These categories of histamine H1 antagonists are noted for sedative effects, EXCEPT:

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Drugs Affecting Cardiovascular System Questions

Question 1 of 5

These categories of histamine H1 antagonists are noted for sedative effects, EXCEPT:

Correct Answer: A

Rationale: The correct answer is A, Piperidines like Loratadine and Fexofenadine are noted for their non-sedating effects due to their low penetration of the blood-brain barrier. This is because they have a low affinity for the central nervous system H1 receptors. In contrast, choices B, C, and D contain antihistamines that are known for their sedative effects due to their high penetration of the blood-brain barrier and high affinity for central nervous system H1 receptors. Therefore, Piperidines are the exception among the listed categories in not causing sedation.

Question 2 of 5

Lipoprotein is:

Correct Answer: A

Rationale: Rationale for Correct Answer (A): 1. A lipoprotein is a conjugated protein with a lipid component, facilitating lipid transportation in the blood. 2. Lipoproteins play a crucial role in transporting lipids such as cholesterol and triglycerides in the bloodstream. 3. They consist of proteins (apolipoproteins) and lipids, enabling solubility of lipids for transport. 4. Lipoproteins are classified based on density (e.g., HDL, LDL), reflecting their lipid and protein composition. Summary of Incorrect Choices: B: This describes vitamins, not lipoproteins. Vitamins are organic substances essential for bodily functions but are not lipoproteins. C: Endocrine gland secretions are hormones, not lipoproteins. Hormones regulate bodily functions and are not directly related to lipid transportation. D: Lipoproteins are not mediators of the inflammatory process. Inflammation involves immune responses, not lipid transport.

Question 3 of 5

This fibric acid derivative increases blood levels of high density lipoproteins (HDL):

Correct Answer: C

Rationale: Step-by-step rationale for why Choice C: Gemfibrozil (Loprol) is correct: 1. Gemfibrozil is a fibric acid derivative known to increase HDL levels. 2. It works by activating lipoprotein lipase, which increases the breakdown of triglycerides and raises HDL levels. 3. Cholestyramine (A) is a bile acid sequestrant that does not affect HDL levels. 4. Lovastatin (B) is a statin that primarily lowers LDL levels. 5. Probucol (D) is an antioxidant that mainly lowers LDL levels and does not significantly impact HDL levels.

Question 4 of 5

Which of the following statements refers to etidronate:

Correct Answer: A

Rationale: Step-by-step rationale for why choice A is correct: 1. Etidronate is a biphosphonate drug used to reduce osteoclast activity in conditions like Paget's disease. 2. It inhibits bone resorption by osteoclasts without significantly affecting osteoblasts. 3. Monitoring serum phosphorus levels daily (choice B) is not necessary for etidronate. 4. Etidronate is a first-generation biphosphonate, not a 2nd generation (choice C). 5. Bioavailability of etidronate is poor and decreases with increasing doses, so choice D is incorrect.

Question 5 of 5

The drug is one of the most potent diuretics:

Correct Answer: B

Rationale: Step 1: Furosemide is a loop diuretic, which acts on the ascending loop of Henle to inhibit sodium and chloride reabsorption, leading to potent diuresis. Step 2: Loop diuretics like Furosemide are more potent compared to other diuretics like thiazides (Hydrochlorothiazide) or potassium-sparing diuretics (Amiloride). Step 3: Acetazolamide is a carbonic anhydrase inhibitor that works in the proximal tubule and has a different mechanism of action, making it less potent than loop diuretics. Step 4: Therefore, the correct answer is B, Furosemide, as it is a potent diuretic acting on the loop of Henle. Other choices are less potent due to their mechanisms of action and sites of action.

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