Product image of Oxaliplatine Sun (Oxaliplatin) supplied by GNH India

Oxaliplatine Sun

Active Ingredient:
Oxaliplatin
Origin:
EU

Oxaliplatine Sun (Oxaliplatin)

Oxaliplatin, the active ingredient in Oxaliplatine Sun, is a platinum compound (alkylating-like agent) presented as a solution for injection for intravenous use. It is employed in the adjuvant treatment of stage III colon cancer and as first‑line therapy for metastatic colorectal cancer in adult patients. GNH India supplies Oxaliplatine Sun as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide.

GNH India supplies Oxaliplatine Sun as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Sun Pharmaceutical Industries Europe B.V.

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Indications & Clinical Uses

Oxaliplatin is used in colorectal cancer treatment pathways, providing cytotoxic therapy for specific disease stages.

  • Stage III colon cancer (adjuvant): Improves disease‑free survival after surgical resection.
  • Metastatic colorectal cancer (first‑line): Reduces tumor burden and prolongs overall survival.
  • Combination regimens (e.g., FOLFOX): Enhances efficacy when paired with fluoropyrimidines and leucovorin.

How It Works

  • Oxaliplatin forms covalent cross‑links between adjacent guanine bases on DNA, creating intra‑ and interstrand adducts that block DNA replication and transcription. The resulting DNA damage triggers cell‑cycle arrest and apoptosis, preferentially affecting rapidly dividing tumor cells while sparing most normal tissues.

Side Effects

Oxaliplatin may cause a range of adverse reactions, from mild to severe, that require monitoring during therapy.

Common Side Effects

  • Peripheral neuropathy: tingling or numbness, often dose‑related.
  • Nausea and vomiting: may occur during or after infusion.
  • Diarrhea: watery stools, sometimes requiring antidiarrheal medication.
  • Fatigue: generalized tiredness during treatment cycles.
  • Myelosuppression: reduced blood cell counts, increasing infection risk.
  • Elevated liver enzymes: mild transaminase rise detected in labs.

Serious or Rare Side Effects

  • Severe neuropathy: persistent loss of sensation that may be irreversible.
  • Acute allergic reactions: rash, bronchospasm, or anaphylaxis during infusion.
  • Hemolytic anemia: destruction of red blood cells.
  • Cardiotoxicity: rare heart rhythm disturbances.
  • Severe neutropenia or thrombocytopenia: markedly low white‑cell or platelet counts.
  • Renal impairment: acute kidney injury in susceptible patients.

Precautions & Warnings

Before initiating Oxaliplatin therapy, clinicians should assess patient suitability and monitor for known risks.

  • Renal function: evaluate creatinine clearance and adjust if impaired.
  • Hepatic function: check liver enzymes and bilirubin levels.
  • Pre‑existing neuropathy: consider alternative regimens if significant.
  • Hematologic status: obtain baseline complete blood count.
  • Pregnancy and lactation: avoid use; discuss risks with a specialist.
  • Store at 2‑8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Oxaliplatin may interact with other agents, influencing efficacy or toxicity. Monitoring and dose adjustments are often required.

Major Interactions (Avoid)

  • Nephrotoxic drugs (e.g., cisplatin, aminoglycosides): increase risk of kidney injury.
  • Myelosuppressive agents (e.g., high‑dose cyclophosphamide): exacerbate bone‑marrow suppression.

Moderate Interactions (Monitor Closely)

  • Antiemetics (e.g., ondansetron): may affect oxaliplatin clearance.
  • Calcium and magnesium infusions: can reduce neurotoxicity but require timing coordination.
  • Warfarin: potential alteration of INR values.
  • NSAIDs: may worsen renal function when combined.
  • Proton pump inhibitors: possible impact on drug absorption dynamics.

Frequently Asked Questions

Oxaliplatine Sun contains oxaliplatin, which is indicated for the adjuvant treatment of stage III colon cancer after surgery and as a first‑line option for metastatic colorectal cancer, often as part of combination regimens such as FOLFOX.

Oxaliplatin creates covalent cross‑links between DNA bases, preventing DNA replication and transcription. This DNA damage triggers cell‑cycle arrest and apoptosis, primarily affecting rapidly dividing cancer cells.

The prescribed dose of Oxaliplatine Sun is determined by the treating oncologist based on the patient’s clinical condition, body surface area, and treatment protocol. Specific dosing regimens are not provided here.

Oxaliplatin is classified as pregnancy‑category unknown and is generally avoided in pregnant or nursing women because of potential fetal or infant toxicity. Consultation with a specialist is essential before exposure.

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

Oxaliplatin differs from cisplatin and carboplatin by its distinct side‑effect profile, notably a higher incidence of peripheral neuropathy but lower nephrotoxicity. It is often preferred in colorectal cancer regimens, whereas cisplatin is commonly used for lung, ovarian and head‑and‑neck cancers.

Oxaliplatine Sun should be stored at 2‑8 °C, protected from light, and kept in its original packaging. It must not be frozen or shaken, and any unused solution should be discarded according to local regulations.

Oxaliplatin is given as an intravenous infusion, typically over 2 hours, under the supervision of qualified healthcare professionals. Infusion rates and pre‑medication protocols are determined by the treating physician.

The most serious risks include severe peripheral neuropathy that may be irreversible, acute allergic reactions such as anaphylaxis, and significant myelosuppression leading to infection, bleeding or anemia.

Patients with pre‑existing severe neuropathy, uncontrolled renal or hepatic impairment, active infections, or known hypersensitivity to oxaliplatin or other platinum compounds should avoid this therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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