This information is intended for use by health professionals
Prednisolone 2.5mg Tablets
Each tablet contains 2.5 mg prednisolone.
For the full list of excipients, see section 6.1.
Yellow, 7mm, round, flat, tablet, with a score line on one side, imprinted with “A610” on one side and “2.5” on the other.
Allergy and anaphylaxis: bronchial asthma, drug hypersensitivity reactions, serum sickness, angioneurotic oedema, anaphylaxis, incapacitating allergies unresponsive to conventional treatment.
Arteritis/collagenosis: giant cell arteritis/polymyalgia rheumatica, mixed connective tissue disease, polyarteritis nodosa, polymyositis.
Blood disorders: haemolytic anaemia (auto-immune), leukaemia (acute and chronic lymphocytic), lymphoma, multiple myeloma, idiopathic thrombocytopenic purpura.
Cardiovascular disorders: post-myocardial infarction syndrome, rheumatic fever with severe carditis.
Endocrine disorders: primary and secondary adrenal insufficiency, congenital adrenal hyperplasia.
Gastro-intestinal disorders: regional ileitis (Crohn's disease), ulcerative colitis, persistent coeliac syndrome (coeliac disease unresponsive to gluten withdrawal), auto-immune chronic active hepatitis, multisystem disease affecting liver, biliary peritonitis.
Hypercalcaemia: sarcoidosis, vitamin D excess.
Infections (with appropriate chemotherapy): helminthic infestations, Herxheimer reaction, infectious mononucleosis, miliary tuberculosis, mumps orchitis (adult), tuberculous meningitis, rickettsial disease.
Muscular disorders: polymyositis, dermatomyositis.
Neurological disorders: infantile spasms, Shy-Drager syndrome, sub-acute demyelinating polyneuropathy.
Ocular disease: scleritis, posterior uveitis, retinal vasculitis, pseudo-tumours of the orbit, giant cell arteritis, malignant ophthalmic Graves disease.
Renal disorders: lupus nephritis, acute interstitial nephritis, minimal change glomerulonephritis, nephrotic syndrome.
Respiratory disease: allergic pneumonitis, asthma, occupational asthma, pulmonary aspergillosis, pulmonary fibrosis, pulmonary alveolitis, aspiration of foreign body, aspiration of stomach contents, pulmonary sarcoid, drug induced lung disease, adult respiratory distress syndrome, spasmodic croup, fulminating or disseminated pulmonary tuberculosis when used concurrently with appropriate antituberculosis chemotherapy.
Rheumatic disorders: rheumatoid arthritis, polymyalgia rheumatica, juvenile chronic arthritis, psoriatic arthritis, systemic lupus erythematosus, dermatomyositis, mixed connective tissue disease.
Skin disorders: pemphigus vulgaris, exfoliative dermatitis, bullous pemphigoid, systemic lupus erythematosus, pyoderma gangrenosum.
Miscellaneous: sarcoidosis, hyperpyrexia, Behçets disease, immunosuppression in organ transplantation.
Adults and the elderly
The lowest effective dose should be used for the minimum period.
Prednisolone should only be used when specifically indicated, at the lowest dose possible and for the shortest possible time.
The initial dosage of Prednisolone may vary from 5mg to 60mg daily depending on the disorder being treated. Divided daily dosage may be used. Administration as a once daily dose in the morning or on alternate days can reduce the risk of adrenocortical suppression (see Section 4.4 Special warnings and precautions for use). In some patients this may not be possible e.g. patients with rheumatoid arthritis with pronounced morning stiffness where an evening dose may need to be given.
The following therapeutic guidelines should be kept in mind for all therapy with corticosteroids:
The lowest dose to produce an acceptable result should be given. Initial dosage should be adjusted until the desired clinical response has been achieved. The dose should be gradually reduced until the lowest dose which will maintain an adequate clinical response is reached. As a guide, the daily dose should be reduced by 2.5 – 5 mg every second to fifth day (more rapidly at the higher initial dose levels) until the lowest possible maintenance dose is reached. Preferably this should not exceed 10 mg per day. Use of the lowest effective dose will tend to minimise side-effects. The incidence of side-effects increases with dose and duration of treatment (see Section 4.4 'Special warnings and special precautions for use').
