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  2. Salicylate poisoning - Wikipedia

    en.wikipedia.org/wiki/Salicylate_poisoning

    The acutely toxic dose of aspirin is generally considered greater than 150 mg per kg of body mass. [12] Moderate toxicity occurs at doses up to 300 mg/kg, severe toxicity occurs between 300 and 500 mg/kg, and a potentially lethal dose is greater than 500 mg/kg. [ 13 ]

  3. Hydromorphone - Wikipedia

    en.wikipedia.org/wiki/Hydromorphone

    Rapidly decreasing the dose may result in opioid withdrawal. [7] Generally, use during pregnancy or breastfeeding is not recommended. [11] Hydromorphone is believed to work by activating opioid receptors, mainly in the brain and spinal cord. [7] Hydromorphone 2 mg IV is equivalent to approximately 10 mg morphine IV. [9] Hydromorphone was ...

  4. Iron-deficiency anemia - Wikipedia

    en.wikipedia.org/wiki/Iron-deficiency_anemia

    The dosing of oral iron replacement therapy is as much as 100–200 mg per day in adults and 3–6 mg per kilogram in children. [41] This is generally spread out as 3–4 pills taken throughout the day. [65] The various forms of treatment are not without possible adverse side effects.

  5. Iron poisoning - Wikipedia

    en.wikipedia.org/wiki/Iron_poisoning

    Dosing of deferoxamine should be determined through consultation with a toxicologist but is typically continuously infused at 15 mg/kg to 35 mg/kg per hour and not exceeding the maximum daily dose of 6 grams for adults. [3] In pediatric patients, doses should not exceed 15 mg/kg per hour.

  6. Aspirin - Wikipedia

    en.wikipedia.org/wiki/Aspirin

    A study of a group with a mean dosage of aspirin of 270 mg per day estimated an average absolute risk increase in intracerebral hemorrhage (ICH) of 12 events per 10,000 persons. [218] In comparison, the estimated absolute risk reduction in myocardial infarction was 137 events per 10,000 persons, and a reduction of 39 events per 10,000 persons ...

  7. Mirtazapine - Wikipedia

    en.wikipedia.org/wiki/Mirtazapine

    A single 15 mg dose of mirtazapine to healthy volunteers has been found to result in over 80% occupancy of the H 1 receptor and to induce intense sleepiness. [92] After a short period of chronic treatment, however, the H 1 receptor tends to sensitize and the antihistamine effects become more tolerable. Many patients may also dose at night to ...

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