Adverse effects of phenoxybenzamine include all of the following EXCEPT:

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ATI Pharmacology Across the Lifespan Questions

Question 1 of 5

Adverse effects of phenoxybenzamine include all of the following EXCEPT:

Correct Answer: D

Rationale: Phenoxybenzamine is an alpha-adrenergic blocker used primarily in the management of pheochromocytoma. The correct answer, option D, bronchospasm, is not an adverse effect associated with phenoxybenzamine use. Option A, postural hypotension, is a common adverse effect of alpha-adrenergic blockers like phenoxybenzamine due to their vasodilatory effect, leading to a sudden drop in blood pressure upon standing. Option B, tachycardia, can also occur as a compensatory response to the vasodilation-induced hypotension. Option C, miosis, is not an expected adverse effect of phenoxybenzamine. In fact, alpha-blockers can cause mydriasis (pupil dilation) due to the blockade of alpha receptors in the iris. In an educational context, understanding the adverse effects of pharmacological agents is crucial for safe and effective patient care. By knowing the expected side effects of medications, healthcare providers can anticipate, monitor, and manage potential complications, thereby enhancing patient safety and treatment outcomes. It is essential for nursing students and healthcare professionals to have a comprehensive understanding of pharmacology to make informed clinical decisions and provide quality care.

Question 2 of 5

Characteristics of carvedilol include all of the following EXCEPT:

Correct Answer: A

Rationale: Carvedilol is a non-selective beta-adrenergic blocker with alpha-blocking properties. The correct answer, A) Beta₁-selective antagonist, is incorrect because carvedilol is not beta₁-selective; rather, it blocks both beta₁ and beta₂ receptors. Carvedilol also possesses alpha₁-blocking effects, making option B incorrect. Option C, carvedilol's ability to attenuate oxygen free radical-initiated lipid peroxidation, is a true characteristic of the drug. This property is beneficial in conditions like heart failure where oxidative stress plays a role. Option D, which states that carvedilol inhibits vascular smooth muscle mitogenesis, is also true. This action contributes to its antihypertensive effects. Educationally, understanding the pharmacological properties of carvedilol is crucial for nursing practice. Nurses need to know that carvedilol is a non-selective beta-blocker with additional alpha-blocking effects, as this guides its clinical use in conditions like heart failure and hypertension. Understanding these characteristics helps nurses make informed decisions regarding medication administration and patient care.

Question 3 of 5

Which of the following hypnotic drugs is related to ethanol derivatives?

Correct Answer: A

Rationale: In this question from the ATI Pharmacology Across the Lifespan exam, the correct answer is A) Chloral hydrate. Chloral hydrate is related to ethanol derivatives because it is metabolized in the body to form trichloroethanol, which has sedative and hypnotic effects similar to ethanol. This relationship is important to understand in pharmacology as it helps in predicting the drug's effects and potential interactions. Option B) Zopiclone is a nonbenzodiazepine hypnotic drug that acts on the GABA receptor but is not related to ethanol derivatives like chloral hydrate. Option C) Flurazepam is a benzodiazepine sedative-hypnotic drug that works by enhancing the effects of GABA in the central nervous system and is not related to ethanol derivatives. Option D) Thiopental is a barbiturate that acts as a central nervous system depressant but is not related to ethanol derivatives like chloral hydrate. Understanding the relationship between drugs and their derivatives is crucial in pharmacology to predict drug actions, side effects, and potential interactions. Knowing that chloral hydrate is related to ethanol derivatives helps in understanding its mechanism of action and its potential effects on the body. This knowledge is essential for healthcare professionals to make informed decisions when prescribing medications and providing patient care.

Question 4 of 5

Which of the following hypnotic drugs is ultra short-acting?

Correct Answer: B

Rationale: The correct answer is B) Midazolam. Midazolam is an ultra short-acting hypnotic drug commonly used for sedation, anesthesia induction, and brief procedures due to its rapid onset and short duration of action. This drug acts quickly to induce sleep or sedation but is rapidly metabolized by the body, leading to a short duration of effect. Option A) Zopiclone is a non-benzodiazepine hypnotic used for treating insomnia with a longer duration of action compared to ultra short-acting drugs like midazolam. Option C) Phenobarbital is a barbiturate with a longer duration of action and slower onset compared to ultra short-acting drugs like midazolam. Option D) Chloral hydrate is also a sedative-hypnotic drug with a duration of action longer than ultra short-acting drugs like midazolam. In an educational context, understanding the pharmacokinetics of hypnotic drugs is crucial for healthcare professionals to make informed decisions about drug selection based on the desired onset and duration of action for specific clinical scenarios. Knowing the differences between ultra short-acting drugs like midazolam and longer-acting agents helps ensure safe and effective medication management for patients requiring sedation or sleep induction.

Question 5 of 5

Zolpidem and zaleplon have effectiveness similar to that of hypnotic benzodiazepines in the management of sleep disorders.

Correct Answer: A

Rationale: Zolpidem and zaleplon are non-benzodiazepine sedative-hypnotic medications commonly used to manage sleep disorders. The correct answer, A) TRUE, is supported by the fact that both zolpidem and zaleplon are considered to have effectiveness similar to hypnotic benzodiazepines in managing sleep disorders, particularly insomnia. Zolpidem and zaleplon act on the same GABA-A receptor complex as benzodiazepines but are more selective in their binding, leading to fewer side effects such as daytime drowsiness and rebound insomnia. They also have a shorter half-life compared to benzodiazepines, making them less likely to cause dependence or tolerance. Option B) FALSE is incorrect because zolpidem and zaleplon do indeed have similar efficacy to hypnotic benzodiazepines in managing sleep disorders, as supported by clinical studies and practice guidelines. Option C) None and Option D) All of the above are also incorrect as they do not accurately address the specific comparison between zolpidem, zaleplon, and hypnotic benzodiazepines in the context of managing sleep disorders. In an educational context, it is important for healthcare providers to be aware of the differences between these medication classes to make informed decisions when treating patients with sleep disorders. Understanding the similarities and distinctions in effectiveness, safety profiles, and side effect profiles of these medications is crucial for optimizing patient care and outcomes in the management of sleep disorders.

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