Page 12 - RxExam's Naplex Theory Book Part 2
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                                Dose               Special Notes

                Filgrastim      3. PBPC:           3). A CBC and platelet count should be obtained before instituting
                (Injection)     10 mcg/kg/day SC‚  Filgrastim (Neupogen) therapy‚ and monitored twice weekly during
                                either as a bolus   therapy.
                                or a continuous
                                infusion.          4). For patients receiving bone marrow transplant (BMT)‚ the first dose
                                                   of Filgrastim (Neupogen) should be administered at least 24 hours
                                4. Congenital      after cytotoxic chemotherapy and at least 24 hours after bone marrow
                                neutropenia:       infusion.
                                6 mcg/kg BID SC
                                every day.         5). Nausea, vomiting, hypertension, rash, cutaneous vasculitis, acute
                                                   respiratory distress syndrome, splenic rupture, alveolar hemorrhage
                                5. Idiopathic or   and hemoptysis, sickle cell crisis and sweet's syndrome (acute febrile
                                Cyclic Neutropenia   neutrophilic dermatosis) are reported with Filgrastim (Neupogen)
                                5 mcg/kg as a      therapy.
                                single injection SC
                                every day.

                Pegfilgrastim   Febrile neutropenia:  1). Pegfilgrastim (Neulasta) is a covalent conjugate of recombinant
                (Injection)                        methionyl human G-CSF (Filgrastim) and monomethoxypolyethylene
                                6 mg via SC given   glycol.
                                once per
                                chemotherapy       2). Pegfilgrastim (Neulasta) is indicated to decrease the incidence of
                                cycle.             infection, as manifested by febrile neutropenia, in patients with non-
                                                   myeloid malignancies receiving myelosuppressive anti-cancer drugs
                                                   associated with a clinically significant incidence of febrile neutropenia.

                                                   3). The 6 mg fixed-dose formulation should not be used in infants,
                                                   children, and smaller adolescents weighing less than 45 kg.

                                                   4). Pegfilgrastim (Neulasta) should NOT be administered in the period
                                                   between 14 days before and 24 hours after administration of cytotoxic
                                                   chemotherapy.

                                                   5). Nausea, vomiting, hypertension, rash, cutaneous vasculitis, acute
                                                   respiratory distress syndrome, splenic rupture, alveolar hemorrhage
                                                   and hemoptysis, sickle cell crisis and sweet's syndrome (acute febrile
                                                   neutrophilic dermatosis) are reported with Filgrastim (Neupogen)
                                                   therapy.

                Sargramostim    250 mcg/m²/day     1). Sargramostim (Leukine) is a recombinant human granulocyte
                (Injection)     administered IV or  macrophage colony stimulating factor (Rhu GM-CSF) produced by
                                SC depend on the   recombinant DNA technology in a yeast (S. cerevisiae) expression
                                conditon treated.   system. GM-CSF is a hematopoietic growth factor which stimulates
                                                   proliferation and differentiation of hematopoietic progenitor cells.



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