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  2. Desloratadine - Wikipedia

    en.wikipedia.org/wiki/Desloratadine

    Onset of action: within 1 hour [6] ... 27 hours, [6] 33.7 hours in elderly patients [3] Duration of action: up to 24 hours [6 ... Desloratadine sold under the brand ...

  3. Antihistamine - Wikipedia

    en.wikipedia.org/wiki/Antihistamine

    An H 3-antihistamine is a classification of drugs used to inhibit the action of histamine at the H 3 receptor. H 3 receptors are primarily found in the brain and are inhibitory autoreceptors located on histaminergic nerve terminals, which modulate the release of histamine .

  4. Bilastine - Wikipedia

    en.wikipedia.org/wiki/Bilastine

    Bilastine is an antihistamine medication used to treat hives (), allergic rhinitis and itchy inflamed eyes (allergic conjunctivitis) caused by an allergy. [6] It is a second-generation antihistamine and takes effect by selectively inhibiting the histamine H 1 receptor, preventing these allergic reactions. [7]

  5. Loratadine - Wikipedia

    en.wikipedia.org/wiki/Loratadine

    Its metabolite desloratadine, which is largely responsible for the antihistaminergic effects, binds to plasma proteins by 73–76%. [ 15 ] Loratadine's peak effect occurs after 1–2 hours, and its biological half life is on average eight hours (range 3 to 20 hours) with desloratadine 's half-life being 27 hours (range 9 to 92 hours ...

  6. Rupatadine - Wikipedia

    en.wikipedia.org/wiki/Rupatadine

    The efficacy of rupatadine as treatment for allergic rhinitis (AR) and chronic idiopathic urticaria (CIU) has been investigated in adults and adolescents (aged over 12 years) in several controlled studies, showing a rapid onset of action and a good safety profile even in prolonged treatment periods of a year. [5] [6] [7]

  7. Pharmacodynamics - Wikipedia

    en.wikipedia.org/wiki/Pharmacodynamics

    The duration of action of a drug is the length of time that particular drug is effective. [5] Duration of action is a function of several parameters including plasma half-life, the time to equilibrate between plasma and target compartments, and the off rate of the drug from its biological target. [6]

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