• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/61

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

61 Cards in this Set

  • Front
  • Back
additive effects
combination of 2 or more drugs w similar actions is equal to the sum of individual effects of the same drugs given alone. 1+1=2
Adverse drug event
undesirable occurrence related to administering or failing to administer a medication
Adverse drug reaction
unexpected, unintended, undesired, or excessive response to a medication given at therapeutic dosages (as opposed to overdose).
Agonist
a drug that binds to and stimulates the activity of one or more receptors in the body
allergic reaction
an immunologic hypersensitivity reaction resulting from the unusual sensitivity of a patient to a particular medication
Antagonist
a drug that binds to and inhibits the activity of one or more receptors in the body (inhibitors )
antagonistic effects
the effect of the combination of 2 or more drugs is less than the sum of the individual effects of the same drugs given alone; usually caused by an antagonizing (blocking/reducing) effect of one drug on another
Bioavailability
a measure of the extent of drug absorption for a given drug and route
biotransformation
(metabolism). occurs mainly in the liver . produces a metabolite that is either inactive or active from a parent drug
Blood-Brain barrier
barrier system that restrics the passage of various chemicals and microscopic entities between the bloodstream and the central nervous system. it still allows for passage of essentials (oxygen)
Chemical name
the name that describes the chemical composition and molecular structure of a drugm
Contraindication
any condition, especially one related to a disease state or patient characteristic, including recent drug therapy, that renders a particular form of treatment improper or undesirable.
Cytochrome
the general name for a large class of enzymes that play a significant role in drug metabolism and drug interactions
Dependence
compulsive or chronic need for a drug
dissolution
solid drug disintegration in the GI Tract in which drugs become more soluble before being absorbed into circulation
drug
any chemical that affects the physiologic processes of a living organism
drug actions
process involved in the interaction between a drug and body cells . aka mechanism of action
drug classification
method of grouping drugs; based on drug or therapeutic use
drug effects
physiologic reactions if the body to a drug. therapeutic or toxic. how the body is affected as a whole by the drug. (onset, peak, & duration )
drug induced teratogenesis
(pregnancy)development of congenital anomalies or defects in the developing fetus caused by the effects of drugs
drug interactions
alteration in the pharmacologic or pharmacokinetic activity of a given drug caused by presence of one or more additional drugs; related to the enzymes required for metabolism of involved drugs
duration of action
the length of time the concentration if a drug in the blood or tissues is sufficient to elicit a response
Enzymes
*break down*protein molecules that catalyze one of more of a variety of biochemical reactions, including those related to the body's physiologic processes as well as those related to drug metabolism
First-pass effect
initial metabolism in the liver of a drug absorbed from the GI tract before the drug reaches systemic circulation through bloodstream
Generic Name
the name given to a drug by the U.S. adopted names counci. nonproprietary name. shorter, simpler, not protected by a trademark
G6PD (Glucose-6-phosphate dehydrogenase deficiency)
hereditary condition in which red blood cells break down when the body is exposed to certain drugs
Half-life
pharmacokinetics, the time required for half of an administered dose of drug to be eliminated by the body. the time it takes for the blood level of a drug to be reduced by 50%
Idiosyncratic reaction
abnormal and unexpected response to a medication, other than an allergic reaction, that I'd peculiar to an individual patient.
Incompatibility
characteristic that causes 2 parenteral drugs or solutions to undergo a reaction, that is peculiar to an individual patient
Intraarterial
within an artery
Intraarticular
within a joint
intrathecal
within a sheath (spinal cord)
Medication error
any preventable adverse drug event
Medication use process
prescribing, dispensing, and administering of medications, and the monitoring of their effects
Metabolite
Chemical form of a drug that's the product of one or more metabolic reaction s involving the parent drug. Active have pharmacologic activity. Inactive do not
Onset of action
the time required for a drug to elicit a therapeutic response after dosing
Parent drug
chemical form of a drug that is administered before it is metabolized by the body's biochemical reactions into its active or inactive metabolites
peak effect
time time required for a drug to retea changed its maximum therapeutic response in the body
peak level
maximum concentration of a drug in the body after administration, usually measured in a blood sample for therapeutic drug monitoring.
pharmaceutics
the science of preparing and dispensing drugs, including dosage form design
Pharmacodynamics
the study of biochemical and physiologic interactions of drugs at their sites of activity. it examines the physicochemical properties of drugs and their pharmacologic interactions with body receptors
Pharmacoeconomics
the study of ececonomic factors impacting the cost of drug therapy
Pharmacogenomics
study of the influence of genetic factors on drug response, including the nature of genetic aberrations that result in the absence, overabundance, or insufficiency of drug metabolizing enzymes.
Pharmacognosy
the study of drugs that are obtained from natural plant and animal sources
pharmacokinetics
Represent the drug ABSORPTION into , DISTRIBUTION and METABOLITES within, and EXCRETION from the body. the study of what happens to a drug from the time it is put into the body until the parent drug and all metabolites have left the body
Pharmacology
broadest term for the study or science of drugs
Pharmacotherapeutics
the treatment of pathologic conditions through the use of drugs.
Prodrug
An inactive drug dosage form that is converted to an active metabolite by various biochemical reactions once inside the body
Receptor
A molecular structure within or on the outer surface of a cell. Receptors bind specific substances (drug molecules) and one or more corresponding cellular effects ( drug actions) occurs as a result of this drug-receptor interaction
steady state
the physiologic state in which the amount of drug removed via elimination is equal to the amount of drug absorbed w each dose
Substrates
substances on which an enzyme acts
Synergistic effects
drug interactions in which the effect of a combination of two orbmore drugs with similar actions is greater than the sum of the individual effects of the same drugs given alone
therapeutic drug monitoring
the process of measuring drug levels to identify a patient's drug exposure and to allow adjustments of dosages with the goals of maximizing therapeutic effects and minimizing toxicity
therapeutic effect
the desired or intended effect of a particular medication
therapeutic index
the ratio between the toxic and therapeutic concentrations of a drug
Tolerance
reduced response to a drug after prolonged use
Toxic
the quality of being poisonous
Toxicity
the condition of producing adverse bodily effects due to poisonous qualities
Toxicology
the study of poisons, including toxic drug effects and applicable treatments
Trade name
the commercial name given to a drug product by it its manufacturer; also called a proprietary name
Trough level
lowest concentration of drug reached in body after it falls from its peak level, usually measured in a blood sample for therapeutic drug monitoring