Methylprednisolone (IV Pulse)
Brand names: Solu-Medrone, Depo-Medrone
Intravenous pulse methylprednisolone is a high-dose glucocorticoid regimen given as short infusions for severe or organ-threatening inflammatory and autoimmune disease, including systemic vasculitis, lupus flares and other rheumatological emergencies.
ClinCalc Pro is rebuilding its dose data from primary open sources — the manufacturer SmPC (eMC), the WHO Model Formulary and other official references — under clinician review. This drug's structured dose is not yet published here. Confirm all doses against the product SmPC and your local formulary before prescribing.
Clinical monograph
How it works
Methylprednisolone is a synthetic glucocorticoid that binds intracellular corticosteroid receptors to suppress pro-inflammatory gene transcription and broadly dampen cellular and humoral immune responses.
Prescribing in practice
- Rapid administration of large doses has been associated with cardiac arrhythmia and rare sudden cardiovascular collapse, so infuse over an adequate period with monitoring rather than as a bolus.
- Pulse dosing markedly raises infection risk and can precipitate hyperglycaemia, fluid retention, hypertension and mood or sleep disturbance, so screen for active infection beforehand.
- Never stop chronic corticosteroid cover abruptly and consider adrenal suppression and gastroprotection in patients on continued oral steroids.
Monitoring
Monitor blood pressure, blood glucose, electrolytes and signs of infection during and after each pulse, with closer observation in patients who have cardiac or renal comorbidity.
Counselling the patient
- Report symptoms of infection, palpitations or marked mood change promptly.
- Carry a steroid alert card if on ongoing steroid therapy.
- Expect possible flushing, altered sleep or raised blood sugar around infusion days.
Evidence & guidelines
Pulsed intravenous corticosteroids are long-established in UK practice for induction of remission in severe autoimmune and vasculitic disease, reflected in NICE and specialist society guidance.
Reference: BSR guidelines; EUROLUPUS trial; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. Monograph status: clinician-reviewed (2026-07-04).
Related
Curated clinical cross-links plus same-class fallbacks.
- Cutaneous Lupus Erythematosus · BAD; EULAR
- Osteoporosis / Fragility Fracture · NOGG 2021; NICE NG147; NG224
- Arteritic AION (Giant Cell Arteritis) · RCOphth; BSR
- Osteoarthritis Hip / Knee Management · NICE NG226 (2022)
- Lupus Nephritis · EULAR/ERA-EDTA 2019; KDIGO 2024
- Rheumatoid Arthritis Management · NICE CG79 2018 / EULAR 2022