
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drug distribution
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the transport of a drug in the body by the bloodstream to its site of action
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topical routes
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skin,eyes,ears,nose,lungs,vagina
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parenteral routes
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intravenous,im,subq,id,intrathecal,intraarticular
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non first pass routes
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aural,buccal,inhalation,intraarterial,im,intranasal,intraocular,intravaginal,intravenous,subq,sublingual,transdermal
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first pass routes
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hepatic artery,oral,portal vein,rectal
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first pass effect
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the metabolism of a drug and its passage from the live into the circulation
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a drugs route of administration effects
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the rate and extent of absorption of that drug
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oral meds rely on - to break down drug for absorption
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gastric, intestinal enzymes and ph
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pharmacokinetics: absorption
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the rate at which a drug leaves its site of administration and the extent to which absorption occurs
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pharmacognosy
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study of natural drug sources
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pharmacotherapeutics
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the use of drugs and the clinical indications for drugs to prevent and treat diseases
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pharmacodynamics
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the study of what the drug does to the body
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4 phases of pharmacokinetics
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absorption,distribution,metabolism,excretion
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pharmacokinetics
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the study of what the body does to drugs
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pharmaceutics
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the study of how various drug forms influence pharmacokinetic and pharmacodynamic activities
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drug
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any chemical that affects the physiologic processes of a living organism
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nursing process
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assessment dx planning implmentation, evaluation
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trade name
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drug has a registered trademark
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chemical name
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describes a drug's chemical composition and molecular structure
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generic name
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name given to a drug also called nonproprietary name
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dissolution
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process of how solid forms of drugs disintegrate in the gastrointestinal tract, become soluable and get absorbed into circulation
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bioavailability
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term used to quantify the extent of drug absorption
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antagonist
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drug binds to and inhibits the activity of one or more biochemical receptor types in the body resulting in inhibitory or antagonistic drug effects
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antagonistic effect
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a drug interaction that results in combined drug effects that are less that those that could be achieved if either drug were given alone
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agonist
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drug that binds to and stumulates the activity of one or more biochemical receptor types in the body resulting in stimulatory or agonstic drug effects
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ADE adverse drug event
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an injury caused by a medication or failure to administer an intended medication
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additive effect
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result of a drug interaction that occurs when two drugs with similar actions are given together. also called synergistic effect
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med error
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any preventable event that may cause or lead to inappropriate medication use or pt harm while the med is in the control of the health care professional pt or consumer
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5 rights
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rigth drug, right dose, right time, right route, right pt
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drug order must contain 6 elements
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pt name, date order written, name of med, dosage, route of delivery, signature of prescriber
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drug polymorphism
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variation in response to drug because of a pt's age, gender, size and body compostion
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infusion time
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total ml divided by ml/hr =infusion time then mulitply decimal by 60 to get minutes.
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1 pt
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500 ml
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1 tsp
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5 ml or zi
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30ml
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2 T
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2 T
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30 ml
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gri
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60/65 mg
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gr xv
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1g
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Hgb
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hemoglobin
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HCT
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hematocrit
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BUN
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blood, urea, nitrogen
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BE
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barium enema
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T & C
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type and crossmatch
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N/C
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nasal cannula
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tid
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3 times a day
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bid
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2 times a day
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qid
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four times a day
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pc
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after meals
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ac
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before meals
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BRP
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bathroom privilages
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excretion of ped pt
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kidneys immature affects glomerular filtration rate and tubular secretion decreased perfusion rate of the kidneys.
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metabolism in ped pt.
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liver immature
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distribution in ped pt.
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greater TBW means fat is decreased so decreased level of protein binding immature blood-brain barrier
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drug
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an chemical that affects the physiologic processes of a living organism
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considerations in absorption in ped pt.
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ph less acidic gastric emptying slow topical absorption faster IM faster and irregular
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category x
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fetal abnormalities reported and positive evidence of fetal risk in humans is available from studies should not be used in pregnant women
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category D
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possible fetal risk in humans reported consider benefits VS risk may in some cases warrant use
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category C
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adverse effects reported on animal fetuses. info on humans not avaioable.