Particular care should be exercised in patients who have received higher than 7.5mg prednisolone daily or equivalent for more than 3 weeks, owing to a greater risk of suppression of the hypothalamic-pituitary-adrenal (HPA) axis in these patients. The speed with which dose can be reduced is also dependent on risk of relapse of the disease being treated. After prolonged treatment, tapering of dose below 7.5 mg (regarded as “equivalent” to physiological levels of glucocorticoids) should be conducted particularly cautiously.
More rapid withdrawal of systemic corticosteroid treatment that has been given for less than 3 weeks is appropriate if it is considered that the disease is unlikely to relapse. Withdrawal of doses of up to 40mg daily of prednisolone, or equivalent that have been administered for less than 3 weeks is unlikely to lead to clinically relevant HPA-axis suppression, in the majority of patients. In the following patient groups, gradual withdrawal of systemic corticosteroid therapy should be considered even after courses lasting 3 weeks or less:
• patients who have had repeated courses of systemic corticosteroids, particularly if taken for greater than 3 weeks.
• when a short course has been prescribed within one year of cessation of long-term therapy (months or years).
• patients who may have reasons for adrenocortical insufficiency other than exogenous corticosteroid therapy.
• patients receiving doses of systemic corticosteroid greater than 40mg daily of prednisolone (or equivalent).
• patients repeatedly taking doses in the evening.
(See Section 4.4 'Special warnings and special precautions for use' and Section 4.8 'Undesirable effects')
During prolonged therapy, dosage may need to be temporarily increased during periods of stress or during exacerbations of the disease (see Section 4.4 'Special warnings and special precautions for use')
If there is lack of a satisfactory clinical response to Prednisolone Tablets, the drug should be gradually discontinued and the patient transferred to alternative therapy.
Intermittent dosage regimen A single dose of Prednisolone Tablets in the morning on alternate days or at longer intervals is acceptable therapy for some patients. When this regimen is practical, the degree of pituitary-adrenal suppression can be minimised.
Specific dosage guidelines The following recommendations for some corticosteroid-responsive disorders are for guidance only. Acute or severe disease may require initial high dose therapy with reduction to the lowest effective maintenance dose as soon as possible. Dosage reductions should not exceed 5-7.5mg daily during chronic treatment.
Allergic and skin disorders Initial doses of 5-15mg daily are commonly adequate.
Collagenosis Initial doses of 20-30mg daily are frequently effective. Those with more severe symptoms may require higher doses.
Rheumatoid arthritis The usual initial dose is 10-15mg daily. The lowest daily maintenance dose compatible with tolerable symptomatic relief is recommended.
Blood disorders and lymphoma An initial daily dose of 15-60mg is often necessary with reduction after an adequate clinical or haematological response. Higher doses may be necessary to induce remission in acute leukaemia.
Use in elderly Treatment of elderly patients, particularly if long-term, should be undertaken with caution bearing in mind the more serious consequences of the common side-effects of corticosteroids in old age (see also 'Special warnings and special precautions for use').
Use in children: Although appropriate fractions of the adult dose may be used, dosage will usually be determined by clinical response as in adults (see also Section 4.4 'Special warnings and special precautions for use' and Section 4.8 'Undesirable effects'). Alternate day dosage is preferable where possible.
Method of administration
Prednisolone tablets should be taken following a meal to reduce the risk of gastric irritation.
Hypersensitivity to the active substance or to any of the excipients listed in section 6.1.
Systemic fungal infection.
Administration of live vaccines is contraindicated in patients receiving corticosteroids in immunosuppressive doses.
In those conditions when treatment with prednisolone can save lives, none of the contraindications generally applies.
Since the complications of glucocorticoid therapy are dependent on the dose and duration of treatment, a risk / benefit assessment must be made in each case regarding dose and duration of treatment, as well as whether daily or intermittent treatment should be used.
The lowest possible corticosteroid dose needed to control the disease being treated should be used. When dose reduction is possible, it should be gradual.
