Product image of Oxaliplatin Sun Pharmaceutical Industries Europe B.V. (Oxaliplatin) supplied by GNH India

Oxaliplatin Sun Pharmaceutical Industries Europe B.V.

Active Ingredient:
Oxaliplatin
Origin:
EU

Oxaliplatin Sun Pharmaceutical Industries Europe B.V. (Oxaliplatin)

Oxaliplatin, the active ingredient in Oxaliplatin Sun Pharmaceutical Industries Europe B.V., is a platinum compound presented as a sterile solution for intravenous use. It is employed in the treatment of colorectal cancer, typically administered to adult patients undergoing combination chemotherapy regimens.

GNH India supplies Oxaliplatin Sun Pharmaceutical Industries Europe B.V. as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres, hospitals and pharmacies worldwide.

Manufacturer / TM Owner

Sun Pharmaceutical Industries Europe B.V.

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Indications & Clinical Uses

Oxaliplatin is a platinum‑based chemotherapeutic agent used primarily within the colorectal cancer treatment pathway.

  • Colorectal cancer: Enhances tumor response when combined with fluoropyrimidine‑based regimens.
  • Gastric cancer: Contributes to disease control in combination chemotherapy protocols.
  • Pancreatic cancer: Used off‑label in some combination regimens to improve response rates.

How It Works

  • Oxaliplatin forms reactive platinum complexes that covalently bind to DNA, creating intra‑ and interstrand cross‑links that inhibit DNA replication and transcription. This DNA damage triggers cell‑cycle arrest and apoptosis, particularly in rapidly dividing tumor cells.

Side Effects

Adverse reactions to oxaliplatin may vary in frequency and severity.

Common Side Effects

  • Nausea and vomiting: Frequently reported during or after infusion.
  • Peripheral neuropathy: Tingling or numbness, often dose‑related.
  • Diarrhoea: May range from mild to moderate severity.
  • Fatigue: Generalised tiredness experienced during treatment cycles.
  • Myelosuppression: Reduced blood cell counts, increasing infection risk.

Serious or Rare Side Effects

  • Severe hypersensitivity reactions: Including anaphylaxis and bronchospasm.
  • Acute neurotoxicity: Sudden onset of muscle cramps or respiratory difficulty.
  • Cardiotoxicity: Rare arrhythmias or myocardial injury.
  • Hemolytic‑uremic syndrome: Extremely rare but potentially life‑threatening.
  • Tumour lysis syndrome: May occur in high‑burden disease settings.

Precautions & Warnings

When handling oxaliplatin, clinicians and patients should observe several safety measures.

  • Renal function monitoring: Assess creatinine clearance before each cycle.
  • Neuropathy assessment: Evaluate sensory changes regularly to adjust dosing.
  • Hematologic monitoring: Perform complete blood counts prior to infusion.
  • Hypersensitivity vigilance: Observe for signs of allergic reaction during administration.
  • Pregnancy and lactation: Contra‑indicated unless benefits outweigh risks; discuss with obstetric specialist.
  • Store at below 25°C: Keep in original packaging, protect from light and moisture.

Avoid Interactions

Oxaliplatin may interact with other agents, influencing efficacy or toxicity.

Major Interactions (Avoid)

  • Anticoagulants: Increased bleeding risk when combined with oxaliplatin.
  • High‑dose vitamin C: May reduce platinum‑induced cytotoxicity.

Moderate Interactions (Monitor Closely)

  • Other neurotoxic chemotherapy (e.g., paclitaxel): Heightened peripheral neuropathy.
  • Renal‑clearing drugs (e.g., cisplatin): Cumulative nephrotoxicity potential.
  • Immunosuppressants: Enhanced infection susceptibility.
  • Proton pump inhibitors: Possible alteration of drug excretion.
  • Herbal supplements (e.g., St. John’s wort): May affect metabolic pathways.

Frequently Asked Questions

Oxaliplatin is a platinum‑based chemotherapy drug used primarily to treat colorectal cancer. It is administered as part of combination regimens, often with fluoropyrimidines, to improve tumour response and survival outcomes in adult patients.

Oxaliplatin creates platinum‑DNA adducts that cause intra‑ and interstrand cross‑links, blocking DNA replication and transcription. This damage triggers cell‑cycle arrest and apoptosis, especially in rapidly dividing cancer cells.

The prescribed dose of Oxaliplatin is determined by the treating oncologist based on the specific cancer type, patient weight, renal function and treatment protocol. Exact dosing regimens are individualized and should follow the prescriber’s instructions.

Oxaliplatin is generally contraindicated in pregnancy and breastfeeding because of potential fetal and infant toxicity. Use only if the potential benefit justifies the risk, and discuss any concerns with a qualified obstetric or oncology specialist.

To order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Oxaliplatin differs from cisplatin and carboplatin in its side‑effect profile, notably causing less nephrotoxicity but more peripheral neuropathy. Its DNA‑cross‑linking pattern offers distinct efficacy in colorectal cancer, making it a preferred option in many modern combination protocols.

Oxaliplatin should be stored below 25 °C, protected from light and moisture, and kept in its original packaging. It must be reconstituted and administered by qualified healthcare professionals following aseptic technique.

Oxaliplatin is supplied as a sterile solution for intravenous infusion. It is typically infused over a period of 2 hours under medical supervision, with pre‑medication to reduce nausea and infusion‑related reactions as needed.

Serious risks include severe hypersensitivity reactions, acute neurotoxicity, cardiotoxicity, hemolytic‑uremic syndrome and tumour lysis syndrome. Patients should be monitored closely for any signs of these events during and after infusion.

Oxaliplatin is contraindicated in patients with known hypersensitivity to platinum compounds, severe pre‑existing neuropathy, uncontrolled infections, or significant renal impairment. It should also be avoided in pregnant or breastfeeding women unless absolutely necessary.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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