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Questions and Answers
What is the primary reason for dosage adjustment in patients with eliminating organ dysfunction?
What is the primary reason for dosage adjustment in patients with eliminating organ dysfunction?
What is the term for the resulting concentration of a drug when another dose is administered before the previous dose is completely removed from the body?
What is the term for the resulting concentration of a drug when another dose is administered before the previous dose is completely removed from the body?
What is the primary factor that determines the rate of drug accumulation?
What is the primary factor that determines the rate of drug accumulation?
What is the purpose of a loading dose?
What is the purpose of a loading dose?
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What is the ratio of drug half-life to dosing interval that determines the degree of drug accumulation?
What is the ratio of drug half-life to dosing interval that determines the degree of drug accumulation?
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How many half-lives does it take for drug accumulation to reach steady state?
How many half-lives does it take for drug accumulation to reach steady state?
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What is the term for the minimum concentration of a drug in the body?
What is the term for the minimum concentration of a drug in the body?
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What is the formula to calculate the loading dose of a drug?
What is the formula to calculate the loading dose of a drug?
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What is the correct formula to calculate the elimination rate constant (k)?
What is the correct formula to calculate the elimination rate constant (k)?
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How is the dosing interval determined given a half-life (t1/2) of 6.3 hours for gentamycin?
How is the dosing interval determined given a half-life (t1/2) of 6.3 hours for gentamycin?
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What is the desired peak concentration for gentamycin every 12 hours?
What is the desired peak concentration for gentamycin every 12 hours?
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Which principle states that the drug plasma concentration is constant when the administration rate equals the elimination rate?
Which principle states that the drug plasma concentration is constant when the administration rate equals the elimination rate?
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What is the necessary condition for a steady state to be established?
What is the necessary condition for a steady state to be established?
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How is the maintenance dose calculated using the steady state principle?
How is the maintenance dose calculated using the steady state principle?
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When does the rate of drug elimination begin to increase during constant-rate IV infusion?
When does the rate of drug elimination begin to increase during constant-rate IV infusion?
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What is the typical time required to reach steady state, in terms of half-lives?
What is the typical time required to reach steady state, in terms of half-lives?
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What primarily determines the plasma concentration of a drug at steady state?
What primarily determines the plasma concentration of a drug at steady state?
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In the context of first-order kinetics, what happens to the clearance of a drug if its concentration is halved?
In the context of first-order kinetics, what happens to the clearance of a drug if its concentration is halved?
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What is the relationship between total clearance (ClT) and the rate of drug elimination?
What is the relationship between total clearance (ClT) and the rate of drug elimination?
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If two drugs have identical clearance but different volumes of distribution, which drug will have a longer half-life?
If two drugs have identical clearance but different volumes of distribution, which drug will have a longer half-life?
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If a drug has a total clearance (ClT) of 4 L/hr and a volume of distribution (Vd) of 20L, what is the elimination rate constant (k)?
If a drug has a total clearance (ClT) of 4 L/hr and a volume of distribution (Vd) of 20L, what is the elimination rate constant (k)?
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How does a larger volume of distribution (Vd) affect the rate constant (k) for a given clearance (ClT)?
How does a larger volume of distribution (Vd) affect the rate constant (k) for a given clearance (ClT)?
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What determines the peak and trough concentrations of a drug in the plasma?
What determines the peak and trough concentrations of a drug in the plasma?
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Which statement accurately describes the relationship between total clearance (ClT) and the disappearance rate of the drug?
Which statement accurately describes the relationship between total clearance (ClT) and the disappearance rate of the drug?
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