Prelone
Noun | 1. | Prelone - a glucocorticoid (trade names Pediapred or Prelone) used to treat inflammatory conditions |
单词 | prelone | |||||||||||
释义 | Prelone
Preloneprednisoloneprednisolone acetateprednisolone sodium phosphatePharmacologic class: Corticosteroid (intermediate-acting) Therapeutic class: Anti-inflammatory, immunosuppressant Pregnancy risk category C ActionExerts potent anti-inflammatory (glucocorticoid) and weak sodium-retaining (mineralocorticoid) activity. Glucocorticoid activity causes profound and varied metabolic effects. AvailabilityOral solution: 5 mg/ml Suspension for injection (acetate): 25 mg/ml, 40 mg/ml, 50 mg/ml Suspension (ophthalmic): 0.12%, 0.125%, 1% Syrup: 5 mg/5 ml, 15 mg/5 ml Tablets: 5 mg Tablets (orally disintegrating, sodium phosphate): 10 mg, 15 mg, 30 mg Indications and dosages➣ Severe inflammation; immunosuppression Adults: Dosage individualized based on diagnosis, severity of condition, and response. Usual dosage ranges from 5 to 60 mg P.O. (prednisolone) daily in two to four divided doses, or 4 to 60 mg I.M. (acetate) daily in divided doses, or 5 to 50 mg P.O. (sodium phosphate) daily in divided doses. ➣ Acute exacerbation of multiple sclerosis Adults: 200 mg P.O. daily for 1 week, followed by 80 mg every other day for 1 month ➣ Refractory bronchial asthma Children: 1 to 2 mg/kg/day (sodium phosphate) as a single dose or in divided doses; may continue for 3 to 10 days or until symptoms resolve or patient achieves peak expiratory flow rate of 80% of personal best ➣ Nephrotic syndrome in children Children: 60 mg/m2 P.O. (sodium phosphate solution) daily in three divided doses for 4 weeks, then 4 weeks of alternate-day therapy at single doses of 40 mg/m2 ➣ Various allergic conditions and dermatologic, endocrine, GI, hematologic, neoplastic, nervous system, ophthalmic, respiratory, and rheumatic disorders Adults: Variable and individualized depending on condition being treated and patient response. Initially, 10 to 60 mg (ODT) P.O. daily. Children: Variable and individualized depending on condition being treated. Initial dosage range is 0.14 to 2 mg/kg/day P.O. in three or four divided doses. ➣ Steroid-responsive inflammatory eye conditions Adults: In severe cases, initially one to two drops (acetate or sodium phosphate) instilled into conjunctival sac q hour during day and q 2 hours at night. In mild or moderate inflammation or in severe cases that respond favorably, one to two drops q 3 to 12 hours. Contraindications• Hypersensitivity to drug, other corticosteroids, alcohol, bisulfite, or tartrazine (with some products) • Systemic fungal infections • Active untreated infections (except in selected patients with meningitis) • Acute superficial herpes simplex, keratitis, fungal or viral eye diseases, tuberculosis of eye, or after uncomplicated removal of superficial corneal foreign body (ophthalmic use) • Idiopathic thrombocytopenic purpura (with I.M. use) • Live-virus vaccines (with immunosuppressive prednisolone dosages) PrecautionsUse 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, ocular herpes simplex, immunosuppression, emotional instability • pregnant or breastfeeding patients • children younger than age 6 (younger than age 2 when treated for nephrotic syndrome; younger than age 1 month when treated for aggressive lymphomas and leukemias with ODT form). AdministrationSee Be aware that prednisolone has many different formulations that may be given by various routes: P.O., I.M., or ophthalmic. Before administering, make sure formulation can be given by prescribed route. • Don't break ODT tablets. • Place ODT tablet on tongue and either swallow tablet whole or allow it to dissolve in mouth with or without water. • Inject I.M. form deep into gluteal muscle. Rotate injection sites. • Avoid subcutaneous injection. See In systemic therapy, don't discontinue drug abruptly, even if inhaled steroid is added. • Know that additional corticosteroids are needed during stress or trauma. Adverse reactionsCNS: headache, nervousness, depression, euphoria, personality changes, psychosis, vertigo, paresthesia, insomnia, restlessness, seizures, meningitis, increased intracranial pressure, hypertrophic cardiomyopathy in premature infants CV: hypotension, hypertension, vasculitis, thrombophlebitis, thrombo-embolism, fat embolism, arrhythmias, heart failure, shock EENT: cataracts, glaucoma, visual disturbances, exacerbation of ocular infection, secondary ocular infections, globe perforation at corneal or scleral thinning site, transient stinging or burning of eyes, dry eyes, corneal ulcers, mydriasis (all with ophthalmic use); 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 (with long-term use) GI: nausea, vomiting, abdominal distention, rectal bleeding, dry mouth, esophageal candidiasis, esophageal ulcer, pancreatitis, peptic ulcer GU: amenorrhea, irregular menses Hematologic: purpura Metabolic: sodium and fluid retention, hypokalemia, hypocalcemia, hyper-glycemia, decreased carbohydrate tolerance, growth retardation (in children), diabetes mellitus, cushingoid effects (with long-term use), hypothal-amic-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, bron-chospasm Skin: urticaria, rash, pruritus, contact dermatitis, acne, striae, poor wound healing, thin fragile skin, bruising, hir-sutism, petechiae, subcutaneous