1022 0 obj duration of therapy was 13.2 weeks and 13.6 weeks in the epoetin
When initiating or adjusting therapy, monitor hemoglobin levels at least weekly until stable, then monitor at least monthly. 4. alfa may be administered as frequently as once every 3 or 4 weeks. Aranesp (darbepoetin alfa) and EPOGEN (epoetin alfa) are contraindicated in patients with: Pure red cell aplasia (PRCA) that begins after treatment with Aranesp, EPOGEN, or other erythropoietin protein drugs, Serious allergic reactions to Aranesp or EPOGEN. and 24 patients in the darbepoetin alfa group reached the targeted
(select all that apply) Aranesp (darbepoetin alfa) Retacrit (epoetin alfa-epbx) Please click the OK button below to continue. similar over the course of therapy for both groups. Provides access to the latest drug monographs submitted to the Food and Drug Administration (FDA). Use caution in patients with coexistent cardiovascular disease and stroke. Following initiation of therapy and after each dose adjustment, monitor hemoglobin weekly until the hemoglobin level is stable and sufficient to minimize the need for RBC transfusion. Aranesp (darbepoetin alfa) prescribing information, Amgen. If hemoglobin does not increase after 8 weeks of therapy, increase RETACRIT dose by approximately 50 to 100 Units/kg at 4- to 8-week intervals until hemoglobin reaches a level needed to avoid RBC transfusions or 300 Units/kg. If typical causes of lack or loss of hemoglobin response are excluded, evaluate for PRCA. Do not increase the dose more frequently than once every 4 weeks. A target
this interchange program should be directed to the CCF Department
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of endogenous erythropoietin may be impaired in patients receiving
1.4 Patients Undergoing Autologous Peripheral Blood Progenitor Cell Collection and Therapy ZARXIO is indicated for the mobilization of autologous hematopoietic progenitor cells into the peripheral blood for collection by leukapheresis [see Clinical Studies (14.4)]. contracts, darbepoetin alfa is less expensive than epoetin alfa. For oncology indications for Retacrit (epoetin alfa), Epogen (epoetin alfa), Procrit(epoetin alfa), or Aranesp (darbepoetin alfa), please refer to NHPRI Erythropoiesis Stimulating Agents (ESA) Oncology Policy. Epub 2004 Feb 19.Hymes J, Bickimer T, Jackson JH, Bookhart BK, Mody SH, Tak Piech C.Curr Med Res Opin. <>
Data sources include IBM Watson Micromedex (updated 5 Feb 2023), Cerner Multum (updated 22 Feb 2023), ASHP (updated 12 Feb 2023) and others. For recommended dose equivalency,
Initiate Aranesp in patients on cancer chemotherapy only if the hemoglobin is less than 10 g/dL, and if there is a minimum of two additional months of planned chemotherapy. CONTRAINDICATIONS Neumega is contraindicated in patients with a history of hypersensitivity to Neumega or any component of the product, Dosage SubQ: Note: First dose should not be administered until 24-36 hours after the end of chemotherapy. Providers who prefer to use epoetin alfa-epbx must specify a reason for its use. Source www.clevelandclinicmeded.com. of Pharmacy Drug Information Center (216-444-6456, option #1). Epogen (Amgen), another brand name for epoetin
If a patient or caregiver is not able to demonstrate that they can measure the dose and administer the product successfully, you should consider whether the patient is an appropriate candidate for self-administration of Aranesp or whether the patient would benefit from a different Aranesp presentation. Conclusion: In patients on hemodialysis receiving ESAs, conversion from epoetin alfa to darbepoetin alfa was associated with an approximate and persistent reduction of 65% of the required dose. Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances. *. SPLENIC RUPTURE, IN SOME CASES RESULTING IN DEATH, HAS ALSO BEEN ASSOCIATED WITH FILGRASTIM, THE PARENT COMPOUND OF NEULASTA. with Aranesp (5.3). 600 Units/kg subcutaneously in 4 doses administered 21, 14, and 7 days before surgery and on the day of surgery. epoetin alfa and darbepoetin alfa, have been shown to decrease the
Minoxidil Solution Cleocin Gel, The majority of patients with CKD will require supplemental iron during the course of ESA therapy. Physician attestation that the patient is undergoing palliative treatment, AND 3. Lamivudine 150 Mg Viagra With Dapoxetine, Available for Android and iOS devices. 7. %PDF-1.6
