GNH USA

Europe — EMA

Irinotecan Accord

GNH USA supplies Irinotecan Accord (Irinotecan), a topoisomerase I inhibitor for advanced colorectal cancer. EU‑sourced GMP‑compliant. Request a quote.

Irinotecan

Request sourcing

1
Pack/s

What is Irinotecan?

Irinotecan, the active ingredient in Irinotecan Accord, is a topoisomerase I inhibitor presented as an intravenous formulation for intravenous use. It is employed in the treatment of metastatic and advanced colorectal cancer, targeting tumor cells that rely on topoisomerase I activity.

GNH USA supplies Irinotecan Accord as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres, hospitals and pharmacies worldwide. The company adheres to stringent quality standards and provides regulatory‑approved batches for clinical use, including both private and public health systems.

What is Irinotecan used for?

Irinotecan is a topoisomerase I inhibitor used in colorectal cancer chemotherapy.

Metastatic colorectal cancer: improves overall survival when combined with fluoropyrimidine therapy. Advanced colorectal cancer: reduces tumor burden in patients with disease progression. Colorectal cancer (adjuvant setting): investigated in clinical trials for high‑risk patients.

What are the side effects of Irinotecan?

Irinotecan may cause a range of adverse reactions.

Common Side Effects: - Neutropenia: reduced white blood cell count increasing infection risk. - Diarrhea: often severe and may require antidiarrheal therapy. - Nausea and vomiting: typical chemotherapy‑related symptoms. - Alopecia: hair loss that is usually reversible. - Fatigue: generalized tiredness during treatment. - Anemia: decreased red blood cell levels.

Serious or Rare Side Effects: - Febrile neutropenia: fever with low neutrophil count requiring urgent care. - Severe colitis: intense inflammation of the colon. - Cholinergic syndrome: abdominal cramps, sweating, and bradycardia. - Hypersensitivity reactions: rash, itching, or anaphylaxis. - Hepatotoxicity: elevated liver enzymes or liver injury. - Pulmonary toxicity: rare lung inflammation.

What precautions apply to Irinotecan?

Before initiating Irinotecan therapy, clinicians should assess patient-specific factors. - Hepatic function: adjust dose in patients with liver impairment. - Blood counts: monitor complete blood count regularly for neutropenia. - Hydration: ensure adequate fluid intake to mitigate severe diarrhea. - Concomitant CYP3A4 inhibitors: avoid strong inhibitors that may increase exposure. - Pregnancy: use only if potential benefit justifies potential risk to the fetus. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze.

What does Irinotecan interact with?

Irinotecan can interact with several drug classes, requiring careful management.

Major Interactions (Avoid): - Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): may raise SN‑38 levels. - CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce efficacy. - Live vaccines: risk of infection due to immunosuppression.

Moderate Interactions (Monitor Closely): - Anticoagulants (e.g., warfarin): increased bleeding risk. - Other myelosuppressive agents: additive bone‑marrow suppression. - Fluoroquinolones: potential for enhanced neutropenia. - Loperamide: may mask early signs of severe diarrhea.

Frequently asked questions

What is Irinotecan Accord used for?+
Irinotecan Accord contains the chemotherapeutic agent irinotecan, which is indicated for the treatment of metastatic and advanced colorectal cancer. It works as part of a chemotherapy regimen to target rapidly dividing tumor cells.
How does irinotecan work in the body?+
Irinotecan is converted to the active metabolite SN‑38, which binds to the DNA‑topoisomerase I complex. This prevents the re‑ligation of single‑strand DNA breaks during replication, leading to DNA damage, cell‑cycle arrest, and tumor cell death.
What is the usual dose of Irinotecan Accord?+
The dose of Irinotecan Accord is determined by the prescribing oncologist based on the patient’s clinical condition, body surface area, and treatment protocol. Specific dosing regimens are not disclosed here and should follow the prescriber’s instructions.
Is Irinotecan Accord safe during pregnancy or breastfeeding?+
Irinotecan is classified as a prescription‑only antineoplastic agent and may pose risks to a developing fetus or nursing infant. It should only be used during pregnancy or lactation if the potential benefit justifies the potential risk, after thorough medical evaluation.
How do I order Irinotecan Accord from GNH USA?+
To place an order, submit an enquiry on the Irinotecan Accord product page at gnh-usa.com, specifying the required quantity. GNH USA supplies 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.
How does Irinotecan Accord compare with other colorectal cancer drugs?+
Irinotecan belongs to the topoisomerase I inhibitor class, differing from agents such as oxaliplatin (a platinum‑based drug) or fluoropyrimidines. It is often combined with fluoropyrimidines for synergistic effect and is chosen based on tumor genetics, prior therapy, and patient tolerance.
What are the storage and handling requirements for Irinotecan Accord?+
Irinotecan Accord should be stored at 2‑8 °C, kept refrigerated, protected from light, and should not be frozen or shaken. Follow the manufacturer’s instructions for reconstitution and handling in a sterile environment.
How is Irinotecan Accord administered?+
Irinotecan Accord is administered intravenously by a qualified healthcare professional. The infusion is typically given over a set period, as directed by the treatment protocol, and may be combined with other chemotherapy agents.
What are the most serious risks associated with Irinotecan Accord?+
The most serious risks include severe neutropenia with fever (febrile neutropenia), life‑threatening diarrhea or colitis, cholinergic syndrome, and rare hypersensitivity reactions. Prompt medical attention is required if any of these symptoms occur.
Who should not use Irinotecan Accord?+
Patients with known hypersensitivity to irinotecan or its components, severe hepatic impairment, uncontrolled infections, or those receiving contraindicated drug combinations should not use Irinotecan Accord. The prescribing physician will assess suitability on an individual basis.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Irinotecan
Route
Intravenous Use
Manufacturer
Accord Healthcare B.V.
Origin
EU

Related products