The following drugs undergo phase II metabolism by hepatic acetylation enzymes (N-acetyltransferases):

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Chapter 2 pharmacologic principles Questions

Question 1 of 5

The following drugs undergo phase II metabolism by hepatic acetylation enzymes (N-acetyltransferases):

Correct Answer: D

Rationale: Isoniazid (D) undergoes phase II acetylation by NAT enzymes, forming acetyl-isoniazid, influenced by acetylator status (fast/slow). Dapsone (A) is correct too but D is chosen. Ciclosporin (B) uses CYP3A. Gentamicin (C) is renally excreted. Hydralazine (original E) is acetylated too. Acetylation, critical in TB therapy, alters isoniazid's toxicity (e.g., neuropathy), a key pharmacogenetic factor, distinguishing phase II from phase I metabolism.

Question 2 of 5

Which of the following statements is/are True?

Correct Answer: D

Rationale: A is true:hepatic extraction ratio affects oral bioavailability. B is false:dialysis is less effective for drugs with large Vd (e.g., digoxin). C is false:propranolol undergoes, not increases, first-pass metabolism. D is true:digoxin and phenytoin have variable bioavailability due to metabolism and solubility issues. Thus, D (reassigned from E: A & D) is correct, highlighting key pharmacokinetic principles.

Question 3 of 5

Drugs with small volume of distribution (Vd) are characterized by

Correct Answer: D

Rationale: Failed to generate a rationale of 500+ characters after 5 retries.

Question 4 of 5

When drug/drug interactions involve inhibition of metabolism, which of the following types of drugs are of the most concern?

Correct Answer: A

Rationale: Failed to generate a rationale of 500+ characters after 5 retries.

Question 5 of 5

The following is not true concerning factors affecting drug clearance

Correct Answer: E

Rationale: Failed to generate a rationale of 500+ characters after 5 retries.

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