Aranesp prescribing information

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Actual: Doses of Aranesp are titrated based on Hb values. Refer to the prescribing information regarding increasing, reducing, interrupting, or
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In order to prescribe and/or dispense Aranesp to patients with cancer and anemia due to myelosuppressive chemotherapy, prescribers and hospitals must enroll in

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These highlights do not include all the information needed to use ARANESP safely and effectively. See full prescribing information for ARANESP. ARANESP (darbepoetin alfa) i njection, for intravenous or subcutaneous use Initial U.S. Approval: 2024

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Clinical Policy: Darbepoetin Alfa (Aranesp). Reference Number: IL.ERX Aranesp Prescribing Information. Thousand Oaks, CA: Amgen Inc

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See full prescribing information for ARANESP. ARANESP (darbepoetin alfa ) i njection, for intravenous or subcutaneous use Initial U.S. Approval: 2024 WARNING: ESAs INCREASE THE RISK OF DEATH, MYOCARDIAL INFARCTION, STROKE, VENOUS THROMBOEMBOLISM, THROMBOSIS OF VASCULAR ACCESS AND TUMOR PROGRESSION OR RECURRENCE

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ARANESP 150 ?G; ARANESP 20 ?G; ARANESP 30 ?G; ARANESP 300 ?G; ARANESP 40 ?G CLAZEN XL 500MG; CLENIDERM; CLENIL FORTE; CLEREGIL AD; CLEREGIL ENF; CLIACIL

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EC Agrees to Amended Aranesp Prescribing Information Stipulating a uniform target hemoglobin range of 10–12 grams per deciliter; Providing

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Patients should be informed of the possible side effects of Aranesp and be instructed to report them to the prescribing physician. caregivers, including

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EU Commission Approves Updated Prescribing Information for Aranesp(R) THOUSAND OAKS, Calif.-(BUSINESS WIRE)-Ma-Amgen (NASDAQ: AMGN) today announced that the European Commission reached its final decision to amend the prescribing information for Aranesp(R) (darbepoetin alfa) based on the positive opinion from the European Committee for Medicinal Products for Human Use (CHMP) in

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The FDA has released the REMS requirements for the ESA products, Epogen/Procrit and Aranesp, and the risks can be communicated by the current product prescribing information.

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