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

Oxaliplatina Hikma

Active Ingredient:
Oxaliplatin
Origin:
EU

Oxaliplatina Hikma (Oxaliplatin)

Oxaliplatin, the active ingredient in Oxaliplatina Hikma, is a platinum‑based chemotherapy agent presented as a sterile solution for intravenous use. It is employed in the treatment of colorectal cancer and other gastrointestinal malignancies, typically in adult patients. GNH India supplies Oxaliplatina Hikma as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres and hospitals worldwide.

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

Manufacturer / TM Owner

Hikma Farmacêutica (Portugal), S.A.

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Indications & Clinical Uses

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

  • Colorectal cancer: improves survival when used in combination regimens for metastatic or adjuvant therapy.
  • Gastric cancer: contributes to tumor response as part of combination chemotherapy.
  • Pancreatic cancer: used in selected protocols to enhance disease control.
  • Ovarian cancer: may be incorporated into multi‑drug regimens for refractory disease.
  • Esophageal cancer: added to standard regimens to increase response rates.
  • Small‑cell lung cancer: occasionally used off‑label within clinical trials.

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, particularly in rapidly proliferating tumor cells, while sparing most normal tissues at therapeutic doses.

Side Effects

Oxaliplatin may cause a range of adverse reactions, from mild to severe.

Common Side Effects

  • Nausea and vomiting: frequent gastrointestinal upset during or after infusion.
  • Peripheral neuropathy: tingling or numbness in hands and feet, often dose‑related.
  • Diarrhea: watery stools that may require supportive care.
  • Fatigue: generalized tiredness during treatment cycles.
  • Myelosuppression: reduced blood cell counts, increasing infection risk.
  • Elevated liver enzymes: transient changes in hepatic function tests.

Serious or Rare Side Effects

  • Severe hypersensitivity reactions: anaphylaxis or bronchospasm during infusion.
  • Acute hemolytic anemia: rapid destruction of red blood cells.
  • Severe neutropenia with fever: risk of life‑threatening infection.
  • Cardiotoxicity: arrhythmias or myocardial ischemia in rare cases.
  • Renal impairment: acute kidney injury requiring monitoring.
  • Thrombotic microangiopathy: rare clotting disorder affecting small vessels.

Precautions & Warnings

Oxaliplatin requires careful monitoring and patient counseling before and during therapy.

  • Renal function: assess baseline creatinine and adjust if impairment is present.
  • Hepatic function: evaluate liver enzymes and bilirubin prior to dosing.
  • Neuropathy risk: monitor for early signs of peripheral neuropathy and adjust dose as needed.
  • Hematologic status: perform complete blood counts before each cycle to detect myelosuppression.
  • Pregnancy and lactation: avoid use unless benefits outweigh potential fetal or infant risks.
  • Storage: Store below 25°C: keep in the original packaging, protect from light and moisture.

Avoid Interactions

Oxaliplatin can interact with several drug classes, affecting efficacy or safety.

Major Interactions (Avoid)

  • Nephrotoxic agents (e.g., cisplatin, aminoglycosides): increase risk of kidney damage.
  • Highly protein‑bound drugs (e.g., warfarin): may displace oxaliplatin and alter plasma levels.

Moderate Interactions (Monitor Closely)

  • Antiemetics (e.g., ondansetron): may be required to control infusion‑related nausea.
  • Antioxidants (e.g., vitamin C, E): theoretical reduction of platinum‑induced cytotoxicity.
  • CYP450 inducers/inhibitors: limited data, monitor for unexpected toxicity.
  • Radiotherapy: concurrent use may enhance neurotoxicity.
  • Blood transfusions: can affect laboratory monitoring of blood counts.

Frequently Asked Questions

Oxaliplatina Hikma is a platinum‑based chemotherapy indicated for the treatment of colorectal cancer and other gastrointestinal malignancies, often in combination with other anticancer agents as part of standard oncologic regimens.

Oxaliplatin creates platinum‑DNA adducts that cross‑link DNA strands, disrupting replication and transcription. This damage triggers cell‑cycle arrest and apoptosis, preferentially affecting rapidly dividing tumor cells.

The dose of oxaliplatin is individualized by the prescribing oncologist based on cancer type, treatment protocol, patient weight, renal function and other clinical factors. Specific dosing regimens are not provided here.

Oxaliplatin is classified as contraindicated in pregnancy because it may harm the developing fetus. It is also not recommended while breastfeeding, as it can be excreted in milk and affect the infant.

To place an order, submit an enquiry on the product page at gnhindia.com with the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and import documentation.

Oxaliplatin differs from cisplatin and carboplatin by its distinct side‑effect profile, notably a higher incidence of peripheral neuropathy but lower nephrotoxicity. Choice of agent depends on tumor type, patient tolerance and therapeutic goals.

Oxaliplatina Hikma should be stored below 25°C in its original packaging, protected from light and moisture. It must be reconstituted and administered by qualified healthcare professionals under aseptic conditions.

The product is supplied as a sterile solution for intravenous infusion. It is typically infused over a period of 2 hours, following institutional protocols and under the supervision of an oncology specialist.

Serious risks include severe hypersensitivity reactions, acute hemolytic anemia, profound neutropenia with fever, cardiotoxicity, renal impairment and rare thrombotic microangiopathy. Prompt medical attention is required if these occur.

Patients with known hypersensitivity to oxaliplatin or other platinum compounds, severe pre‑existing neuropathy, significant renal or hepatic impairment, and pregnant or breastfeeding women should not receive this medication unless the potential benefit outweighs the risk.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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