Severe inflammation; immunosuppression Adults: Dosage individualized based on diagnosis, severity of condition, and response. Amphotericin B, mezlocillin, piperacillin, thiazide and loop diuretics, ticarcillin: additive hypokalemia Aspirin, other nonsteroidal anti-inflammatory drugs: increased risk of GI discomfort and bleeding Cardiac glycosides: increased risk of digitalis toxicity due to hypokalemia Cyclosporine: therapeutic benefits in organ transplant recipients, but with increased risk of toxicity Erythromycin, indinavir, itraconazole, ketoconazole, ritonavir, saquinavir: increased prednisone blood level and effects Hormonal contraceptives: impaired metabolism and increased effects of prednisone Isoniazid: decreased isoniazid blood level Live-virus vaccines: decreased antibody response to vaccine, increase risk of adverse effects Oral anticoagulants: reduced anticoagulant requirements, opposition to anticoagulant action Phenobarbital, phenytoin, rifampin: decreased prednisone efficacy Salicylates: reduced salicylate blood level Somatrem: inhibition of somatrem's growth-promoting effects Theophylline: altered pharmacologic effects of either drug Drug-diagnostic tests. CNS: headache, nervousness, depression, euphoria, personality changes, psychosis, vertigo, paresthesia, insomnia, restlessness, seizures, meningitis, increased intracranial pressure CV: hypotension, hypertension, vasculitis, heart failure, thrombophlebitis, thromboembolism, fat embolism, arrhythmias, shock EENT: posterior subcapsular cataracts (especially in children), glaucoma, nasal irritation and congestion, rebound congestion, sneezing, epistaxis, nasopharyngeal and oropharyngeal fungal infections, perforated nasal septum, anosmia, dysphonia, hoarseness, throat irritation (all with long-term use) GI: nausea, vomiting, abdominal distention, rectal bleeding, esophageal candidiasis, dry mouth, esophageal ulcer, pancreatitis, peptic ulcer GU: amenorrhea, irregular menses Hematologic: purpura Metabolic: sodium and fluid retention, hypokalemia, hypocalcemia, hyperglycemia, decreased carbohydrate tolerance, diabetes mellitus, growth retardation (in children), cushingoid effects (with long-term use), hypothalamic-pituitary-adrenal suppression (with systemic use longer than 5 days), adrenal suppression (with high-dose, long-term use) Musculoskeletal: muscle weakness or atrophy, myalgia, myopathy, osteoporosis, aseptic joint necrosis, spontaneous fractures (with long-term use), osteonecrosis, tendon rupture Respiratory: cough, wheezing, bronchospasm Skin: rash, pruritus, contact dermatitis, acne, striae, poor wound healing, hirsutism, thin fragile skin, petechiae, bruising, subcutaneous fat atrophy, urticaria, angioedema Other: bad taste, increased or decreased appetite, weight gain (with long-term use), facial edema, aggravation or masking of infections, hypersensitivity reaction Drug-drug. • Hypersensitivity to drug, other corticosteroids, alcohol, bisulfite, or tartrazine (with some products) • Systemic fungal infections • Live-virus vaccines (with immunosuppressant doses) • Active untreated infections (except in selected meningitis patients) Use cautiously in: • diabetes mellitus, glaucoma, renal or hepatic disease, hypothyroidism, cirrhosis, diverticulitis, nonspecific ulcerative colitis, recent intestinal anastomoses, inflammatory bowel disease, thromboembolic disorders, seizures, myasthenia gravis, heart failure, hypertension, osteoporosis, hypothyroidism, ocular herpes simplex, immunosuppression, emotional instability • pregnant or breastfeeding patients • children under age 6. Calcium, potassium, thyroid I uptake, thyroxine, triiodothyronine: decreased levels Cholesterol, glucose: increased levels Nitroblue tetrazolium test for bacterial infection: false-negative result Drug-herbs. Alfalfa: activation of quiescent systemic lupus erythematosus Echinacea: increased immune-stimulating effects Ephedra (ma huang): decreased drug blood level Ginseng: potentiation of immunomodulating effect Licorice: