Excretion Flashcards

1
Q

Correct definition of clearance is:

A. Clearance is the volume of any organ in body cleared of drug per unit of time.
B. Clearance is the volume of blood/plasma cleared of drug per unit of time.
C. The volume of blood or any organ where the drug can be found.
D. The amount of drug eliminating from the body per unit of time.

A

B. Clearance is the Volume of blood/plasma cleared of drug per unit of time.

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2
Q

Which is NOT a correct clearance equation?

A. CL=VK
B. CL=QE
C. CL= Dose/concentration
D. CL= Rate/Cp

A

C. CL=Dose/Concentration

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3
Q

Which clearance equation relates to compartment model?

A. CL=VK
B. CL=QE
C. CL=Dose/concentration
D. CL=Rate/Cp

A

A. CL=VK

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4
Q

Main driving force of Glomerular filtration is:

A. Passive diffusion
B. Facilitated diffusion
C. Active transport
D. Hydrostatic pressure

A

E. Hydrostatic pressure

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5
Q

Active tubular secretion is measured by:

A. Para-amino hippuric acid (PAH)
B. Acetaminophen
C. Creatinine
D. Cytochrome P450

A

A. Para-amino hippuric acid (PAH)

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6
Q

Correct definition of clearance is:

A. The volume of body are cleared of drug per unit of time
B. The Volume of blood/plasma cleared of drug per unit of time
C. The amount of drug eliminating from the blood per unit of time
D. The rate at which drug is eliminating from the body

A

B. The Volume of blood/plasma cleared of drug per unit of time

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7
Q

Which is not correct equation for clearance?

A. CL=VK
B. CL=QE
C. CL=Dose/Concentration
D. CL=Rate/Cp

A

CL=Dose/Concentration

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8
Q

Which of the following equation follows the compartment model?

A. CL=QE
B. CL=Rate/Cp
C. CL=VK
D. CL=Dose/AUC

A

C. CL.VK

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9
Q

Which drug is not cleared by kidney (renal clearance)?

A. Non-volatile
B. Water soluble drugs
C. Low molecular weight drug
D. Volatile drug

A

D. Volatile drug

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10
Q

Which is not a part of renal clearance process?

A. Glomerular filtration
B. Active transportation
C. Tubular Reabsorption
D. Active tubular secretion

A

B. Active transportation

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11
Q

The major driving force for glomerular filtration is:

A. Hydrostatic pressure
B. Active transporter
C. Passive diffusion
D. Osmotic pressure

A

A. Hydrostatic pressure

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12
Q

Active tubular secretion is measured by:

A. Cytochrome P450
B. Insulin
C. Creatinine
D. Para-amino hippuric acid (PAH)

A

D. Para amino hippuric acid (PAH)

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13
Q

Creating is reliable indicator of:

A. Kidney function
B. Liver function
C. Heart function
D. Brain function

A

A. kidney function

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14
Q

Organ clearance is determined by ______________ and ____________.

A

Q and E

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15
Q

The study of the time course of drug absorption, distribution, metabolism, and excretion is called:

A. pharmacodynamics.
B. drug concentration.
C. pharmacokinetics.
D. kinetic homogeneity

A

C. Pharmacokinetics

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16
Q

The EC50 refers to the drug concentration at which:

A. one-half the maximum response is achieved.
B. the maximal effect is achieved.
C. tolerance is likely to be observed.

A

A. One-half the maximum response is achieved

17
Q

For a drug with a narrow therapeutic index, the plasma concentration required for therapeutic effects is near the concentration that produces toxic effects.

A. True
B. False

A

A. True

18
Q

The units for clearance are:

A. concentration/half-life.
B. dose/volume.
C. half-life/dose.
D. volume/time

A

D. Volume/time

19
Q

Which of the following pharmacokinetic processes are part of “Drug Disposition”? (Select all that apply)

a. excretion
b. metabolism
c. distribution
d. absorption

A

a. excretion
b. metabolism
c. distribution

20
Q

Drug elimination is divided into two major components: (2)

A
  1. Excretion

2. Biotransformation

21
Q

Is the most important PK parameter.

A

Clearance