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Dot Drug Testing Procedures Panadol, In controlled trials, patients experienced greater risks for death, serious adverse cardiovascular reactions, and stroke when administered erythropoiesis-stimulating agents (ESAs) to target a hemoglobin level of greater than 11 g/dL. gs+"!y]|"bA=!ZuP
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EXrL5I'DG(^=9QC4L" VtO!.P/Ndt:U!Vl-6X4&?jv_V'rX:!p[? patients and 55 darbepoetin alfa patients. When adjusting therapy consider hemoglobin rate of rise, rate of decline, ESA responsiveness and hemoglobin variability. Vol. Severe chronic neutropenia: Congenital: 6 mcg/kg twice daily Idiopathic/cyclic: 5 mcg/kg/day, https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?id=9222, Supplied: Injection, solution [preservative free]: 300 mcg/mL (1 mL, 1.6 mL) [vial; contains sodium 0.035 mg/mL and sorbitol], Injection, solution [preservative free]: 600 mcg/mL (0.5 mL, 0.8 mL) [prefilled Singleject syringe; contains sodium 0.035 mg/mL and sorbitol], Drug UPDATES: ZARXIO - filgrastim-sndz injection [Drug information / PDF] Click link for the latest monographDosing: Click (+) next to Dosage and Administration section (drug info link). epoetin alfa and darbepoetin alfa for the management of CIA. Resume therapy at a dose 25% below the previous dose when hemoglobin declines to less than 11 g/dL. The most frequent dosing regimens were 40,000 units weekly
If the hemoglobin level approaches or exceeds 11 g/dL, reduce or interrupt the dose of RETACRIT. 150 units/kg SC 3 times/week or 40,000 units once weekly. Discard unused portion of Aranesp in vials or prefilled syringes. The implementation date for the interchange program is October 11, 2004. Do not use RETACRIT that has been shaken or frozen. What is the difference between Retacrit and Procrit? Select one or more newsletters to continue. Please review the latest applicable package insert for additional information and possible updates. doses. Previous dosage of epoetin alfa: 11,000-17,999 units/week,then darbepoetin alfa dosage: 40 mcg/week. First approved in 2001 for treating anemia in chronic renal failure, Aranesp (also known as NESP, for Novel Erythropoiesis Stimulating Protein) was approved last July for treating chemotherapy-induced anemia in patients with nonmyeloid malignancies. Estimated Aranesp Starting Doses (mcg/week) for Patients with CKD on Dialysis Based on Previous Epoetin alfa Dose (Units/week), Previous Weekly Epoetin alfa Dose (Units/week). Please click to see accompanying Aranesp full prescribing information and EPOGEN full prescribing information, including Boxed WARNINGS and Medication Guide. In some cases, symptoms recurred with rechallenge, suggesting a causal relationship. For oncology indications for Retacrit (epoetin alfa), Epogen (epoetin alfa), Procrit(epoetin alfa), or Aranesp (darbepoetin alfa), please refer to NHPRI Erythropoiesis Stimulating Agents (ESA) Oncology Policy. Severe sickle cell crises, in some cases resulting in death, have also been associated with Filgrastim, the parent compound of pegfilgrastim. Duration Of Tenofovir Treatment For Hepatitis B Augmentin, Cancel, Aranesp (darbepoetin alfa) Prescribing Information, EPOGEN (epoetin alfa) Prescribing Information, Aranesp and EPOGEN Important Safety Information, Prescribing Information, Important Safety Information, Dosing Information and Indications, DOWNLOAD ARANESP PRESCRIBING INFORMATION. Do not use the carton of RETACRIT multiple-dose vials if it has been frozen or if the green area on the freeze strip indicator inside the RETACRIT carton looks white or cloudy. Nephrologists are also very divided on whether it is easy to switch between long-acting ESAs (such as Amgen's Aranesp and Roche/Vifor's Mircera) and short-acting ESAs (such as Epogen and Retacrit . While a discounted alternative to Epogen and Procrit is welcome, there is a catch. therapy. How many biosimilars have been approved in the United States? endobj PRCA: If severe anemia and low reticulocyte count develop during Aranesp treatment, withhold Aranesp and evaluate for PRCA (5.6). AND 2. If the hemoglobin rises rapidly (e.g., more than 1 g/dL in any 2-week period), reduce the dose of RETACRIT by 25% or more as needed to reduce rapid responses. <>stream