Immunosuppressive effects / increased infection sensitivity
Glucocorticoids, including prednisolone, may cause increased susceptibility to infection, masking symptoms of infection, and new infections may occur during treatment.
Infections caused by viruses, bacteria, fungi, protozoa or helminths may be associated with the use of corticosteroids alone or corticosteroids in combination with other immunosuppressive agents that affect cellular immunity, humoral immunity or the function of neutrophils. The infections can be mild, but also difficult and in some cases fatal. The risk of infectious complications increases with increasing dose.
Glucocorticoids should not be given during infections without concomitant causal treatment.
Chickenpox and measles can be more serious or even fatal in non-immunized children and adults treated with corticosteroids. Children, or adults who have not had these diseases, and who take immunosuppressive doses of corticosteroids, should be advised to avoid exposure to chickenpox and measles, and to seek care when exposed.
The use of prednisolone in active tuberculosis should be limited to those cases of fulminant or disseminated tuberculosis where the corticosteroid is used to treat the disease in combination with appropriate tuberculosis therapy. If corticosteroids are indicated in patients with latent tuberculosis or tuberculin reactivity, careful monitoring is necessary as the disease can be reactivated. In long-term corticosteroid therapy, these patients should receive tuberculosis prophylaxis.
High dose corticosteroids may interfere with active immunization.
Vaccination with live vaccine should be done under close supervision and not in patients on long-term treatment with corticosteroids in immunosuppressive doses.
Since rare cases of skin reactions and anaphylactic / anaphylactoid reactions have occurred in patients treated with corticosteroids, appropriate precautions should be taken prior to administration, especially if the patient has previously had an allergic reaction to any drug.
Long-term treatment with pharmacological doses of corticosteroid may lead to secondary adrenal insufficiency. The risk can be reduced by giving the treatment every other day (see section 4.2).
Patients who receive corticosteroid maintenance therapy and are exposed to unusual stresses (e.g. infection, surgery or trauma) need higher corticosteroid doses before, during and after the stressful situation.
Abrupt termination of treatment may lead to acute adrenal insufficiency which may be fatal. The risk of secondary adrenal insufficiency can be reduced by gradually decreasing the dose. This type of relative insufficiency may persist for months after the end of treatment, so hormone replacement therapy should be reintroduced in stressful situations occurring during this time period. Since the secretion of mineral corticoids may be impaired, salts and / or mineral corticoids should be administered simultaneously.
A "steroid withdrawal syndrome", apparently without associated with adrenal insufficiency, may also occur following abrupt withdrawal of glucocorticoids. This syndrome causes symptoms such as anorexia, nausea, vomiting, lethargy, headache, fever, joint pain, desquamation, myalgia, weight loss and / or hypotension. These effects are believed to be due to the sudden change in glucocorticosteroid concentration rather than to low corticosteroid levels.
Patients with hypothyroidism or liver cirrhosis will have an enhanced effect of corticosteroids.
Pheochromocytoma-related crisis, which may be fatal, has been reported following systemic corticosteroid administration. Corticosteroids should only be administered to patients with suspected or identified pheochromocytoma following consideration of individual risk / benefit.
Metabolism and nutrition
Corticosteroids, including prednisolone, can raise blood sugar levels, exacerbate existing diabetes and increase the risk of developing diabetes in patients on long-term corticosteroid therapy.
Potentially serious mental disorders may occur during treatment with corticosteroids including prednisolone. It can be anything from euphoria, sleep disorders, mood swings, personality changes and severe depression to psychotic manifestations. Existing emotional instability and psychotic tendencies can also be exacerbated by corticosteroids (see section 4.8). The symptoms typically begin within a few days or weeks after the start of treatment. Most reactions return after dose reduction or withdrawal, but specific treatment may be necessary.
Psychiatric effects have been reported with the withdrawal of corticosteroids, the frequency is unknown. Patients / caregivers should be encouraged to seek medical care if the patient shows mental symptoms, especially if depression or suicidal thoughts are suspected. Patients / caregivers should be aware that mental disorders may occur either during or immediately after dose reduction / discontinuation of systemic steroids.
