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

Oxaliplatin Accord Healthcare

Active Ingredient:
Oxaliplatin
Origin:
EU

Oxaliplatin Accord Healthcare (Oxaliplatin)

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

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

Manufacturer / TM Owner

Accord Healthcare B.V.

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Indications & Clinical Uses

Oxaliplatin is a platinum‑based chemotherapy drug that interferes with DNA replication in several cancer types.

  • Colorectal cancer: improves the efficacy of combination regimens and helps achieve tumour shrinkage.
  • Gastric cancer: used as part of multimodal treatment protocols.
  • Pancreatic cancer: contributes to disease control when combined with other agents.
  • Ovarian cancer: employed in platinum‑sensitive treatment strategies.
  • Esophageal cancer: added to multidrug regimens to enhance response rates.
  • Small‑cell lung cancer: incorporated into combination chemotherapy for better outcomes.

How It Works

  • Oxaliplatin forms reactive platinum‑DNA adducts that cause intra‑ and interstrand cross‑links, disrupting 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 elicit 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: loose stools that may require supportive care.
  • Fatigue: generalized tiredness during treatment cycles.
  • Thrombocytopenia: reduced platelet count, increasing bleeding risk.

Serious or Rare Side Effects

  • Severe hypersensitivity reactions: anaphylaxis or bronchospasm.
  • Acute neurotoxicity: sudden onset of muscle cramps or spasms.
  • Hematologic toxicity: neutropenia or anemia requiring intervention.
  • Hepatotoxicity: elevated liver enzymes indicating liver stress.
  • Cardiotoxicity: rare arrhythmias or chest discomfort.
  • Renal impairment: decreased kidney function in susceptible patients.

Precautions & Warnings

When using Oxaliplatin, clinicians should assess patient suitability and monitor for adverse events throughout therapy.

  • Renal function: evaluate baseline creatinine and adjust dosing if impaired.
  • Hepatic function: monitor liver enzymes before and during treatment.
  • Neuropathy risk: assess pre‑existing peripheral neuropathy and adjust therapy as needed.
  • Hematologic monitoring: perform regular complete blood counts to detect cytopenias.
  • Pregnancy and lactation: avoid use unless benefits outweigh risks; discuss with obstetric specialist.
  • Store at ambient temperature: keep in original container, protect from moisture and light.

Avoid Interactions

Oxaliplatin may interact with other medicines, altering efficacy or safety. Proper review of concomitant drugs is essential.

Major Interactions (Avoid)

  • Nephrotoxic agents (e.g., cisplatin, aminoglycosides): increase risk of kidney injury.
  • Anticoagulants (warfarin, DOACs): heightened bleeding risk due to thrombocytopenia.

Moderate Interactions (Monitor Closely)

  • Antiemetics (5‑HT3 antagonists): may require dose adjustment of anti‑emetic regimen.
  • Immunosuppressants (steroids, azathioprine): potential additive bone‑marrow suppression.
  • Radiotherapy: combined neurotoxicity risk, especially with peripheral nerve exposure.
  • CYP450 inducers/inhibitors: may modestly affect plasma levels, requiring observation.
  • Herbal supplements (e.g., St. John’s wort): possible alteration of drug metabolism.

Frequently Asked Questions

Oxaliplatin Accord Healthcare is a platinum‑based chemotherapy agent indicated for the treatment of several solid tumours, most commonly colorectal cancer, often in combination with other chemotherapy drugs as part of a standard treatment regimen.

Oxaliplatin exerts its anticancer effect by forming platinum‑DNA adducts that create cross‑links within and between DNA strands. These cross‑links block DNA replication and transcription, leading to cell‑cycle arrest and programmed cell death, especially in rapidly dividing cancer cells.

The specific dose of oxaliplatin is determined by the prescribing oncologist based on the patient’s diagnosis, body surface area, renal function and treatment protocol. Dosing regimens are individualized and should follow established clinical guidelines.

Oxaliplatin is classified as contraindicated in pregnancy because it can cross the placenta and may cause fetal harm. It is also not recommended while breastfeeding, as it may be excreted in milk and affect the infant. Consultation with a specialist is essential.

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 required import documentation.

Oxaliplatin differs from cisplatin and carboplatin in its chemical structure, which results in a distinct toxicity profile—most notably a higher incidence of peripheral neuropathy but lower nephrotoxicity. Efficacy is comparable in colorectal cancer, where oxaliplatin‑based regimens are often preferred.

Oxaliplatin should be stored at ambient temperature, protected from moisture and light, and kept in its original packaging until reconstitution. Once prepared for infusion, it must be used within the time frame specified in the product labeling.

Oxaliplatin is supplied as a sterile powder for intravenous infusion. It is reconstituted with a suitable diluent and administered by a healthcare professional, typically over a period of 2 hours, according to the prescribed treatment schedule.

Serious risks include severe hypersensitivity reactions, acute neurotoxicity, significant hematologic toxicity such as neutropenia or thrombocytopenia, and rare cases of cardiotoxicity or renal impairment. 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 infections, or significant renal or hepatic dysfunction. It should also be avoided in pregnant or breastfeeding individuals unless absolutely necessary.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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