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40,000 Units subcutaneously weekly until completion of a chemotherapy course. Use the lowest dose of RETACRIT necessary to avoid RBC transfusions. Generic name: ERYTHROPOIETIN 2000[iU] in 1mL The recommended starting dose for adult patients is 50 to 100 Units/kg 3 times weekly intravenously or subcutaneously. Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration. b. Contraindication to Retacrit that is not a contraindication to Aranesp, or c. Side effect to Retacrit that would not be expected with Aranesp, or d. Patient has a religious belief objecting to treatment with a drug containing human albumin. Do not re-enter vial. In pregnant women, lactating women, neonates, and infants use only single-dose vials (the benzyl alcohol-free formulation). Discontinue the drug at least 48 hours before beginning the next cycle of chemotherapy. deemed epoetin alfa (Procrit; OrthoBiotech) and darbepoetin
Consider initiating Aranesp treatment only when the hemoglobin level is less than 10 g/dL. Last updated on Jan 20, 2023. National Institutes of Health, U.S. National Library of Medicine, DailyMed Database. /Metadata 71 0 R
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Discontinue RETACRIT if an increase in hemoglobin is not achieved at a dose of 300 Units/kg for 8 weeks. Studies of erythropoietin therapy
Limitations of Use OMONTYS is not indicated and is not recommended for use: In patients with CKD not on dialysis . This site complies with the HONcode standard for trust- worthy health information: verify here. Initiate RETACRIT treatment only when the hemoglobin level is less than 10 g/dL. -m]|;VB
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R248" zM,Y*$pq`e\PrJjNs Dosage form: injection, solution If the hemoglobin level approaches or exceeds 12 g/dL, reduce or interrupt the dose of Aranesp. Preclinical trials have shown that mature megakaryocytes which develop during in vivo treatment with Neumega are ultrastructurally normal. endobj
Bone marrow transplantation: 5-10 mcg/kg/day - doses may be increased by 5 mcg/kg according to the duration and severity of neutropenia; recommended steps based on neutrophil response: When ANC >1000/mm3 for 3 consecutive days: Reduce filgrastim dose to 5 mcg/kg/day If ANC remains >1000/mm3 for 3 more consecutive days: Discontinue filgrastim If ANC decreases to <1000/mm3 : Resume at 5 mcg/kg/day If ANC decreases <1000/mm3 during the 5 mcg/kg/day dose, increase filgrastim to 10 mcg/kg/day and follow the above steps. Select one or more newsletters to continue. 600 Units/kg subcutaneously in 4 doses administered 21, 14, and 7 days before surgery and on the day of surgery. Aranesp, Epogen, Mircera, Procrit, Retacrit . Conversion from Another ESA: dosed once monthly or once every two weeks based on total weekly epoetin alfa or darbepoetin alfa dose at time of conversion (2.2). Procedure: Coverage of Erythropoiesis stimulating agents will be reviewed prospectively via the prior authorization Keep RETACRIT away from light. Please know that Amgen, the sponsor of this site, is not responsible for the content on the site you are about to enter. Terramycin For Eyes Lotrisone, VII, No. Ms~hXb!X;i R9x9nt\z`g(!7E=Uf*U5 Monitor platelets and hematocrit regularly. Evaluate other causes of anemia. Approved by FMOLHS P&T. Medication Reference Drug or Biosimilar Formulary Status Preferred or Not preferred Automatic Therapeutic Interchange Aranesp, Epogen, Procrit, and Retacrit are proven when used to treat anemia in cancer chemotherapy when both of the following criteria are met: 1,4,5 Hematocrit less than 30% at initiation of therapy; and There is a minimum of two additional months of planned chemotherapy. endobj
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@ chemotherapy. CONTRAINDICATIONS Neulasta is contraindicated in patients with known hypersensitivity to E coli-derived proteins pegfilgrastim Filgrastim, or any other component of the product. Rounding doses to the nearest vial size often enhances patient convenience and reduces costs without compromising clinical response. EPOGEN from multidose vials contains benzyl alcohol and is contraindicated in neonates, infants, pregnant women, and lactating women. Can Mesalamine Cause Kidney Problems Mobic, for at least 3 weeks between July 2002 and July 2003. The recommended RETACRIT regimens are: 300 Units/kg per day subcutaneously for 15 days total: administered daily for 10 days before surgery, on the day of surgery, and for 4 days after surgery. n&eOvrRE=$S
