Pharmacology Flashcards
Calculation of Volume of Distribution
Total amount of drug in body/ (plasma concentration of drug x weight)
Volume of distribution in pre-term versus full-term infants
Preterm infants have a higher volume of distribution compared to full-term infants
Do highly protein-bound drugs have a large or small volume of distribution
Small
Most important enzyme system for phase 1 reactions
Cytochrome P450
What is the most common phase 2 reaction?
Glucuronidation
(Phase 2 is conjugation of a drug with an endogenous compound)
Zero order kinetics
Excrete a constant amount of drug per unit time regardless of the concentration; half life dependent on dosage; fraction of drug that is eliminated is not constant
Drugs that have zero order kinetics
Aspirin, chloramphenicol, ethanol, and diazepam
First order kinetics
Excrete a certain percentage of drug per unit time so the rate of drug elimination is directly proportional to the serum drug concentration; half-life is independent of drug dosage; the fraction of drug that is eliminated is constant
Loading dose calculation
(Volume of distribution x plasma concentration of drug) / (fraction of drug which is active x active of drug which is bioavailable)
Do preterm infants have faster or slower clearance compared to term infants
Slower
Calculation of clearance of drug
Elimination rate constant x volume of distribution
Or
(Dose/interval)/ average steady state concentration
Elimination half life concentration
(0.693 x Vd)/ clearance of drug
Drugs that increase bilirubin levels by binding albumin and displacing unconjugated bilirubin from albumin
Ceftriaxone, sulfonamides, indomethacin
Drugs that decrease bilirubin by increasing P450 metabolism and increasing the conjugation of bilirubin
Phenobarbital, rifampin
Drugs that induce cytochrome P450
Chronic alcohol use, phenytoin, phenobarbital, rifampin, griseofulvin, carbamazipime, dexamethasone