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Corticosteroids Pregnancy: Methylprednisolone crosses the placenta. There is no evidence that corticosteroids increase the incidence of congenital abnormalities such as cleft palate in man, but when administered for long periods or repeatedly during pregnancy they may increase the risk of intra-uterine growth retardation, and the risk of low birth weight appears dose related. Adequate human reproductive studies have not been done with methylprednisolone sodium succinate, so use during pregnancy only after careful assessment of the benefit-risk ratio to mother and fetus. Infants born to mothers who received substantial doses during pregnancy must be observed and evaluated for signs of adrenal insufficiency. Corticosteroids are excreted in small amounts in breast milk, but doses up to 40 mg daily of methylprednisolone are unlikely to cause systemic effects in the infant.

Methylprednisolone (Respiratory)

Brand names: Solu-Medrone

Methylprednisolone is a systemic corticosteroid used in respiratory practice for severe asthma or COPD exacerbations and inflammatory or interstitial lung disease, given orally or intravenously. This entry covers its systemic respiratory use rather than any inhaled product.

Auto-extracted from the source labelling — not yet independently clinician-verified. These values were distilled from the UK SPC (or the US label where noted) but have not had a clinician sign-off. Confirm against the current SmPC before prescribing.

Adult dose

Dose: Status asthmaticus: 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). General adult dosing across indications: initial dosage varies from 10 to 500 mg depending on the clinical problem being treated, with larger doses for short-term management of severe, acute conditions.
Route: Intravenous or intramuscular; the preferred method for emergency use is intravenous injection given over a suitable time interval. Doses up to 250 mg should be given intravenously over at least 5 minutes; doses exceeding 250 mg should be given intravenously over at least 30 minutes. Not recommended for intrathecal or epidural use.
Frequency: Repeated as dictated by patient response; subsequent doses may be given intravenously or intramuscularly at intervals dictated by the patient's response and clinical condition
Dosage requirements are variable and must be individualised on the basis of the disease being treated, its severity and the patient's response over the entire duration of treatment, with a risk/benefit decision made in each case on an ongoing basis. Determine the maintenance dose by decreasing the initial dosage in small decrements at appropriate intervals until the lowest dose maintaining an adequate clinical response is reached. After long-term therapy the drug must be withdrawn gradually rather than abruptly. Following the initial emergency period, consider a longer-acting injectable or an oral preparation. Other stated adult regimens: intravenous pulses of 250 mg/day or above for a few days (usually <=5 days) may be suitable during exacerbations or conditions unresponsive to standard therapy (rheumatic disorders, systemic lupus erythematosus, oedematous states such as glomerulonephritis or lupus nephritis); acute exacerbations of multiple sclerosis — 500 mg/day or 1 g daily for 3 days (or pulses of 500 or 1000 mg/day for 3 or 5 days), given as an intravenous infusion over at least 30 minutes; graft rejection following transplantation — up to 1 g/day, with 500 mg to 1 g most commonly used for acute rejection, limited to 48-72 hours until the patient stabilises; anaphylactic reactions — give adrenaline or noradrenaline first for immediate haemodynamic effect, followed by intravenous methylprednisolone with other accepted procedures; cerebral oedema due to brain tumour — see the SPC's Schedule A and Schedule B tapering tables (Schedule A: pre-operative 20 mg IM every 3-6 h, during surgery 20-40 mg IV hourly, then post-operatively 20 mg IM 3-hourly for 24 h, then 16, 12, 8 and 4 mg IM 3-hourly for 24 h each, then 4 mg IM 6-hourly then 12-hourly for 24 h each; Schedule B: pre-operative 40 mg IM 6-hourly for 2-3 days, post-operative 40 mg IM 6-hourly for 3-5 days, then 20 mg orally 6-hourly for 1 day, 12 mg 6-hourly for 1 day, 8 mg 8-hourly for 1 day, 4 mg 12-hourly for 1 day and 4 mg for 1 day, aiming to discontinue after a total of 10 days). Elderly: methylprednisolone is primarily used in acute short-term conditions and there is no information to suggest a change in dosage is warranted, but plan treatment bearing in mind the more serious consequences of common corticosteroid side effects in old age, with close clinical supervision. Use the lowest effective dose for the minimum period. For intravenous infusion, the initially prepared solution may be diluted with 5% dextrose in water, isotonic saline, or 5% dextrose in isotonic saline; administer separately from other drugs and only in the solutions mentioned. Corticosteroid therapy is an adjunct to, not a replacement for, conventional therapy. NOTE ON INTERACTIONS: section 4.5 was not fetched from this SPC, and the openFDA record in this bundle is for 'Dyural 40 Kit' — a kit whose interactions section describes bupivacaine and epinephrine, not methylprednisolone — so it has deliberately NOT been used and no interaction list is given here.

