Sections View Full Chapter Figures Tables Videos Annotate Full Chapter Figures Tables Videos Supplementary Content +++ Abbreviations ++Table Graphic Jump Location|Download (.pdf)|PrintACCPAmerican College of Chest PhysiciansAPAAntiphospholipid antibody syndromeCKDChronic kidney diseaseESAErythropoietin-stimulating agentFFPFresh frozen plasmaHITHeparin-induced thrombocytopeniaK/DOQIThe Kidney Disease Outcomes Quality InitiativeLMWHLow-molecular-weight heparinNCCNNational Comprehensive Cancer NetworkPCCProthrombin complex concentratePPIProton pump inhibitorVTEVenous thromboembolism++Table Graphic Jump LocationTable 11.1.1 Iron Products for Treatment of AnemiaView Table||Download (.pdf)Table 11.1.1 Iron Products for Treatment of AnemiaDrugDosingCommentsOral IronFerrous fumarate200 mg (66 mg elemental)325 mg (106 mg elemental)150–200 mg elemental per day for most patientsK/DOQI guidelines suggest 200 mg elemental per day for dialysis patientsCommon adverse effects are constipation, diarrhea, nausea, vomiting, and darkened stoolsFood, PPIs, and antacids decrease absorptionTaking with a vitamin C source (orange juice or 50–100 mg ascorbic acid tablet) can improve tolerability and absorption (Hum Nutr Appl Nutr. 1986;40:97)Sustained release formulations may bypass site of absorptionHemoglobin will rise slowly, generally 2 g/L over 2–3 weeksA trial of IV iron or 1-3 months of PO iron can be considered for any CKD patient with TSAT ≤30% and ferritin ≤500 ng/mL (Kidney Int Suppl. 2012;2:279.)Ferrous gluconate246 mg (28 mg elemental)300 mg (34 mg elemental)325 mg (36 mg elemental)Ferrous sulfate325 mg (65 mg elemental)220 mg/5 mL (44 mg/5 mL elemental)300 mg/mL (60 mg/5 mL elemental)Parental IronaFerumoxytol (Feraheme)30 mg/mL (17 mL)CKD: 510 mg IV push every 3–8 daysCommon indications for IV iron therapy include ongoing blood loss, intolerance of or difficulty absorbing PO iron and cancer or dialysis patients taking ESAs who do not respond to or cannot take PO ironAnaphylactic reactions have occurred with both irondextran and sodium ferric gluconate, the reported frequency is 8.7 and 3.3 events per million, respectively (Am J Kidney Dis. 1999;33:464)A 25 mg test dose is recommended by NCCN guidelines for sodium ferric gluconate in patients with history of anaphylaxis to irondextranDelayed (1–2 days) infusion reactions reported with irondextran including arthralgias, dizziness, chills, and feverIrondextran (INFeD, Dexferrum)50 mg/ml (1, 2 mL)Cancer: 25 mg test dose, followed 1 h later by 100 mg over 5 minutesLabeled dosing = 0.0442 (desired Hgb – observed Hgb) × LBW + (0.26 × LBW)bIron sucrose (Venofer)20 mg/mL (5, 10 mL)CKD: 100–200 mg over 2–5 minutes 1–3 times per week up to 1 g cumulative doseCancer: 200 mg infused over 1 h every 2–3 weeksSodium ferric gluconate (Ferrlecit)12.5 mg/mL (5 mL)CKD: 125 mg over 1 h per dialysis session × 8 dosesCancer: 125 mg over 1 h weekly × 8 dosesaParenteral iron product strengths reflect elemental iron content.bLBW, lean body weight.++Table Graphic ... Your Access profile is currently affiliated with [InstitutionA] and is in the process of switching affiliations to [InstitutionB]. Please select how you would like to proceed. Keep the current affiliation with [InstitutionA] and continue with the Access profile sign in process Switch affiliation to [InstitutionB] and continue with the Access profile sign in process Get Free Access Through Your Institution Learn how to see if your library subscribes to McGraw Hill Medical products. Subscribe: Institutional or Individual Sign In Error: Incorrect UserName or Password Username Error: Please enter User Name Password Error: Please enter Password Sign in Forgot Password? Forgot Username? Download the Access App: iOS | Android Sign in via OpenAthens Sign in via Shibboleth You already have access! Please proceed to your institution's subscription. Create a free profile for additional features.