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

Oxaliplatin Aqvida

Active Ingredient:
Oxaliplatin
Origin:
EU

Oxaliplatin Aqvida (Oxaliplatin)

Oxaliplatin, the active ingredient in Oxaliplatin Aqvida, is a platinum‑based chemotherapy agent 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 by healthcare professionals in hospital or oncology centre settings.

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

Manufacturer / TM Owner

Aqvida Gmbh

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Indications & Clinical Uses

Oxaliplatin Aqvida is a platinum‑based chemotherapeutic that acts on the DNA replication pathway in malignant cells.

  • Colorectal cancer: used in combination regimens to inhibit tumour growth and improve survival.
  • Gastric cancer: incorporated into multi‑drug protocols to enhance response rates.
  • Pancreatic cancer: added to standard chemotherapy backbones to increase disease control.
  • Ovarian cancer: employed in selected cases as part of combination therapy to achieve cytoreduction.

How It Works

  • Oxaliplatin forms reactive platinum complexes that covalently bind to DNA bases, creating intra‑ and interstrand cross‑links that impede DNA replication and transcription. The resulting DNA damage triggers cell‑cycle arrest and apoptosis, preferentially affecting rapidly dividing cancer cells while sparing most normal tissues.

Side Effects

Oxaliplatin may cause a range of adverse reactions, from mild to severe, depending on patient factors and treatment context.

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 bleed risk.

Serious or Rare Side Effects

  • Severe hypersensitivity reactions: anaphylaxis or bronchospasm.
  • Acute neurotoxicity: sudden onset of muscle cramps or dysesthesia.
  • Hematologic toxicity: profound neutropenia or anemia.
  • Hepatotoxicity: elevated liver enzymes indicating liver stress.
  • Renal impairment: decreased kidney function requiring monitoring.

Precautions & Warnings

When using Oxaliplatin Aqvida, clinicians should assess patient suitability and monitor for known risks.

  • Renal function: evaluate creatinine clearance before each infusion.
  • Hepatic function: check liver enzymes and bilirubin levels regularly.
  • Neuropathy monitoring: assess sensory changes before and during therapy.
  • Hematologic surveillance: perform complete blood counts to detect cytopenias.
  • Premedication: consider anti‑emetics and antihistamines as per protocol.
  • Store at 2‑8°C: keep refrigerated, protect from light, do not freeze.

Avoid Interactions

Oxaliplatin may interact with several concomitant medicines, altering efficacy or safety.

Major Interactions (Avoid)

  • Aminoglycoside antibiotics: increased risk of nephrotoxicity.
  • High‑dose vitamin C: may reduce platinum‑drug cytotoxicity.
  • Live vaccines: immunosuppression can lead to uncontrolled infection.

Moderate Interactions (Monitor Closely)

  • Anticoagulants (e.g., warfarin): heightened bleeding risk due to thrombocytopenia.
  • NSAIDs: may exacerbate renal toxicity.
  • CYP‑inducing agents: potential impact on drug clearance, though oxaliplatin is not primarily metabolised by CYP enzymes.

Frequently Asked Questions

Oxaliplatin Aqvida is an intravenous platinum‑based chemotherapy indicated for the treatment of several solid tumours, most commonly colorectal cancer, and is used in combination with other anticancer agents to improve response rates and overall survival.

Oxaliplatin creates platinum‑DNA adducts that cross‑link DNA strands, blocking replication and transcription. This DNA damage triggers cell‑cycle arrest and apoptosis, preferentially targeting rapidly dividing tumour cells while sparing most normal tissues.

The dosing regimen for Oxaliplatin Aqvida is determined by the prescribing oncologist based on the specific cancer type, treatment protocol, patient weight, renal function and overall health status. Clinicians set the dose and infusion schedule according to established guidelines.

Oxaliplatin is classified as contraindicated in pregnancy because it can cross the placenta and cause fetal toxicity. It is also not recommended while breastfeeding, as it may be excreted in milk and affect the infant. Women of child‑bearing potential should use effective contraception during treatment.

To place an order, submit an enquiry on the Oxaliplatin Aqvida 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, leading to a distinct toxicity profile. It is associated with less nephrotoxicity and ototoxicity but has a higher incidence of peripheral neuropathy. Clinicians often choose oxaliplatin for colorectal regimens where its efficacy and side‑effect balance are advantageous.

Oxaliplatin Aqvida should be stored refrigerated at 2‑8 °C, protected from light, and must not be frozen. The solution should be inspected for particulate matter before use and handled with aseptic technique in a controlled‑temperature environment.

The product is supplied as a sterile solution for intravenous infusion. It is administered by a qualified healthcare professional, typically over 2 hours, using an infusion pump or controlled drip, following institutional protocols for pre‑medication and monitoring.

Serious risks include severe hypersensitivity reactions, acute neurotoxicity, profound neutropenia or thrombocytopenia leading to infection or bleeding, and hepatic or renal impairment. Prompt recognition and supportive care are essential to mitigate these potentially life‑threatening events.

Patients with known hypersensitivity to oxaliplatin or other platinum compounds, those with severe pre‑existing neuropathy, uncontrolled renal or hepatic dysfunction, and pregnant or breastfeeding women should not be treated with Oxaliplatin Aqvida.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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