Principles of drug interactions Flashcards

1
Q

usually the drugs forms chemical bonds with specific sites, called _______ within the body

A

Receptor

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2
Q

the study of the interactions between drugs and their receptors and the series of events that result in a pharmacologic response

A

pharmacodynamics

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3
Q

drugs that interact with a receptor to stimulate a response

A

agonists

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4
Q

drugs that attach to a receptor but do not stimulate a response

A

antagonists

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5
Q

drugs that interact with a receptor to stimulate a response but inhibit other responses

A

partial agonists

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6
Q

route that the drug is administered directly into the gastrointestinal (GI) tract by the oral, rectal, or nasogastric tube

A

enteral

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7
Q

route bypasses the GI tract with the use of subcutaneous, intramuscular, or intravenous injection

A

parenteral

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8
Q

route involves drugs being absorbed through the skin and mucous membranes. methods include: inhalation, sublingual (under the tongue), and topical (on the skin) administration

A

percutaneous

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9
Q

the study of the mathematic relationship among the ADME features of individual medicines over time

A

pharmacokinetics

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10
Q

the rate of absorption when a drug is administered by a parenteral route depends

A

on the rate blood flow through the tissues

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11
Q

have the slowest absorption rate, especially is peripheral circulation is impaired

A

subcutaneous (subcut) injections

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12
Q

are more rapidly absorbed because of greater blood flow per unit weight of muscle as compared with subcutaneous tissue

A

intramuscular (IM) injections

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13
Q

organs with the most extensive blood supplies

A

heart, liver, kidneys, brain

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14
Q

areas with less extensive blood supplies

A

muscle, skin, fat

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15
Q

two factors that influence drug distribution

A

protein binding and lipid fat solubility

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16
Q

most drugs are transported in combination with plasma protein specially ________

A

Albumin

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17
Q

have a high affinity for adipose tissue, which serves as a repository site for these agents

A

lipid-soluble drugs

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18
Q

is the process whereby the body inactivates drugs

A

metabolism

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19
Q

the two primary routes of excretion

A

GI tract into the feces and renal tubules into the urine

20
Q

other routes of excretion

A

evaporation through the skin, exhalation from the lungs, and secretion into saliva and breast milk

21
Q

is defined as the amount of time required for 50% of the drug to be eliminated from the body

22
Q

half-life of 36 hours

23
Q

half-life of 5 hours

24
Q

peak action

A

is the time at which the drugs reaches the highest concentrations on the target receptor sites, thereby inducing the maximal pharmacologic response for the dose given

25
time-response curve
demonstrates the relationship between the administration of a drug and the associated response
26
examples of drugs that are important to be measured to ensure that the drug level is between therapeutic range
anticonvulsants, aminoglycoside antibiotics
27
the classes of medicines that account for the largest number of ADRs
antibiotics, cardiovascular medicines, cancer chemotherapy agents, analgesics, and anti-inflammatory agents
28
idiosyncratic reaction
occurs when something unusual or abnormal happens when a drug is first administered
29
life-threatening reaction that cause respiratory distress and cardiovascular collapse
anaphylactic reaction
30
occur when the action of one drug is altered by the action of another drug
drug interaction
31
antacids
inhibit the dissolution of ketoconazole tablets by increasing the gastric pH
32
Aluminum-containing antacids
inhibit the absorption of tetracycline
33
the anticoagulant action of warfarin is increased by
administration with furosemide, which is a loop diuretic
34
furosemide
displaces warfarin from albumin-binding sites, thereby increasing the amount of unbound anticoagulant
35
medications known to bind to enzymes and to slow the metabolism of other drugs
verapamil, chloramphenicol, ketoconazole, amiodarone, cimetidine, erythromycin
36
inhibits the metabolism of theophylline
erythromycin
37
common drugs that bind to an enzyme that increases its metabolism of the drug (enzyme inducers)
phenobarbital, carbamazepine, rifampin, phenytoin
38
rapidly metabolized drugs
disopyramide, doxycycline, griseofulvin, warfarin, metronidazole, mexiletine, quinidine, theophylline, verapamil
39
acetazolamide
elevates urine pH and quinidine
40
the alkaline urine produced by acetazolamide causes
quinidine to be reabsorbed in the renal tubules, which potentially increases the physiologic and toxic effects of quinidine
41
two drugs with similar actions are taken for an increased effect. hydrocodone + acetaminophen = added analgesic effect
additive effect
42
the combined effect of two drugs is greater than the sum of the effect of each drug given together aspirin + codeine = much greater analgesic effect
synergistic effect
43
one drug interferes with the action of another | tetracycline + antacid = decreased absorption of the tetracycline
antagonistic effect
44
the ________ of the first drug from protein-binding sites (bound drugs are inactive) by a second drug increases the activity of the first drug because more unbound drug is available warfarin + valproic acid = increased anticoagulant effect
displacement
45
the first drug inhibits the metabolism or excretion of the second drug, thereby causing increased activity of the second drug probenecid + ampicillin = prolonged antibacterial activity of ampicillin because probenecid blocks the renal excretion of ampicillin
interference
46
the first drug is chemically incompatible with the second drug, thereby causing deterioration when the drugs are mixed in the same syringe or solution or are administered together at the same site; signs include haziness, formation of a precipitate, or a change in the color of the solution when the drugs are mixed ampicillin + gentamicin = ampicillin inactivates gentamicin
incompatibility