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

Oxaliplatin Stada

Active Ingredient:
Oxaliplatin
Origin:
EU

Oxaliplatin Stada (Oxaliplatin)

Oxaliplatin, the active ingredient in Oxaliplatin Stada, is a platinum‑based chemotherapy presented as a sterile solution for intravenous use. It is employed in the treatment of colorectal cancer, typically in combination with other agents, and is administered to adult patients under specialist supervision.

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

Manufacturer / TM Owner

Stadapharm Gmbh

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Indications & Clinical Uses

Oxaliplatin is a platinum‑based chemotherapeutic that interferes with DNA replication in rapidly dividing cells.

  • Colorectal cancer: improves progression‑free survival when used in combination regimens.
  • Gastric cancer: contributes to tumor response as part of multi‑drug protocols.
  • Pancreatic cancer: adds cytotoxic effect within combination therapy schedules.

How It Works

  • Oxaliplatin forms reactive platinum complexes that covalently bind to DNA, creating intra‑ and interstrand cross‑links that block DNA synthesis and trigger apoptosis in rapidly proliferating tumor cells. The drug’s activity is independent of the cellular mismatch‑repair status, enhancing its effectiveness across a range of gastrointestinal malignancies.

Side Effects

Oxaliplatin may cause a range of adverse reactions, varying in frequency and severity.

Common Side Effects

  • Nausea and vomiting: gastrointestinal upset commonly reported during infusion.
  • Peripheral neuropathy: tingling or numbness in extremities, often dose‑related.
  • Diarrhea: loose stools occurring during or after treatment cycles.
  • Fatigue: general tiredness that may affect daily activities.
  • Myelosuppression: reduced blood cell counts, increasing infection risk.

Serious or Rare Side Effects

  • Severe hypersensitivity reactions: including anaphylaxis, requiring immediate medical attention.
  • Acute pulmonary toxicity: respiratory distress or infiltrates on imaging.
  • Severe neutropenia or thrombocytopenia: markedly low white‑cell or platelet counts.
  • Cardiac arrhythmias: irregular heart rhythms observed during infusion.
  • Renal impairment: acute kidney injury in susceptible patients.

Precautions & Warnings

When handling Oxaliplatin Stada, clinicians should observe several safety measures to protect patients and staff.

  • Renal function assessment: evaluate baseline creatinine and monitor during therapy.
  • Neuropathy monitoring: assess sensory changes before each cycle and adjust dose if needed.
  • Hematologic surveillance: perform regular complete blood counts to detect myelosuppression.
  • Infusion site care: rotate sites and observe for phlebitis or extravasation.
  • Pregnancy and lactation: avoid use in pregnant or breastfeeding women unless benefits outweigh risks.
  • Store at ambient temperature: keep vials in original packaging, protect from light and moisture.

Avoid Interactions

Oxaliplatin can interact with other medicines, affecting its efficacy or safety profile.

Major Interactions (Avoid)

  • Aminoglycoside antibiotics: may increase nephrotoxic potential.
  • High‑dose vitamin C: can reduce platinum‑drug cytotoxicity.

Moderate Interactions (Monitor Closely)

  • Anticoagulants: heightened bleeding risk due to thrombocytopenia.\n- Other neurotoxic agents (e.g., vincristine): may exacerbate peripheral neuropathy.
  • CYP‑inducing agents: potential alteration of drug clearance, requiring dose review.
  • Radiotherapy: concurrent use may amplify tissue toxicity.
  • Electrolyte imbalances (hypomagnesemia): can worsen neurotoxic effects.

Frequently Asked Questions

Oxaliplatin Stada is an injectable platinum‑based chemotherapy indicated for the treatment of colorectal cancer and, in combination regimens, for certain gastric and pancreatic cancers. It is used under the direction of oncologists as part of multi‑drug protocols to improve tumor response and progression‑free survival.

Oxaliplatin creates platinum‑DNA adducts that cause intra‑ and interstrand cross‑links, blocking DNA replication and transcription. This DNA damage triggers programmed cell death (apoptosis) in rapidly dividing tumor cells, making the drug effective against a range of gastrointestinal malignancies.

The dosing regimen for Oxaliplatin Stada is individualized by the prescribing oncologist based on factors such as cancer type, treatment protocol, patient weight, renal function and prior therapy. Clinicians determine the appropriate dose and schedule 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 for breastfeeding mothers, as it may be excreted in breast 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 (including cold‑chain if needed) and 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. Clinicians often select oxaliplatin for colorectal cancer regimens where its efficacy and tolerability balance is advantageous.

Oxaliplatin Stada vials should be stored at ambient temperature, protected from light and moisture, and kept in their original packaging until use. Do not freeze. Follow standard aseptic techniques during preparation and administration to maintain product integrity.

The drug is supplied as a sterile solution for intravenous infusion. It is administered by a qualified healthcare professional, typically over a period of 2 hours, using an infusion pump or controlled drip set, following institutional protocols for chemotherapy delivery.

Serious risks include severe hypersensitivity reactions, acute pulmonary toxicity, profound neutropenia or thrombocytopenia, and dose‑limiting peripheral neuropathy. Patients should be monitored closely for signs of respiratory distress, infection, bleeding or worsening neuropathic symptoms during and after treatment.

Oxaliplatin Stada is contraindicated in patients with known hypersensitivity to platinum compounds, severe pre‑existing neuropathy, uncontrolled renal impairment, or active infections that could be worsened by myelosuppression. 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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