单词 | carboplatin |
释义 | carboplatincarboplatin[¦kär·bō′plat·ən]carboplatincarboplatin[kahr″bo-plat´in]carboplatinPharmacologic class: Alkylating agent Therapeutic class: Antineoplastic Pregnancy risk category D FDA Box Warning• Give under supervision of physician experienced in cancer chemotherapy, in facility with adequate diagnostic and treatment resources. • Bone marrow suppression is dose-related and may be severe, resulting in infection and bleeding. Anemia may be cumulative and warrant transfusions. • Vomiting is a common adverse effect. • Anaphylactic-like reactions may occur within minutes of administration. ActionInhibits DNA synthesis by causing cross-linking of parent DNA strands; interferes with RNA transcription, causing growth imbalance that leads to cell death. Cell-cycle-phase nonspecific. AvailabilityInjection: 50-mg, 150-mg, and 450-mg vials Indications and dosages➣ Initial treatment of advanced ovarian cancer or palliative treatment of ovarian cancer unresponsive to other chemotherapeutic modalities Adults: Initially, 300 mg/m2 I.V. (given with cyclophosphamide) at 4-week intervals. For refractory tumors, 360 mg/m2 I.V. as a single dose; may be repeated at 4-week intervals, depending on response. However, single dose shouldn't be repeated until neutrophil count is at least 2,000/mm3 and platelet count at least 100,000/mm3. Subsequent dosages are based on blood counts. Dosage adjustment• Renal impairment • Reduced bone marrow reserve Off-label uses• Advanced endometrial cancer • Advanced or recurrent squamous cell carcinoma of head and neck • Relapsed and refractory acute leukemia • Small-cell lung cancer • Testicular cancer Contraindications• Hypersensitivity to drug, cisplatin, or mannitol • Pregnancy or breastfeeding PrecautionsUse cautiously in: • hearing loss, electrolyte imbalances, renal impairment, active infections, diminished bone marrow reserve • females of childbearing age. Administration• Premedicate with antiemetics, as prescribed. • When preparing and administering drug, follow facility protocol for handling cytotoxic drugs. • Reconstitute powder for injection by adding sterile water for injection, 0.9% sodium chloride injection, or 5% dextrose injection, as appropriate, to provide 10-mg/ml solution. Drug may be further diluted to concentrations as low as 0.5 mg/ml. • Don't use with needles or I.V. sets containing aluminum. • Administer I.V. infusion over at least 15 minutes. • Make sure patient maintains adequate fluid intake. • Know that drug is given in combination with other agents. ![]() Adverse reactionsCNS: weakness, dizziness, confusion, peripheral neuropathy, cerebrovascular accident CV: heart failure, embolism EENT: visual disturbances, ototoxicity GI: nausea, vomiting, constipation, diarrhea, abdominal pain, stomatitis GU: gonadal suppression, nephrotoxicity Hematologic: anemia, leukopenia, thrombocytopenia, neutropenia Hepatic: hepatitis Metabolic: hypocalcemia, hypokalemia, hypomagnesemia, hyponatremia Respiratory: bronchospasm Skin: alopecia, rash, urticaria, erythema, pruritus Other: altered taste, hypersensitivity reactions, anaphylaxis InteractionsDrug-drug. Live-virus vaccines: decreased antibody response to vaccine, increased risk of adverse reactions Myelosuppressants: additive bone marrow depression Nephrotoxic or ototoxic drugs (such as aminoglycosides, loop diuretics): additive nephrotoxicity or ototoxicity Phenytoin: decreased phenytoin blood level Drug-diagnostic tests. Alkaline phosphatase (ALP), aspartate aminotransferase (AST), blood urea nitrogen, creatinine: increased values Electrolytes, hematocrit, hemoglobin. neutrophils, platelets, red blood cells, white blood cells: decreased values Patient monitoring• Assess for signs and symptoms of hypersensitivity reactions. • Monitor CBC to help detect drug-induced anemia and other hematologic reactions. • Monitor ALP, AST, and total bilirubin levels. • Evaluate fluid and electrolyte balance. Patient teaching• Instruct patient to report signs and symptoms of allergic response and other adverse reactions, such as breathing problems, mouth sores, rash, itching, and reddened skin. • Advise patient to report unusual bleeding or bruising. • Caution patient to avoid driving and other hazardous activities until he knows how drug affects concentration and alertness. • Urge patient to avoid activities that can cause injury. Advise him to use soft toothbrush and electric razor to avoid gum and skin injury. • Instruct patient to drink plenty of fluids to ensure adequate urinary output. • Provide dietary counseling and refer patient to dietitian as needed if GI adverse effects significantly limit food intake. • As appropriate, review all other significant and life-threatening adverse reactions and interactions, especially those related to the drugs and tests mentioned above. car·bo·plat·in(kar'bō-pla-tin),carboplatin(kär′bō-plăt′n)carboplatinA chemotherapeutic agent used to manage advanced ovarian, lung, head and neck and other cancers; it interacts with DNA in a manner similar to that of alkylating agents.Adverse effects Myelosuppression, nausea, vomiting diarrhoea, hair loss, pain, neurologic complaints. carboplatinOncology A chemotherapeutic for advanced ovarian and other CAs Adverse effects Cytopenias, nausea, diarrhea, hair loss, pain, neurologic complaintscar·bo·plat·in(kahr'bō-plat'in)carboplatinAn anticancer drug. A brand name is Paraplatin. |
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