Section 04 · Monograph

Methylprednisolone

Reviewed Nov 2026FDA label
Solu-MedrolCorticosteroid
Forms
IV: 40, 125, 500, 1000mg vials
Dose
500-1000mg/day x3-5d (relapse)
MOA
Broad anti-inflammatory/immunosuppressive

Indications

  • Treatment of acute exacerbations (relapses) of multiple sclerosisFDA-labeled
  • Broad anti-inflammatory and immunosuppressive indications across many specialtiesFDA-labeled

Mechanism of Action

  • Synthetic glucocorticoid
  • Binds intracellular glucocorticoid receptors, modulating gene transcription to suppress inflammatory cytokine production, reduce leukocyte migration, and stabilize the blood-brain barrier during acute relapses

Full Dosing

Adult / usual

  • MS relapse: 500-1000 mg IV once daily for 3-5 days, sometimes followed by an oral prednisone taper
  • Oral dosing highly variable by indication

Contraindications

  • Systemic fungal infections
  • Known hypersensitivity to methylprednisolone or components

Drug Interactions

  • CYP3A4 inducers (e.g., rifampin, phenytoin) may decrease effect
  • CYP3A4 inhibitors may increase effect
  • NSAIDs increase GI ulceration risk
  • May reduce efficacy of vaccines

Adverse Effects

  • Insomnia
  • Mood changes/irritability
  • Hyperglycemia
  • Increased appetite
  • GI upset
  • Fluid retention
  • Hypertension
  • Increased infection risk with prolonged use
  • Osteoporosis with long-term use
  • Adrenal suppression with prolonged use

Monitoring Parameters

  • Blood glucose during treatment, especially in diabetics
  • Blood pressure
  • Signs of infection
  • Mood/behavioral changes
  • Bone density with long-term repeated courses

Pregnancy & Lactation

  • Crosses placenta in small amounts; short courses generally considered lower risk
  • Present in breast milk in small amounts; generally compatible with breastfeeding at low-to-moderate doses

References

  1. Methylprednisolone FDA prescribing information — DailyMed (NIH)

Same class

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