πŸ“Š Biopharmaceutics and Pharmacokinetic
Q. The time period for which the plasma concentration of drug remains above minimum effective concentration is known as ______________
  • (A) Onset of time
  • (B) Onset of action
  • (C) Duration of drug of action
  • (D) Therapeutic range
πŸ’¬ Discuss
βœ… Correct Answer: (C) Duration of drug of action
πŸ“Š Biopharmaceutics and Pharmacokinetic
Q. In vitro determination of bioavailability by dissolution rate is not the best way to determine therapeutic efficacy.
  • (A) True
  • (B) False
  • (C) none
  • (D) all
πŸ’¬ Discuss
βœ… Correct Answer: (B) False
πŸ“Š Biopharmaceutics and Pharmacokinetic
Q. What is the equation for bioavailability?
  • (A) [AUC]std Dstd τtest / [AUC]test Dtest τstd
  • (B) [AUC]test Dtest τstd / [AUC]std Dstd τtest
  • (C) [AUC]test Dstd τtest / [AUC]std Dtest τstd
  • (D) 1 / [AUC]std Dtest τstd
πŸ’¬ Discuss
βœ… Correct Answer: (C) [AUC]test Dstd τtest / [AUC]std Dtest τstd
πŸ“Š Biopharmaceutics and Pharmacokinetic
Q. Which of the following is not an important parameter of plasma level time studies?
  • (A) Cmax
  • (B) Tax
  • (C) The area under the plasma level-time curve
  • (D) Steady state level
πŸ’¬ Discuss
βœ… Correct Answer: (D) Steady state level
πŸ“Š Biopharmaceutics and Pharmacokinetic
Q. Which of the following is the pharmacodynamics method of studying bioavailability?
  • (A) Acute pharmacologic response
  • (B) Plasma-level time studies
  • (C) Urinary excretion studies
  • (D) Stool excretion studies
πŸ’¬ Discuss
βœ… Correct Answer: (A) Acute pharmacologic response