GNH USA

Europe — EMA

Irinotecan Accord

GNH USA supplies Irinotecan Accord (Irinotecan), a topoisomerase I inhibitor for metastatic colorectal cancer and other solid tumors. Request a quote.

Irinotecan Hydrochloride Trihydrate

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What is Irinotecan Hydrochloride Trihydrate?

Irinotecan, the active ingredient in Irinotecan Accord, is a topoisomerase I inhibitor presented as an injectable solution for intravenous use. It is used in the treatment of metastatic colorectal cancer and other solid tumors in adult patients.

GNH USA supplies Irinotecan Accord as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide.

What is Irinotecan Hydrochloride Trihydrate used for?

Irinotecan Accord is a topoisomerase I inhibitor used in oncology to target malignant cells. - Metastatic colorectal cancer: used in combination regimens to inhibit tumor growth and improve survival. - Advanced colorectal cancer: employed as part of first‑line or later‑line therapy to control disease progression. - Other solid tumors: provided in selected cases where topoisomerase I inhibition offers antineoplastic benefit.

What are the side effects of Irinotecan Hydrochloride Trihydrate?

Irinotecan Accord may cause a range of adverse reactions.

Common Side Effects: - Diarrhea: often severe and may require antidiarrheal therapy. - Nausea and vomiting: managed with antiemetics. - Neutropenia: monitor blood counts regularly. - Fatigue: may affect daily activities. - Alopecia: hair loss can occur during treatment. - Abdominal pain: may accompany gastrointestinal upset.

Serious or Rare Side Effects: - Febrile neutropenia: risk of infection requiring prompt medical attention. - Severe diarrhea (colitis): can lead to dehydration and electrolyte imbalance. - Cholinergic syndrome: characterized by sweating, salivation, and bronchospasm. - Hypersensitivity reactions: including rash, fever, or anaphylaxis. - Hepatic toxicity: elevated liver enzymes indicating liver injury.

What precautions apply to Irinotecan Hydrochloride Trihydrate?

Prior to initiating Irinotecan Accord, several safety considerations are recommended. - Dose adjustment in hepatic impairment: reduce dose according to liver function tests. - Monitor blood counts: perform regular CBC to detect neutropenia early. - Assess for diarrhea: initiate antidiarrheal measures at first sign. - Avoid in pregnancy: contraindicated due to fetal risk (Category D). - Store at controlled room temperature: keep in original container, protect from light and moisture.

What does Irinotecan Hydrochloride Trihydrate interact with?

Irinotecan may interact with other medicines, requiring careful management.

Major Interactions (Avoid): - Strong CYP3A4 inducers: may lower irinotecan exposure and efficacy. - Concurrent use of other topoisomerase I inhibitors: increases risk of overlapping toxicity. - Live vaccines: immunosuppression can lead to infection.

Moderate Interactions (Monitor Closely): - Anticoagulants: heightened bleeding risk. - UGT1A1 inhibitors: can raise SN‑38 levels and toxicity. - Drugs causing electrolyte imbalance: may worsen irinotecan‑related diarrhea.

Frequently asked questions

What is Irinotecan Accord used for?+
Irinotecan Accord is an intravenous chemotherapy agent indicated for the treatment of metastatic colorectal cancer and selected other solid tumors in adult patients. It is typically used as part of combination regimens to improve disease control and overall survival.
How does Irinotecan work?+
Irinotecan is a pro‑drug that is converted inside cells to SN‑38, an active metabolite that binds to the DNA‑topoisomerase I complex. This prevents the re‑ligation of single‑strand DNA breaks during replication, causing permanent DNA damage and triggering cancer cell death.
What is the usual dose of Irinotecan Accord?+
The dosing of Irinotecan Accord is individualized and determined by the prescribing oncologist based on factors such as cancer type, treatment protocol, patient weight, and organ function. Specific regimens are not disclosed here.
Is Irinotecan Accord safe in pregnancy or breastfeeding?+
Irinotecan is classified as Pregnancy Category D, indicating evidence of fetal risk. It is contraindicated during pregnancy and should not be used by breastfeeding mothers because it may be excreted in milk and harm the infant.
How do I order Irinotecan Accord from GNH USA?+
To request Irinotecan Accord, submit an enquiry on the 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 Irinotecan compare with the main alternative drug or class?+
The primary alternative within the same class is topotecan, another topoisomerase I inhibitor. Irinotecan generally has a broader indication profile, especially for colorectal cancer, and is often combined with fluoropyrimidines. Topotecan is used more frequently for small‑cell lung cancer and ovarian cancer, with differing toxicity patterns.
How should Irinotecan Accord be stored and handled?+
Irinotecan Accord should be stored at controlled room temperature, below 25 °C, in its original packaging to protect from light and moisture. The product must be reconstituted and administered by qualified healthcare professionals following aseptic technique.
How is Irinotecan Accord given or administered?+
Irinotecan Accord is administered intravenously by a qualified healthcare provider, usually as an infusion over a specified period. The exact infusion rate and schedule are determined by the treating physician and may be adjusted based on patient tolerance and response.
What are the most serious risks to watch for with Irinotecan Accord?+
The most serious risks include severe neutropenia with fever (febrile neutropenia), life‑threatening diarrhea or colitis, cholinergic syndrome, hypersensitivity reactions, and hepatic toxicity. Prompt medical evaluation is essential if any of these events occur.
Who should not use Irinotecan Accord?+
Irinotecan Accord should not be used in patients with known hypersensitivity to irinotecan or its excipients, in pregnant women, or in individuals with severe hepatic impairment without dose adjustment. Caution is also advised for patients with pre‑existing severe bone‑marrow suppression.
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 Polska Sp. Z O.O.
Origin
EU

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