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A comparison of cetirizine and terfenadine in the management of solar urticaria.

Abstract
Many solar urticaria patients may benefit from the use of antihistamines. Historically, the value of such therapy was limited by sedation. Newer agents such as terfenadine and cetirizine that are relatively non-sedating appear to be better tolerated by patients. The latter drug, in addition to its antihistamine effect, also appears to inhibit eosinophil migration, which terfenadine and other potent H1 antagonists do not significantly affect. Eosinophils have been reported as early migrating cells in induced solar urticaria, raising the possibility that the dual action of cetirizine may provide a greater potential benefit in the management of solar urticaria. Six patients with idiopathic solar urticaria were entered into a double-blind, phototest study to compare cetirizine and terfenadine. Using the minimal urticarial dose as a phototest end-point, both drugs were equally effective in raising the threshold of sensitivity in 4 patients. Two patients failed to respond to either therapy, which is in keeping with the known variable response to histamine blockade in solar urticaria. At the dosage used, cetirizine therapy appears to be no more effective than terfenadine.
AuthorsD Bilsland, J Ferguson
JournalPhotodermatology, photoimmunology & photomedicine (Photodermatol Photoimmunol Photomed) Vol. 8 Issue 2 Pg. 62-4 (Apr 1991) ISSN: 0905-4383 [Print] England
PMID1684515 (Publication Type: Clinical Trial, Comparative Study, Journal Article, Randomized Controlled Trial)
Chemical References
  • Histamine H1 Antagonists
  • Hydroxyzine
  • Terfenadine
  • Cetirizine
Topics
  • Adult
  • Aged
  • Cetirizine
  • Double-Blind Method
  • Female
  • Histamine H1 Antagonists (administration & dosage, adverse effects)
  • Humans
  • Hydroxyzine (administration & dosage, adverse effects, analogs & derivatives)
  • Male
  • Middle Aged
  • Sunlight (adverse effects)
  • Terfenadine (administration & dosage, adverse effects)
  • Urticaria (drug therapy, etiology)

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