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Systemic Corticosteroid — Acute Dermatoses Pregnancy: 88% of prednisolone is inactivated as it crosses the placenta. There is no evidence that corticosteroids increase the incidence of congenital abnormalities such as cleft lip/palate in man, but when administered for prolonged periods or repeatedly during pregnancy they may increase the risk of intra-uterine growth retardation; cataracts have been observed in infants born to mothers treated with long-term prednisolone during pregnancy. Corticosteroids should only be prescribed when the benefits to mother and child outweigh the risks. Lactation: excreted in small amounts in breast milk; if maternal doses greater than 40 mg/day of prednisolone are prescribed, the infant should be monitored for adrenal suppression.

Prednisolone (Systemic)

Brand names: Deltacortril (enteric-coated), Predsol, Dilacort

Used in: COPD Asthma Gout Inflammatory Bowel Disease

Prednisolone is an oral glucocorticoid used across specialties for inflammatory, allergic and immunological conditions.

Auto-extracted from the source labelling — not yet independently clinician-verified. These values were distilled from the UK SPC (or the US label where noted) but have not had a clinician sign-off. Confirm against the current SmPC before prescribing.

Adult dose

Dose: Initial dosage 5 mg to 60 mg daily, depending on the disorder being treated. For allergic and skin disorders, initial doses of 5-15 mg daily are commonly adequate.
Route: Oral (gastro-resistant tablets)
Frequency: Daily — divided daily dosage is usually used
Corticosteroids are palliative symptomatic treatment by virtue of their anti-inflammatory effects; they are never curative. The appropriate individual dose must be determined by trial and error and re-evaluated regularly according to disease activity. In general the initial dosage should be maintained or adjusted until the anticipated response is observed, then gradually reduced to the lowest dose that maintains an adequate clinical response. Dosage reductions should not exceed 5-7.5 mg daily during chronic treatment. Other indication-specific initial doses given in the SPC: collagenosis 20-30 mg daily (higher doses may be needed for more severe symptoms); rheumatoid arthritis usual initial dose 10-15 mg daily; blood disorders and lymphoma initial daily dose 15-60 mg, with higher doses possibly needed to induce remission in acute leukaemia. Acute or severe disease may require initial high-dose therapy with reduction to the lowest effective maintenance dose as soon as possible. Intermittent regimen: a single morning dose on alternate days or at longer intervals is acceptable for some patients and minimises pituitary-adrenal suppression. WITHDRAWAL: in patients who have received more than a physiological dose (approximately 7.5 mg prednisolone or equivalent) for greater than 3 weeks, withdrawal should not be abrupt; once a daily dose equivalent to 7.5 mg is reached, reduction should be slower to allow HPA-axis recovery. Abrupt withdrawal of doses up to 40 mg daily for 3 weeks is unlikely to lead to clinically relevant HPA-axis suppression in most patients. Gradual withdrawal should be considered even after courses of 3 weeks or less in: patients who have had repeated courses (particularly if taken for more than 3 weeks); a short course prescribed within one year of cessation of long-term therapy; patients who may have other reasons for adrenocortical insufficiency; patients on more than 40 mg daily of prednisolone (or equivalent); and patients repeatedly taking doses in the evening. During prolonged therapy the dosage may need to be temporarily increased during periods of stress or exacerbation. Elderly: treatment, particularly if long-term, should be planned bearing in mind the more serious consequences of the common side-effects of corticosteroids in old age. Children: the SPC states that although appropriate fractions of the actual dose may be used, dosage will usually be determined by clinical response as in adults, and alternate day dosage is preferable where possible — NO numeric paediatric dose is given, so verify paediatric dosing against a children's formulary.

Dose auto-extracted from UK Summary of Product Characteristics (SPC) via the eMC; US FDA prescribing information (openFDA / DailyMed) — cross-check; US labelling may differ from UK — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.

Contraindications

  • Hypersensitivity to prednisolone or to any of the excipients
  • Systemic infections unless specific anti-infective therapy is employed
  • Ocular herpes simplex, because of possible perforation
  • Rare hereditary problems of galactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorption (product-specific excipient contraindication)

Side effects

  • Psychiatric reactions (common): irritability, depressed and labile mood, suicidal thoughts, psychotic reactions, mania, delusions, hallucinations, aggravation of schizophrenia, anxiety, sleep disturbance and cognitive dysfunction including confusion and amnesia
  • Increased susceptibility to, and severity of, infections; opportunistic infections; recurrence of dormant tuberculosis; oesophageal candidiasis
  • Suppression of the hypothalamo-pituitary adrenal axis, cushingoid facies, impaired carbohydrate tolerance, manifestation of latent diabetes mellitus
  • Sodium and water retention, hypokalaemic alkalosis, potassium loss, weight gain, obesity, hyperglycaemia, dyslipidaemia, increased appetite
  • Eye disorders: glaucoma, papilloedema, posterior subcapsular and nuclear cataracts
  • Very rare: calciphylaxis

Clinical monograph

How it works

It activates glucocorticoid receptors to broadly suppress inflammation and immune responses through changes in gene expression.

Prescribing in practice

  • Do not stop abruptly after more than a short course — taper to avoid adrenal insufficiency, and issue a steroid card.
  • Prolonged or high-dose use causes hyperglycaemia, hypertension, osteoporosis, increased infection risk, mood change and gastrointestinal effects; consider bone and gastric protection.
  • Take it in the morning to mimic the natural cortisol rhythm; review the need to continue regularly.

Monitoring

Monitor blood glucose, blood pressure and weight; with longer courses consider bone health and infection risk.

Counselling the patient

  • Carry a steroid card and do not stop suddenly.
  • Report signs of infection, marked thirst, or mood changes.
  • Take it in the morning, with food.

Evidence & guidelines

Systemic corticosteroids are used for many inflammatory and allergic conditions at the lowest effective dose for the shortest duration, with appropriate protection and tapering.

Reference: BAD Atopic Eczema Systemic Guidelines 2020; BAD Pemphigus Guidelines; NOGG Bone Protection Guidelines 2017; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).

Related

Curated clinical cross-links plus same-class fallbacks.