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  2. Chloropyramine - Wikipedia

    en.wikipedia.org/wiki/Chloropyramine

    Oral administration: In adults, 25 mg can be taken 3 to 4 times daily (up to 150 mg); in children over 5 years old, 25 mg can be taken 2 to 3 times daily. For external application, the skin or the eye conjunctiva can be treated up to several times a day by applying a thin layer of cream or ointment containing 1% chloropyramine hydrochloride.

  3. 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 ...

  4. Ebastine - Wikipedia

    en.wikipedia.org/wiki/Ebastine

    Ebastine is a second-generation H1 receptor antagonist that is indicated mainly for allergic rhinitis and chronic idiopathic urticaria. [5] It is available in 10 and 20 mg tablets [6] and as fast-dissolving tablets, [7] as well as in pediatric syrup.

  5. Acrivastine - Wikipedia

    en.wikipedia.org/wiki/Acrivastine

    Acrivastine is a medication used for the treatment of allergies and hay fever. It is a second-generation H1-receptor antagonist antihistamine (like its base molecule triprolidine) and works by blocking histamine H1 receptors. [1]

  6. Hydroxyzine - Wikipedia

    en.wikipedia.org/wiki/Hydroxyzine

    Hydroxyzine can also be used for the treatment of allergic conditions, such as chronic urticaria, atopic or contact dermatoses, and histamine-mediated pruritus. [ medical citation needed ] These have also been confirmed in both recent and past studies to have no adverse effects on the liver, blood, nervous system, or urinary tract.

  7. Chlorphenamine - Wikipedia

    en.wikipedia.org/wiki/Chlorphenamine

    [24] [25] The smaller the K d value, the greater the binding affinity of the ligand for its target. In addition to acting as an inverse agonist at the H 1 receptor, chlorphenamine has been found to act as a serotonin reuptake inhibitor (K d = 15.2 nM for the serotonin transporter ).

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