When considering the half-life of naloxone, what are the implications for this medication therapy?

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Principles of Pharmacology Questions

Question 1 of 5

When considering the half-life of naloxone, what are the implications for this medication therapy?

Correct Answer: A

Rationale: The correct answer is A because the half-life of naloxone is relatively short, typically around 30-81 minutes. This short half-life means that the effects of naloxone wear off quickly, necessitating repeated doses to maintain its therapeutic effects in reversing opioid overdose. Choice B is incorrect because an increase in dosage is not necessarily required due to the short half-life of naloxone. Choice C is incorrect because as long as naloxone is still effective in reversing opioid overdose, there is no need for a different antidote solely based on the decreasing serum levels of naloxone. Choice D is incorrect because naloxone is an effective antidote for opioid overdose when administered correctly, despite its short half-life.

Question 2 of 5

Drugs that have a significant first-pass effect:

Correct Answer: C

Rationale: The correct answer is C because drugs with a significant first-pass effect are extensively metabolized by the liver upon oral administration, leading to reduced bioavailability and potentially minimal therapeutic effects. This is due to the high enzymatic activity in the liver that rapidly breaks down the drug before it reaches the systemic circulation. Choices A, B, and D are incorrect because drugs with a significant first-pass effect are not limited to oral administration only, do not bypass hepatic circulation, and are not necessarily converted to more active and fat-soluble forms by the liver.

Question 3 of 5

The NP chooses to give cephalexin every 8 hours based on knowledge of the drug’s:

Correct Answer: B

Rationale: The correct answer is B: Biological half-life. The biological half-life of a drug determines the duration of action and how frequently it needs to be administered. Cephalexin has a short half-life of around 1 hour, so it needs to be given every 8 hours to maintain therapeutic levels. Explanation for why the other choices are incorrect: A: Propensity to go to the target receptor - While this is important for drug efficacy, it does not dictate the dosing frequency. C: Pharmacodynamics - While pharmacodynamics refers to how a drug works in the body, it does not directly impact the dosing interval. D: Safety and side effects - While safety and side effects are important considerations, they do not determine the dosing frequency.

Question 4 of 5

Phenytoin requires a trough level be drawn. Peak and trough levels are done:

Correct Answer: D

Rationale: The correct answer is D because peak levels indicate the highest concentration of the drug in the bloodstream after administration and trough levels indicate the lowest concentration before the next dose. By measuring both, healthcare providers can ensure the drug is within the therapeutic range for efficacy and safety. Choice A is incorrect as a wide therapeutic range does not negate the need for monitoring levels. Choice B is incorrect as the duration of drug administration does not determine the need for level monitoring. Choice C is incorrect as receptor saturation does not directly relate to the need for peak and trough level monitoring.

Question 5 of 5

Drugs that are receptor antagonists, such as beta blockers, may cause:

Correct Answer: B

Rationale: Step 1: Receptor antagonists block the action of agonist drugs by binding to the receptors. Step 2: Beta blockers are receptor antagonists that block beta-adrenergic receptors. Step 3: Abrupt discontinuation of beta blockers can lead to an exaggerated response due to unopposed stimulation of beta receptors. Step 4: This can cause rebound effects like increased heart rate and blood pressure. Step 5: Therefore, an exaggerated response if abruptly discontinued is the correct answer. Summary: A: Down-regulation of drug receptors is incorrect because antagonists blocking receptors do not lead to down-regulation. C: Partial blockade of agonist drug effects is incorrect as antagonists fully block agonist effects. D: Exaggerated response to competitive drug agonists is incorrect as antagonists reduce the response to agonists.

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