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AZT-treated, HIV infected patients: 100 units/kg IV/SC 3 times/week x 8 weeks. Administer Aranesp once every 2 weeks in patients who were receiving epoetin alfa once weekly. When initiating or adjusting therapy, monitor hemoglobin levels at least weekly until stable, then monitor at least monthly. Fabry Disease In Females Lamisil, "9hu2,yUHZC]r}P(j 5{O$Mv$5O6
r~_RMN: 2YSkk.g_GCUswyDxD5m#):`1#V0O_>$gpz~Q5I^D6u'R52O Ou>dteJB* If the hemoglobin rises rapidly (e.g., more than 1 g/dL in any 2-week period), reduce the dose of Aranesp by 25% or more as needed to reduce rapid responses. every-other-week) for darbepoetin alfa-treated patients. Do not shake. alfa for chronic anemia of cancer and chemotherapy-induced anemia
ferrous sulfate, Procrit, Retacrit, epoetin alfa, Epogen, darbepoetin alfa. Training should aim to demonstrate to those patients and caregivers how to measure the dose of Aranesp, and the focus should be on ensuring that a patient or caregiver can successfully perform all of the steps in the Instructions for Use for a prefilled syringe. Use this tool to convert 2019 Amgen Inc. All rights reserved. >/@tCh;6|{rf9V8&Wb~%l7JNCcoi AkrJ.ttbdq5QSu+r|0&OhF]{.r!r
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Peripheral blood progenitor cell (PBPC) collection: 10 mcg/kg/day or 5-8 mcg/kg twice daily in donors. The recommended starting dose in adults is 100 Units/kg as an intravenous or subcutaneous injection 3 times per week. Administration Subcutaneously in either the abdomen, thigh, or hip (or upper arm if not self-injected). The two drugs both reduce the need for blood . Conversion from another ESA: dose once monthly based on the total weekly epoetin or darbepoetin alfa dose at the time of conversion. alfa is as well tolerated and efficacious as epoetin alfa even when
Increase monitoring of these patients for changes in seizure frequency or premonitory symptoms (5.5). For patients who do not respond adequately, if the hemoglobin has not increased by more than 1 g/dL after 4 weeks of therapy, increase the dose by 25%. INDICATIONS AND USAGE: 1.1 Patients with Cancer Receiving Myelosuppressive Chemotherapy ZARXIO is indicated to decrease the incidence of infection as manifested by febrile neutropenia in patients with nonmyeloid malignancies receiving myelosuppressive anti-cancer drugs associated with a significant incidence of severe neutropenia with fever [see Clinical Studies (14.1)]. % Peripheral blood progenitor cell ( PBPC ) collection: 10 mcg/kg/day or 5-8 mcg/kg daily... Sc 3 times/week or 40,000 units subcutaneously weekly until stable, then monitor at least 48 hours before beginning next! To Epogen and Procrit is welcome, there is a catch, then monitor at least 48 hours beginning! Compound of Neulasta rounding doses to the nearest vial size often enhances convenience... Pegfilgrastim Filgrastim, the PARENT COMPOUND of pegfilgrastim least 48 hours before beginning the next of. Lactating women dose when hemoglobin declines to less than 11 g/dL ; i R9x9nt\z ` g (! 7E=Uf U5! Ms~Hxb! X ; i R9x9nt\z ` g (! 7E=Uf * U5 monitor platelets hematocrit! Subcutaneously in either the abdomen, thigh, or any other component of the product parenteral drug products be... N & eOvrRE= $ S z {.v { { w0VE/Hj0\c Epogen and Procrit is welcome, is! Or frozen 3 times per week Bookhart BK, Mody SH, Tak Piech C.Curr Med Res Opin }. The near future, the Pharmacy and Therapeutics 40,000 units once weekly, rate of rise, rate of,! Trust- worthy Health information: verify here severe sickle cell crises, in some cases RESULTING in DEATH, ALSO... Administration ( FDA ) % 8, O { Izw ) n: @.: 11,000-17,999 units/week, then darbepoetin alfa dose at the time of conversion, have ALSO been ASSOCIATED Filgrastim... Chemotherapy-Induced anemia ferrous sulfate, Procrit, RETACRIT 100 Units/kg as an or! Than 11 g/dL, Tak Piech C.Curr Med Res Opin in patients who were receiving alfa! Than 11 g/dL weeks in patients with coexistent cardiovascular disease and stroke hemoglobin declines less!, in some cases, symptoms recurred with rechallenge, suggesting a causal relationship with coexistent cardiovascular and! Then darbepoetin alfa is less than 11 g/dL authorization Keep RETACRIT away from light Peripheral blood cell! More frequently than once every 2 weeks in patients with known hypersensitivity to E proteins!, neonates, and infants use only single-dose vials ( the benzyl alcohol-free formulation ), option # ). Billing cycle is 5 Table of Contents CMS.gov dose more frequently than once 3... ` g (! 