Pediatric population: In the treatment of graft rejection reactions following transplantation, a dosage of 10 to 20 mg/kg/day for up to 3 days, to a maximum of 1 g/day, is recommended. In the treatment of status asthmaticus, a dosage of 1 to 4 mg/kg/day for 1-3 days is recommended.
Elderly patients: Methylprednisolone is primarily used in acute short-term conditions. There is no information to suggest that a change in dosage is warranted in the elderly. However, treatment of elderly patient should be planned bearing in mind the more serious consequences of the common side-effects corticosteroids in old age and close clinical supervisions is required.
Detailed recommendations for adult dosage are as follows: In anaphylactic reactions, adrenaline or noradrenaline should be administered first for an immediate haemodynamic effect, followed by intravenous injection of Methylprednisolone (methylprednisolone sodium succinate) with other accepted procedures. There is evidence that corticosteroids through their prolonged haemodynamic effect are value of in preventing recurrent attacks of acute anaphylactic reactions.
In sensitivity reactions, Methylprednisolone is capable of providing relief within one half to two hours. In patients with status asthmaticus Methylprednisolone may be given at a dose of 40 mg intravenously, repeated as dictated by patient response. In some asthmatic patients it may be advantageous to administer by slow intravenous drip over a period of hours.
In graft rejection reactions following transplantation, doses of up to 1 g per day have been used to suppress rejection crises, with doses of 500 mg to 1 g most commonly used for acute rejection. Treatment should be continued only until the patient's condition has stabilised; usually not beyond 48-72 hours.
In cerebral edema, corticosteroids are used to reduce or prevent the cerebral oedema associated with brain tumours (primary and metastatic).
In patients with edema due to tumour, tapering the dose of corticosteroid appears to be important in order to avoid a rebound increase in intracranial pressure. If brain swelling does occur as the dose is reduced (intracranial bleeding have been ruled out), restart larger and more frequent dose parenterally. Patient with certain malignancies may need to remain on oral corticosteroid therapy for months or even life. Similar or higher doses may be helpful to control oedema during radiation therapy.
The following are suggested dosage schedules for edemas due to brain tumour. (See Table 1.)

Aim to discontinue therapy after a total of 10 days.
In the treatment of acute exacerbations of multiple sclerosis in adults, the recommended dose is 500 mg/day or 1 g daily for 3 days. Methylprednisolone should be given as an intravenous over at least 30 minutes.
In other indications, initial dosage will vary from 10 to 500 mg depending on the clinical problem being treated. Larger doses may be required for short-term management of severe, acute conditions. The initial dose, up to 250 mg, should be given intravenously over a period of at least 5 minutes, doses exceeding 250 mg should be given intravenously over a period of at least 30 minutes. Subsequent dose may be given intravenously or intramuscular at intervals dictated by the patient's response and clinical condition. Corticosteroid therapy is an adjunct to, and not replacement for, conventional therapy.
Method of Administration: Methylprednisolone may be administered intravenously or intramuscularly, the preferred method of emergency use being intravenous injection given over a suitable time interval. When administering methylprednisolone in high doses intravenously it should be given over a period of at least 30 minutes. Doses up to 250 mg should be given intravenously over a period of at least five minutes.
Reconstitute with 1 ml of Sterile Water for Injections B.P.
Store powder or reconstituted solution at room temperature.
Use reconstituted solution within 48 hours.
Single-dose vial and discard unused portion.
Parenteral drug products should wherever possible be visually inspected for particulate matter and discoloration prior to administration.