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Safe Administration and Key Precautions for Iron Dextran Injection

Iron Dextran injection is a powerful therapeutic agent for treating iron deficiency anemia when oral iron is insufficient or not tolerated. However, its administration is not without risks, primarily serious hypersensitivity reactions, including anaphylaxis. Therefore, strict adherence to safety guidelines and thorough patient monitoring are paramount.

Before initiating Iron Dextran therapy, a comprehensive patient assessment is crucial. This includes reviewing the patient's medical history for any prior allergic reactions to medications, asthma, or other sensitivities. Establishing a documented iron deficiency state that is not amenable to oral iron therapy is a prerequisite for its use.

The cornerstone of safe Iron Dextran administration is the test dose. A small initial dose, typically 0.5 mL, is administered either intravenously or intramuscularly. Patients must be closely observed for at least one hour following the test dose for any signs of an allergic reaction, such as difficulty breathing, rash, itching, dizziness, or a drop in blood pressure. If any reaction occurs, the remainder of the dose should not be administered, and appropriate medical management should be initiated.

Once the test dose is tolerated, the full therapeutic dose can be administered. The rate of infusion for intravenous administration should be slow, generally not exceeding 50 mg of iron per minute. For intramuscular injections, deep intramuscular administration into the upper outer quadrant of the buttock is recommended to minimize tissue irritation and discoloration, often using a Z-track technique. Daily doses should not exceed specific limits based on patient weight and age to prevent adverse effects.

Continuous monitoring during and after administration is essential. Healthcare providers must be prepared with resuscitation equipment and trained personnel to manage potential anaphylactic reactions promptly. Patients should be advised to report any immediate or delayed adverse symptoms to their healthcare provider. Delayed reactions, occurring 1-2 days post-administration, may include flu-like symptoms such as fever, chills, muscle aches, and joint pain. While these are usually transient, they warrant medical attention.

Suppliers of high-quality pharmaceutical ingredients, like NINGBO INNO PHARMCHEM CO.,LTD., play a vital role in ensuring the availability of safe and effective Iron Dextran for healthcare professionals. Understanding the nuances of iron dextran buy and purchase procedures ensures that medical facilities can procure this essential medication reliably.

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NINGBO INNO PHARMCHEM CO.,LTD. was established in 2007. It is committed to the R&D, production and sales of raw materials, pharmaceutical intermediates and fine chemicals. We striving to create a high-efficiency and high-quality integrated chemical service platform to better serve domestic and foreign customers.

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WHY CHOSE US?

1. 20 years of R&D, manufacturing and sales experience, serving customers in 60 countries and regions around the world;

2. Own R&D laboratory, pilot platform and large-scale production workshop, which can meet the audit requirements of global customers;

3. We can satisfy customers' perfect transition from small scale lab requirements (gram level) to commercialization requirements (hundred tons level).

FAQ

  • A: We don't have Minimum Order Quantity, exact quantity should be provided before quotation for us to calculate the exact cost.

  • A: We don't provide free samples due to lots of request and expensive international courier's cost, we can deduct the sample charge after commercial order placed.

  • A: Our payment terms: Small or sample order: T/T IN ADVANCE. Commercial order: First order should be by T/T IN ADVANCE or L/C at sight, and following orders T/T 30~90days is acceptable subject to approval of credit application.

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NINGBO INNO PHARMCHEM CO.,LTD.
Address: No.163 Ruiqing Rd.,Ningbo 315000 China
Phone: 86-574-87319282
Fax: 86-574-27912196
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