Central and peripheral nervous system
Corticosteroids should be used with caution in patients with seizures.
Side effects of glucocorticoids on the cardiovascular system, for example dyslipidemia and hypertension, can predispose in treated patients with existing cardiovascular risk factors for additional cardiovascular events at high doses and prolonged treatment times. Corticosteroids should therefore be introduced to these patients only after careful consideration, and risk-modifying measures as well as extra cardiac monitoring should be considered as needed. Low dose and treatment every other day can reduce the complications of corticosteroid treatment.
Since cortisone has been reported to increase the blood clotting tendency in rare cases, thereby accelerating the development of intravascular thrombosis, thromboembolism and thrombophlebitis, corticosteroids should be used with caution in patients with thromboembolic disorders.
High doses of corticosteroids can cause acute pancreatitis.
There are no conclusive data that states that corticosteroids cause ulcers. Glucocorticoid therapy can mask peritonitis and other signs and symptoms associated with gastrointestinal conditions such as perforation, obstruction or pancreatitis. In combination with NSAIDs, the risk of gastrointestinal ulcers is increased.
Corticosteroids should therefore be used with caution in non-specific ulcerative colitis if there is a likelihood of imminent perforation, abscess or other pyogenic infection, diverticulitis, newly created anastomoses, or active or latent peptic ulcer.
Liver and biliary tract
Diseases of the liver and bile ducts have been reported rarely and in the majority of these cases the condition was reversible after discontinuation of treatment. Appropriate monitoring measures are required.
Acute myopathy has been reported with high corticosteroid doses, most often in patients with neuromuscular transmission disorders (e.g., myasthenia gravis), or in patients concomitantly treated with anticholinergics, e.g. neuromuscular blocking drugs (such as pancuronium) (see section 4.5). This acute myopathy is generalized, may involve eye and respiratory muscles, and may lead to tetraparesis. Elevated creatine kinase may occur. Clinical improvement or recovery after discontinuation of corticosteroid therapy may take weeks or years.
Corticosteroids should be used with caution in patients with osteoporosis.
Kidneys and urinary tract
Corticosteroids should be used with caution in patients with renal insufficiency.
Acute renal crisis (renal crisis in scleroderma)
Caution is required in patients with systemic sclerosis as an increased incidence of (possibly fatal) renal crisis in scleroderma, with hypertension and decreased urine output, has been observed with a daily prednisolone dose of 15 mg or more. Therefore, blood pressure and renal function (S-creatinine) should be routinely monitored. In case of suspected renal crisis, blood pressure should be kept under close control.
Effects on electrolytes and fluid balance
Systemic corticosteroids should be used with caution in patients with heart failure or hypertension. Medium and high doses of hydrocortisone or cortisone can lead to increased blood pressure, salt and water retention and increased potassium secretion. These effects are less likely with synthetic derivatives, except when used in high doses. Dietary restrictions with lower salt intake and potassium supplementation may be necessary.
All corticosteroids increase calcium excretion.
Syncope disorder can be reported in systemic and topical use of corticosteroids. If a patient comes with symptoms such as blurred vision or other visual disturbances, consideration should be given to referring the patient to ophthalmologist for investigation of possible causes. These may include cataracts, glaucoma or rare diseases such as central serous chorioretinopathy (CSCR), which have been reported following the use of systemic and topical corticosteroids.
Use in children
Corticosteroids cause growth inhibition in infants, children and adolescents, therefore avoid long-term treatment with pharmacological doses. If long-term treatment is required, the infant / child's growth and development should be closely monitored (see section 4.2). Infants and children who are on long-term corticosteroid therapy are at particular risk of developing elevated intracranial pressure.
Patients with rare hereditary problems of galactose intolerance, total lactase deficiency or glucose-galactose malabsorption should not take this medicine.
This medicine contains less than 1 mmol sodium (23 mg) per tablet, that is to say essentially 'sodium-free'.
The following combinations with Prednisolone Pfizer may require dose adjustment.
Phenobarbital, phenytoin, carbamazepine:
Phenobarbital (which is also the metabolite of primidone), phenytoin and carbamazepine alone and in combination, induces the metabolism of hydrocortisone, prednisolone and methylprednisolone (shown in children with asthma) with increased dose requirements as a result. The interaction probably applies to the whole group of glucocorticoids.