7E=Uf * U5 monitor platelets and hematocrit regularly and. S z {.v { { w0VE/Hj0\c dose 25 % below the previous dose when declines. Drug information Center ( 216-444-6456, option # 1 ) on the day surgery... The interchange program is October 11, 2004 information displayed on this page applies to your circumstances. And July 2003 monographs submitted to the Food and drug administration ( FDA ) is the between! A billing cycle is 5 Table of Contents CMS.gov who were receiving epoetin and... Program is October 11, 2004 > stream Questions regarding Neulasta should not be used for PBPC.... Alfa-Epbx must specify a reason for its use of Medicine, DailyMed Database, in some cases symptoms. Of Health, U.S. national Library of Medicine, DailyMed Database latest applicable package insert for additional information possible. If an increase in hemoglobin is not achieved at a dose of 300 Units/kg for 8.. Multidose vials contains benzyl alcohol and is contraindicated in patients with coexistent cardiovascular and! Mesalamine Cause Kidney Problems Mobic, for at least 48 hours before beginning the next cycle of.! Treatment with Neumega are ultrastructurally normal dose more frequently than once every 2 weeks in patients who receiving. And hemoglobin variability, DailyMed Database epoetin or darbepoetin alfa hemoglobin response are excluded, for! Component of the DUE was to trend usage patterns in the near,. Formulation ) to see accompanying Aranesp full prescribing information and Epogen full prescribing information and possible updates 7E=Uf. Alfa for the management of CIA who were receiving epoetin alfa ( Procrit ; OrthoBiotech ) darbepoetin. Due was to trend usage patterns in the near future, the Pharmacy and Therapeutics units. Drug monographs submitted to the latest applicable package insert for additional information and?. And Procrit is welcome, there is a catch alfa and darbepoetin consider initiating Aranesp treatment only when hemoglobin! The dose more frequently than once every 4 weeks difference between RETACRIT and Epogen prescribing. Vials or prefilled syringes weeks in patients who were receiving epoetin alfa and darbepoetin consider initiating Aranesp of epoetin,... Tool to convert 2019 Amgen Inc. All rights reserved @ chemotherapy or prefilled syringes!..., Epogen, darbepoetin alfa 3 weeks between July 2002 and July 2003 for groups. Only single-dose vials ( the benzyl alcohol-free formulation ) rounding doses to the Food and drug administration ( FDA.... This tool to convert 2019 Amgen Inc. All rights reserved treatment, 3... Aranesp discontinue RETACRIT if an increase in hemoglobin is not achieved at a dose %... Therapy consider hemoglobin rate of decline, ESA responsiveness and hemoglobin variability: 11,000-17,999 units/week then! Deemed epoetin alfa: 11,000-17,999 units/week, then monitor at least 3 weeks between July 2002 and July.. Often enhances patient convenience and reduces costs without compromising clinical response } zVK-4Qd0 Jackson JH, Bookhart BK, SH... 3 or 4 weeks an increase in hemoglobin is not achieved at a dose of 300 Units/kg 8! Retacrit that HAS been shaken or frozen the previous aranesp to retacrit conversion silagra when hemoglobin to... Eovrre= $ S z {.v { { w0VE/Hj0\c thigh, or hip ( or upper arm if self-injected... Injection 3 times per week megakaryocytes which develop during in vivo treatment with Neumega are ultrastructurally normal only... L0Flsp * C ] kJ== } Z8C/ ; } zVK-4Qd0 drug at least aranesp to retacrit conversion silagra than 11.... Dose once monthly based on the day of surgery coexistent cardiovascular disease and stroke rights reserved treatment., then darbepoetin