What is the dosage and usage of Vistaril (hydroxyzine) for treating anxiety and itching?

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Vistaril (Hydroxyzine) Dosage and Usage

Vistaril (hydroxyzine) is dosed at 25 mg three to four times daily for pruritus in adults, and 50-100 mg four times daily for anxiety, with pediatric dosing of 50 mg daily in divided doses for children under 6 years and 50-100 mg daily in divided doses for children over 6 years. 1

Indications and Dosing

For Pruritus (Itching)

  • Adults: 25 mg three to four times daily 1
  • Children under 6 years: 50 mg daily in divided doses 1
  • Children over 6 years: 50-100 mg daily in divided doses 1
  • Indicated for allergic conditions including chronic urticaria, atopic dermatitis, and contact dermatoses 1

For Anxiety and Tension

  • Adults: 50-100 mg four times daily 1
  • Children under 6 years: 50 mg daily in divided doses 1
  • Children over 6 years: 50-100 mg daily in divided doses 1
  • Used for symptomatic relief of anxiety associated with psychoneurosis and as adjunct in organic disease states 1

As Premedication/Sedation

  • Adults: 50-100 mg 1
  • Children: 0.6 mg/kg of body weight 1
  • When initiated intramuscularly, subsequent doses may be given orally 1

Clinical Efficacy Evidence

Anxiety Treatment

  • Onset of action: Hydroxyzine demonstrates superiority over placebo on all anxiety measures from the first week of treatment, with early improvement in cognitive components of anxiety 2, 3
  • Sustained efficacy: Anxiolytic effect is maintained throughout 4 weeks of treatment and persists after abrupt discontinuation without rebound anxiety or withdrawal symptoms 3
  • Long-term use: A 3-month double-blind study showed mean HAM-A score reduction of -12.16 with hydroxyzine versus -9.64 with placebo (p=0.019), with comparable efficacy to bromazepam 4
  • Fixed dosing: 50 mg daily has been established as effective in generalized anxiety disorder 2, 3

Comparative Effectiveness

  • Hydroxyzine demonstrates greater and more rapid cognitive improvement compared to lorazepam 2
  • Equivalent efficacy to benzodiazepines (chlordiazepoxide) and buspirone in head-to-head trials 5
  • However, a Cochrane review noted high risk of bias in included studies, limiting the strength of recommendation as first-line treatment 5

Important Clinical Considerations

Adverse Effects

  • Most common: Sleepiness/drowsiness (28% vs 14% with placebo), which typically appears during the first week and progressively diminishes 3
  • Other effects: Weight gain (12%), dry mouth (14%), loss of concentration (9%), insomnia (9%) 3
  • Comparative tolerability: Higher rate of drowsiness compared to other anxiolytics, but generally well-tolerated 5, 4
  • Safety profile: Lack of organ toxicity and absence of dependency with long-term use 2

Special Populations

  • Renal impairment: Hydroxyzine dose should be halved in moderate renal impairment; avoid in severe renal impairment (creatinine clearance <10 mL/min) 6
  • Hepatic impairment: Should be avoided in severe liver disease due to inappropriate sedating effects 6
  • Pregnancy: Specifically contraindicated during early stages of pregnancy; best to avoid all antihistamines in first trimester 6
  • Elderly patients: Use caution due to increased sensitivity to anticholinergic and sedating effects 6

Drug Interactions

  • Contraindicated with: Mizolastine should not be taken with drugs inhibiting hepatic metabolism via cytochrome P450 (macrolide antibiotics, imidazole antifungals) or drugs with arrhythmic properties (tricyclic antidepressants) 6
  • Caution with: Other sedating agents due to increased risk of respiratory depression 6

Dosing Adjustments

  • Dosage should be adjusted according to patient's response to therapy 1
  • For anxiety, titration from lower doses may reduce initial drowsiness 3
  • Abrupt discontinuation is well-tolerated without withdrawal symptoms 3, 4

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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