Pharm Qiz 2 Flashcards

0
Q

Define hyperreactive?

A

Low dose for expected results. O.5mg versed makes the patient blue for example(BIG REACTION TO SMALL DOSE)

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1
Q

What is the only volatile agent that is not a racemic mixture?

A

Sevoflurane

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2
Q

Define hypersensitive

A

Allergic reaction to a drug

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3
Q

Define hyporeactive

A

Large dose for expected results, 380 mg dilaudid

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4
Q

Define tolerance

A

hypo-reactivity secondary to chronic exposure

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5
Q

Define cross tolerance

A

hypo-reactivity between drugs of different classes, for example ether or alcohol, propofol and alcohol both affect GABA so it might take more drug to achieve the effect.

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6
Q

Define tachyphylaxis

A

hypo-reactivity with only a few drug doses, the first time one receives fentanyl its the best it will ever be

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7
Q

Three ways one develops tolerance

A
  1. cellular tolerance, neuronal adaptation(crack smoker having neuro changes)
  2. Enzyme induction(drinks alcohol everyday)
  3. Neurotransmitter depletion(big coffee drinkers deplete their catecholamine stores, so it would take more catecholamine support for them
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8
Q

Define immunity

A

hypo-reactivity due to the formation of antibodies

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9
Q

Define idosyncrasy

A

unusual drug effects in small percentage of patients regardless of dose

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10
Q

Define additive effects

A

2 drugs together have total effects of each drug added together, 1/2 mac Des + 1/2 mac of N20 = 1 mac

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11
Q

Define synergistic effect?

A

2 drugs interact to have effect greater than each effect if drug was given alone, 1/2 mac drug “a” + 1.2 mac drug “b” = 2 mac

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12
Q

Define agonist in relation to a drug effect

A

binds to receptor and activates, there is a conformational change at the receptor site

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13
Q

Define antagonist as related to a drug receptor

A

drug binds but does not activate or generate a response

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14
Q

What are two types of antagonist?

A
  1. competitive

2. non competitive

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15
Q

Explain competitive antagonist

A

agonist can replace the antagonist on the receptor site, it takes greater does of antagonist to prevent being swept off the receptor site by the agonist

16
Q

Explain noncompetative antagonist

A

Irreversible binding, large doses of agonist can’t overcome the antagonist on the receptor site

17
Q

In the two compartment model of pharmokinetics what happens?

A

Drug is administered IV into the central compartment, distributes to the peripheral compartment, and then returns to the central compartment for clearance

18
Q

Define the central compartment

A
  1. intravascular fluid
  2. highly perfused tissue(heart, lung, brain,kidneys and liver)
  3. 75% of cardiac output but only 10% of the blood mass
19
Q

Define peripheral compartment

A

Everything else, majority of body weight, minority of cardiac output

  • theoretical calculated volume
  • rate of drug transfer from central compartment to peripheral compartment can vary with age
  • peripheral drug compartment can exaggerate repeated drug doses
20
Q

What do log graphs show concerning decreases in drug plasma versus time after IV bolus?

A

alpha shows distribution with a rapid fall off of concentration, while beta elimination will show a more slow decline

21
Q

What is elimination 1/2 time?

A
  • most common method of describing a drugs pharmakinetic behavior
  • its the time necessary for the plasma concentration to decrease by half
  • Inversely proportional to clearance
  • 5 elimination1/2 times necessary for 97% clearance of a drug
22
Q

What is elimination 1/2 life?

A

time necessary to eliminate 1/2 of the drug from the body, elimination 1/2 life is not = elimination 1/2 time if plasma concentration decreases do not = drug elimination