Atarax 25 mg in Topeka

Atarax 25 mg in Topeka

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Active Ingredients: Hydroxyzine


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  • Function: Antidepressant
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    Wahlgren et al 8 performed a randomized, double-blind, placebo-controlled, crossover study of terfenadine, 60 mg twice daily, and clemastine fumarate, 2 mg twice daily for 3 days with intervening 4-day washout periods.

    The study was randomized with a double-dummy protocol, with each patient receiving 3 courses in random order: 1 active terfenadine and placebo clemastine fumarate; 2 placebo terfenadine and active clemastine fumarate; and 3 placebo terfenadine and placebo clemastine fumarate.

    Twenty-five adults fulfilling the criteria of Hanifin and Rajka 23 were enrolled in the study.

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    Age, sex, disease duration, and history of atopy were provided. Patients were permitted to use topical hydrocortisone and emollients during the study. The quantity of topical hydrocortisone used during the 4-day washout period after each treatment course was comparable between groups.

    Patients recorded pruritus using visual analog scales and a computerized method for self-recording. The sedative effect of clemastine fumarate was significantly greater than terfenadine or placebo, yet its antipruritic effect did not differ.

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    Hannuksela et al 9 conducted a randomized, double-blind, placebo-controlled, parallel study of cetirizine hydrochloride, a nonsedating antihistamine, at 10 mg, 20 mg, or 40 mg taken once daily for 4 weeks.

    The study included 178 adults, patient characteristics, such as mean age, sex, weight, and prior use of emollients and hydrocortisone were provided. All groups were comparable at baseline.

    The criteria of Hanifin and Rajka 23 were not used in patient selection. Of the 178 patients, 51 were excluded from the statistical analysis of efficacy: adverse reactions 20, noncompliance 19, protocol violations 5, use of a forbidden drug 5, lost to follow-up 1, and did not fulfill the inclusion criteria 1.

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    The active group included 26, 34, and 35 patients who received 10 mg, 20 mg, and 40 mg of cetirizine hydrochloride daily for 4 weeks, respectively. The placebo group had 32 subjects.

  • Berth-Jones and Graham-Brown 7 conducted a randomized, due-blind, placebo-controlled, crossover study of 28 costs given 120 mg of terfenadine twice lot for 1 week.
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  • Patients used emollients and hydrocortisone cream during the study and the containers were weighed before and after the trial. Pruritus was assessed using visual analog scales by both investigators and patients. At the end of the trial, the investigators' pruritus scores of the active and placebo groups at all doses were significantly decreased compared with baseline values.

    However, none of the active groups showed a statistically significant improvement compared with the placebo group.

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