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  2. Prednisolone - Wikipedia

    en.wikipedia.org/wiki/Prednisolone

    Prednisolone is a corticosteroid drug with predominant glucocorticoid and low mineralocorticoid activity, making it useful for the treatment of a wide range of inflammatory and autoimmune conditions [17] such as asthma, [18] uveitis, pyoderma gangrenosum, rheumatoid arthritis, urticaria, [19] angioedema, [19] ulcerative colitis, pericarditis ...

  3. List of corticosteroids - Wikipedia

    en.wikipedia.org/wiki/List_of_corticosteroids

    Most esters of these corticosteroids are not included in this list; for esters, see here instead. The most common structural modifications in synthetic corticosteroids include 1(2)- dehydrogenation , 6α-, 9α-, 16α-, and 16β- substitution (with a halogen or methyl group ), 16α,17α- acetonidation , and 17α- and 21- esterification .

  4. Drug nomenclature - Wikipedia

    en.wikipedia.org/wiki/Drug_nomenclature

    Drug nomenclature is the systematic naming of drugs, especially pharmaceutical drugs.In the majority of circumstances, drugs have 3 types of names: chemical names, the most important of which is the IUPAC name; generic or nonproprietary names, the most important of which are international nonproprietary names (INNs); and trade names, which are brand names. [1]

  5. List of steroids - Wikipedia

    en.wikipedia.org/wiki/List_of_steroids

    List of – steroidal antiandrogens; List of estrogens – estrogens; List of progestogens – progestogens; List of corticosteroids – corticosteroids, including both glucocorticoids and mineralocorticoids; List of neurosteroids – excitatory, inhibitory, mixed, neurotrophic, antineurotrophic, and other neurosteroids, as well as pheromones ...

  6. Methylprednisolone - Wikipedia

    en.wikipedia.org/wiki/Methylprednisolone

    Methylprednisolone acetate suspension (Depo-Medrol) is a 6-methyl derivative of prednisolone that melts at 215 degrees Celsius with some decomposition. [23] Methylprednisolone sodium succinate (Solu-Medrol) is the sodium succinate ester of methylprednisolone.

  7. Glucocorticoid - Wikipedia

    en.wikipedia.org/wiki/Glucocorticoid

    Name Glucocorticoid potency Mineralocorticoid potency Terminal half-life (hours) Cortisol (hydrocortisone) 1 1 8 Cortisone: 0.8 0.8 8 Prednisone: 3.5–5 0.8 16–36 Prednisolone: 4 0.8 16–36 Methylprednisolone: 5–7.5 0.5 18–40 Dexamethasone: 25–80 0 36–54 Betamethasone: 25–30 0 36–54 Triamcinolone: 5 0 12–36 Deflazacort: 6.5 ...

  8. 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 ...

  9. 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 ...

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