Chap 2 Drugs and The body

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________ is the process by which a drug works or affects the body.

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1

________ is the process by which a drug works or affects the body.

Pharmacodynamics

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2

________ is the major process through which drugs are absorbed into the body.

Passive diffusion

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3

________: removal of a drug from the body; primarily occurs in the kidneys, but can also occur through the skin, lungs, bile, or feces.

Excretion

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4

________ involves a conjugation reaction that makes the drug more polar and easier to excrete.

Phase II biotransformation

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5

________ is an oxidation, reduction, or hydrolysis of the drug via the cytochrome P450 system, abundant in the liver.

Phase I biotransformation

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6

Men have more vascular muscles than women, causing drugs to reach ________ faster.

peak levels

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7

________: specific areas on cell membranes that react with certain chemicals to cause an effect within the cell.

Receptor sites

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8

________: movement of a drug to body tissues; the places where a drug may be distributed depend on the drugs solubility, perfusion of the area, cardiac output, and binding of the drug to plasma proteins.

Distribution

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9

Drugs taken orally are usually absorbed from the ________ into the portal venous system, with aspirin and alcohol absorbed from the lower end of the stomach.

small intestine

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10

________: the study of genetically determined variations in the response to drugs.

Pharmacogenomics

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11

(________) Poor blood flow to a certain area, such as a patient's lower limb infection, can reduce drug effectiveness.

Diabetes

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12

Skin, ________, lungs, bile, and feces are routes of used to excrete.

saliva

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13

________ (used on tips of spears in Amazon) blocks acetylcholine receptor sites, preventing muscle stimulation & causing paralysis.

Curare

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14

________: property of a chemotherapeutic agent that affects only systems found in foreign cells without affecting healthy human cells (e.g., specific antibiotics can affect certain proteins or enzyme systems used by bacteria but not by human cells)

Selective toxicity

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15

________: the movement of substances across a cell membrane against the concentration gradient; this process requires the use of energy.

Active transport

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16

________ is another process the body commonly uses in drug excretion.

Filtration

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17

________ can influence drug excretion.

Urine acidity

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18

________: the passage of water and water- soluble components from the plasma into the renal tubule.

Glomerular filtration

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19

________ are thought to work by reacting with specific receptor sites or by interfering with enzyme systems in the body.

Drugs

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20

Drugs may work by replacing a missing body chemical, by stimulating or depressing ________, or by interfering with the functioning of foreign cells.

cellular activity

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21

During distribution: One drug competes for the protein- binding site of another drug, so the second drug can not be transported to the ________.

reactive tissue

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22

________ can affect the absorption of many oral drugs.

GI disorders

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23

________ and low blood pressure alter the distribution of a drug, preventing it from being delivered to the reactive tissue, thus rendering the drug nontherapeutic.

Vascular diseases

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24

Because the warfarin is biotransformed to an inactive state more quickly, ________ will be needed to achieve the desired effect.

higher doses

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25

Loading dose: use of a higher dose than what is usually used for treatment to allow the drug to reach the ________ sooner.

critical concentration

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26

________: synthetic chemicals used to interfere with the functioning of foreign cell populations, causing cell death; this term is frequently used to refer to the drug therapy of neoplasms, but it also refers to drug therapy affecting any foreign cell.

Chemotherapeutic agents

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27

________ is most common, non- invasive, and cost- effective, with patients able to easily continue regimens at home.

Oral

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28

The ________ is a protective system to keep foreign invaders and poisons away from the CNS.

blood brain barrier

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29

Liver or kidney diseases affect the way that a drug is biotransformed and excreted and can lead to ________ when the usual dose is given.

toxic reactions

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30

________: liver enzymes tightly packed together in the hepatic intracellular structure, responsible for the biotransformation of chemicals, including drugs.

Hepatic microsomal system

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31

________ tend to be faster than subcutaneous due to more capillaries.

IM injections

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32

________ deposit the drug just under the skin, where it is absorbed into circulation at varying speeds based on fat content of injection site and local circulation.

Subcutaneous injections

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33

________ may arise due to increased biotransformation /resistance to drug effects, causing the body to need larger doses to achieve a therapeutic effect.

Tolerance

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34

________: the time it takes for the amount of drug in the body to decrease to one half of the peak level it previously achieved.

Half life

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35

the movement of substances across a cell membrane against the concentration gradient; this process requires the use of energy

active transport

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36

synthetic chemicals used to interfere with the functioning of foreign cell populations, causing cell death; this term is frequently used to refer to the drug therapy of neoplasms, but it also refers to drug therapy affecting any foreign cell

chemotherapeutic agents

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37

the concentration a drug must reach in the tissues that respond to the particular drug to cause the desired therapeutic effect

critical concentration

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38

movement of a drug to body tissues; the places where a drug may be distributed depend on the drugs solubility, perfusion of the area, cardiac output, and binding of the drug to plasma proteins

distribution

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39

a phenomenon in which drugs given orally are carried directly to the liver after absorption, where they may be largely inactivated by liver enzymes before they can enter the general circulation; oral drugs frequently are given in higher doses than drugs given by other routes because of this early breakdown

first-pass effect

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40

the passage of water and water-soluble components from the plasma into the renal tubule

glomerular filtration

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41

the time it takes for the amount of drug in the body to decrease to one half of the peak level it previously achieved

half-life

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42

liver enzymes tightly packed together in the hepatic intracellular structure, responsible for the biotransformation of chemicals, including drugs

hepatic microsomal system

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43

use of a higher dose than what is usually used for treatment to allow the drug to reach the critical concentration sooner

loading dose

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44

movement of substances across a semipermeable membrane with the concentration gradient; this process does not require energy

passive diffusion

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45

the study of the interactions between the chemical components of living systems and the foreign chemicals, including drugs, that enter living organisms; the way a drug affects a body

pharmacodynamics

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46

the study of genetically determined variations in the response to drugs

pharmacogenomics

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47

the way the body deals with a drug, including absorption, distribution, biotransformation, and excretion

pharmacokinetics

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48

documented effect of the mind on drug therapy; if a person perceives that a drug will be effective, the drug is much more likely to actually be effective

placebo effect

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49

specific areas on cell membranes that react with certain chemicals to cause an effect within the cell

receptor sites

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50

property of a chemotherapeutic agent that affects only systems found in foreign cells without affecting healthy human cells (e.g., specific antibiotics can affect certain proteins or enzyme systems used by bacteria but not by human cells)

selective toxicity

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51
  • One drug prevents or accelerates absorption of the other drug

At the site of absorption*

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52

One drug competes for the protein-binding site of another drug, so the second drug cannot be transported to the reactive tissue

During distribution

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53
  • One drug stimulates or blocks the metabolism of the other drug

During biotransformation*

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54

One drug competes for excretion with the other drug, leading to accumulation and toxic effects of one of the drugs

During excretion

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55
  • One drug may be an antagonist of the other drug or may cause effects that oppose those of the other drug, leading to no therapeutic effect

At the site of action*

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