Product image of Oxaliplatin Eugia (Oxaliplatin) supplied by GNH India

Oxaliplatin Eugia

Active Ingredient:
Oxaliplatin
Origin:
EU

Oxaliplatin Eugia (Oxaliplatin)

Oxaliplatin, the active ingredient in Oxaliplatin Eug, is a platinum‑based chemotherapy presented as a sterile solution for intravenous infusion use. It is employed in the treatment of certain solid tumours, most notably colorectal cancer, and is administered under the supervision of oncologists.

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

Manufacturer / TM Owner

Eugia Pharma (Malta) Ltd

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Indications & Clinical Uses

Oxaliplatin Eug is a platinum‑based agent used in the management of malignancies that are treated with DNA‑cross‑linking chemotherapy.

  • Colorectal cancer: enhances tumor response when combined with fluoropyrimidine regimens.
  • Gastric cancer: contributes to disease control as part of combination protocols.
  • Pancreatic cancer: used in multi‑drug regimens to improve progression‑free survival.

How It Works

  • Oxaliplatin exerts cytotoxic activity by forming covalent adducts with DNA, creating intra‑ and interstrand cross‑links that disrupt DNA replication and transcription. The resulting 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

  • Peripheral neuropathy: tingling or numbness, often dose‑related.
  • Nausea and vomiting: may require anti‑emetic prophylaxis.
  • Diarrhoea: can be mild to moderate.
  • Fatigue: generalised tiredness during treatment cycles.
  • Myelosuppression: reduced blood cell counts.
  • Elevated liver enzymes: mild transaminitis.

Serious or Rare Side Effects

  • Severe hypersensitivity reactions: including anaphylaxis.
  • Acute neurotoxicity: sudden onset of muscle cramps or spasms.
  • Persistent peripheral neuropathy: may be long‑lasting after treatment.
  • Hemolytic‑uremic syndrome: rare but serious renal complication.
  • Cardiac arrhythmias: uncommon electrophysiological disturbances.
  • Severe myelosuppression: febrile neutropenia or pancytopenia.

Precautions & Warnings

When handling Oxaliplatin Eug, clinicians should observe several safety measures.

  • Renal function assessment: evaluate baseline creatinine and eGFR before infusion.
  • Hepatic function monitoring: check liver enzymes and bilirubin regularly.
  • Neuropathy surveillance: assess sensory changes at each visit.
  • Hematologic monitoring: perform complete blood counts prior to each cycle.
  • Premedication: consider antihistamines or steroids to reduce infusion reactions.
  • Store at below 25°C: keep in the original container, protect from light and moisture.

Avoid Interactions

Oxaliplatin may interact with other medicines, altering efficacy or safety.

Major Interactions (Avoid)

  • Nephrotoxic agents: concurrent use can worsen renal impairment.
  • High‑dose vitamin C: may reduce platinum‑drug activity.
  • Live vaccines: immunosuppression increases infection risk.

Moderate Interactions (Monitor Closely)

  • Anticoagulants: heightened bleeding risk during thrombocytopenia.
  • Other neurotoxic chemotherapy: additive peripheral neuropathy.
  • CYP‑modulating drugs: may affect supportive‑care medication metabolism.

Frequently Asked Questions

Oxaliplatin Eug is a platinum‑based chemotherapy indicated for the treatment of certain solid tumours, most commonly colorectal cancer, and is used as part of combination regimens in gastric and pancreatic cancer under oncologist supervision.

Oxaliplatin forms covalent bonds with DNA, creating cross‑links that block replication and transcription. This DNA damage triggers cell‑cycle arrest and apoptosis, preferentially affecting rapidly dividing cancer cells.

The dose of Oxaliplatin Eug is individualized by the prescribing oncologist based on factors such as cancer type, treatment protocol, patient weight, renal function and overall health status.

Oxaliplatin is classified as contraindicated in pregnancy because it can cross the placenta and cause fetal toxicity. Breastfeeding is not recommended while receiving treatment, as the drug may be excreted in milk.

To order, submit an enquiry on the Oxaliplatin Eug product page at gnhindia.com, providing the required quantity and institutional credentials. GNH India will verify the buyer, then respond with pricing, availability, shipping details and any necessary import documentation.

Oxaliplatin differs from cisplatin and carboplatin by having a diaminocyclohexane carrier ligand, which reduces nephrotoxicity and increases activity against colorectal tumours, though it is associated with a higher incidence of peripheral neuropathy.

Oxaliplatin Eug should be stored below 25°C, protected from light and moisture, and kept in its original packaging. Reconstitution must be performed in a controlled environment using aseptic technique.

The product is supplied as a sterile solution for intravenous infusion. It is administered by a qualified healthcare professional, typically over 2 hours, with appropriate pre‑medication and monitoring for infusion reactions.

Serious risks include severe hypersensitivity reactions, acute neurotoxicity, persistent peripheral neuropathy, and profound myelosuppression that can lead to febrile neutropenia or infection.

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

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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