Histaderm is unrelated chemically to the phenothiazines, reserpine, meprobamate, or the benzodiazepines. Histaderm is not a cortical depressant, but its action may be due to a suppression of activity in certain key regions of the subcortical area of the central nervous system. Primary skeletal muscle relaxation has been demonstrated experimentally. Bronchodilator activity, and anti- histaminic and analgesic effects have been demonstrated experimentally and confirmed clinically. An antiemetic effect, both by the apomorphine test and the veriloid test, has been demonstrated. Pharmacological and clinical studies indicate that Histaderm in therapeutic dosage does not increase gastric secretion or acidity and in most cases has mild antisecretory activity. Histaderm is rapidly absorbed from the gastrointestinal tract and Histaderm's clinical effects are usually noted within 15 to 30 minutes after oral administration.
Other names for this medication:
Hydroxyzine,
Atarax,
Ataraxone,
Bestalin,
Dalun,
Fasarax,
Hiderax,
Hidroxizina,
Histaderm,
Hydroxyzinum,
Iterax,
Neurax,
Neurolax,
Otarex,
Ucerax,
Vistaril,
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Anclog,
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Vergon,
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Warin,
Sulfamethoxazole,
Perative,
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