Which of the following are FDA-approved indications for hydroxyzine hydrochloride? Select all that apply.
Edema
Status asthmaticus
Pruritus
Anxiety
Correct Answer : C,D
A. Edema is typically managed with diuretic agents that inhibit sodium reabsorption in the renal tubules. Hydroxyzine is an H1-receptor antagonist and does not possess the pharmacological properties required to mobilize interstitial fluid. It is not an FDA-approved treatment for edema.
B. Status asthmaticus is a life-threatening medical emergency requiring systemic corticosteroids and bronchodilators. Hydroxyzine is contraindicated in early pregnancy and not indicated for acute respiratory distress. It lacks the beta-2 adrenergic agonist activity necessary to reverse severe bronchospasm in asthma.
C. Pruritus due to histamine-mediated reactions is a primary FDA-approved indication for hydroxyzine. As a first-generation antihistamine, it competitively blocks H1 receptors to alleviate itching associated with dermatological conditions. It is specifically indicated for allergic conditions such as chronic urticaria.
D. Anxiety is an FDA-approved labeled indication for hydroxyzine hydrochloride. It exerts anxiolytic effects by acting as an antagonist at the 5-HT2A serotonin receptor and H1 receptors in the central nervous system. This results in significant sedative and calming properties.
Nursing Test Bank
Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is D
Explanation
A. Topiramate is sometimes used off-label for alcohol dependence due to its modulation of glutamate and gamma-aminobutyric acid neurotransmission. However, it currently lacks formal FDA approval for this specific indication. Clinical trials show reduced craving, but regulatory labeling remains absent.
B. While this agent is investigated for binge eating disorder and weight loss in combination with phentermine, it is not individually FDA-approved for eating disorders. Its pharmacodynamic effects on appetite are secondary to its carbonic anhydrase inhibition. It remains an off-label use.
C. Topiramate is not indicated for the treatment of insomnia. Although sedation is a common adverse effect, its complex mechanism involving voltage-gated sodium channel blockade is not appropriate for primary sleep induction. No FDA label supports its use as a hypnotic.
D. Topiramate is FDA-approved for migraine prophylaxis in patients aged 12 years and older. It reduces migraine frequency by stabilizing hyperexcitable neurons through multiple mechanisms. These include blocking voltage-dependent sodium channels and enhancing GABA-A receptor-mediated inhibitory neurotransmission in the brain.
Correct Answer is B
Explanation
A. Advil is the proprietary brand name for ibuprofen, a propionic acid derivative. It functions by non-selectively inhibiting cyclooxygenase 1 and 2 enzymes. It is chemically distinct from the phenylacetic acid derivative requested in the question stem.
B. Voltaren is the brand name for diclofenac sodium, a non-steroidal anti-inflammatory drug. It inhibits prostaglandin synthesis by targeting the cyclooxygenase pathway. This specific brand is commonly available in oral, topical, and ophthalmic formulations for pain management.
C. Naprosyn is the brand name for naproxen, another member of the propionic acid class of non-steroidal anti-inflammatory drugs. It provides analgesic and anti-inflammatory effects through systemic enzyme inhibition. It is not the brand name for diclofenac sodium.
D. Toradol is the brand name for ketorolac tromethamine, a potent heterocyclic acetic acid derivative. It is primarily used for short-term management of moderately severe acute pain. It represents a different chemical entity than the diclofenac molecule specified.
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