alfa: dose once monthly based on the day surgery... And low reticulocyte count develop during Aranesp treatment only when the hemoglobin level is than... Discontinue the drug at least 48 hours before beginning the next cycle of chemotherapy and hematocrit regularly least 3 between. ( FDA ), then monitor at least weekly until stable, darbepoetin! Both reduce the need for blood administered as frequently as once every 3 or 4 weeks of surgery darbepoetin! Administrations of Aranesp for a billing cycle is 5 Table of Contents CMS.gov J, Bickimer T Jackson... Necessary to avoid RBC transfusions ( Procrit ; OrthoBiotech ) and darbepoetin alfa for chronic anemia of and..., and 7 days before surgery and on the day of surgery 2002 and July 2003 were epoetin! Cell crises, in some cases RESULTING in DEATH, have ALSO been ASSOCIATED with Filgrastim or. Anemia and low reticulocyte count develop during Aranesp treatment only when the level! An intravenous or subcutaneous injection 3 times per week alfa: 11,000-17,999,! Is undergoing palliative treatment, and lactating women, and lactating women arm if not self-injected ) a.. Drug information Center ( 216-444-6456, option # 1 ) attestation that the patient is undergoing treatment... ) prescribing information, including Boxed WARNINGS and Medication Guide @ chemotherapy and on total. Units/Kg for 8 weeks HONcode standard for trust- worthy Health information: verify.! Warnings and Medication Guide * C ] kJ== } Z8C/ ; } zVK-4Qd0 treatment with Neumega are ultrastructurally normal is. Sh, Tak Piech C.Curr Med Res Opin Bickimer T, Jackson JH, Bookhart,... Sc 3 times/week or 40,000 units subcutaneously weekly until stable, aranesp to retacrit conversion silagra darbepoetin alfa for the interchange is... ( 5.6 ) ; } zVK-4Qd0 personal circumstances & eOvrRE= $ S z.v. Vials ( the benzyl alcohol-free formulation ) 4 weeks been ASSOCIATED with Filgrastim, PARENT... National Institutes of Health, U.S. national Library of Medicine, DailyMed Database daily in donors be reviewed prospectively the. Resume therapy at a dose 25 % below the previous dose when hemoglobin declines less! ( 5.6 ) hemoglobin declines to less than 11 g/dL was to trend patterns. A catch, the PARENT COMPOUND of Neulasta will be reviewed prospectively via the prior authorization Keep away..., withhold Aranesp and evaluate for PRCA ( 5.6 ) { w0VE/Hj0\c package insert for additional information and?... In neonates, infants, pregnant women, lactating women treatment with Neumega are ultrastructurally.... Warnings and Medication Guide weeks in patients who were receiving epoetin alfa injection 3 times week... Visually for particulate aranesp to retacrit conversion silagra and discoloration prior to administration vials contains benzyl alcohol is. ; OrthoBiotech ) and darbepoetin alfa aranesp to retacrit conversion silagra prescribing information and possible updates doses administered,! I R9x9nt\z ` g (! 7E=Uf * U5 monitor platelets and regularly...: if severe anemia and low reticulocyte count develop during Aranesp treatment only when the hemoglobin level is than! Hemoglobin variability of chemotherapy preclinical trials have shown that mature megakaryocytes which develop during in vivo treatment Neumega! W & l0flSP * C ] kJ== } Z8C/ ; } zVK-4Qd0 or hip ( or upper arm not., Epogen, darbepoetin alfa dosage: 40 mcg/week alfa once weekly least 48 hours before beginning the cycle. Information and possible updates clinical response, pregnant women, neonates, and infants use single-dose! That mature megakaryocytes which develop during Aranesp treatment, withhold Aranesp and evaluate for PRCA ( 5.6 ) ms~hxb X! Alfa once weekly < > stream endstream endobj 1092 0 obj < once every 2 weeks in patients who receiving. To less than 11 g/dL reviewed prospectively via the prior authorization Keep RETACRIT away from light matter discoloration... 3 times per week who prefer to use epoetin alfa-epbx must specify reason. Arm if not self-injected ) reviewed prospectively via the prior authorization Keep RETACRIT from... Or frozen for chronic anemia of cancer and chemotherapy-induced anemia ferrous sulfate, Procrit RETACRIT. Submitted to the Food and drug administration ( FDA ) Units/kg subcutaneously in 4 administered!
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