Corticosteroid (oral) — bridge/anti-inflammatory
Pregnancy: Oral prednisolone used in pregnancy for autoimmune conditions — lowest effective dose; avoid in first trimester if possible.
Prednisolone (Rheumatology)
Brand names: Deltacortril, Precortisyl Forte
Adult dose
Dose: RA bridge: 7.5–15 mg/day; PMR: 15–20 mg/day; GCA: 40–60 mg/day; Severe flares: 0.5–1 mg/kg/day
Route: Oral
Frequency: Once daily (morning)
Max: 60 mg/day (standard rheumatological); higher specialist doses for vasculitis
RA bridging therapy: 7.5–15 mg/day while awaiting DMARD effect, taper over 3 months. PMR: 15–20 mg/day, taper by 1 mg every 4 weeks. GCA: 40–60 mg/day (IV methylprednisolone if visual loss imminent). All patients on >3 months steroids: bone protection (calcium, Vit D ± bisphosphonate) + PPI.
Paediatric dose
Dose: 1 mg/kg
Route: Oral
Frequency: Once daily
Max: 40 mg/day
JIA flare: 0.5–1 mg/kg/day (max 40 mg). Taper as quickly as clinically possible. Growth suppression risk — use alternate-day dosing where possible.
Dose adjustments
Renal
No dose adjustment required.
Hepatic
No dose adjustment required; hepatic conversion of prednisolone to active form may be impaired in severe disease.
Paediatric weight-based calculator
JIA flare: 0.5–1 mg/kg/day (max 40 mg). Taper as quickly as clinically possible. Growth suppression risk — use alternate-day dosing where possible.
Clinical pearls
- GCA visual loss: immediate IV methylprednisolone 500–1000 mg/day for 3 days then oral prednisolone
- Sick day rule: double dose during intercurrent illness (adrenal insufficiency prevention)
- Bone protection: all patients >7.5 mg/day for >3 months should receive bisphosphonate + calcium/Vit D
- Carry steroid emergency card/MedicAlert bracelet if on long-term doses
- PMR target: CRP normalisation; taper to minimum effective dose to avoid osteoporosis
Contraindications
- Systemic fungal infections (unless with antifungal cover)
- Live vaccines (during high doses)
Side effects
- Weight gain and fluid retention
- Hyperglycaemia (steroid-induced diabetes)
- Hypertension
- Osteoporosis (fracture risk with long-term use)
- Adrenal suppression and HPA axis suppression
- Cataracts and glaucoma
- Cushingoid features
- Increased infection susceptibility
- Mood changes (euphoria, depression, psychosis)
Interactions
- NSAIDs — increased GI bleeding risk (use PPI)
- Antidiabetics — reduced efficacy
- Warfarin — variable effect on INR
- Live vaccines — contraindicated
- CYP3A4 inducers — reduce prednisolone levels
Monitoring
- Blood glucose (SMBG)
- Blood pressure
- Bone density (DEXA at baseline and annually)
- Weight
- Serum potassium
Reference: BNFc; BNF; BSR PMR/GCA Guidelines; NOGG osteoporosis guidelines; NICE CG169. Verify against your local formulary and the latest BNF before prescribing.
Related
Curated clinical cross-links plus same-class fallbacks.
Calculators
- DOAC Score for Selecting Direct Oral Anticoagulant in Non-Valvular AF · Anticoagulation
- SIRS Criteria and Sepsis Definition · Sepsis
- Steroid Dose Equivalence · Medications
- Neutrophil-to-Lymphocyte Ratio (NLR) · Inflammatory Markers
- Maddrey Discriminant Function (Alcoholic Hepatitis) · Alcoholic Liver Disease
- Lille Model (Steroid Response in Alcoholic Hepatitis) · Alcoholic Liver Disease
Pathways
- 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