Pharm: Ch 2 Basic Concepts and Processes Key Terms Flashcards

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1
Q

process that occurs from the time a drug enters the body to the time it enters the bloodstream to be circulated

A

Absorption

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2
Q

any undesired responses to medication administration

A

Adverse effects

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3
Q

drug that produces effects similar to those produced by naturally occurring hormones, neurotransmitters, and other substances

A

Agonist

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4
Q

drug that inhibits cell function by occupying receptor sites

A

Antagonist

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5
Q

substance that relieves, prevents, or counteracts the effect of a poison

A

Antidote

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6
Q

portion of a drug dose that reaches the systemic circulation and is available to act on body cells

A

Bioavailability

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7
Q

when drugs are altered from their original form into a new form by the body; also referred to as metabolism

A

Biotransformation (Metabolism)

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8
Q

Drug distribution into the central nervous system (CNS) is limited because the blood–brain barrier, composed of capillaries with tight walls, limits the movement of drug molecules into brain tissue. Only drugs that are lipid soluble or have a transport system can cross the blood–brain barrier and reach therapeutic concentrations in brain tissue.

A

Blood-brain barrier

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9
Q

transport of drug molecules within the body; after a drug is injected or absorbed into the bloodstream, it is carried by the blood and tissue fluids to its sites of action, metabolism, and excretion

A

Distribution

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10
Q

Frequency, size, and number of doses- major determinants of drug actions and responses, both therapeutic and adverse.

A

Dosage

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11
Q

drugs or metabolites that are excreted in bile, reabsorbed from the small intestine, returned to the liver, metabolized, and eventually excreted in urine

A

Enterohepatic recirculation

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12
Q

production of larger amounts of drug-metabolizing enzymes by liver cells; process accelerates drug metabolism because larger amounts of the enzymes (and more binding sites) allow larger amounts of a drug to be metabolized during a given time

A

Enzyme induction

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13
Q

process in which a molecule binds to enzymes and inhibits their activity

A

Enzyme inhibition

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14
Q

elimination of a drug from the body; effective excretion requires adequate functioning of the circulatory system and of the organs of excretion (kidneys, bowel, lungs, and skin)

A

Excretion

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15
Q

initial metabolism of some oral drugs as they are carried from the intestine to the liver by the portal circulatory system prior to reaching the systemic circulation for distribution to site of action

A

First-pass effect

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16
Q

immune-mediated reaction to a drug

A

Hypersensitivity

17
Q

dose larger than the regular prescribed daily dosage of a medication; used to attain a therapeutic blood level

A

Loading dose

18
Q

quantity of drug that is needed to keep blood levels and/or tissue levels at a steady state or constant level

A

Maintenance dose

19
Q

toxic or damaging effect of a substance on the kidney; potentially serious because renal damage interferes with drug excretion, causing drug accumulation and increased adverse effects

A

Nephrotoxicity

20
Q

the study of how a person’s genetic heritage leads to variable responses to drugs; more generally refers to genetic polymorphisms that occur in a patient population, such as an ethnic group, as opposed to an individual person

A

Pharmacogenomics

21
Q

reactions between living systems and drugs; drug actions on target cells and the resulting alterations in cellular biochemical reactions and functions

A

Pharmacodynamics

22
Q

drug movement through the body to reach sites of action, metabolism, and excretion

A

Pharmacokinetics

23
Q

the occurrence of two or more clearly different forms (or phenotypes) in a species important in drug therapy because it explains the functionally different response to drugs in a general patient population or a specific individual

A

Polymorphism

24
Q

initially inactive drugs that exert no pharmacologic effects until they are metabolized

A

Prodrugs

25
Q

Drug molecules bound to plasma proteins (mostly Albumin) are pharmacologically inactive because the complex’s large size prevents them from leaving the bloodstream through the small openings in capillary walls and reaching their sites of action, metabolism, and excretion.

A

Protein binding

26
Q

laboratory measurement of the amount of a drug in the blood at a particular time

A

Serum drug level

27
Q

time required for the serum concentration of a drug to decrease by 50%; also called elimination half-life

A

Serum half-life