CH 2: Pharmacologic Principles Flashcards

(64 cards)

1
Q

Drug interactions in which the effect of a combination of two or more drugs with similar actions is equivalent to the same of the individual effects of the same drugs given alone.

Example: 1 + 1 = 2 (compare with synergistic effects)

A

Additive effects

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2
Q

Any undesirable occurrence related to administering or failing to administer a prescribed medication

A

Adverse drug event

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3
Q

Any unexpected, unintended, undesired, or excessive response to a medication given at therapeutic dosages (as opposed to overdose)

A

Adverse drug reaction

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4
Q

A general term for any undesirable effects that are a direct response to one or more drugs

A

Adverse effects

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5
Q

A drug that binds to and stimulates the activity of one or more receptors in the body

A

Agonist

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6
Q

An immunologic hypersensitivity reaction resulting form the unusual sensitivity of a patient to a particular medication; a type of adverse drug event

A

Allergic reaction

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7
Q

A drug that binds to and inhibits the activity of one or more receptors in the body. Also called receptors

A

Antagonists

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8
Q

Drug interactions in which the effect of a combination of two or more drugs is less than the sum of the individual effects of the same drugs given alone (1 + 1 equals less than 2); it is usually caused by an antagonizing (blocking or reducing) effect of one drug on another

A

Antagonistic effects

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9
Q

A measure of the extent of drug absorption for a given drug and route (from 0% to 100%)

A

Bioavailability

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10
Q

One or more biochemical reactions involving a parent drug; occurs mainly in the liver and produces a metabolite that is either inactive or active. Known as a metabolism

A

Biotransformation

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11
Q

The barrier system that restricts the passage of various chemicals and microscopic entities (e.g., bacteria, viruses) between the bloodstream and the central nervous system. It still allows for the passage of essential substances such as oxygen.

A

Blood-brain barrier

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12
Q

The name that describes the chemical composition and molecular structure of a drug

A

Chemical name

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13
Q

Any condition, especially one related to a disease state or patient characteristic, including current or recent drug therapy, which renders a particular form of treatment improper or undesirable

A

Contraindication

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14
Q

The general name for a large class of enzymes that plays a significant role in drug metabolism and drug interactions

A

Cytochrome P-450

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15
Q

A state in which there is a compulsive or chronic need, as for a drug

A

Dependence

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16
Q

The process by which solid forms of drugs disintegrate in the gastrointestinal tract and become soluble before being absorbed into the circulation

A

Dissolution

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17
Q

Any chemical that affects the physiologic processes of a living organism

A

Drug

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18
Q

The processes involved in the integration between a drug and body cells (e.g., the action of a drug on a receptor protein); also called mechanism of action.

A

Drug actions

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19
Q

A method of grouping drugs; may be based on structure or therapeutic use

A

Drug classification

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20
Q

The physiologic reactions of the body to a drug. Can be therapeutic or toxic and describe how the body is affected as a whole by the drug

A

Drug effects

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21
Q

The development of congenital anomalies or defects in the developing fetus cause by the toxic effects of drugs

A

Drug-induced teratogenesis

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22
Q

Alteration in the pharmacologic or pharmacokinetic activity of a given drug caused by the presence of one or more additional drugs; it is usually related to effects on the enzymes required for metabolism of the involved drugs

A

Drug interaction

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23
Q

The length of time the concentration of a drug in the blood or tissues is sufficient to elicit a response

A

Duration of action

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24
Q

Protein molecules that catalyze one or more of a variety of biochemical reactions, including those related to the body’s physiologic processes, as well as those related to drug metabolism

