A) Mixed order
B) Saturated kinetics
C) Capacity Limited
D) All of the above
Correct Answer
verified
Multiple Choice
A) Active tubular secretion
B) Active tubular reabsorption
C) Both of the above
D) None of the above
Correct Answer
verified
Multiple Choice
A) Accumulation Index
B) Apparent volume of drug distribution
C) Accumulation factor
D) None of the above
Correct Answer
verified
Multiple Choice
A) When absorption is solubility or dissolution rate-limited
B) When absorption involves carrier-mediated transport systems
C) When a presystemic gut wall or hepatic metabolism attains saturation
D) Saturation of binding sites on plasma proteins
Correct Answer
verified
Multiple Choice
A) Direct Linear plot
B) Lineweaver -Burke plot or Klotz Plot
C) Graphical Method
D) All of the above
Correct Answer
verified
Multiple Choice
A) Liver
B) Lungs
C) Kidneys
D) Muscles
Correct Answer
verified
Multiple Choice
A) Linear Pharmacokinetics
B) Non-linear Pharmacokinetics
C) Both of the above
D) None of the above
Correct Answer
verified
Multiple Choice
A) Two compartment model with elimination from the central compartment
B) Two compartment model with elimination from the peripheral compartment
C) Two compartment model with elimination from only plasma and blood
D) Two compartment model with elimination from both the compartments
Correct Answer
verified
Multiple Choice
A) Linearity
B) Non-linearity
C) Both of the above
D) None of the above
Correct Answer
verified
Multiple Choice
A) Carbamazepine
B) Propranolol
C) Penicillin
D) Thiopental
Correct Answer
verified
Multiple Choice
A) Dose dependent
B) Dose independent
C) Both of the above
D) None of the above
Correct Answer
verified
Multiple Choice
A) First-order kinetics
B) Second order kinetics
C) Pseudo order kinetics
D) None of the above in
Correct Answer
verified
Multiple Choice
A) Size
B) Route
C) Both of free above
D) None of the above
Correct Answer
verified
Multiple Choice
A) Capacity limited Process
B) Dose volume
C) Enzyme induction
D) None of the above
Correct Answer
verified
Multiple Choice
A) rate of process is half (1 /2) the maximum rate.
B) the elimination of most drugs follows first order kinetic
C) the elimination of most drugs follows zero order kinetic
D) the elimination of most drugs follows second order kinetic
Correct Answer
verified
Multiple Choice
A) The pharmacokinetic parameters of a drug will not change when multiple doses of drug are administered
B) The graph of the relationship between the different factors involved (dose, blood plasma concentrations, elimination, etc.) gives a straight line.
C) the plasma drug concentration changes either more or less than would be expected from a change in dose rate.
D) None of the above
Correct Answer
verified
Multiple Choice
A) Nonlinearity may arise due to pathological alteration at any one of the various pharmacokinetic steps, such as absorption, distribution and/or elimination.
B) Nonlinearity may arise due to Capacity-limited metabolism.
C) Nonlinearity may arise due to alteration in protein binding characteristics
D) All of the above
Correct Answer
verified
Multiple Choice
A) True
B) False
C) none
D) all
Correct Answer
verified
Multiple Choice
A) -dC/dt = Vmax C/Km+C
B) dC/dt = Vmax C/Km+C
C) -dC/dt = Vmax C/Km
D) -dC/dt = Km+C / Vmax C
Correct Answer
verified
Multiple Choice
A) dose dependent
B) enzyme capacity limited
C) saturation pharmacokinetics
D) All of the above
Correct Answer
verified
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