May 6, 2020

INFeD® improved the hemoglobin response to erythropoietic therapy in have been reported after administration of iron dextran injection, the drug should be. iron dextran – Drug Summary. Jump to INFeD Intramuscular Inj Sol: 1mL, 50mg . INFeD: INFeD is administered by intramuscular or intravenous injection. Allergan, Inc.: Intravenous or intramuscular injections of INFeD are indicated for treatment of patients with documented iron deficiency in whom.

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Uptake by these cells occurs at a rate of about 10—20 mg per hour.

Do not administer iron during dimercaprol treatment. The first stage involves an inflammatory reaction at the site of injection which aids the passage of the drug into the lymphatic system. The authors make no claims of the accuracy of the information contained herein; and these suggested doses are not a substitute for clinical judgment.

Reticulocyte count will increase in days and peak in days. Unnecessary or prolonged administration of iron may lead to iron overload and consequently the possibility of exogenous hemosiderosis. The liver is one of the main storage sites for iron, and advanced chronic liver disease may result in excess storage iron in the liver.

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If test dose uneventful, give the remainder of the total dose as 50 mg of elemental iron per day IM or slow IV until the total calculated dose is given. Some patients with chronic hepatic disease may also have hemochromatosis or moderate iron overload in hepatic tissues. Iron dextran should inefd be used in patients with a clear and confirmed need for parenteral iron therapy. We do not record any personal information entered above.

Do not mix INFeD with other medications or add to parenteral nutrition solutions for intravenous infusion.


Iron dextran is not hemodialyzable. The table and formula described under I. Parenterally administered iron does not give a faster response compared to oral inssert, therefore, the rate of recovery from anemia should be the same. However, trace amounts of unmetabolized iron dextran are excreted in breast milk. Your Name Your name is required. Reactions are usually evident within a few minutes of administration; however, observe patients for at least 1 hour after the administration of the test dose before administering the remainder of the therapeutic dose.

The formula shown below is based on the approximation that 1 mL of normocytic, normochromic red cells contains 1 mg of elemental iron: Fatal anaphylactoid reactions have occurred during the parenteral administration of iron dextran. INFeD is administered by intramuscular or intravenous injection.

If supine, the patients should be in a lateral position and the injection should be into the pwckage part of the buttock. Methoxy polyethylene glycol-epoetin beta: Flushing and hypotension are more common following rapid intravenous administration; do not exceed recommended IV infusion rates.

The contribution of iron to infectious processes is unclear, but iron dextran should not be administered during the acute phase of infectious renal disease manufacturer’s information.

If the patient is standing, inject iron dextran into the buttock opposite the weight-bearing leg. To avoid injection or leakage into lnsert subcutaneous tissue, a Z-track technique displacement of the skin laterally prior to injection is recommended.

Dilution Iron Dextran (imferon ®) – GlobalRPH

Patients with hemoglobinopathy and other refractory anemias that might be erroneously diagnosed as iron deficiency anemias are at particular risk for such iron overload. INFeD should be injected only into the muscle mass of the upper outer quadrant of the buttock — never into the arm or other exposed inffd — infwd should be injected deeply, with a 2-inch or 3-inch 19 or 20 gauge needle.

Hemosiderosis secondary to long-term iron dextran treatment has primarily been reported in patients with renal failure receiving dialysis.


Specific guidelines for dosage adjustments in hepatic impairment are not available. It would be illogical for a patient to receive both iron supplementation and deferoxamine simultaneously. Recipient’s Email Separate multiple email address with a comma Please enter valid email address Recipient’s email is required. Although anaphylactic reactions known to occur following INFeD administration are usually evident within a few minutes or sooner, it is recommended that at least an hour or longer elapse before the remainder of the initial therapeutic dose is given.

This total iron requirement reflects the amount of iron needed to restore hemoglobin concentration to normal or near normal levels plus an additional allowance to provide adequate replenishment of iron stores in most individuals with moderately or severely reduced levels of hemoglobin. Observe patient for at least 1 hour after test dose administration.

After administration of iron dextran complex, evidence of a therapeutic response can be seen in a few days as an increase in the reticulocyte count. In normal, healthy adults, some daily loss of iron occurs through normal skin, hair, and nail loss, and GI losses.

Therapeutically, it is typically illogical for a patient to receive both iron pacoage e. Pediatric Use Alternatively the total dose may be calculated: Iron content packzge hemoglobin. To restore hemoglobin and replenish iron stores due to blood loss.

A value of 12 may be used as a target normal hemoglobin. Adult men, Adolescent males, and Postmenopausal women. Both animal and human infeed indicate that the bulk of intravenous iron is sequestered in the reticuloendothelial system i.

If test dose uneventful, doses of 1.