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|Sodium Ferric Gluconate |
Drugs search, click the first letter of a drug name: | A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z | 1 | 2 | 3 | 4 | 5 | 6 | 8 | 9 Home Sodium Ferric GluconatePronouncation: (SO-dee-uhm FER-ick GLUE-koe-nate)Class: Parenteral iron Trade Names: Mechanism of ActionPharmacologyProvides iron to replenish hemoglobin and depleted iron stores. Indications and UsageTreatment of iron deficiency anemia in patients undergoing chronic hemodialysis and supplemental erythropoietin. ContraindicationsAll anemias not associated with iron deficiency; evidence of iron overload; hypersensitivity to any component of the product. Dosage and AdministrationDosage is expressed as mg of elemental iron. AdultsIV Iron Replacement Dose: 10 mL (iron 125 mg) diluted in 100 mL of 0.9% sodium chloride. Infuse over 1 h. Most patients require a minimum cumulative dose of 1 g over 8 sessions at sequential dialysis treatments. ChildrenIV Iron Replacement Dose: 0.12 mL/kg (elemental iron 1.5 mg/kg) diluted in 25 mL 0.9% sodium chloride and given by IV infusion over 1 h at 8 sequential dialysis sessions (max, 125 mg/dose). Storage/StabilityStore ampules at controlled room temperature (59° to 86°F). Protect from freezing. Use immediately after dilution in saline. Drug InteractionsACE inhibitorsMay potentiate adverse reactions. Oral iron preparationsMay have reduced absorption. IncompatibilityDo not mix with other medications or add to parenteral nutrition solutions. Laboratory Test InteractionsNone well documented. Adverse ReactionsCardiovascularHypotension (29%); hypertension (13%); syncope (6%); tachycardia (5%); angina pectoris; bradycardia; MI; pulmonary edema; vasodilation. CNSDizziness (13%); fatigue, paresthesia (6%); agitation; malaise; nervousness; somnolence (postmarketing). DermatologicPruritus (6%); increased sweating; rash. EENTAbnormal vision; conjunctivitis; ear disorder. GIDiarrhea, nausea, vomiting (35%); anorexia; dry mouth; dyspepsia; eructation; flatulence; GI disorder; melena; rectal disorder (postmarketing). GenitourinaryUTI. HematologicAbnormal erythrocytes (11%); anemia; hemorrhage; leukocytosis; lymphadenopathy; sepsis (postmarketing). LocalInjection-site reactions (33%). Metabolic-NutritionalHyperkalemia (6%); generalized edema (5%); edema; hypervolemia; hypoglycemia; hypokalemia; leg edema; peripheral edema. MusculoskeletalLeg cramps (10%); arthralgia; myalgia. MiscellaneousCramps (25%); chest pain, pain (10%); fever (5%); abscess; arm pain; back pain; chills; flu-like syndrome; hypersensitivity; hypertonia; infection; rigors (postmarketing). PrecautionsPregnancyCategory B . LactationUndetermined. ChildrenSafety and efficacy are not established for children younger than 6 yr of age. ElderlyUse with caution, usually starting at the low end of the dosing range because of the greater frequency of decreased hepatic, renal, or cardiac function, and concomitant diseases or other drug therapy. HypersensitivityRare cases of serious hypersensitivity reported. Benzyl alcoholThis product contains benzyl alcohol and should not be used in premature infants and neonates. Flushing and hypotension reactionsAssociated with too rapid administration. Do not exceed 125 mg/h (2.1 mg/min). HemosiderosisUnwarranted therapy with parenteral iron will cause excess storage of iron and possibly cause exogenous hemosiderosis, especially in patients with hemoglobinopathies and other refractory anemias. HypotensionHypotension associated with lightheadedness, malaise, fatigue, weakness, or severe chest, back, flank, or groin pain reported. This reaction has not been associated with hypersensitivity and usually resolves within 1 to 2 h. OverdosageSymptomsAccumulation of iron in iron storage sites, abdominal pain, diarrhea, vomiting, pallor, cyanosis, lassitude, drowsiness, hyperventilation (caused by acidosis), CV collapse. Patient Information
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