prolonged drug activity Drug-behaviors. Alcohol use: increased risk of gastric irritation and GI ulcers Check for signs and symptoms of depression and psychosis. • Assess blood glucose level carefully in diabetic patient. zoloft contraindications Multicentric reticulohistiocytosis (MRH) is a rare histiocytic proliferative disorder of uncertain etiology, characterized by mucocutaneous papulonodular lesions and progressive, symmetric erosive arthritis. MRH can coexist with various autoimmune disorders, tuberculosis, and malignancy. It usually occurs in the elderly and is very rare in children. This is probably the first case in which disease manifestation appeared in infancy in the form of skin lesions. The patient had recurrent ulceration of cutaneous lesions, which is unusual in MRH. Early diagnosis and aggressive treatment are essential to prevent progressive irreversible course and development of arthritis mutilans. Various drugs, such as steroids, nonsteroidal anti-inflammatory drugs, immunosuppressants, interleukin inhibitors, and tumor necrosis factor-α antagonist, have been tried with variable responses. Sertraline weight loss diet The aim of our study was to investigate the efficacy of prednisone to preserve pancreatic beta-cell function in patients with recent- onset Type I diabetes mellitus IDDM. cheap valtrex 1000mg Prednisone is a common synthetic corticosteroid medication that was initially synthesized in 1955. Upon ingestion of prednisone, it doesn't elicit. Prednisone is a steroid used as a replacement for cortisol, which is a hormone produced by ourPrednisone is a steroid drug belonging to the class of corticosteroids used to treat ulcerative colitis. The aim of our study was to investigate the efficacy of prednisone to preserve pancreatic beta-cell function in patients with recent-onset Type I diabetes mellitus (IDDM). Twenty-five patients with IDDM, aged 24 /- 6 years, entered the trial within 8 weeks of the onset of diabetes. They were allocated, according to a single blind randomized protocol, to one of the following treatments: (A) prednisone (15 mg/day), (B) indomethacin (100 mg/day), (C) placebo. All treatments lasted 8 months and all patients achieved satisfactory metabolic control with a multi-injection regimen (three injections/day) within a few weeks, and maintained it throughout the entire period of observation. Only minor side effects were observed in the prednisone-treated patients. A lower insulin requirement was observed in the prednisone group than in other patients at 12 months (0.33 /- 0.11 vs 0.57 /- 0.06 U/kg/day, P less than 0.05), 18 months (0.34 /- 0.11 vs 0.64 /- 0.06, P less than 0.05) and 24 months (0.38 /- 0.10 vs 0.63 /- 0.05, P less than 0.05). Endogenous insulin release, evaluated as urinary C-peptide, was higher in the prednisone group than in other patients at 3, 6, 9, 12, 18 and 24 months (P less than 0.05). Prednisone is a steroid used as a replacement for cortisol, which is a hormone produced by our adrenal gland. This drug is used in the treatment of various diseases. As prednisone is a steroid, sudden withdrawal of the drug can have an adverse effect on the health of the patient. Prednisone is a steroid drug belonging to the class of corticosteroids used to treat ulcerative colitis, some types of arthritis, allergies, migraine headache, asthma, Crohn's disease, and disorders related to blood, skin, kidney, eyes, etc., because of its anti-inflammatory properties. Prednisone is used as a replacement for cortisol (a steroid produced by the adrenal glands in our body), when adrenal glands fail to produce enough hormone required for our body. Prednisone provides relief in case of most of the diseases that involve internal inflammation such as inflammation of digestive tract, severe poison ivy dermatitis, severe asthma, and systemic lupus erythematosus, etc. Prednisone is primarily a steroid and so, it does have both positive as well as negative effects on our health. 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