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  2. Prednisolone - Wikipedia

    en.wikipedia.org/wiki/Prednisolone

    Prednisolone has a relatively short half-life, ranging 2–4 hours. It also has a large therapeutic window, considering the dosage required to produce a therapeutic effect is a few times higher than what the body naturally produces. [14] Prednisolone is 70–90% plasma protein bound, it binds to proteins such as albumin. [14]

  3. Prednisolone acetate - Wikipedia

    en.wikipedia.org/wiki/Prednisolone_acetate

    Prednisolone acetate is acutely toxic with an LD50 of >240 mg/kg for a rat and 3500 mg/kg for a mouse. Effects may present delayed. Target organs include adrenal cortex, bones, and eyes. It is also a known teratogen. [3] Class B PPE should be worn when working with this chemical. Any contact with this chemical should be taken seriously and the ...

  4. Prednisolone sodium phosphate - Wikipedia

    en.wikipedia.org/wiki/Prednisolone_sodium_phosphate

    "Prednisolone sodium phosphate". Drug Information Portal. U.S. National Library of Medicine. This page was last edited on 29 January 2023, at 00:02 (UTC). Text ...

  5. Methylprednisolone - Wikipedia

    en.wikipedia.org/wiki/Methylprednisolone

    Serious side effects include iatrogenic Cushing's syndrome, hypertension, osteoporosis, diabetes, infection, and skin atrophy. [9] Chemically, methylprednisolone is a synthetic pregnane steroid hormone derived from hydrocortisone and prednisolone. It belongs to a class of synthetic glucocorticoids and more generally, corticosteroids. It acts as ...

  6. Corticosteroid - Wikipedia

    en.wikipedia.org/wiki/Corticosteroid

    The neuropsychiatric effects are partly mediated by sensitization of the body to the actions of adrenaline. Therapeutically, the bulk of corticosteroid dose is given in the morning to mimic the body's diurnal rhythm; if given at night, the feeling of being energized will interfere with sleep. An extensive review is provided by Flores and Gumina ...

  7. Glucocorticoid - Wikipedia

    en.wikipedia.org/wiki/Glucocorticoid

    Then change to oral hydrocortisone or cortisone as a single morning dose, and gradually decrease by 2.5 mg each week. When the morning dose is less than replacement, the return of normal basal adrenal function may be documented by checking 0800 cortisol levels prior to the morning dose; stop drugs when 0800 cortisol is 10 μg/dl.

  8. Deflazacort - Wikipedia

    en.wikipedia.org/wiki/Deflazacort

    The review noted that the drug has a high therapeutic index, being used at initial oral doses ranging from 6 to 90 mg, and probably requires a 50% higher dose to induce the same demineralizing effect as prednisolone. Thus it has "a smaller impact on calcium metabolism than any other synthetic corticosteroid, and therefore shows a lower risk of ...

  9. Prednisolone tebutate - Wikipedia

    en.wikipedia.org/wiki/Prednisolone_tebutate

    Drug class: Corticosteroid; Glucocorticoid: Identifiers; IUPAC name ... Prednisolone tebutate is a synthetic glucocorticoid corticosteroid and a corticosteroid ester. [1]

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