Product image of Ifosfamide Baxter Healthcare (Ifosfamide) supplied by GNH India

Ifosfamide Baxter Healthcare

Active Ingredient:
Ifosfamide
Origin:
EU

Ifosfamide Baxter Healthcare (Ifosfamide)

Ifosfamide, the active ingredient in Ifosfamide Baxter Healthcare, is a alkylating agent (nitrogen mustard) presented as an injectable solution for intravenous use. It treats a range of solid tumours and haematologic malignancies in adult and paediatric patients.

GNH India supplies Ifosfamide Baxter Healthcare as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide.

Manufacturer / TM Owner

Baxter Healthcare Ltd.

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Indications & Clinical Uses

Ifosfamide is employed in oncology as a DNA‑alkylating agent for several tumour types.

  • Testicular cancer: used in combination regimens to achieve tumour shrinkage and improve survival.
  • Soft tissue sarcoma: incorporated into multi‑drug protocols to control disease progression.
  • Ovarian cancer: administered as part of salvage chemotherapy for resistant disease.
  • Lymphoma: utilized in refractory cases to induce remission.
  • Wilms tumor: given in pediatric protocols to enhance cure rates.
  • Neuroblastoma: applied in high‑risk treatment schedules to reduce tumour burden.

How It Works

  • Ifosfamide is a nitrogen‑mustard alkylating agent that forms covalent bonds with DNA bases, leading to intra‑ and interstrand cross‑links. These cross‑links obstruct DNA replication and transcription, triggering cell‑cycle arrest and apoptosis in rapidly dividing cancer cells. The drug is activated intracellularly by hepatic cytochrome P450 enzymes to its cytotoxic metabolites.

Side Effects

Ifosfamide may cause a range of adverse reactions, which are monitored during therapy.

Common Side Effects

  • Nausea and vomiting: frequent gastrointestinal upset during treatment.
  • Myelosuppression: reduced white blood cells, red cells and platelets.
  • Fatigue: generalized tiredness often reported by patients.
  • Alopecia: temporary hair loss during cycles.

Serious or Rare Side Effects

  • Hemorrhagic cystitis: bladder irritation that may cause bleeding.
  • Neurotoxicity: confusion, seizures or encephalopathy in severe cases.
  • Nephrotoxicity: impaired kidney function requiring monitoring.

Precautions & Warnings

When using Ifosfamide, clinicians should observe several safety measures.

  • Hydration: ensure adequate intravenous fluids to reduce risk of bladder toxicity.
  • Mesna co‑administration: provide uroprotective agent to prevent hemorrhagic cystitis.
  • Renal function monitoring: assess serum creatinine and electrolytes before each dose.
  • Neurological assessment: watch for signs of encephalopathy or seizures.
  • Pregnancy category D: avoid use in pregnant women unless benefits outweigh risks.
  • Store at ambient temperature: keep in original container, protect from light and moisture.

Avoid Interactions

Ifosfamide can interact with other medicines, affecting efficacy or safety.

Major Interactions (Avoid)

  • CYP3A4 inhibitors (e.g., ketoconazole, ritonavir): may increase toxic metabolite levels.
  • Nephrotoxic agents (e.g., cisplatin, aminoglycosides): heighten risk of kidney injury.

Moderate Interactions (Monitor Closely)

  • CYP inducers (e.g., rifampin, phenytoin): may reduce therapeutic effect.
  • Anticoagulants (e.g., warfarin): monitor coagulation parameters due to potential bleeding risk.
  • Other myelosuppressive drugs: increase likelihood of severe bone‑marrow suppression.

Frequently Asked Questions

Ifosfamide Baxter Healthcare is an intravenous alkylating chemotherapy used for several malignancies, including testicular cancer, soft tissue sarcoma, ovarian cancer, lymphoma, Wilms tumor and neuroblastoma. It is typically given as part of multi‑drug regimens to improve tumour control and patient outcomes.

Ifosfamide is converted by liver enzymes into active metabolites that alkylate DNA, creating cross‑links that block replication and transcription. This DNA damage triggers cell‑cycle arrest and apoptosis, preferentially affecting rapidly dividing cancer cells while sparing most normal tissues.

The dosage of Ifosfamide is individualized by the prescribing oncologist based on the specific cancer type, patient weight, renal function and treatment protocol. Dosing schedules are determined in a clinical setting and should not be altered without medical supervision.

Ifosfamide is classified as Pregnancy Category D, indicating evidence of risk to the fetus. It should be avoided in pregnant women unless the potential benefit justifies the risk. Breastfeeding is not recommended while receiving Ifosfamide because the drug can be excreted in milk.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if needed) and necessary import documentation.

Ifosfamide shares a similar mechanism with other nitrogen‑mustard agents such as cyclophosphamide, but it has a distinct toxicity profile, including a higher risk of hemorrhagic cystitis and neurotoxicity. Choice of agent depends on tumour type, prior therapy, and individual patient tolerance.

Ifosfamide Baxter Healthcare should be stored at ambient temperature, below 25 °C, in its original packaging. Protect the product from direct light, moisture and extreme temperatures to maintain stability and potency.

Ifosfamide is given by intravenous infusion, usually over a period of 1–3 hours depending on the protocol. Administration is performed in a clinical setting with appropriate monitoring for infusion reactions and supportive care measures such as hydration and mesna.

The most serious risks include hemorrhagic cystitis, which can cause bladder bleeding; neurotoxicity, presenting as confusion, seizures or encephalopathy; and nephrotoxicity, leading to impaired kidney function. Prompt detection and supportive measures are essential to mitigate these complications.

Ifosfamide is contraindicated in patients with known hypersensitivity to the drug or its components, those with severe renal impairment, and pregnant women unless the therapeutic benefit outweighs the fetal risk. Caution is also advised for individuals with pre‑existing neurological disorders.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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