Prednisone
General
- Type: Corticosteroids, systemic
- Dosage Forms:1, 2, 5, 10, 20, 50, 5/5ml
- Common Trade Names: Sterapred, Sterapred DS, Rayos
Adult Dosing
For all doses of prednisone, it is best given with food. Also, ideally best when given in AM to coincide with natural cortisol release. No need to taper if short course less than 1 week, otherwise consider taper.
- Corticosteroid-responsive conditions
- 5-60mg PO QD
- Dose varies based on condition
- Asthma, acute
- 40-80mg/day PO divided QD-bid
- Most practitioners give 60mg PO x 1, followed by 40mg PO QD x 4 days (for a 80-100kg adult)
- If patient can tolerate PO, no need to give steroids IV, but if asthma is severe, and bipap / intubation likely, best to keep patient NPO and give methylprednisolone IV
- 40-80mg/day PO divided QD-bid
- Adrenal Insufficiency
- 4-5mg/ m^2 PO QD
- Taper dose gradually to discharge when appropriate
- Multiple Sclerosis, acute exacerbation
- 200mg PO QD x1 week, then 80mg po qod x1 mo
- Give with food, also prescribe PPI for gastric protection. Taper dose gradually to discharge
- Alcoholic Hepatitis, acute
- 40mg PO QD
- PCP, Adjunct treatment
- 40mg PO BID x5 days, then 40mg PO QD x5 days, then 20mg PO QD x11 days
- Start within 72hrs of antimicrobial treatment
- Always consider discussion with HIV consultants prior to given steroids, as they will be managing patient in hospital
Pediatric Dosing
For all doses of prednisone, it is best tolerated with food. Ideally best when given in AM to coincide with natural cortisol release. No need to taper if short course less than 1 week, otherwise consider taper.
- Corticosteroid-responsive conditions
- 0.05-2mg/kg/day PO divided QD-QID
- Dose varies based on condition
- Asthma, acute
- 1-2mg/day PO divided QD-bid Max 60mg/day
- If patient can tolerate PO, no need to give steroids IV, but if asthma is severe, and Bipap / intubation likely, best to keep patient NPO and give methylprednisolone IV
- Adrenal Insufficiency
- 4-5mg/ m^2 PO QD Taper dose gradually to discharge when appropriate
- Nephrotic Syndrome
- 2mg / kg PO QD
- Max 80mg / day. Use for 1st 3 episodes
- PCP, adjunct treatment (children <40kg)
- 1mg/kg PO BID x5days, then 0.5mg/kg PO BID x5days, then 0.5mg PO QD x 11 days. Start within 72 hrs of antimicrobial treatment (Children >40kg)
- 40mg PO BID x5 days, then 20mg PO BID x5 days, then 20mg PO QD x 11 days. Start within 72 hrs of antimicrobial treatment (Adolescents)
- 40mg PO BID x5 days, then 40mg PO QD x5 days, then 20mg PO QD x 11 days. Start within 72 hrs of antimicrobial treatment
Special Populations
- Pregnancy Rating: Category C
- Lactation: Probably safe "Limited information in animals and/or humans demonstrates no risk/minimal risk of adverse effects to infant/breast milk production; caution advised" -Epocrates
- Renal Dosing
- Adult - No adjustment
- Pediatric - No adjustment
- Hepatic Dosing
- Adult - Not defined
- Pediatric - Not defined
Contraindications
- Allergy to class/drug
- Systemic fungal infection
- Recent varicella or measles infection
- Caution in TB, immunosuppressed, hypertension, CHF, DM, PUD, seizure disorder, psychiatric disorder, osteoporosis,
Adverse Reactions
Serious
- Adrenal insufficiency
- Cushing syndrome
- Immunosuppression
- Infection, fractures, thromboembolism[1]
- hypertension
- CHF
- Diabetes mellitus
- GI perf / ulcer
- Osteopenia / osteoporosis
- tendon rupture
- pseudotumor cerebri
- Increased ICP
- Seizures
- Glaucoma
Common
- Sodium and fluid retention
- diaphoresis
- headache
- Vertigo
- Insomnia
- Nervousness, mood swings
- Muscle weakness
- BP elevation
- glucose intolerance
- Menstrual irregularities
Pharmacology
- Half-life: 18-36h (biological) 3.4-3.8h (chemical)
- Metabolism: Liver CYP450; 3A4 substrate. Prodrug is converted to prenisolone
- Excretion: Urine
- Mechanism of Action: Exact mechanism unknown, inhibits inflammatory cytokines, produces multiple glucocorticoid and mineralcorticoid effects
Indications by Condition
The following table is automatically generated from disease/condition pages across WikEM.
| Indication | Dose | Context | Route | Population |
|---|---|---|---|---|
| Acute allergic reaction | 60mg initially, then 40mg PO daily x 5 days | Corticosteroid (outpatient) | PO | Adult |
| Acute asthma exacerbation | 40-60 mg PO daily x5 days | Corticosteroid | PO | Adult |
| Acute asthma exacerbation | 1-2 mg/kg/day (max 60 mg) x3-10 days | Corticosteroid (pediatric) | PO | Pediatric |
| Acute asthma exacerbation (peds) | 1-2mg/kg/day (max 60mg) in 1-2 divided doses x 3-5 days | Systemic corticosteroid alternative to dexamethasone | PO | Pediatric |
| Acute rheumatic fever | 1-2mg/kg/day PO | Moderate-to-severe carditis | PO | Pediatric |
| COPD exacerbation | 60 mg PO x1, then 40 mg PO daily x5 days | Corticosteroid (preferred, oral) | PO | Adult |
| Crohn's disease | 40-60mg daily with taper once remission induced | Moderate flare | PO | Adult |
| Giant cell arteritis | 1mg/kg/day (max 80mg) | Initial treatment; alternative to IV pulse dose | PO | Adult |
| Gout and pseudogout | 30-50mg initially, taper over 10 days | Alternative when NSAIDs and colchicine contraindicated | PO | Adult |
| Henoch-Schonlein purpura | 1mg/kg/day | Severe arthralgias, abdominal or scrotal disease | PO | Pediatric |
| Hypercalcemia | 60mg daily | Steroid-sensitive tumors (lymphoma, multiple myeloma) | PO | Adult |
| Nephrotic syndrome | 2mg/kg/day PO (max 60mg) x 4-6 weeks, then taper | Initial treatment, minimal change disease | PO | Pediatric |
| Pericarditis | 0.2-0.5 mg/kg/day x2 weeks, then taper | Steroid (if NSAID contraindicated or refractory) | PO | Adult |
| Polymyalgia rheumatica | 15mg daily x 2-4 weeks | Initial treatment; dramatic response expected within days | PO | Adult |
| Sudden sensorineural hearing loss | 1mg/kg/day PO (max 60mg) x 10-14 days | First-line, oral glucocorticoid | PO | Adult |
| Ulcerative colitis | 40mg daily x 2 weeks, then taper by 5mg/week | Moderate-severe flare | PO | Adult |
See Also
References
Epocrates
- ↑ Waljee, A. K., Rogers, M. A. M., Lin, P., Singal, A. G., Stein, J. D., Marks, R. M., … Nallamothu, B. K. (2017). Short term use of oral corticosteroids and related harms among adults in the United States: population based cohort study. Bmj. doi: 10.1136/bmj.j1415
