GNH USA

Europe — EMA

Irinotecano Accord

GNH USA supplies Irinotecano Accord (Irinotecan), a topoisomerase I inhibitor for metastatic colorectal cancer in adults. Request a quote for global supply.

Irinotecan Hydrochloride Trihydrate

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What is Irinotecan Hydrochloride Trihydrate?

Irinotecan Hydrochloride Trihydrate, the active ingredient in Irinotecano Accord, is a topoisomerase I inhibitor presented as a sterile injectable solution for intravenous use. It is employed in the treatment of metastatic colorectal cancer and advanced colorectal cancer in adult patients.

GNH USA supplies Irinotecano Accord as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres worldwide.

What is Irinotecan Hydrochloride Trihydrate used for?

Irinotecano Accord is a topoisomerase I inhibitor used in colorectal cancer treatment pathways.

Metastatic colorectal cancer: improves survival when combined with standard chemotherapy regimens. Colorectal cancer (advanced): reduces tumor burden and disease progression. Colorectal cancer (first‑line): administered with fluorouracil and leucovorin as part of a standard combination protocol.

What are the side effects of Irinotecan Hydrochloride Trihydrate?

Irinotecano Accord may cause a range of adverse reactions.

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

Serious or Rare Side Effects: - Febrile neutropenia: fever with low neutrophils requiring urgent care. - Severe colitis: intense abdominal pain and bloody diarrhea. - Cholinergic syndrome: abdominal cramps, sweating, and bradycardia. - Hypersensitivity reactions: rash, bronchospasm, or anaphylaxis. - Hepatotoxicity: elevated liver enzymes indicating liver injury.

What precautions apply to Irinotecan Hydrochloride Trihydrate?

Prior to initiating therapy, clinicians should evaluate patient‑specific risk factors.

Monitor blood counts: perform complete blood count before each infusion. Assess liver function: adjust dosing if bilirubin or transaminases are elevated. Hydration: ensure adequate fluid intake to mitigate severe diarrhea. Avoid concurrent strong CYP3A4 inhibitors: may increase irinotecan exposure. Pregnancy: contraindicated unless potential benefit justifies risk. Store at 2-8°C: keep refrigerated, protect from light, do not freeze.

What does Irinotecan Hydrochloride Trihydrate interact with?

Irinotecano Accord can interact with several drug classes.

Major Interactions (Avoid): - Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): may raise plasma levels. - UGT1A1 inhibitors (e.g., atazanavir): increase risk of toxicity. - Concurrent myelosuppressive agents: amplify bone‑marrow suppression.

Moderate Interactions (Monitor Closely): - CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce efficacy. - Anticholinergic drugs: may exacerbate cholinergic syndrome. - Anticoagulants: monitor for altered bleeding risk.

Frequently asked questions

What is Irinotecano Accord used for?+
Irinotecano Accord contains irinotecan, a chemotherapy agent indicated for the treatment of metastatic colorectal cancer and advanced colorectal cancer. It is administered intravenously as part of combination regimens to slow tumor growth and improve patient survival.
How does irinotecan work in cancer therapy?+
Irinotecan is converted inside cells to the active metabolite SN‑38, which inhibits topoisomerase I. This enzyme normally relieves DNA supercoiling during replication; its inhibition causes DNA strand breaks, halting replication and triggering apoptosis of rapidly dividing cancer cells.
What is the usual dose of Irinotecano Accord?+
The specific dose and schedule of Irinotecano Accord are determined by the prescribing oncologist based on factors such as disease stage, patient weight, liver function, and prior therapies. Only a qualified healthcare professional should set the dosing regimen.
Is Irinotecano Accord safe during pregnancy or breastfeeding?+
Irinotecan is classified as contraindicated in pregnancy unless the potential benefit outweighs the risk to the fetus. It is also not recommended during breastfeeding because it can be excreted in milk and may harm the infant. Consultation with a specialist is essential.
How do I order Irinotecano Accord from GNH USA?+
To place an order, submit an enquiry on the Irinotecano Accord product page at gnh-usa.com, specifying the required quantity. GNH USA 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.
How does Irinotecano Accord compare with other colorectal cancer drugs?+
Irinotecan belongs to the topoisomerase I inhibitor class, offering a distinct mechanism from fluoropyrimidines or oxaliplatin. It is often combined with these agents to enhance efficacy. Compared with other options, irinotecan provides a valuable alternative for patients who have progressed on or are unsuitable for other regimens.
What are the storage and handling requirements for Irinotecano Accord?+
Irinotecano Accord should be stored refrigerated at 2‑8 °C, protected from light, and must not be frozen or shaken. Keep the product in its original packaging until use to maintain stability and sterility.
How is Irinotecano Accord administered?+
The medication is given as an intravenous infusion, typically over 30 to 90 minutes depending on the protocol. Administration is performed by qualified healthcare personnel in a clinical setting, with monitoring for infusion‑related reactions and vital signs.
What are the most serious risks associated with Irinotecano Accord?+
The most critical 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 develop during or after treatment.
Who should not receive Irinotecano Accord?+
Patients with known hypersensitivity to irinotecan or its excipients, those with uncontrolled infections, severe hepatic impairment, or who are pregnant without a clear therapeutic justification should not receive Irinotecano Accord. A thorough clinical assessment is necessary before initiating therapy.
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 Hydrochloride Trihydrate
Route
Intravenous Use
Manufacturer
Accord Healthcare S.L.U.
Origin
EU

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