Practice Test Review! Flashcards

1
Q

What abbreviations can you not use at UCH

A

ad, aid, qod, as, al, ad, au, os, ol, od, ou

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2
Q

which requires FDA evaluation: health claims or structural/function claims

A

health claims

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3
Q

3 things that determine drug category

A

medical use, abuse potential, potential for dependency

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4
Q

what does a drug in category 2 require

A

a doc to write in ink the script, cannot phone in

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5
Q

most common means of absorption

A

lipid diffusion passive

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6
Q

four factors that affect drug membrane passage

A

molecular size, lipid solubility, degree of ionization, concentration gradient

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7
Q

what means of administration fall into the following categories of bioavailability: 100, 75-100, 0-100

A

100- IV, 75-100: IM, subQ, sublingual, inhalation, transdermal, 0-100 is oral

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8
Q

how long does IV and inhalation take to effect

A

seconds to minutes- FASTEST

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9
Q

how long does sublingual, IM, subQ, and buccal take to take effect

A

5-15 minutes- intermediate

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10
Q

immediate release oral formulation- time to effect?

A

15-30 minutes

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11
Q

time to effect for transdermal, oral (enteric coated or sustained release drugs) and IM and SC (if depot forms)

A

HOURS- slowest

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12
Q

Formula for Loading dose

A

Cp(desired)*Vd

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13
Q

when pH<pKa, which is ionized (acids or bases?)

A

bases are ionized

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14
Q

when pH> pKa, which is ionized?

A

acids are ionized

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15
Q

4 areas of tight junctions where drugs have to pass THROUGH cells

A

GI, BBB, placenta, renal tubules (for REabsorption)

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16
Q

Volume of plasma/blood and what it means for that drug

A

3-5 L, drugs are highly bound to plasma proteins

17
Q

volume of extracellular water and what it means for that drug

A

12-15 L, drugs are water soluble and don’t enter cells

18
Q

volume of total body water and what it means for that drug

A

42 L,d rugs that freely enter cells

19
Q

other compartments of body volume and what it means for that drug

A

> 50, highly lipid soluble and get sequestered at tissue sites

20
Q

3 reactions that happen with phase 1

A

oxidations reductions and hydrolysis

21
Q

fluoxetine and cimetidine effect on CYP450

A

inhibit

22
Q

low extraction drugs- do they have good or bad hepatic metabolism

A

poorly metabolized by the liver

23
Q

high lipid water coefficient means its excreted (quickly or slowly?)

A

slowly- hangs in cells and tissues

24
Q

glomerulus filtration rate

A

120 mL/min

25
Q

RZBF

A

600 mL/min

26
Q

passive reabsoption int he kidneys depends on what

A

pH

27
Q

active secretion (reabsorption) in the kidneys rate

A

120-600 mL/mi

28
Q

time to reach steady state

A

4-5 half lives* time of each half life

29
Q

degree of fluctuations in plasma between doses equation

A

time between doses/time of each half life

30
Q

time to reach steady state is dependent on ____ and independent of ____

A

half life, drug dosage

31
Q

elimination kinetics equation:

A

Ln(C2/C1)=(-ke)*t

32
Q

fold fluctuation equation

A

2^x where x= number of half lives in the dosing interval

33
Q

to determine Vd on a graph look at:

A

Cp at time zero and do amount of drug in the body/concentration of drug in plasma

34
Q

CYP2A4-5

A

most drug metabolism

35
Q

CYP2D6

A

metabolizes codeine into morphine

36
Q

CYP2C9

A

metabolizes warfarin

37
Q

CYP2C10

A

Asians have lots of polymorphisms

38
Q

CYP2E1

A

metabolizes acetometophin in phase 1 reactions– hepatotoxicity