Product image of Oxaliplatine Fresenius Kabi (Oxaliplatin) supplied by GNH India

Oxaliplatine Fresenius Kabi

Active Ingredient:
Oxaliplatin
Origin:
EU

Oxaliplatine Fresenius Kabi (Oxaliplatin)

Oxaliplatin, the active ingredient in Oxaliplatine Fresenius Kabi, is a platinum-based chemotherapy agent presented as an intravenous solution for infusion use. It is employed in the treatment of certain gastrointestinal cancers, primarily colorectal and gastric malignancies, often in combination with other cytotoxic drugs.

GNH India supplies Oxaliplatine Fresenius Kabi as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres worldwide.

Manufacturer / TM Owner

Fresenius Kabi Nv/Sa

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Indications & Clinical Uses

Oxaliplatin is used in chemotherapy regimens targeting gastrointestinal tumor types.

  • Colorectal cancer: combined with fluoropyrimidines to inhibit tumor growth and improve survival in metastatic and adjuvant settings.
  • Gastric cancer: incorporated into multi‑drug protocols to enhance response rates in advanced disease.
  • Pancreatic cancer: used off‑label within combination regimens to augment cytotoxic activity in selected patients.

How It Works

  • Oxaliplatin exerts its antineoplastic effect by forming covalent platinum‑DNA adducts that create intra‑ and interstrand cross‑links, disrupting DNA replication and transcription. The resulting DNA damage triggers cell‑cycle arrest and apoptosis, particularly in rapidly dividing tumor cells. Its diaminocyclohexane carrier ligand enhances cytotoxicity and contributes to a distinct spectrum of activity compared with other platinum compounds.

Side Effects

Oxaliplatin may cause a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Nausea and vomiting: gastrointestinal upset occurring during or after infusion.
  • Peripheral neuropathy: tingling or numbness in hands and feet, often dose‑related.
  • Fatigue: generalized tiredness affecting daily activities.
  • Myelosuppression: reduced white blood cells, platelets, or red cells.
  • Diarrhea: loose stools that may require supportive care.

Serious or Rare Side Effects

  • Severe neutropenia with fever: risk of infection requiring urgent medical attention.
  • Pulmonary toxicity: acute or chronic lung injury presenting with dyspnea.
  • Anaphylactic reactions: sudden hypersensitivity that can be life‑threatening.
  • Hepatic dysfunction: elevated liver enzymes or bilirubin indicating liver injury.
  • Persistent neuropathy: long‑lasting sensory deficits that may be irreversible.

Precautions & Warnings

When using Oxaliplatin, clinicians should observe several precautionary measures to minimize risks.

  • Renal function: assess baseline creatinine and monitor during therapy to avoid accumulation.
  • Hepatic function: evaluate liver enzymes before each cycle, adjusting dose if impairment is present.
  • Pre‑existing neuropathy: avoid or reduce dose in patients with significant peripheral nerve disorders.
  • Pregnancy and lactation: contraindicated; avoid use in pregnant or breastfeeding women.
  • Concomitant ototoxic drugs: limit use of aminoglycosides or loop diuretics to reduce hearing loss risk.
  • Store at ambient temperature: keep in original container, protect from light and moisture, do not freeze.

Avoid Interactions

Oxaliplatin can interact with other medicines, influencing efficacy or toxicity.

Major Interactions (Avoid)

  • Nephrotoxic agents (e.g., cisplatin, aminoglycosides): increase risk of kidney injury.
  • Ototoxic drugs (e.g., high‑dose furosemide): amplify hearing loss potential.
  • High‑dose radiation therapy: may exacerbate tissue toxicity when combined.

Moderate Interactions (Monitor Closely)

  • Anticoagulants (e.g., warfarin, DOACs): heightened bleeding risk due to thrombocytopenia.
  • Myelosuppressive chemotherapy (e.g., 5‑FU, irinotecan): additive bone‑marrow suppression.
  • CYP450 modulators (e.g., rifampin, carbamazepine): may alter plasma levels of co‑administered drugs.

Frequently Asked Questions

Oxaliplatine, containing the active ingredient oxaliplatin, is employed in oncology to treat gastrointestinal malignancies, most notably colorectal and gastric cancers. It is typically given as part of combination chemotherapy regimens such as FOLFOX, where it works alongside fluoropyrimidines and other agents to improve tumor response and patient survival.

Oxaliplatin belongs to the platinum‑based class of anticancer drugs. After intravenous administration, it forms covalent bonds with DNA, creating intra‑ and interstrand cross‑links that block DNA replication and transcription. This DNA damage triggers cell‑cycle arrest and programmed cell death, especially in rapidly dividing cancer cells.

The exact dose of Oxaliplatine is individualized by the prescribing oncologist. Factors such as the patient’s body surface area, renal and hepatic function, treatment intent (curative vs. palliative), and the specific chemotherapy protocol all influence the calculated dose and schedule.

Oxaliplatine is classified as contraindicated in pregnancy and lactation because it can cross the placenta and be excreted in breast milk, posing a risk of fetal or infant toxicity. Women of child‑bearing potential should use effective contraception during treatment and for a period after the last dose.

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

Compared with cisplatin and carboplatin, oxaliplatin has a distinct diaminocyclohexane carrier ligand that yields a different toxicity profile. It is less nephrotoxic and ototoxic than cisplatin but more likely to cause peripheral neuropathy. Its efficacy is particularly strong in colorectal cancer, where it is often preferred over other platinum drugs.

Oxaliplatine should be stored at ambient temperature, below 25 °C, in its original sealed container. The product must be protected from light, moisture, and freezing. Once reconstituted, it should be used according to the manufacturer’s stability guidelines and discarded if any discoloration or particulate matter appears.

Oxaliplatine is supplied as an intravenous solution that is infused directly into a vein, usually over a period of 2 hours. The infusion is performed in a clinical setting by qualified healthcare professionals, with appropriate monitoring of vital signs and infusion‑related reactions throughout the administration.

The most critical adverse events include severe neutropenia with fever, which can lead to life‑threatening infections; acute pulmonary toxicity presenting as shortness of breath; and persistent peripheral neuropathy that may become irreversible. Prompt recognition and medical intervention are essential for these serious complications.

Oxaliplatine is contraindicated in patients with known hypersensitivity to platinum compounds, pre‑existing severe peripheral neuropathy, uncontrolled renal or hepatic impairment, and in pregnant or breastfeeding women. Caution is also advised for individuals receiving concurrent ototoxic or nephrotoxic medications.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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