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  2. Fexofenadine - Wikipedia

    en.wikipedia.org/wiki/Fexofenadine

    The safety profile of fexofenadine is quite favorable, as no cardiovascular or sedative effects have been shown to occur even when taking 10 times the recommended dose. [25] Research on humans ranges from a single 800-mg dose, to a twice-daily, 690-mg dose for a month, with no clinically significant adverse effects, when compared to a placebo.

  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. Bilastine - Wikipedia

    en.wikipedia.org/wiki/Bilastine

    Ninety six percent of the administered dose is eliminated within 24 hours. [25] In relation to its antihistamine effect, oral doses of 20 mg daily of bilastine, measured as skin wheal-and-flare surface areas for 24 h, bilastine is capable of inhibiting 50% of the surface areas – throughout the whole administration interval. [25]

  5. Pseudoephedrine - Wikipedia

    en.wikipedia.org/wiki/Pseudoephedrine

    A dose–response relationship was established, with larger doses (>170 mg) showing greater increases in heart rate and faster time trials than with smaller doses (≤170 mg) (SMD = 0.85 for heart rate and SMD = -0.24 for time trials, respectively). [20]

  6. Tapentadol - Wikipedia

    en.wikipedia.org/wiki/Tapentadol

    The CDC Opioid Guidelines Calculator estimates a conversation rate of 50mg of tapentadol equaling 10 mg of oral oxycodone in terms of opioid receptor activation. [ 18 ] Common side effects include euphoria , constipation , nausea , vomiting , headaches, loss of appetite , drowsiness , dizziness , itching , dry mouth , and sweating . [ 19 ]

  7. Ebastine - Wikipedia

    en.wikipedia.org/wiki/Ebastine

    Ebastine is a H 1 antihistamine with low potential for causing drowsiness.. It does not penetrate the blood–brain barrier to a significant amount and thus combines an effective block of the H 1 receptor in peripheral tissue with a low incidence of central side effects, i.e. seldom causing sedation or drowsiness.