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Patients with pre-eclampsia or fluid retention require close monitoring. Dosage reductions should not exceed 5 – 7.

Although concomitant therapy with salicylate and corticosteroids does not appear to increase the incidence or severity of GI ulceration, the possibility of this effect should be considered. May suppress reactions to skin tests. Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme at: www. Because of interference with antibody formation, systemic administration is usually contraindicated in the presence of acute bacterial and viral infections.

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For the administration of higher doses in particular haematological forms, dermatologic forms, etc. Basic principles and indications for corticosteroid therapy should apply. While on corticosteroid therapy patients should not be vaccinated against smallpox.

How dose reduction should be carried out depends largely on whether the disease is likely to relapse as the dose of systemic corticosteroids is reduced. After a favorable response is noted, the proper maintenance dosage should be determined by decreasing the initial drug dosage in small increments at appropriate time intervals until the lowest dosage which will maintain an adequate clinical response is reached. Once opened: in case of administration of partial doses, the opened container must be discarded once the required dose is removed. Tumorigenicity: direct tumour-inducing effects of the glucocorticoids are not known, but the particular risk that malignancies in patients undergoing immunosupression with these or other drugs will spread more rapidly is a well-recognised problem. Plasma half-life is about 3 hours in adults and somewhat less in children. The American Journal of Emergency Medicine.

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Increased intra-ocular pressure, may suppress reactions to skin tests. Amongst the different subpopulations the occurrence of scleroderma renal crisis varies. The “Steroid Dementia Syndrome”: A Possible Model of Human Glucocorticoid Neurotoxicity”. Corticosteroids should not be stopped and the dose may need to be increased.

Abrupt cessation of prolonged, high dosage therapy may produce adrenal insufficiency or sufficient severity to be threatening to life. Alternate day dosage is preferable where possible. Patients without a definite history of chickenpox should be advised to avoid close personal contact with chickenpox or herpes zoster and if exposed they should seek urgent medical attention.

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Oestrogens may potentiate the effects of glucocorticoids and dosage adjustments may be required if oestrogens are added to or withdrawn from a stable dosage regimen. Glucocorticoids cause profound and varied metabolic effects. Prednisolone is extensively metabolised, mainly in the liver, but the metabolic pathways are not clearly defined. Caution must be observed in ulcerative colitis if a possibility exists of intestinal perforation and peritonitis. The toxicity of cardiac glycosides is increased if hypokalaemia occurs with corticosteroids.

In less severe disease processes in which corticoid therapy is indicated, it may be possible to initiate treatment with alternate-day therapy. In rare cases the concomitant treatment with corticosteroids and fluoroquinolones may increase the risk of tendon rupture. Suppression of the hypothalamo-pituitary adrenal axis3, cushingoid facies, impaired carbohydrate tolerance with increased requirement for antidiabetic therapy, manifestation of latent diabetes mellitus. Prednisone can be used in the treatment of decompensated heart failure to increase renal responsiveness to diuretics, especially in heart failure patients with refractory diuretic resistance with large dose of loop diuretics. Allergic and skin disorders Initial doses of 5-15 mg daily are commonly adequate.

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For detailed instructions for use refer to the Patient Information Leaflet in every pack. The dose is then reduced in steps to be withdrawn 10 days after initiation of prednisone therapy. Therapeutic and Adverse Effects of Glucocorticoids”. Prednisolone sodium phosphate is a synthetic glucocorticoid with the same general properties as prednisolone itself and other compounds classified as corticosteroids. The following side effects may be associated with the long-term systemic use of corticosteroids.

100, 500, 1000 and 5000 tablets in an amber PVC bottle. Live vaccines should not be given to individuals with impaired immune responsiveness caused by high doses of corticosteroids. Prednisolone Tablets should be stored in a dry place below 25ºC and protected from light. Treatment is unlikely to be needed in cases of acute overdosage. Mechanisms of muscle atrophy induced by glucocorticoids”.

