Depo-Medrol (Methylprednisolone Acetate) Dosing
For systemic effect, Depo-Medrol dosing ranges from 40-120 mg intramuscularly weekly for most chronic conditions, with single doses of 80-120 mg for acute conditions like severe asthma or allergic reactions, while intra-articular doses range from 4-80 mg depending on joint size. 1
Systemic Intramuscular Dosing
Acute Conditions
- Severe asthma exacerbations or allergic rhinitis: 80-120 mg IM as a single dose, with relief expected within 6-48 hours and lasting several days to 2 weeks 1
- Acute severe dermatitis (poison ivy): 80-120 mg IM single dose, with relief within 8-12 hours 1
- Acute multiple sclerosis exacerbations: 160 mg daily for 1 week, followed by 64 mg every other day for 1 month 1
Chronic Maintenance Therapy
- Rheumatoid arthritis maintenance: 40-120 mg IM weekly 1
- Dermatologic conditions: 40-120 mg IM weekly for 1-4 weeks 1
- Chronic contact dermatitis: Repeat injections at 5-10 day intervals as needed 1
- Seborrheic dermatitis: 80 mg weekly 1
- Adrenogenital syndrome: 40 mg IM every 2 weeks 1
Conversion from Oral Therapy
- Daily equivalent: Single IM injection of Depo-Medrol equal to total daily oral Medrol dose 1
- Weekly equivalent: Multiply daily oral dose by 7 and give as single weekly IM injection 1
Intra-Articular Dosing by Joint Size
Large Joints (Knees, Ankles, Shoulders)
Medium Joints (Elbows, Wrists)
- Dose range: 10-40 mg per injection 1
Small Joints (Metacarpophalangeal, Interphalangeal, Sternoclavicular, Acromioclavicular)
- Dose range: 4-10 mg per injection 1
Other Local Injection Indications
Bursitis
- Dose: Aspirate fluid, then inject appropriate dose based on bursa size 1
Tendinitis, Tenosynovitis, Epicondylitis
- Dose range: 4-30 mg injected into tendon sheath (not tendon substance) 1
- Repeat: May require repeated injections for recurrent/chronic conditions 1
Ganglia
- Dose: Inject directly into cyst; single injection often causes marked decrease in size 1
Dermatologic Lesions (Intralesional)
- Dose range: 20-60 mg injected into lesion 1
- Frequency: 1-4 injections with intervals varying by lesion type 1
Critical Modifications for Comorbidities
Diabetes
- Monitoring requirement: Increase blood glucose monitoring to 2-4 times daily during treatment, with temporary adjustment of diabetes medications typically required 2
- Caution: Significant hyperglycemia can occur even with single injections 2
Hypertension
- Monitoring requirement: Check blood pressure every 2-3 days during treatment, as hypertension can develop or worsen rapidly 2
Osteoporosis
- Immediate intervention: Start calcium 1,000-1,200 mg/day and vitamin D 600-800 IU/day for any patient with pre-existing osteoporosis receiving even a single injection 2
- Prophylaxis consideration: Consider bisphosphonate prophylaxis if multiple injections are anticipated 2
- Risk threshold: Doses >5 mg daily prednisone equivalent (approximately 4 mg methylprednisolone) for >3 months increase osteoporosis and fracture risk 3
Dose Equivalency Reference
- Methylprednisolone 4 mg = Prednisone 5 mg = Hydrocortisone 20 mg 4, 1
- This equivalency applies to oral/IV routes; relative properties may differ greatly with IM or intra-articular injection 1
Common Pitfalls to Avoid
Technical Errors
- Failure to enter joint space: Most common cause of treatment failure; confirm entry by aspirating synovial fluid before injection 1
- Injection into tendon substance: Always inject into tendon sheath, not the tendon itself, to avoid tendon rupture 1
- Excessive intralesional volume: Avoid injecting enough material to cause blanching, which may result in tissue slough 1
Safety Concerns
- Inadvertent intrathecal injection: Epidural injections have 2.5% risk of inadvertent subarachnoid placement and 40% risk of interspinous ligament injection 5
- Polyethylene glycol toxicity: Depo-Medrol contains approximately 30 mg polyethylene glycol per mL, which can cause sterile meningitis, arachnoiditis, or pachymeningitis if placed near the neuraxis 5
- Never use intraspinally: The polyethylene glycol vehicle makes Depo-Medrol inappropriate for epidural or intrathecal use 5
Monitoring Failures
- Underestimating rebound flaring: Discontinuation can cause worse flaring than the original presentation; never use as bridge to chronic therapy without a clear steroid-sparing plan 2
- Neglecting osteoporosis prevention: All patients receiving repeated injections need calcium and vitamin D supplementation 2, 4
Pediatric Dosing Considerations
- Initial dose varies by disease severity: Dosage must be individualized based on disease severity and patient response rather than strict adherence to age or body weight ratios 1
- Reduction permitted but not mandatory: Recommended dosage may be reduced for pediatric patients, but severity of condition should govern dosing 1
When Rapid Effect Is Required
- Use IV methylprednisolone sodium succinate instead: If rapid hormonal effect of maximum intensity is required, the highly soluble IV formulation is indicated rather than the depot IM formulation 1