fat atrophy, urticaria, angioedema Other: aggravation or masking of infections, increased or decreased appetite, weight gain (with long-term use), facial edema and erythema, edema, hypersensitivity reaction InteractionsDrug-drug. Amphotericin B, mezlocillin, piperacillin, thiazide and loop diuretics, ticarcillin: additive hypokalemia Anticholinesterase drugs: decreased anticholinesterase effect (when prednisolone is used for myasthenia gravis) 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 prednisolone blood level and effects Hormonal contraceptives: impaired metabolism and increased effects of prednisolone Isoniazid: decreased isoniazid blood level Live-virus vaccines: decreased antibody response to vaccine, increased risk of adverse effects Oral anticoagulants: reduced anticoagulant requirement, opposition to anticoagulant action Phenobarbital, phenytoin, rifampin: decreased prednisolone efficacy Salicylates: reduced salicylate blood level Somatrem: inhibition of somatrem's growth-promoting effects Theophylline: altered pharmacologic effects of either drug Skin tests: suppressed results Drug-diagnostic tests. Calcium, potassium, thyroid 131I uptake, thyroxine, tri-iodothyronine: decreased levels Cholesterol, glucose: increased levels Nitroblue tetrazolium test for bacterial infection: false-negative result Skin tests: suppressed results 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 Patient monitoring• Monitor weight, blood pressure, and electrolyte levels. • Watch for cushingoid effects (moon face, central obesity, buffalo hump, hair thinning, high blood pressure, frequent infections). See Assess patient for depression and psychosis. • Monitor blood glucose level carefully in diabetic patient. • Evaluate for signs and symptoms of infection, which drug may mask or exacerbate. See Monitor for signs and symptoms of early adrenal insufficiency (fatigue, weakness, joint pain, fever, anorexia, shortness of breath, dizziness, syncope). • Assess musculoskeletal status for joint, tendon, and muscle pain. Patient teaching• Tell patient to take oral dose with food or milk to reduce GI upset. • Instruct patient to remove ODT tablet from blister just before taking. • Instruct patient to place ODT tablet on tongue and either swallow tablet whole or allow it to dissolve in mouth with or without water. Caution patient not to cut, split, or break tablet. See Teach patient to recognize and immediately report cushingoid effects and signs and symptoms of early adrenal insufficiency. See Advise patient and significant other to immediately report depression or psychosis. • Explain that drug increases risk of infection. Instruct patient to contact prescriber at first sign of infection. See Caution patient not to suddenly stop drug (including ophthalmic forms). Instruct him to discuss any changes in therapy with prescriber. See Tell patient to immediately report bleeding or joint, muscle, tendon, or abdominal pain. • Inform patient that he may need higher dosage during periods of stress. Encourage him to wear or carry medical identification stating this. • Tell patient to avoid vaccinations during therapy. Mention that others in household shouldn't receive oral polio vaccine because they could pass poliovirus to him. • Caution patient not to take over-the-counter drugs or herbs during therapy. • Teach patient how to use eye drops. Caution him not to touch dropper tip to eye or any other surface. • As appropriate, review all other significant and life-threatening adverse reactions and interactions, especially those related to the drugs, tests, herbs, and behaviors mentioned above. prednisoLONE(pred-niss-oh-lone) prednisolone,Flo-Pred(trade name),Orapred(trade name),Orapred ODT(trade name),Pediapred(trade name),Prelone(trade name)ClassificationTherapeutic: anti inflammatories steroidalIndications
ActionTherapeutic effectsPharmacokineticsTime/action profile (anti-inflammatory activity)
Contraindications/PrecautionsAdverse Reactions/Side EffectsAdverse reactions/side effects are much more common with high-dose/long-term therapyCentral nervous system
Ear, Eye, Nose, Throat
Cardiovascular
Gastrointestinal
Dermatologic
Endocrinologic
Fluid and Electrolyte
Hematologic
Metabolic
Musculoskeletal
Miscellaneous
InteractionsDrug-Drug interactionAdditive hypokalemia with thiazide and loop diuretics, amphotericin B, piperacillin, or ticarcillin.Hypokalemia may ↑ risk of digoxin toxicity.May ↑ requirement for insulin or oral hypoglycemic agents.Phenytoin, phenobarbital, and rifampin stimulate metabolism; may ↓ effectiveness.Oral contraceptives may ↓ metabolism.↑ risk of adverse GI effects withNSAIDs (including aspirin ).At chronic doses that suppress adrenal function, may ↓ antibody response to and ↑ risk of adverse reactions from live-virus vaccines.May ↑ risk of tendon rupture from fluoroquinolones.Route/DosageAvailability (generic available)Nursing implicationsNursing assessment
Potential Nursing DiagnosesRisk for infection (Side Effects)Disturbed body image (Side Effects) Deficient knowledge, related to medication regimen (Patient/Family Teaching) Implementation
Patient/Family Teaching
Evaluation/Desired Outcomes
Prelone(prē′lōn′)Prelone®Prednisone, see there.Prelone
Synonyms for Prelone
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