A

Enzymes

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25
The initial metabolism in the liver of a drug absorbed form the gastrointestinal tract before the drug reaches systemic circulation through the bloodstream
First-pass effect
26
The name given to a drug by the United States Adopted Name Council. Also called the nonproprietary name. Much shorter and simpler- not protected by trademark
Generic name
27
A hereditary condition in which red blood cells break down when the body is exposed to certain drugs
Glucose-6-phospahte dehydrogenase (G6PD) deficiency
28
In pharmacokinetics, the time required for half of an administered dose of drug to be eliminated by the body, or the time it takes for the blood level of a drug to be reduced by 50%
Half-life
29
An abnormal and unexpected response to a medication, other than an allergic reaction, that is peculiar to an individual patient
Idiosyncratic reaction
30
The characteristic that causes two parental drugs or solutions to undergo a reaction when mixed or given together that results in the chemical deterioration of at the least one of the drugs
Incompatibility
31
Within an artery
Intraarterial
32
Within a joint
Intraarticular
33
Within a sheath (e.g., the theca of the spinal cord, as in an intrathecal injection into the subarachnoid space)
Intrathecal
34
Any preventable adverse drug even involving inappropriate medication us by a patient or health care professional; in may or may not cause patient harm
Medication error
35
The prescribing, dispensing, and administering of medications, and the monitoring of their effects
Medication use process
36
Chemical form of a drug that is the product of one or more biochemical (metabolic) reactions involving a parent drug. Active- are those that have pharmacologic activity of their own, even if the parent drug is inactive Inactive- lack of pharmacologic activity and are simply drug waste products awaiting excretion from he body
Metabolite
37
Time required for a drug to elicit a therapeutic response after dosing
Onset of action
38
A transporter protein that moves drugs out of cells and into the gut, urine, or bile
P-glycoprotein
39
The chemical form of a drug that is administered before it is metabolized by the body not its active or inactive metabolite. No pharmacologically active itself is called a prodrug. Prodrug is then metabolized to pharmacologically active metabolites
Parent drug
40
The time required for a drug to reach its maximum therapeutic response in the body
Peak effect
41
The maximum concentration of a drug in the body after administration, usually measured in a blood sample for therapeutic drug monitoring
Peak level
42
The science of preparing and dispensing drugs, including dosage form design
Pharmaceutics
43
The study of the biochemical and physiologic interactions of drugs at their sites of activity. It examines the effect of the drug on the body
Pharmacodynamics
44
The study of economic factors impacting the cost of drug therapy
Pharacoeconomics
45
The study of the influence of genetic factors on drug response that result in the absence, overabundance, or insufficiency of drug-metabolizing enzymes
Pharmacogenomics
46
The study of dugs that are obtained form natural plant and animal sources
Pharmocognosy
47
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. Represent the drug absorption into, distribution and metabolism within, and excretion from the body.
Pharmacokinetics
48
The broadest term for the study or science of drugs
Pharmacology
49
The treatment of pathologic conditions through the use of drugs
Pharmacotherapeutics
50
An inactive drug dosage form that is converted to an active metabolite by various biochemical reactions once it is inside the body
Prodrug
51
The first form of a drug, or first in a class of drugs. Will be denoted as a "key drug"
Prototypical drug
52
A molecular structure within or on the outer surface of a cell. They bind specific substances (drug molecules) and one or more corresponding cellular effects (drug action) occur as a result of this drug-receptor interaction
Receptor
53
The physiologic state in which the amount of drug removed via elimination is equal to the amount of drug absorbed with each dose
Steady state
54
Substances (e.g., drugs or natural biochemicals in the body) on which an enzyme acts
Substrates
55
Drug interaction in which the effect of a combination of two or more drugs with similar actions is greater that the sum of the individual effect of the same drugs given alone. Example: 1 + 1 is greater than 2 (compare with additive effects)
Synergistic effects
56
The process of measuring drug levels to identify a patient's drug exposure to allow adjustment of dosages with the goals of maximizing therapeutic effects and minimizing toxicity
Therapeutic drug monitoring
57
The desired or intended effect of a particular medication
Therapeutic effect
58
The ratio between the toxic and therapeutic concentration of a drug
Therapeutic index
59
Reduced response to a drug after prolonged use
Tolerance
60
The quality of being poisonous (i.e., injurious to health or dangerous to life)
Toxic
61
The condition of producing adverse bodily effects due to poisonous qualities
Toxicity
62
The study of poisons, including toxic drug effects, and applicable treatments
Toxicology
63
The commercial name given to a drug products by its manufacturer; also called the proprietary name
Trade name
64
The lowest concentration of drug reached in the body after it falls from its peak level usually measures in a blood sample for therapeutic drug monitoring
Trough level