单词 | neupogen |
释义 | NeupogenNeu·po·genN5078850 (no͞o′pə-gĕn′, -gən, nyo͞o′-)NeupogenNeupogen[noo´po-jen]filgrastimPharmacologic class: Granulocyte colony-stimulating factor Therapeutic class: Hematopoietic stimulator, antineutropenic Pregnancy risk category C ActionInduces formation of neutrophil progenitor cells by binding directly to receptor on surface granulocyte, stimulating cell proliferation and differentiation. Also potentiates effects of mature neutrophils and reduces fever and risk of infection associated with severe neutropenia. AvailabilitySingleJect prefilled syringes: 300 mcg, 480 mcg Vial for injection: 300 mcg/ml, 480 mcg/1.6 ml Indications and dosages➣ To prevent infection after myelosuppressive chemotherapy Adults: 5 mcg/kg/day by subcutaneous injection or I.V. infusion over 15 to 30 minutes, or continuous subcutaneous or continuous I.V. infusion, increased by 5 mcg/kg with each chemotherapy cycle if needed ➣ Neutropenia after bone marrow transplantation Adults: 10 mcg/kg/day I.V. over 4 or 24 hours or as a continuous subcutaneous infusion over 24 hours ➣ To enhance peripheral blood progenitor cell collection in autologous hematopoietic stem cell transplantation Adults: 10 mcg/kg/day by subcutaneous injection or as continuous subcutaneous infusion, starting 4 days before first leukapheresis procedure and continuing until last day of leukapheresis ➣ Neutropenia in congenital neutropenia Adults: 6 mcg/kg subcutaneously b.i.d. ➣ Neutropenia in idiopathic or cyclic neutropenia Adults: 5 mcg/kg/day subcutaneously Off-label uses• AIDS • Aplastic anemia • Hairy cell leukemia • Myelodysplasia Contraindications• Hypersensitivity to drug, its components, or Escherichia coli-derived proteins PrecautionsUse cautiously in: • patients receiving lithium or other drugs that can potentiate neutrophil release • breastfeeding patients. Administration• Know that drug may be injected into venous return line of dialysis tubing after dialysis is completed. See To dilute for I.V. administration, use dextrose 5% in water. Never use saline solution, because it may cause drug to precipitate. • Administer single dose intermittently over 15 to 30 minutes or by continuous infusion over 4 to 24 hours. • Don't mix with other drugs, and don't shake. • Don't give within 24 hours of chemotherapy, bone marrow transplantation, or radiation therapy. Adverse reactionsCNS: headache, weakness CV: chest pain, hypotension, transient supraventricular tachycardia, myocardial infarction, arrhythmias EENT: sore throat GI: nausea, vomiting, diarrhea, constipation, abdominal pain, splenomegaly, stomatitis GU: bleeding Hematologic: leukocytosis, sickle cell crisis, thrombocytopenia, splenic rupture Metabolic: hyperuricemia Musculoskeletal: bone, joint, muscle, arm, or leg pain Respiratory: dyspnea, cough Skin: pruritus, rash, erythema, alopecia, cutaneous necrotic vasculitis Other: fever, mucositis, pain at injection site, edema, hypersensitivity reactions InteractionsDrug-drug. Lithium: increased neutrophil production Topotecan: prolonged neutropenia Vincristine: increased risk of severe atypical peripheral neuropathy Drug-diagnostic tests. Alkaline phosphatase, creatinine, lactate dehydrogenase, uric acid: increased levels Platelets: decreased count Patient monitoring• Obtain CBC with platelet count before starting therapy; monitor these counts often thereafter. • Monitor cardiovascular status carefully. • Assess for signs and symptoms of sickle cell crisis and splenic rupture. Patient teaching• Teach patient how to recognize and promptly report signs and symptoms of allergic response. • Caution patient to avoid driving and other hazardous activities until he knows how drug affects concentration and alertness. • Advise patient to discuss possible need for iron supplements, vitamin B12, and folic acid with prescriber. • Teach patient how to monitor blood pressure at home. • Advise patient to minimize GI upset by eating small, frequent servings of food and drinking adequate fluids. • Tell female patient to inform prescriber if she is breastfeeding. • Inform patient that he'll undergo regular blood testing during therapy. • As appropriate, review all other significant and life-threatening adverse reactions and interactions, especially those related to the drugs and tests mentioned above. Neupogen®Filgrastim Oncology An agent used to ↓ neutrophil recovery time and duration of fever after chemotherapy for AML. See Acute myelogenous leukemia.NeupogenA brand name for FILGRASTIM. |
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