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Methylprednisolone chemical structure
Methylprednisolone

(6α, 11β)-11,17,21-trihydroxy-6-methyl-pregna-1,4-diene-3,20 -dione
IUPAC name
CAS number
83-43-2
ATC code

D07AA01 ., ., .

PubChem
6741
DrugBank
APRD00342
Chemical formula {{{chemical_formula}}}
Molecular weight 374.471 g/mol
Bioavailability
Metabolism liver primarily, kidney, tissues; CYP450: 3A4 substrate
Elimination half-life urine; Half-life: 18-26h (biological)
Excretion {{{excretion}}}
Pregnancy category C
Legal status
Routes of administration IV, IM, IV Infusion, oral

Methylprednisolone is a synthetic glucocorticoid drug. It is sold in the USA and Canada under the brand names Medrol and Solu-Medrol.[1]

Like most adrenocortical steroids, methylprednisolone is typically used for its anti-inflammatory effects. However, glucocorticoids have a wide range of effects, including changes to metabolism and immune responses. The list of medical conditions for which methlyprednisolone is prescribed is rather large, and is similar to other corticosteroids such as prednisolone. Common uses include arthritis therapy and short-term treatment of bronchial inflammation or acute bronchitis due to various respiratory diseases. It is used both in the treatment of acute periods and long-term controlling of autoimmune diseases, most notably SLE.

Methylprednisolone has serious side effects if taken long-term, including weight gain, glaucoma, osteoporosis and psychosis, especially when overdosed. The most serious side effect occurs after the adrenal glands cease natural production of cortisone, which methylprednisolone will replace. Abrupt cessation of the drug after this occurs can result in a condition known as Addisonian crisis, which can be fatal. To prevent this, the drug is usually prescribed with a tapering dosage, including a pre-dosed "dose pack" detailing a specific number of pills to take at designated times over a six day period.

Alternative treatments to many of the conditions currently indicated for methlyprednisolone are actively being researched. Additionally, new drugs such as budesonide are being created, which provide similar benefits but without the adrenal suppression problems.

and its prescribed for spinal cord injuries(traumas).It has been proven that a dose of 30 mg/ kg IV followed by IV drip at 5.4 mg / kg / hr for 23 hours: improves sensory and motor recovery if given within 8 hours of the injury.