Non-steroidal anti-inflammatory drugs:
1) The incidence of gastrointestinal bleeding and ulceration may increase if corticosteroids are given with NSAIDs.
2) Corticosteroids may increase the clearance of high doses of acetylsalicylic acid, which may lead to lower salicylate levels in the serum. Salicylate levels in serum may increase upon discontinuation of corticosteroid therapy, which could lead to an increased risk of toxic effects of salicylate.
Glucocorticoids increase blood sugar levels. Patients with diabetes mellitus receiving concomitant insulin and / or oral hypoglycaemic agents may need to adjust the dose of such treatment.
Estrogens (also oral contraceptives containing estrogens):
estrogens increase the concentration of transcortin. The effect of glucocorticoids that bind to transcortin can be enhanced and dose adjustments may be needed if estrogens are added or removed from a stable treatment regimen.
Potassium Reducing Agents:
Potassium-reducing diuretics (e.g., thiazides, furosemide, ethacrynic acid) and other drugs that reduce the amount of potassium such as amphotericin B, xanthines and beta2-agonists, may potentiate the potassium-lowering effect of glucocorticoids. Serum potassium should be closely monitored in patients receiving glucocorticoids and potassium reducing agents.
Rifampicin induces the microsomal oxidation of glucocorticoids (hydrocortisone, prednisolone, methylprednisolone). This leads to an increased steroid need during rifampicin treatment and reduced steroid need after such treatment.
Prednisolone also has a potential effect which results in increased acetylation rate and clearance of isoniazid.
There are reports of altered effects of anticoagulants given concurrently with prednisolone. Prothrombin time (INR) should be monitored during treatment.
CYP3A inhibitors, including medicinal products containing cobicistat:
These are expected to increase the risk of systemic side effects. The combination should be avoided unless the benefit outweighs the increased risk of systemic side effects of corticosteroids, and if so, patients should be monitored for systemic adverse events of corticosteroids.
Anticholinergic, neuromuscular blockers:
Corticosteroids may affect the effect of anticholinergics.
1) Acute myopathy has been reported with concomitant use of high doses of corticosteroids and anticholinergics such as neuromuscular blockers (see section 4.4).
2) Antagonism with the neuromuscular blocking effect of pancuronium and vecuronium has been reported in patients taking glucocorticosteroids. This interaction can be expected with all competitive neuromuscular blockers.
Interaction between glucocorticoids and anticholinesterases such as ambenonium, neostigmine and pyridostigmine may lead to significant potency in myasthenia gravis.
If possible, treatment with anticholinesterase should be discontinued at least 24 hours before administration of glucocorticoid.
Animal studies have shown that corticosteroids impair fertility (see section 5.3).
In animal studies, corticosteroids have been shown to give rise to various types of malformations (palate gap, skeletal malformations, see section 5.3).
The relevance in humans is unknown.
After long-term treatment, reduced placental and birth weight have been observed in humans and animals.
In addition, there is a risk of adrenal insufficiency in the newborn during long-term treatment. Therefore, during pregnancy, corticosteroids should be given after special consideration.
Prednisolone passes into breast milk, but the risk of affecting the baby seems unlikely with therapeutic doses.
The effect of corticosteroids on the ability to drive and use machines has not been systematically investigated.
Side effects such as dizziness, visual disturbances and fatigue are possible after treatment with corticosteroids. In such adverse reactions, patients should not drive or use machines.
The following side effects have been observed and reported during treatment with Prednisolone Pfizer at the following frequencies: Very common (≥1/10), common (≥1/100 to <1/10), uncommon (≥1/1,000 to <1/100), rare (≥1/10,000 to <1/1000), very rare (<1/10,000), not known (cannot be estimated from the available data).
