Lecture 8 - PRINCIPLES OF PHARMACOTHERAPEUTICS Flashcards

1
Q

What happens to the plasma concentration during repeated administration?

A

If a drug that is eliminated by first-order kinetics, is administered repeatedly, the average plasma concentration of the drug will increase until a mean steady-state level is reached.

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2
Q

When is the different levels of steady state achived?

A
  • Levels will be at the high point of the steady state range shortly after a dose is administered.
  • Levels will be at the low point immediately before administration of the next dose.
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3
Q

How is the mean of plasma concentration during steady state?

A

The mean of plasma concentration during steady-state (Cpss) is 1.44 times higher then the Cmax after the first application.

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4
Q

When is a large loading dose needed?

A

-A large loading dose may be needed initially when the therapeutic concentration of a drug in the plasma must be achieved rapidly.

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5
Q

What is the :Maintenance dose rate?

A

-Maintenance dose rate is the dose of a drug required per unit time to maintain the wanted steady-state level in the plasma to sustain a specific therapeutic effect.

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6
Q

How can the magnitude of fluctuations (shifts/changes) at the steady state can be controlled?

A
  • The magnitude of fluctuations can be controlled by the dosing interval.
  • A shorter dosing interval decreases fluctuations, and a longer dosing interval increases them.
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7
Q

What can may hurt the steady-state level?

A

Too long intervals between application of doses may hurt the steady-state level.

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8
Q

How do you calculate the loading dose?

A
  • To calculate the loading dose, select the desired plasma concentration of drug and multiply by the Vd.
  • After administration of the loading dose , one administers the drug at the maintenance dose rate to maintain the drug concentration at the desired steady-state level.
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9
Q

To remain at steady state, the dose rate must equal the ….

A

To remain at steady state, the dose rate must equal the elimination rate; that is, the rate at which the drug is added to the body must equal the rate at which it is eliminated.

elimination rate = Cl × Drugplasma.

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