Literature DB >> 11270939

New insights into the second generation antihistamines.

G M Walsh1, L Annunziato, N Frossard, K Knol, S Levander, J M Nicolas, M Taglialatela, M D Tharp, J P Tillement, H Timmerman.   

Abstract

Second generation antihistamines are recognised as being highly effective treatments for allergy-based disease and are among the most frequently prescribed and safest drugs in the world. However, consideration of the therapeutic index or the benefit/risk ratio of the H1 receptor antagonists is of paramount importance when prescribing this class of compounds as they are used to treat non-life threatening conditions. There are many second generation antihistamines available and at first examination these appear to be comparable in terms of safety and efficacy. However, the newer antihistamines in fact represent a heterogeneous group of compounds, having markedly differing chemical structures, adverse effects, half-life, tissue distribution and metabolism, spectrum of antihistaminic properties, and varying degrees of anti-inflammatory effects. With regard to the latter, there is growing awareness that some of these compounds might represent useful adjunct medications in asthma therapy. In terms of safety issues, the current second generation grouping includes compounds with proven cardiotoxic effects and others with the potential for adverse drug interactions. Moreover, some of the second generation H1 antagonists have given cause for concern regarding their potential to cause a degree of somnolence in some individuals. It can be argued, therefore, that the present second generation grouping is too large and indistinct since this was based primarily on the concept of separating the first generation sedating compounds from nonsedating H1 antagonists. Although it is too early to talk about a third generation grouping of antihistamines, future membership of such a classification could be based on a low volume of distribution coupled with a lack of sedating effects, drug interactions and cardiotoxicity.

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Year:  2001        PMID: 11270939     DOI: 10.2165/00003495-200161020-00006

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  264 in total

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3.  The effects of terfenadine with and without alcohol on an aspect of car driving performance.

Authors:  J Z Bhatti; I Hindmarch
Journal:  Clin Exp Allergy       Date:  1989-11       Impact factor: 5.018

4.  Effects of cetirizine on human eosinophil and neutrophil activation in vitro.

Authors:  G M Walsh; R Moqbel; A Hartnell; A B Kay
Journal:  Int Arch Allergy Appl Immunol       Date:  1991

Review 5.  The systemic safety of fexofenadine HCl.

Authors:  J Mason; R Reynolds; N Rao
Journal:  Clin Exp Allergy       Date:  1999-07       Impact factor: 5.018

Review 6.  Clinical assessment of antihistamines in rhinitis.

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Journal:  Clin Exp Allergy       Date:  1999-07       Impact factor: 5.018

Review 7.  Antihistamines: models to assess sedative properties, assessment of sedation, safety and other side-effects.

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Journal:  Clin Exp Allergy       Date:  1999-07       Impact factor: 5.018

8.  Loratadine treatment of rhinitis due to pollen allergy reduces epithelial ICAM-1 expression.

Authors:  G Ciprandi; C Pronzato; V Ricca; G Passalacqua; M Danzig; G W Canonica
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9.  Suppression by azelastine hydrochloride of NF-kappa B activation involved in generation of cytokines and nitric oxide.

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Journal:  Jpn J Pharmacol       Date:  1997-02

10.  The effect of azelastine on the infiltration of inflammatory cells into the bronchial mucosa and clinical changes in patients with bronchial asthma.

Authors:  M Hoshino; Y Nakamura
Journal:  Int Arch Allergy Immunol       Date:  1997-11       Impact factor: 2.749

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  17 in total

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Review 4.  Safety of non-antiarrhythmic drugs that prolong the QT interval or induce torsade de pointes: an overview.

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Review 5.  Chronic urticaria: aetiology, management and current and future treatment options.

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6.  Cetirizine: a review of its use in allergic disorders.

Authors:  Monique P Curran; Lesley J Scott; Caroline M Perry
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7.  Synthesis, structure-affinity relationships, and modeling of AMDA analogs at 5-HT2A and H1 receptors: structural factors contributing to selectivity.

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9.  Histamine induces Toll-like receptor 2 and 4 expression in endothelial cells and enhances sensitivity to Gram-positive and Gram-negative bacterial cell wall components.

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10.  The anti-inflammatory effects of levocetirizine--are they clinically relevant or just an interesting additional effect?

Authors:  Garry M Walsh
Journal:  Allergy Asthma Clin Immunol       Date:  2009-12-17       Impact factor: 3.406

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