Product image of Oxaliplatin Accord Healthcare Ireland (Oxaliplatin) supplied by GNH India

Oxaliplatin Accord Healthcare Ireland

Active Ingredient:
Oxaliplatin
Origin:
EU

Oxaliplatin Accord Healthcare Ireland (Oxaliplatin)

Oxaliplatin, the active ingredient in Oxaliplatin Accord Healthcare Ireland, is a platinum‑based chemotherapy presented as a solution for intravenous use. It treats colorectal cancer and other solid tumours in adult patients. GNH India supplies Oxaliplatin Accord Healthcare Ireland as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres, hospitals and pharmacies worldwide.

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

Manufacturer / TM Owner

Accord Healthcare Ireland Limited

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Indications & Clinical Uses

Oxaliplatin is a platinum‑based agent used in the treatment of cancers that involve the gastrointestinal tract and related metastatic disease.

  • Colorectal cancer: improves survival when combined with fluorouracil and leucovorin in adjuvant and metastatic settings.
  • Gastric cancer: used as part of combination regimens for advanced disease.
  • Pancreatic cancer: contributes to response rates when added to multi‑drug protocols.
  • Ovarian cancer: employed in selected regimens for recurrent disease.
  • Esophageal cancer: used in combination chemotherapy for locally advanced tumours.
  • Small‑cell lung cancer: occasionally incorporated into experimental combination protocols.

How It Works

  • Oxaliplatin forms reactive platinum‑DNA adducts that disrupt DNA replication and transcription, leading to cell‑cycle arrest and apoptosis. The drug preferentially forms intra‑strand cross‑links, interfering with the repair mechanisms of rapidly dividing tumor cells while sparing most normal tissues.

Side Effects

Oxaliplatin may cause a range of adverse reactions that vary in frequency and severity.

Common Side Effects

  • Nausea and vomiting: mild to moderate gastrointestinal upset.
  • Peripheral neuropathy: tingling or numbness, often dose‑related.
  • Diarrhoea: watery stools that may require supportive care.
  • Fatigue: generalized tiredness affecting daily activities.
  • Thrombocytopenia: reduced platelet count increasing bleed risk.
  • Elevated liver enzymes: transient rise in ALT/AST.

Serious or Rare Side Effects

  • Severe hypersensitivity reactions: anaphylaxis or bronchospasm.
  • Persistent neurotoxicity: long‑lasting sensory deficits.
  • Myelosuppression: profound neutropenia or anemia.
  • Acute pulmonary toxicity: interstitial pneumonitis.
  • Renal impairment: acute kidney injury in susceptible patients.
  • Cardiotoxicity: rare arrhythmias or myocardial injury.

Precautions & Warnings

When handling Oxaliplatin, clinicians should consider several safety and monitoring measures.

  • Renal function: assess baseline creatinine and adjust if impaired.
  • Hepatic function: monitor liver enzymes before each cycle.
  • Neuropathy risk: evaluate baseline peripheral sensation and adjust dose if neuropathy develops.
  • Hematologic status: check complete blood count prior to infusion.
  • Pregnancy and lactation: avoid use unless benefits outweigh potential fetal risks.
  • Storage: Store below 25°C: keep in the original container, protect from light and moisture.

Avoid Interactions

Oxaliplatin may interact with other medicines, requiring attention to avoid reduced efficacy or increased toxicity.

Major Interactions (Avoid)

  • Nephrotoxic agents: concurrent use with high‑dose cisplatin or aminoglycosides may worsen kidney injury.
  • Anticoagulants: increased bleeding risk when combined with warfarin or direct oral anticoagulants.

Moderate Interactions (Monitor Closely)

  • Antiemetics: serotonin‑receptor antagonists may enhance serotonin syndrome risk.
  • CYP450 inducers: drugs such as rifampicin could alter oxidative metabolism of supportive agents.
  • Immunosuppressants: heightened infection risk when combined with high‑dose steroids.
  • Radiotherapy: concurrent treatment may amplify neuro‑toxic effects.
  • Herbal supplements: St John’s wort may affect plasma levels of concomitant supportive drugs.

Frequently Asked Questions

Oxaliplatin Accord Healthcare Ireland is a platinum‑based chemotherapeutic used primarily in combination regimens for colorectal cancer and other gastrointestinal malignancies. It is administered intravenously as part of multi‑drug protocols to improve response rates and overall survival in adult oncology patients.

Oxaliplatin creates platinum‑DNA adducts that block DNA replication and transcription, causing cell‑cycle arrest and apoptosis in rapidly dividing tumor cells. Its ability to form intra‑strand cross‑links makes it especially effective against cells with limited DNA‑repair capacity.

The specific dose of oxaliplatin is determined by the prescribing oncologist based on the treatment protocol, patient weight, renal function and combination drugs. Dosing regimens vary across different cancer indications and are individualized for each patient.

Oxaliplatin is classified as contraindicated in pregnancy because it can cross the placenta and cause fetal toxicity. It is also not recommended while breastfeeding, as it may be excreted in milk and affect the infant. Use only if the potential benefit justifies the risk.

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.

Oxaliplatin differs from cisplatin and carboplatin in its side‑effect profile, showing less nephrotoxicity but a higher incidence of peripheral neuropathy. Its DNA‑cross‑linking pattern provides distinct activity against colorectal tumours, making it a preferred choice in many modern regimens.

Oxaliplatin should be stored below 25 °C in its original packaging, protected from light and moisture. The solution must be prepared in a sterile environment and used within the stability period indicated by the manufacturer.

Oxaliplatin is given as an intravenous infusion, typically over 2 hours, under the supervision of qualified healthcare professionals. Infusion rates and pre‑medication for nausea or hypersensitivity are determined by the treatment protocol.

The most serious risks include severe peripheral neuropathy, hypersensitivity reactions that can be life‑threatening, and myelosuppression leading to infection or bleeding. Patients should be monitored closely for these events throughout treatment.

Oxaliplatin is contraindicated in patients with known hypersensitivity to platinum compounds, severe pre‑existing neuropathy, uncontrolled renal or hepatic impairment, and in pregnant or lactating women unless the therapeutic benefit outweighs the risk.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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