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category B
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studies indicate no risk to animal fetus info on humans unavailable
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category A
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studies indicate no risk to human fetus
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which stage of pregnancy is the greatest danger for drug induced development defects
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first trimester
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synergistic effect
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a drug interaction that results from combined drug effects that could have been achieved if the drugs where given alone
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substrate
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a substance on which an enzyme acts
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steady state
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a physiologic state in which the amount of drug removed via elimination is equal to the amount of drug absorbed with each dose
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expediteted drug approval
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a hastening the usual IND approval process in response to public health threat
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durham-humphrey amendment
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the act of 1951 differentiated between prescription and otc drugs also which drugs could be refilled without a prescription
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federal food and drug act
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first fed law that attempted to protect the public from danger 1906
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federal food, drug and cosmetic act
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1938 act required drug manufactures to apply for an IND exemption for a safety review before marketing new drugs
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harrison narcotic act
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1914 established the legal term narcotic
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sherley amendment
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1912 prohibited labeling of med with false therapeutic claims intending to defraud the purchaser
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kefauver-harris amendment
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1962 required drug to be proved safe and effective before being approved
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controlled substance act
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1970 promotes research on drug abuse prevention education treatment rehabilitation and enhancement of law enforcement
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orphaned drug act
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1983 aid in the development of drugs for treatment of rare diseases
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autonomy
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self determination and ability to act on one's own
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investigational new drug
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drug not approved by the FDA but available for use in experiments to determine its safety and effects
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2 types of ADR's
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allergic and idiosyncratic
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veracity
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duty to tell the truth
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nonmaleficence
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the duty to do no harm to a client
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justice
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being fair or equal in one's actions
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confidentiality
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duty to respect privileged information about a pt. implications include not talking about a pt in public or outside the context of the health care setting
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beneficence
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the doing or active promotion of good implications include how the patient is best served
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use of otc's may
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delay effective treatment of more chronic disease states, delay treatment of serious life threating disorders, may relieve symptoms of a disorder but not the cause
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stages of development
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infant 0-1yr, toddler 1-3yr, preschooler 3-6yr, school age 6-12yr, adolescent 12-18yr, young adult 18-45yr, middle aged 45-65yr, older adult 65 and up
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opioid drug withdrawl
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peak period 1-3 days /duration 5-7days
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opioids produce
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analgesia, drowsiness, euphoria, tranquility, other mood alterations
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commonly abused substances
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opioids stimulants depressants alcohol nicotine
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drug used for withdrawl of opioid
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clondine, methadone
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amphetamines, cocaine, methylphenidate are what
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stimulants
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effects that lead to abuse of stimulants
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elevation of mood, reduction of fatigue, sense of incresed alertness, invigoration alertness
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methylenedioxyamphetamine
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love drug
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methylendioxymethamphetamine
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ecstasy
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stimulant withdrawl
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peak 1-3 days
duration 5*7days |
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signs of stimulant withdrawl
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social withdrawl, psycomotor retardation, hypersomnia, hyperphagia
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signs of symtoms withdrawl from stimulants
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depression, suicidal thoughts and behaviors, paranoid delusions
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depressants
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drugs that relieve anxiety, irrability,tension
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opioid signs of withdrawl
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drug seeking, mydriasis, diaphoresis, rhinoorrhea, lacrimation diarrhea bp and pulse up
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benzodiazepine and barbiturates are
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depressants
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flunitrazepam (rohypol)
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roofies date rape drug used to enhance a herion high or to ease the coming down from a cocaine high
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depressant withdrawl
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peak period short acting agent 2-4 days.long acting agent 4-7 days
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alcohol (ethanol)
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CNS depression
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flumazenil ( romazicon)
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may be used to reverse the acute sedative effects of benzodiazepines
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3 ethano withdrawl treatment durgs
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diazepam ( valium ), lopazepam ( ativan ), disulfiram ( antabuse ).
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releases epinephrine that creates physiologic stress rather that relaxation
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nicotin
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drug aids in cessation of smoking
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bupropion ( zyban)
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commission E monographs
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comprehensive published herbal recommendations from the german equibalent of the us fda
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legend drugs
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meds not legally available without a prescription
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phytochemical
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the pharmacologically active ingredient in an herbal remedy
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dietary supplement and health education act
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1994 defines dietary supplements and provide the regulatory framwork for their sale.
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opioid analgesic
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synthetic pain-relieving substance that originated from the opium plant.
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narcotic
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any agent that produces insensibility or stupor
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roofies
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pills that are classified as benzodiazepines
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amphetamines
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drugs that stimulate the CNS
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how opioids work
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they block receptors in the cns blocking pain
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stimulants work by
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releasing biogenic amines form their storage sites in the nerve terminals main one is norepinephrine
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how do benzodiazepines and barbiturates work
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they increase the action of gamma-aminobutyric acid
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drug order must contain 6 elements
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pt name, date order written , name of med, dosage size frequency and doses, route of delivery, signature of prescriber
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