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Drug ComparisonGlucocorticoid

Prednisolone vs Dexamethasone

Clinical Comparison

Clinical Context

Prednisolone is the workhorse oral glucocorticoid in UK general practice and hospital medicine. Dexamethasone is reserved for situations requiring high potency with no mineralocorticoid effect (cerebral oedema, croup, anti-emesis) or where its long duration is advantageous.

Drug Profiles

Prednisolone

Glucocorticoid (intermediate-acting)

Mechanism

Binds to intracellular glucocorticoid receptors, translocates to nucleus, upregulates anti-inflammatory genes and suppresses pro-inflammatory cytokine transcription

Indications

  • Acute asthma exacerbation
  • COPD exacerbation
  • Inflammatory bowel disease
  • Autoimmune conditions
  • Allergic reactions
  • Nephrotic syndrome

Common Doses

Acute asthma: 40-50 mg OD for 5 days; Maintenance: 5-15 mg OD; Varies widely by indication

Route

Oral (tabs and soluble), rectal

Onset & Duration

Onset 1-2 hours; biological half-life 12-36 hours

Dexamethasone

Glucocorticoid (long-acting, high potency)

Mechanism

Same as prednisolone but with 6-7x greater glucocorticoid potency and negligible mineralocorticoid activity

Indications

  • Cerebral oedema (brain tumours)
  • Croup (viral laryngotracheobronchitis)
  • Bacterial meningitis (adjunctive)
  • Anti-emetic (chemotherapy-induced)
  • COVID-19 (hospitalised, requiring oxygen)
  • Preterm labour (fetal lung maturation)

Common Doses

Cerebral oedema: 8-16 mg/day; Croup: 0.15-0.6 mg/kg single dose; COVID-19: 6 mg OD for 10 days; Anti-emetic: 4-8 mg

Route

Oral, IV, IM

Onset & Duration

Onset 1-2 hours oral; biological half-life 36-54 hours

Key Differences

Potency (glucocorticoid)

Prednisolone

4x cortisol (moderate)

Dexamethasone

25-30x cortisol (very high) — roughly 6-7x prednisolone

Mineralocorticoid effect

Prednisolone

Moderate — some sodium retention

Dexamethasone

Negligible — no sodium/water retention

Duration of action

Prednisolone

Intermediate (12-36 hours)

Dexamethasone

Long-acting (36-54 hours)

Typical use

Prednisolone

Standard for most inflammatory and autoimmune conditions

Dexamethasone

Cerebral oedema, croup, anti-emetic, COVID-19

Equivalent doses

Prednisolone

5 mg prednisolone

Dexamethasone

0.75 mg dexamethasone

Formulations

Prednisolone

Oral tablets and soluble

Dexamethasone

Oral, IV, and IM

Key Advantages

Prednisolone

  • Standard oral glucocorticoid in UK practice
  • Moderate potency with manageable mineralocorticoid effects
  • Available as soluble tablets for children
  • Extensive evidence across all inflammatory conditions
  • Cheap and widely available

Dexamethasone

  • Very potent — lower doses needed
  • No mineralocorticoid effect — no sodium/water retention
  • Long duration allows less frequent dosing
  • Proven mortality benefit in COVID-19 (RECOVERY trial)
  • IV formulation for acute situations

Key Cautions

Prednisolone

  • Adrenal suppression with prolonged use (>3 weeks needs taper)
  • Hyperglycaemia — may unmask or worsen diabetes
  • Osteoporosis with chronic use (co-prescribe bone protection)
  • Immunosuppression — risk of infection
  • GI ulceration — caution with NSAIDs
  • Psychiatric effects (insomnia, mania, psychosis at high doses)

Dexamethasone

  • Very potent — adrenal suppression even with short courses
  • Higher risk of hyperglycaemia per unit of anti-inflammatory effect
  • Same class risks as prednisolone but at lower doses
  • Not typically used for general inflammatory conditions (too potent)
  • Must taper carefully after prolonged use

Clinical Verdict

Use prednisolone as the standard oral steroid for most inflammatory conditions (asthma, COPD, IBD, autoimmune). Reserve dexamethasone for cerebral oedema, croup, anti-emesis, and situations where mineralocorticoid activity must be avoided.

Medical Disclaimer: This comparison is for educational purposes only and is not a substitute for professional medical advice. Always consult a qualified healthcare professional before making prescribing decisions. Verify all drug information with current clinical guidelines (BNF, NICE, SmPCs).

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