N-acetyl-para-aminophenol is an example of which type of drug name?
Trade
Proprietary
Generic
Chemical
The Correct Answer is D
Choice A reason: Trade names are brand-specific (e.g., Tylenol for acetaminophen). N-acetyl-para-aminophenol is the chemical structure name, not a marketed brand. Trade names are proprietary and vary by manufacturer, while chemical names describe molecular composition, making this choice incorrect for the given term.
Choice B reason: Proprietary names are brand names owned by manufacturers (e.g., Advil for ibuprofen). N-acetyl-para-aminophenol is the chemical name for acetaminophen, not a proprietary or trade name, which is used for marketing purposes, making this choice incorrect for the drug’s nomenclature.
Choice C reason: Generic names are non-proprietary, like acetaminophen for N-acetyl-para-aminophenol. The term given is the chemical name, describing the molecular structure, not the standardized generic name used in clinical practice, making this choice incorrect for classifying N-acetyl-para-aminophenol.
Choice D reason: N-acetyl-para-aminophenol is the chemical name for acetaminophen, describing its molecular structure (an acetyl group on a para-aminophenol backbone). Chemical names are used in scientific contexts, distinct from generic or trade names, making this the correct choice for the drug’s nomenclature.
Nursing Test Bank
Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is C
Explanation
Choice A reason: A 25-year-old man typically has mature liver and kidney function, efficiently metabolizing and excreting CNS depressants like benzodiazepines. Toxicity risk is lower compared to neonates, whose immature systems impair drug clearance, making this choice less critical for close toxicity monitoring.
Choice B reason: A 15-year-old boy has relatively mature metabolic pathways, though not fully adult-like. CNS depressants are cleared more effectively than in neonates, reducing toxicity risk. Adolescents are less vulnerable than infants to accumulation, making this choice less concerning for drug toxicity observation.
Choice C reason: A 3-week-old neonate has immature liver enzymes (e.g., CYP450) and reduced renal clearance, increasing the risk of CNS depressant toxicity (e.g., respiratory depression, sedation). Their low body mass and underdeveloped metabolism necessitate close monitoring, making this the correct choice for heightened toxicity vigilance.
Choice D reason: A 25-year-old woman, like men of the same age, typically has efficient drug metabolism and excretion. CNS depressants pose lower toxicity risk compared to neonates, whose immature systems lead to drug accumulation, making this choice less critical for close toxicity monitoring.
Correct Answer is C
Explanation
Choice A reason: Administering captopril risks angioedema, as the patient’s history of tongue and lip swelling with enalapril (another ACE inhibitor) suggests a class effect due to bradykinin accumulation. This is potentially life-threatening, requiring avoidance, not monitoring, making this choice unsafe and incorrect.
Choice B reason: Fosinopril, another ACE inhibitor, carries the same angioedema risk as captopril and enalapril due to similar bradykinin effects. Switching within the same drug class doesn’t address the patient’s history of adverse reactions, making this choice inappropriate and potentially dangerous.
Choice C reason: Holding captopril and notifying the provider is correct, as the patient’s history of angioedema with enalapril indicates a high risk with captopril, another ACE inhibitor. Alternative classes (e.g., ARBs) should be considered to avoid life-threatening reactions, making this the safest and correct action.
Choice D reason: Angioedema (tongue and lip swelling) is a serious, potentially fatal side effect of ACE inhibitors, not benign. Reassuring the patient minimizes the risk, which could delay intervention. The history warrants avoiding captopril and consulting the provider, making this choice incorrect and unsafe.
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