Infections and infestations
Activation of infection (e.g., tuberculosis)
Blood and lymphatic system
Leukocytosis (due to redistribution of intravascular granulocytes)
Immune system disorders
Inhibition of endogenous ACTH and cortisol secretion, Cushing-like symptoms. Growth retardation (in children)
Steroid withdrawal syndrome (see section 4.4)
Pheochromocytoma-related crisis (see section 4.4)
Metabolism and nutrition disorders
Reduced glucose tolerance (diabetes mellitus may deteriorate and latent diabetes become manifest)
Increased appetite (which can lead to weight gain)
Activation of previous mental disorders (high dose)
Depression, mania in patients without previously known mental illness
Affective disorder (includes euphoria, affective lability, drug-related, suicidal condition)
Psychotic disorder (includes delusions, hallucinations and schizophrenia)
Nervous system disorders
Benign intracranial hypertension
Central serous chorioretinopathy (see section 4.4)
Blurred vision (see section 4.4)
Heart failure (in sensitive patients)
Respiratory, thoracic and mediastinal disorders
Peptic wound (possibly with perforation and bleeding)
Intestinal perforation pancreatitis
Ulcerative esophagitis abdominal distension
Skin and subcutaneous tissue disorders
Impaired wound healing
Musculoskeletal and connective tissue disorders
Aseptic bone necrosis
Renal and urinary disorders
Acute renal crisis (renal crisis in scleroderma) *
Reproductive system and breast disorders
General disorders and administration site conditions
Increased calcium levels in the urine
Elevated alanine aminotransferase
Elevated aspartate aminotransferase
Increased blood alkaline phosphatase
Elevated blood urea
Suppression of skin test reactions1
1 Not MedDRA term.
* Acute renal crisis (scleroderma renal crisis)
The incidence of acute renal crisis varies between the different subpopulations. The greatest risk has been reported in patients with diffuse systemic sclerosis. The minimum risk has been reported in patients with limited systemic sclerosis (2%) and systemic sclerosis with juvenile onset (1%).
** Following high doses.
Reporting of suspected adverse reactions
Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme Website: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.
Reports of acute toxicity and / or death following glucocorticoid overdose are rare.
Possibly, acute overdose may aggravate preexisting disease states such as ulcers, electrolyte disorders, infections and edema.
Treatment: Not usually required. If proper gastric emptying, with charcoal.
In case of overdose, there is no specific antidote, but the treatment is supportive and symptomatic.
Pharmacotherapeutic group: Glucocorticoid
ATC code: H02AB06
Synthetic glucocorticoid with anti-inflammatory, immunosuppressive and antiallergic action.
Prednisolone has, by weight, 4-5 times higher anti-inflammatory effect than cortisone, but affects electrolyte turnover to a lesser extent.
The mechanism of action is not yet fully understood.
Prednisolone is rapidly absorbed into the gastrointestinal tract when given orally. Maximum plasma concentration is achieved after 1 to 2 hours after oral administration. The plasma half-life is normally 2 to 4 hours. Its initial absorption, but not total bioavailability, is affected by food.
Prednisolone is highly bound to plasma proteins and has high affinity for the transcortin.
The volume of distribution and clearance are reported to increase with transition from low to medium doses.
Prednisolone is metabolised primarily in the liver to a biologically inactive compound.
Prednisolone can be reversibly converted to prednisone by 11β-hydroxysteroid dehydrogenase.
The absolute bioavailability of prednisolone is on average 82% compared to intravenously administered prednisolone following a single 10 mg dose. At normal dosing, the effective duration is calculated to be 12-36 hours.
Prednisolone is excreted via the urine as free and conjugated metabolites, along with small amounts of unchanged prednisolone.
More than 90% of the given amount is excreted in the urine. 7-15% is excreted in unchanged form.
In animal experiments, corticosteroids have been shown to give rise to various types of malformations (palate gap, skeletal malformations). After long-term treatment, reduced placental and birth weight have been observed in animals.
Corticosteroids have been shown to reduce fertility when administered to the rat.
Sodium starch glycolate, type A
Iron oxide yellow (E172)
Iron oxide red (E172)
Do not store above 25°C.
Keep the blister packs in the outer carton in order to protect from light.
Blisters of AL/PVC containing packs of 28 tablets
Not all pack sizes may be marketed.
(Trading style: Accord)