GNH USA

Europe — EMA

Irinotecan Hydrochloride Accord Healthcare Ireland

GNH USA supplies Irinotecan Hydrochloride Accord Healthcare Ireland (Irinotecan), an antineoplastic agent for colorectal cancer. Request a quote for supply.

Irinotecan Hydrochloride Trihydrate

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What is Irinotecan Hydrochloride Trihydrate?

Irinotecan Hydrochloride, the active ingredient in Irinotecan Hydrochloride Accord Healthcare Ireland, is a topoisomerase I inhibitor presented as an injectable solution for intravenous use. It treats colorectal cancer, including metastatic disease, in adult patients.

GNH USA supplies Irinotecan Hydrochloride Accord Healthcare Ireland as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres, hospitals, pharmacies and clinics worldwide.

What is Irinotecan Hydrochloride Trihydrate used for?

Irinotecan Hydrochloride is used in the management of colorectal cancer and related disease pathways.

- Colorectal cancer: improves survival by targeting rapidly dividing tumor cells. - Metastatic colorectal cancer: provides systemic therapy for advanced disease. - Advanced colorectal carcinoma: used as part of combination chemotherapy regimens to reduce tumor burden.

What are the side effects of Irinotecan Hydrochloride Trihydrate?

Irinotecan Hydrochloride may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects: - Nausea: mild to moderate upset stomach. - Diarrhea: often severe and may require antidiarrheal therapy. - Fatigue: general tiredness during treatment cycles. - Alopecia: hair loss that is usually reversible. - Neutropenia: reduced neutrophil count increasing infection risk. - Anemia: lowered red blood cell count causing fatigue.

Serious or Rare Side Effects: - Severe neutropenia: profound drop in neutrophils requiring medical intervention. - Febrile neutropenia: fever with low neutrophils, a medical emergency. - Severe diarrhea (colitis): can lead to dehydration and electrolyte imbalance. - Liver enzyme elevation: indicates hepatic stress. - Allergic reactions: rash, itching, or anaphylaxis. - Pulmonary toxicity: rare lung inflammation.

What precautions apply to Irinotecan Hydrochloride Trihydrate?

When using Irinotecan Hydrochloride, clinicians should observe several precautionary measures to ensure patient safety.

- Assess baseline blood counts: obtain a complete blood count before each cycle. - Monitor liver function: check hepatic enzymes regularly. - Adjust dose in hepatic impairment: reduce dosage according to liver function tests. - Avoid concurrent strong CYP3A4 inhibitors: these may increase exposure. - Educate patients on early signs of diarrhea: prompt antidiarrheal therapy is essential. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Irinotecan Hydrochloride Trihydrate interact with?

Irinotecan Hydrochloride interacts with several drugs that can alter its efficacy or toxicity.

Major Interactions (Avoid): - Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may increase toxicity. - Concurrent use of other topoisomerase I inhibitors: additive bone marrow suppression. - High-dose aspirin or NSAIDs: increased risk of gastrointestinal toxicity.

Moderate Interactions (Monitor Closely): - UGT1A1 inhibitors (e.g., atazanavir): may raise plasma levels. - Anticoagulants (e.g., warfarin): monitor INR for bleeding risk. - Radiotherapy to abdomen: may enhance gastrointestinal toxicity.

Frequently asked questions

What is Irinotecan Hydrochloride used for?+
Irinotecan Hydrochloride is an antineoplastic agent indicated for the treatment of colorectal cancer, including metastatic disease, and is commonly used in combination chemotherapy regimens for adult patients.
How does Irinotecan Hydrochloride work?+
The drug inhibits topoisomerase I, preventing DNA re‑ligation during replication. This causes accumulation of DNA breaks, leading to tumor cell apoptosis and inhibition of cancer growth.
What is the usual dose of Irinotecan Hydrochloride?+
The prescribed dose is set by the treating physician based on factors such as body surface area, disease stage and prior therapy. Dosing regimens follow the approved prescribing information and are individualized for each patient.
Is Irinotecan Hydrochloride safe in pregnancy or breastfeeding?+
Irinotecan Hydrochloride is classified as pregnancy category D and can cause fetal harm; it is not recommended during pregnancy. It is also contraindicated while breastfeeding because the drug is excreted in milk and may affect the infant.
How do I order Irinotecan Hydrochloride from GNH USA?+
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 other chemotherapy agents for colorectal cancer?+
Irinotecan belongs to the topoisomerase I inhibitor class, offering a mechanism distinct from fluoropyrimidines or oxaliplatin. It is often combined with 5‑FU and leucovorin, providing synergistic activity and is preferred for patients who have progressed on or are unsuitable for other regimens.
What are the storage and handling requirements for Irinotecan Hydrochloride?+
The injectable solution must be stored refrigerated at 2‑8 °C, protected from light, and should never be frozen or shaken. Before administration, allow the product to reach room temperature and inspect for particulate matter.
How is Irinotecan Hydrochloride administered?+
Irinotecan Hydrochloride is given as an intravenous infusion, typically over 30 to 90 minutes, under the supervision of qualified healthcare professionals. Infusion rates may be adjusted based on patient tolerance and clinical response.
What are the most serious risks associated with Irinotecan Hydrochloride?+
The most critical adverse events include severe neutropenia, febrile neutropenia, and life‑threatening diarrhea (colitis). Prompt monitoring and supportive care are essential to mitigate these risks.
Who should not receive Irinotecan Hydrochloride?+
Patients with known hypersensitivity to irinotecan or its excipients, severe hepatic impairment, uncontrolled infections, or pre‑existing severe bone‑marrow suppression should avoid this medication.
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 Ireland Limited
Origin
EU

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