Heme/Onc Pharm Flashcards
Can be used to prevent mast cell degranulation
Cromolyn sodium Pharmacology Heme/Onc
Treatment of lead poisoning
Dimercaprol and EDTA, succimer in kids Pharmacology Heme/Onc
Heparin (mechanism, use, toxicity)
Activates antithrombin, which inactivates thrombin and Xa; used for immediate coagulation and in pregnant women; some patients develop antibodies to platelet factor 4 (HIT) Pharmacology Heme/Onc
Enoxaparin, dalteparin (mechanism, use, toxicity)
Same actions as heparin, but has a longer half-life, does not have to be monitored as closely, and has a reduced risk of HIT Pharmacology Heme/Onc
Warfarin (mechanism, use, toxicity)
Inactivated gamma-carboxylation of factors II, VII, IX, X, C, and S; used for long-term and non-immediate anticoagulation; can cause tissue necrosis, teratogenic Pharmacology Heme/Onc
Alteplase, reteplase, tenecteplase (mechanism, use, toxicity)
Converts plasminogen to plasmin; used as a thrombolytic Pharmacology Heme/Onc
Aspirin (mechanism, use, toxicity)
Irreversibly inhibits COX-1 and COX-2; anti-platelet and anti-inflammatory; gastric ulcers, tinnitus, Reye’s syndrome in childhood viral infections Pharmacology Heme/Onc
Clopidogrel, ticlodipine, prasugrel, ticagrelor (mechanism, use, toxicity)
Irreversibly blocks ADP receptors on platelets, preventing degranulation; used for acure coronary syndrome; ticlodipine causes neutropenia Pharmacology Heme/Onc
Cilostazol, dipyridamole (mechanism, use, toxicity)
Phosphodiesterase inhibitor, increases cAMP and decreases ADP, preventing platelet degranulation; nausea, headache, facial flushing, hypotension Pharmacology Heme/Onc
Abciximab, eptifibatide, tirofiban (mechanism, use, toxicity)
GPIIb/IIIa inhibitors, preventing platelet aggregation; bleeding, thrombocytopenia Pharmacology Heme/Onc
Methotrexate (mechanism, use, toxicity)
Inhibits dihydrofolate reductase, inhibiting DNA synthesis; myelosuppression, macrovesicular fatty change in liver Pharmacology Heme/Onc
5-fluorouracil (mechanism, use, toxicity)
Pyrimidine analog that is activated and inhibits thymidylate synthase, inhibiting DNA synthesis; myelosuppression, photosensitivity Pharmacology Heme/Onc
Cytarabine (mechanism, use, toxicity)
Pyrimidine analog that inhibits DNA polymerase; leukopenia, thrombocytopenia, megaloblastic anemia Pharmacology Heme/Onc
Azathioprine, 6-mercaptopurine, 6-thioguanine (mechanism, use, toxicity)
Purine analogs that are activated by HGPRT and inhibit purine synthesis; toxicity is increased with allopurinol, causes bone marrow, GI, and liver toxicity Pharmacology Heme/Onc
Dactinomycin (actinomycin D) (mechanism, use, toxicity)
DNA intercalator; used for childhood tumors; myelosuppression Pharmacology Heme/Onc
Doxorubicin (Adriamycin), daunorubicin (mechanism, use, toxicity)
Generates free radicals that cause DNA strand breaks; dilated cardiomyopathy, myelosuppression, alopecia Pharmacology Heme/Onc
Bleomycin (mechanism, use, toxicity)
Generates free radicals that cause DNA strand breaks; pulmonary fibrosis with minimal myelosuppression Pharmacology Heme/Onc
Cyclophosphamide, ifosfamide (mechanism, use, toxicity)
Crosslinks DNA (must be activated by liver); myelosuppression, hemhorragic cystitis (can be minimized with mesna) Pharmacology Heme/Onc
Carmustine, lomustine, semustine, streptozocin (mechanism, use, toxicity)
Used to treat CNS tumors Pharmacology Heme/Onc
Busulfan (mechanism, use, toxicity)
Alkylates DNA; pulmonary fibrosis, hyperpigmentation Pharmacology Heme/Onc
Vincristine, vinblastine (mechanism, use, toxicity)
Block microtubule polymerization; vincristine causes neurotoxicity, vinblastine causes bone marro suppression Pharmacology Heme/Onc
Paclitaxel (mechanism, use, toxicity)
Blocks microtubule breakdown; myelosuppression Pharmacology Heme/Onc
Cisplatin, carboplatin (mechanism, use, toxicity)
Crosslinks DNA; nephrotoxicity (minimize with chloride diuresis, amifostine), acoustic n. damage Pharmacology Heme/Onc
Etoposide, teniposide (mechanism, use, toxicity)
Inhibits topoisomerase II; myelosuppression, GI upset, alopecia Pharmacology Heme/Onc
Hydroxyurea (mechanism, use, toxicity)
Inhibits ribonucleotide reductase; used in cancers and HbSS disease; bone marrow suppression Pharmacology Heme/Onc
Prednisone (mechanism, use, toxicity)
Unknown but may trigger apoptosis in dividing cells; Cushingoid symptoms Pharmacology Heme/Onc
Tamoxifen, raloxifene (mechanism, use, toxicity)
Prevents estrogen receptor binding; used in breast cancer and prevention of osteoporosis; tamoxifen increases the risk of endometrial cancer due to agonist effects Pharmacology Heme/Onc
Trastuzumab (mechanism, use, toxicity)
Antibody against HER-2 receptor; cardiotoxicity Pharmacology Heme/Onc
Imatinib (mechanism, use, toxicity)
Antibody against bcr-abl tyrosine kinase Pharmacology Heme/Onc
Rituximab (mechanism, use, toxicity)
Antibody against CD20; used to treat non-Hodgkin’s lymphoma and rheumatoid arthritis Pharmacology Heme/Onc
Vemurafenib (mechanism, use, toxicity)
B-raf kinase inhibitor (V600 mutation); used in metastatic melanoma Pharmacology Heme/Onc
Bevacizumab (mechanism, use, toxicity)
Antibody against VEGF Pharmacology Heme/Onc