Diazepam belongs to which therapeutic class?
Antidepressant agent
Antianxiety agent
Antiparkinson agent
Antimanic agent
The Correct Answer is B
A. Antidepressants modulate monoamine neurotransmission by inhibiting the reuptake of serotonin or norepinephrine. Diazepam does not possess these pharmacological properties or clinical indications for treating depressive disorders. It is chemically distinct from selective serotonin reuptake inhibitors and tricyclic antidepressants.
B. Diazepam is an antianxiety agent that functions as a benzodiazepine. It enhances the inhibitory effects of gamma-aminobutyric acid by binding to the GABA-A receptor complex. This increases chloride ion conductance, resulting in neuronal hyperpolarization and reduced central nervous system excitability.
C. Antiparkinson agents typically aim to restore dopamine levels or antagonize acetylcholine within the striatum. Diazepam has no effect on dopaminergic pathways or the motor symptoms associated with Parkinson disease. It is not indicated for the management of neurodegenerative movement disorders.
D. Antimanic agents, such as lithium, are utilized to stabilize mood in bipolar disorder through various intracellular signaling pathways. Diazepam lacks the specific clinical efficacy and regulatory approval for treating acute mania. It is primarily used for its sedative, anxiolytic, and muscle relaxant properties.
Nursing Test Bank
Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is D
Explanation
A. Hydromorphone HCl does not act directly on the motor end plate or the spinal cord to reduce skeletal muscle tone. It is not classified as a spasmolytic or neuromuscular blocker. Its primary therapeutic indication is not the relief of muscle spasms.
B. This agent does not inhibit cyclooxygenase 1 or 2 enzymes. It lacks the peripheral anti-inflammatory, antipyretic, and antiplatelet properties characteristic of drugs like ibuprofen or aspirin. It does not reduce prostaglandin synthesis at the site of tissue injury.
C. While it may cause sedation as a side effect, it is not indicated for the clinical management of generalized anxiety disorder. It does not modulate gamma-aminobutyric acid receptors in the same manner as benzodiazepines. Its use is strictly regulated.
D. Hydromorphone HCl is a potent mu-opioid receptor agonist within the central nervous system. It alters the perception of and emotional response to pain by inhibiting ascending pain pathways. This mechanism of action defines its classification as an opioid analgesic.
Correct Answer is D
Explanation
A. Zanaflex is the brand name for tizanidine, a central alpha-2 adrenergic agonist. It reduces spasticity by increasing presynaptic inhibition of motor neurons within the spinal cord. It is pharmacologically distinct from the carbamate derivative specified in the question stem.
B. Lioresal is the proprietary name for baclofen, which acts as a gamma-aminobutyric acid-B receptor agonist. It is primarily indicated for the management of spasticity resulting from multiple sclerosis or spinal cord injuries. It is not the brand for methocarbamol.
C. Amrix is the brand name for the extended-release formulation of cyclobenzaprine hydrochloride. It functions as a skeletal muscle relaxant by acting on the brainstem to reduce tonic somatic motor activity. It is not the proprietary name for methocarbamol.
D. Robaxin is the brand name for methocarbamol, a central nervous system depressant with sedative and skeletal muscle relaxant properties. It inhibits polysynaptic reflex pathways in the spinal cord and subcortical areas. This medication is indicated for musculoskeletal pain relief.
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