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Adrenal cortical atrophy develops during prolonged therapy and may persist for years after stopping treatment. Live vaccines should not be given to individuals with impaired immune responsiveness. Manifestations of allergic conditions which do not react to antihistaminic treatment may be suppressed by adequate doses or as a supplement to primary therapy.

Each 5 ml single-dose container contains 0. Infants of mothers taking higher doses than this may have a degree of adrenal suppression but the benefits of breast feeding are likely to outweigh any theoretical risk. The initial dose may vary up to 60 mg daily depending on the disorder being treated, taken in the morning after food. Glycyrrhizin can delay the clearance of prednisolone. 5 mg to 60 mg per day depending on the specific disease entity being treated. Glucocorticoids improve renal responsiveness to atrial natriuretic peptide by up-regulating natriuretic peptide receptor-A expression in the renal inner medullary collecting duct in decompensated heart failure”.

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The absorption of prednisolone may be reduced by large doses of some antacids such as magnesium trisilicate or aluminium hydroxide. There is however wide inter-subject variation suggesting impaired absorption in some individuals. Dispense in a well-closed container with child-resistant closure. Hirsutism, skin atrophy, bruising, striae, telangiectasia, acne, increased sweating, pruritis, rash, urticaria. The following regimens are for guidance only.

A reduction in the number of circulating lymphocytes may occur. 5 mg daily during chronic treatment. After control has been obtained, dosage should be reduced by small steps of 5 mg prednisone per week until further reductions elucidate symptoms. Symptoms typically emerge within a few days or weeks of starting the treatment. To email a medicine you must be a registered user.

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Rifamycins accelerate metabolism of corticosteroids and thus may reduce their effect. Chickenpox is of particular concern since this normally minor illness may be fatal in immunosuppressed patients. Suppression of the inflammatory response and immune function increases the susceptibility of infections and their severity. However, divided daily dosages may be employed if required. Archived from the original on 4 January 2013. These consist of a high density polythene body and high density polythene cap.

3 to 4 hours in adults. May increase AUC and reduce clearance in oral contraceptives containing ethinylestradiol, mestranol, desogestrel, levonorgestrel, norgestrel or norethisterone. Patients should also be advised that if they are exposed, medical advice should be sought without delay. A ‘withdrawal syndrome’ may also occur including fever, myalgia, arthralgia, rhinitis, conjunctivitis, painful itchy skin nodules and loss of weight.

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In patients with liver failure, blood levels of corticosteroid may be increased, as with other drugs which are metabolised in the liver. Skin atrophy, skin striae, acne, telangiectasia, hyperhidrosis, rash, pruritus, urticaria, hirsutism, Stevens-Johnson syndrome. If glucocorticoids are administered towards the end of pregnancy, there is a risk of atrophy of the fetal adrenal cortex, which may necessitate replacement therapy in the newborn, which has to be slowly reduced. Discontinuation of corticosteroids may result in clinical remission.

Prednisolone is four times as active as hydrocortisone on a weight for weight basis. Prednisolone clearance increased by the use of carbimazole and thiamazole. Glucocorticoids cause profound and varied metabolic effects. Systemic corticosteroids may be stopped abruptly in those whose disease is unlikely to relapse and who have received treatment for 3 weeks or less and who are not included in the patient groups described above. In order to minimise suppression of the hypothalamo-pituitary adrenal axis and growth retardation, treatment should be administered where possible as a single dose on alternate days. Patients receiving diuretics which causes potassium depletion should be watched carefully for signs of hypokalaemia.

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Chorioretinopathy may result in impaired vision, including loss of vision. The dose is then reduced to minimally effective level. Sodium and water retention, hypokalaemic alkalosis, potassium loss, negative nitrogen and calcium balance, glucose intolerance and protein catabolism.

Erythromycin and ketoconazole may inhibit the metabolism of some corticosteroids. Growth and development of infants and children on prolonged corticosteroid therapy should be carefully observed. During prolonged corticosteroid therapy, these patients should receive chemoprophylaxis. In long-term therapy the dose must be the smallest one to achieve a desired effect.