Product image of Ifo-Cell N 1000 (Ifosfamide) supplied by GNH India

Ifo-Cell N 1000

Active Ingredient:
Ifosfamide
Origin:
EU

Ifo-Cell N 1000 (Ifosfamide)

Ifosfamide, the active ingredient in Ifo-Cell N 1000, is an alkylating agent presented as a sterile injectable solution for intravenous use. It interferes with DNA replication and is employed in the treatment of several solid tumours and hematologic malignancies in adult patients.
GNH India supplies Ifo-Cell N 1000 as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide.

Manufacturer / TM Owner

Stadapharm Gmbh

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Indications & Clinical Uses

  • Ifosfamide is an alkylating chemotherapy used in the treatment of several solid tumours and hematologic malignancies.
  • Testicular cancer: provides cytotoxic activity to eradicate malignant germ‑cell tumors.
  • Soft tissue sarcoma: reduces tumor burden and improves surgical outcomes.
  • Lymphoma: contributes to remission in aggressive non‑Hodgkin subtypes.
  • Bladder cancer: used as part of combination regimens for invasive disease.

How It Works

  • Ifosfamide is a DNA cross‑linking alkylating agent that forms covalent bonds between DNA strands, preventing replication and transcription. After intracellular activation by hepatic cytochrome P450 enzymes, the reactive metabolites bind to guanine bases, causing interstrand cross‑links that trigger cell‑cycle arrest and apoptosis in rapidly dividing cancer cells.

Side Effects

Adverse reactions may vary in frequency and severity.

Common Side Effects

  • Nausea and vomiting: often requires anti‑emetic prophylaxis.
  • Fatigue: generalized tiredness during treatment cycles.
  • Alopecia: reversible hair loss.
  • Myelosuppression: decreased blood cell counts.
  • Hemorrhagic cystitis: bladder irritation due to metabolites.
  • Electrolyte disturbances: especially hyponatremia.

Serious or Rare Side Effects

  • Nephrotoxicity: impaired renal function requiring monitoring.
  • Neurotoxicity: encephalopathy or seizures in high doses.
  • Secondary malignancies: risk of therapy‑related cancers.
  • Severe infection: opportunistic infections due to immunosuppression.
  • Anaphylactic reactions: rare hypersensitivity to the formulation.
  • Cardiotoxicity: occasional cardiac dysfunction.

Precautions & Warnings

Safety considerations are essential when handling this cytotoxic agent.

  • Hydration: ensure adequate intravenous fluids to reduce renal toxicity.
  • Mesna co‑administration: protect the bladder from hemorrhagic cystitis.
  • Renal monitoring: assess serum creatinine and electrolytes before each cycle.
  • Hepatic function: evaluate liver enzymes as metabolism occurs hepatically.
  • Myelosuppression monitoring: perform regular complete blood counts.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze.

Avoid Interactions

Potential drug‑drug interactions may affect efficacy or increase toxicity.

Major Interactions (Avoid)

  • Nephrotoxic agents (e.g., cisplatin, aminoglycosides): amplify renal damage.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole): raise active metabolite levels.
  • Other alkylating agents: heighten myelosuppression risk.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampin): may reduce therapeutic effect.
  • Anticoagulants (e.g., warfarin): alter INR, requiring dose adjustment.
  • Concurrent myelosuppressive drugs: increase risk of severe cytopenias.

Frequently Asked Questions

Ifo-Cell N 1000 contains ifosfamide, an alkylating chemotherapy indicated for adult patients with testicular cancer, soft tissue sarcoma, certain lymphomas and invasive bladder cancer. It is administered as part of multi‑agent regimens to achieve tumor reduction and improve surgical outcomes.

Ifosfamide is activated in the liver by cytochrome P450 enzymes to form reactive metabolites that cross‑link DNA strands. These cross‑links block DNA replication and transcription, leading to cell‑cycle arrest and apoptosis of rapidly dividing cancer cells.

The dosing regimen for Ifo-Cell N 1000 is individualized by the treating oncologist based on cancer type, patient weight, renal function and treatment protocol. Only a qualified prescriber can determine the appropriate dose and schedule.

Ifosfamide is classified as contraindicated in pregnancy because of its teratogenic potential and may be excreted in breast milk. Women of child‑bearing potential should use effective contraception, and breastfeeding is generally discouraged during treatment.

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 and any necessary import documentation.

Ifosfamide shares the DNA‑cross‑linking mechanism of other alkylators such as cyclophosphamide, but it has a distinct activation pathway and a higher propensity for hemorrhagic cystitis, requiring co‑administration of mesna. Its spectrum of activity includes sarcomas and bladder cancer where some alternatives are less effective.

Ifo-Cell N 1000 should be stored at 2‑8 °C in a refrigerator, protected from light and never frozen. Keep the vial in its original packaging to maintain sterility and stability until use.

The product is supplied as a sterile injectable solution for intravenous infusion. Administration is performed by qualified healthcare professionals in a clinical setting, typically over a defined period according to the prescribed regimen and with appropriate hydration and supportive care.

Serious risks include nephrotoxicity, neurotoxicity (including seizures), severe myelosuppression leading to infection or bleeding, and hemorrhagic cystitis. Patients should be closely monitored for renal function, neurological status and blood counts throughout therapy.

Patients with severe renal impairment, uncontrolled infections, known hypersensitivity to ifosfamide or its excipients, and those who are pregnant or breastfeeding should not receive Ifo-Cell N 1000. Contraindications are determined by the prescribing physician based on individual health status.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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