Paediatric dose

Route: Intravenous or intramuscular
Frequency: Per day (total daily dose), for 1-3 days in status asthmaticus and for up to 3 days in graft rejection
Max: 1 g/day (stated for the graft rejection regimen of 10 to 20 mg/kg/day for up to 3 days)
The SPC states a RANGE, not a single per-kilogram value, so dosePerKg is left null rather than fabricating a single number. Status asthmaticus: 'a dosage of 1 to 4 mg/kg/day for 1-3 days is recommended'. 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'. Verify against a children's formulary before prescribing.

Dose auto-extracted from UK Summary of Product Characteristics (SPC) via the eMC; US FDA prescribing information (openFDA / DailyMed) — cross-check; US labelling may differ from UK — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.

Contraindications

  • Systemic fungal infections, unless specific anti-infective therapy is employed
  • Cerebral oedema in malaria
  • Known hypersensitivity to methylprednisolone or to any of the excipients
  • Administration of live or live attenuated vaccines is contraindicated in patients receiving immunosuppressive doses of corticosteroids

Side effects

  • Increased susceptibility to and severity of infection with suppression of clinical signs, opportunistic infection, and reactivation of dormant tuberculosis
  • Cushingoid features, hypothalamic-pituitary-adrenal axis suppression and steroid withdrawal syndrome
  • Sodium and fluid retention, hypokalaemic alkalosis, impaired glucose tolerance and increased insulin or oral hypoglycaemic requirements, increased appetite and weight gain
  • A wide range of psychiatric reactions — irritable, euphoric, depressed and labile mood, psychotic reactions including mania, delusions and hallucinations, sleep disturbance and cognitive dysfunction (severe reactions estimated at 5-6% in adults)
  • Eye disorders — blurred vision (rare), posterior subcapsular cataracts, glaucoma, papilloedema with possible optic nerve damage, exophthalmos
  • Drug hypersensitivity including anaphylactic and anaphylactoid reactions; raised intracranial pressure with papilloedema, seizure, headache and dizziness

Clinical monograph

How it works

It is a glucocorticoid that binds the glucocorticoid receptor to suppress airway inflammation and the transcription of multiple inflammatory mediators.

Prescribing in practice

  • Do not stop prolonged or high-dose systemic corticosteroid therapy abruptly because of the risk of adrenal insufficiency; withdraw gradually and provide steroid-sickness advice.
  • Monitor for and manage hyperglycaemia, hypertension, infection risk and mood or sleep disturbance, especially in diabetes.
  • Co-prescribe gastroprotection and consider bone-protection assessment when used with other risk factors or for longer courses.

Monitoring

Monitor blood glucose, blood pressure, weight, mood and signs of infection during treatment, with bone health review for prolonged courses.

Counselling the patient

  • Carry a steroid alert card and do not stop the steroid suddenly.
  • Report signs of infection, mood changes or excessive thirst.
  • Take oral doses with food to reduce stomach upset.

Evidence & guidelines

Established UK guidance supports systemic corticosteroids in acute asthma and COPD exacerbations and in selected inflammatory lung diseases.

Reference: BTS/SIGN Asthma Guidelines 2022; NICE NG80; ABPA ISHAM Guidelines 2013; BTS ILD Guidelines 2008; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).

Related

Curated clinical cross-links plus same-class fallbacks.