Multiple Dose Flashcards

1
Q

What does dosage regimen depend on?

A
  • Strength

- Frequency of drug administration

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2
Q

Plasma drug concentration predictions are based on…

A
  • Pharmacokinetic parameters obtained from single dose
  • Strength
  • Dosage interval (Tau)
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3
Q

What is the principle of superposition?

A

Subsequent doses don’t interfere w/ kinetics of early doses

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4
Q

When can’t you use the principle of superposition?

A
  • If there is interaction at transport level or enzyme level

- If drug affects cardiac output

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5
Q

Window between Cmax and Cmin will be greater for a _____ dosing interval

A

Longer

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6
Q

What is accumulation half life? What determines it?

A
  • Time to reach 1/2 Css

- Determined by elimination half life, NOT absorption rate constant (ka)

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7
Q

What happens to Cmax, Cmin, and C average when dosage interval increases?

A
  • Cmax decreases
  • C average is unchanged
  • Cmin decreases
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8
Q

What does f mean?

A

Fraction of dose remaining in the body

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9
Q

What is n at steady state?

A

Infinity, so would use a formula w/o n

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10
Q

What must be calculated if you want to know max concentration at steady state?

A

tp (time to reach maximum concentration)

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11
Q

What is the dose ratio (DL/D0) when tau (dosage interval) = t1/2?

A

Ratio = about 2

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12
Q

What are some advantages to using single dose data to determine bioequivalence?

A
  • Patient acts as own control
  • Cmin is maintained
  • Assay is more accurate
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13
Q

What are some disadvantages to using single dose data to determine bioequivalence?

A
  • Takes longer time to complete study

- Need more samples

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14
Q

What does multiple dose take into account?

A

IV and oral

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15
Q

What is R for multiple dose? What does it depend and not depend on?

A
  • R = index of drug accumulation
  • Dependent on dosing interval and rate constant
  • Independent of dose
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16
Q

What happens to Cmax if you start at a short dosing interval? Why?

A

Cmax will be high b/c there is less time for elimination