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  2. Fexofenadine - Wikipedia

    en.wikipedia.org/wiki/Fexofenadine

    Fexofenadine was also shown to inhibit histamine-induced wheal and flare to a significantly greater degree than loratadine or desloratadine, [21] but was slightly less effective than levocetirizine. [22] Fexofenadine at doses above 120 mg a day does not appear to provide additional efficacy in the treatment of allergic rhinitis. [23] [24]

  3. Fexofenadine/pseudoephedrine - Wikipedia

    en.wikipedia.org/wiki/Fexofenadine/pseudoephedrine

    It contains fexofenadine, as the hydrochloride, an antihistamine; and pseudoephedrine, as the hydrochloride, a nasal decongestant. [ 2 ] In 2021, it was the 279th most commonly prescribed medication in the United States, with more than 800,000 prescriptions.

  4. Pseudoephedrine - Wikipedia

    en.wikipedia.org/wiki/Pseudoephedrine

    Aleve-D Sinus & Cold (made by Bayer Healthcare) — contains 120 mg pseudoephedrine hydrochloride (also 220 mg naproxen). Allegra-D (made by Sanofi Aventis) — contains 120 mg of pseudoephedrine hydrochloride (also 60 mg of fexofenadine).

  5. H1 antagonist - Wikipedia

    en.wikipedia.org/wiki/H1_antagonist

    50 mg 2–3 hours 2–9 hours CYP2D6, others Yes Doxylamine: 25 mg 2–3 hours 10–12 hours CYP2D6, others Yes Hydroxyzine: 25–100 mg 2 hours 20 hours ADH, CYP3A4, others No Doxepin: 3–6 mg 2–3 hours 17 hours c: CYP2D6, others No (at low doses) Mirtazapine: 7.5–15 mg 2 hours 20–40 hours CYP2D6, others No Quetiapine e: 25–200 mg 1.5 ...

  6. Terfenadine - Wikipedia

    en.wikipedia.org/wiki/Terfenadine

    Terfenadine acts as a peripherally-selective antihistamine, or antagonist of the histamine H 1 receptor. [3] It is a prodrug, generally completely metabolized to the active form fexofenadine in the liver by the enzyme cytochrome P450 3A4.

  7. Quifenadine - Wikipedia

    en.wikipedia.org/wiki/Quifenadine

    Quifenadine (Russian: хифенадин, trade name: Phencarol, Фенкарол) is a 2nd generation antihistamine drug, marketed mainly in post-Soviet countries. [2] [3] Chemically, it is a quinuclidine derivative.

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