Product image of Oxaliplatine Hikma (Oxaliplatin) supplied by GNH India

Oxaliplatine Hikma

Active Ingredient:
Oxaliplatin
Origin:
EU

Oxaliplatine Hikma (Oxaliplatin)

Oxaliplatin, the active ingredient in Oxaliplatine Hikma, is a platinum compound presented as an intravenous solution for intravenous use. It treats colorectal cancer and is employed as adjuvant therapy for stage III colon cancer in adult patients.

GNH India supplies Oxaliplatine Hikma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide, with the product sourced from EU‑regulated manufacturers and meeting global quality standards. The company provides regulatory documentation and logistics support to ensure safe delivery to qualified healthcare institutions.

Manufacturer / TM Owner

Hikma Farmacêutica (Portugal), S.A.

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Indications & Clinical Uses

Oxaliplatin is used in oncology protocols that target colorectal malignancies and related disease stages.

  • Colorectal cancer: administered in combination regimens to inhibit tumor growth and improve response rates.
  • Stage III colon cancer (adjuvant): given after surgical resection to reduce the risk of disease recurrence.
  • Metastatic colorectal cancer: used as part of systemic therapy to control disease spread and prolong survival.

How It Works

  • Oxaliplatin forms covalent DNA cross‑links that block DNA replication and transcription. The resulting DNA damage triggers cellular apoptosis, particularly in rapidly dividing tumor cells, while sparing most normal tissues. Its platinum‑based structure enables the formation of both intra‑ and interstrand cross‑links, disrupting the cell cycle and leading to programmed cell death.

Side Effects

Oxaliplatin may cause a range of adverse reactions, from mild to severe, that require monitoring during therapy.

Common Side Effects

  • Nausea and vomiting: transient gastrointestinal upset.
  • Peripheral neuropathy: tingling or numbness, often dose‑related.
  • Fatigue: generalized tiredness affecting daily activities.
  • Neutropenia: reduced white blood cell count increasing infection risk.
  • Anemia: lowered red blood cell levels causing weakness.
  • Thrombocytopenia: decreased platelets leading to easy bruising.

Serious or Rare Side Effects

  • Severe allergic reactions: anaphylaxis or hypersensitivity requiring immediate care.
  • Pulmonary toxicity: interstitial lung disease or acute respiratory distress.
  • Severe neutropenia with fever: potential sepsis.
  • Hepatic dysfunction: elevated liver enzymes or jaundice.
  • Cardiac arrhythmias: irregular heart rhythms.
  • Tumor lysis syndrome: rapid tumor cell breakdown causing metabolic disturbances.

Precautions & Warnings

Prior to initiating Oxaliplatin therapy, clinicians should assess patient-specific risk factors and monitor relevant parameters.

  • Renal function: evaluate creatinine clearance and adjust dosing if impaired.
  • Pre‑existing neuropathy: avoid or use with caution in patients with baseline nerve damage.
  • Hematologic status: perform baseline CBC and monitor for cytopenias.
  • Electrolyte balance: correct hypomagnesemia and other electrolyte abnormalities.
  • Hypersensitivity: discontinue if severe allergic reaction occurs.
  • Store at ambient temperature: keep in original container, protect from moisture and light.

Avoid Interactions

Oxaliplatin can interact with other agents that affect renal function, hematopoiesis, or immune response.

Major Interactions (Avoid)

  • Concurrent platinum agents: additive toxicity and overlapping side‑effects.
  • Live vaccines: increased risk of infection due to immunosuppression.
  • High‑dose radiation therapy: potentiates tissue damage.

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may worsen renal impairment.
  • Loop diuretics: can exacerbate electrolyte disturbances and nephrotoxicity.
  • Anticoagulants/antiplatelet agents: heightened bleeding risk with thrombocytopenia.
  • Other myelosuppressive chemotherapy: cumulative bone‑marrow suppression.
  • Magnesium supplements: may reduce neurotoxicity but require monitoring.

Frequently Asked Questions

Oxaliplatine Hikma contains oxaliplatin, a platinum‑based chemotherapy agent indicated for the treatment of colorectal cancer, including metastatic disease, and as adjuvant therapy after surgery for stage III colon cancer. It is used in combination with other chemotherapeutic drugs to improve response rates and reduce the risk of disease recurrence.

Oxaliplatin exerts its anticancer effect by forming covalent cross‑links within DNA strands. These cross‑links block DNA replication and transcription, leading to accumulation of DNA damage and triggering programmed cell death (apoptosis) in rapidly dividing tumor cells while sparing most normal tissues.

The specific dose of Oxaliplatine Hikma is determined by the prescribing oncologist based on the patient’s weight, renal function, treatment regimen, and clinical response. Dosing is individualized and administered intravenously under medical supervision.

Oxaliplatin is classified as contraindicated in pregnancy because it may cause fetal harm. Women of child‑bearing potential should use effective contraception during treatment and for a period after the last dose. Breastfeeding is not recommended, as the drug can be excreted in milk and may affect the infant.

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 where applicable), and necessary import documentation.

Oxaliplatin differs from cisplatin and carboplatin in its side‑effect profile, notably causing less nephrotoxicity but a higher incidence of peripheral neuropathy. It is often preferred in colorectal cancer regimens because of its synergistic activity with fluoropyrimidines and favorable efficacy in this tumor type.

Oxaliplatine Hikma should be stored at ambient temperature, below 25 °C, in its original packaging. Protect the product from moisture, direct sunlight, and extreme temperature fluctuations. Follow standard aseptic handling procedures when preparing the intravenous solution.

Oxaliplatine Hikma is administered intravenously by a qualified healthcare professional. The drug is typically diluted in a compatible infusion solution and infused over a prescribed period, often 2 hours, depending on the treatment protocol and patient tolerance.

Serious risks include severe allergic reactions (anaphylaxis), pulmonary toxicity, profound neutropenia with fever (risk of infection), hepatic dysfunction, and cardiac arrhythmias. Patients should be monitored closely for signs of these events, and treatment should be discontinued if life‑threatening reactions occur.

Oxaliplatine Hikma is contraindicated in patients with known hypersensitivity to oxaliplatin or other platinum compounds, those with severe pre‑existing neuropathy, uncontrolled renal impairment, or active infections. Caution is also advised for patients with significant hepatic disease or cardiac conditions.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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