Page 11 - RxExam's Naplex Theory Book Part 2
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                                Dose               Special Notes

                Epoetin beta                       2). Epoetin beta methoxy polyethylene glycol (Mircera) is NOT
                methoxy                            indicated for the treatment of anemia due to cancer chemotherapy.
                propylene glycol
                (Injection)
                                                   3). Patients experienced greater risks for death and serious
                                                   cardiovascular events when administered erythropoiesis-stimulating
                                                   agents (ESAs) to target higher versus lower hemoglobin levels (13.5 vs.
                                                   11.3 g/dL; 14 vs. 10 g/dL) in two clinical studies. Individualize dosing to
                                                   achieve and maintain hemoglobin levels within the range of 10 to 12 g/dL.

                                                   4). ESAs, including Epoetin beta methoxy polyethylene glycol
                                                   (Mircera), shortened overall survival and/or time-to-tumor
                                                   progression in clinical studies in patients with advanced breast, head
                                                   and neck, lymphoid and non-small cell lung malignancies when dose to
                                                   a target hemoglobin of ≥ 12 g/dL.

                                                   5). An increased incidence of deep vein thrombosis, serious
                                                   cardiovascular events and strokes (especially in chronic renal failure
                                                   patients), pure red cell aplasia (PRCA), severe anemia, hypertension
                                                   and seizure are reported side effects of Epoetin beta methoxy
                                                   polyethylene glycol (Mircera).

                B). Colony Stimulating Factors (CSF)

                Filgrastim      1. MC:             1). Filgrastim (Neupogen) is a human granulocyte colony-stimulating
                (Injection)     5 mcg/kg/day‚      factor (G-CSF) produced by recombinant DNA technology. Filgrastim
                                given as a single   (Neupogen) is produced by Escherichia coli (E coli) bacteria into which
                                daily injection by   the human granulocyte colony-stimulating factor gene has been
                                SC bolus injection‚  inserted. Colony-stimulating factors are glycoproteins which act on
                                by short IV infusion  hematopoietic cells by binding to specific cell surface receptors and
                                (15 to 30 minutes)‚  stimulating proliferation‚ differentiation commitment‚ and some end-
                                or by continuous   cell functional activation.
                                SC or continuous
                                IV infusion.       2). Filgrastim (Neupogen) is indicated to reduce the duration of
                                                   neutropenia and neutropenia-related clinical sequelae‚ eg‚ febrile
                                2. BMT:            neutropenia‚ in:
                                10 mcg/kg/day
                                given as an IV     a). Cancer patients receiving myelosuppressive chemotherapy (MC)
                                infusion of 4 or 24  b). Patients with acute myeloid leukemia receiving induction or
                                hours‚ or as a     consolidation chemotherapy (AML)
                                continuous 24-     c). Cancer patients receiving bone marrow transplant (BMT)
                                hour SC infusion.    d). Patients undergoing peripheral blood progenitor cell collection and
                                                   therapy (PBPC)
                                                   e). Patients with congenital‚ cyclic‚ or idiopathic neutropenia.




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