GNH USA

Europe — EMA

Irinotekanijev Klorid Kabi

GNH USA supplies Irinotekanijev Klorid Kabi (Irinotecan), a topoisomerase I inhibitor for colorectal cancer and solid tumors. Request a quote for supply.

Irinotecan Hydrochloride Trihydrate

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What is Irinotecan Hydrochloride Trihydrate?

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

GNH USA supplies Irinotekanijev Klorid Kabi as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide.

What is Irinotecan Hydrochloride Trihydrate used for?

Irinotecan is a topoisomerase I inhibitor used in chemotherapy for gastrointestinal and other solid tumors.

Colorectal cancer: improves survival when combined with standard chemotherapy regimens. Metastatic colorectal cancer: used as part of combination therapy to reduce tumor burden. Other solid tumors: employed in selected cases where topoisomerase I inhibition is indicated.

What are the side effects of Irinotecan Hydrochloride Trihydrate?

Irinotecan may cause a range of adverse reactions that vary in frequency and severity.

Common Side Effects: - Nausea and vomiting - Diarrhea, often severe - Neutropenia (low white blood cell count) - Fatigue and weakness - Alopecia (hair loss) - Mild liver enzyme elevations

Serious or Rare Side Effects: - Febrile neutropenia with risk of infection - Severe colitis or bowel perforation - Hepatic toxicity with jaundice - Anaphylactic or severe allergic reactions - Pulmonary toxicity (interstitial pneumonitis) - Cardiac arrhythmias in susceptible patients

What precautions apply to Irinotecan Hydrochloride Trihydrate?

Before initiating therapy, clinicians should assess patient-specific risk factors and monitor organ function.

Pregnancy: Category D – avoid use unless potential benefit justifies the risk. Breastfeeding: Not recommended; drug may be excreted in milk. Renal impairment: Use with caution and monitor renal function. Hepatic impairment: Adjust monitoring; dose may need modification. Concurrent myelosuppressive agents: Monitor for additive bone‑marrow suppression. Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Irinotecan Hydrochloride Trihydrate interact with?

Irinotecan can interact with several medicines, affecting its efficacy or safety.

Major Interactions (Avoid): - Strong CYP3A4 inhibitors (e.g., ketoconazole) – may increase exposure. - UGT1A1 inhibitors (e.g., atazanavir) – raise risk of neutropenia. - Live vaccines – heightened infection risk due to immunosuppression.

Moderate Interactions (Monitor Closely): - Other myelosuppressive chemotherapy agents – additive bone‑marrow toxicity. - High‑dose radiation therapy – may exacerbate tissue damage.

Frequently asked questions

What is Irinotekanijev Klorid Kabi used for?+
Irinotekanijev Klorid Kabi contains irinotecan, a topoisomerase I inhibitor indicated for the treatment of colorectal cancer, metastatic colorectal cancer and selected solid tumours. It is used as part of combination chemotherapy regimens in adult patients to improve disease control and survival outcomes.
How does Irinotecan work?+
Irinotecan is a pro‑drug that is metabolised inside cells to SN‑38, an active metabolite that binds to the DNA‑topoisomerase I complex. By stabilising this complex, it prevents the re‑ligation of single‑strand DNA breaks during replication, leading to accumulation of DNA damage, cell‑cycle arrest and ultimately tumour cell death.
What is the usual dose of Irinotekanijev Klorid Kabi?+
The dose of Irinotekanijev Klorid Kabi is individualized and determined by the prescribing oncologist based on factors such as cancer type, treatment protocol, patient weight, organ function and prior therapy. No fixed dosing information is provided here; clinicians set the regimen according to established guidelines.
Is Irinotekanijev Klorid Kabi safe in pregnancy or breastfeeding?+
Irinotecan is classified as Pregnancy Category D, indicating evidence of risk to the fetus. It should only be used during pregnancy when the potential benefit justifies the risk. Breastfeeding is not recommended because the drug can be excreted in milk and may harm the infant.
How do I order Irinotekanijev Klorid Kabi from GNH USA?+
To place an order, submit an enquiry on the 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 where required) and any necessary import documentation.
How does Irinotecan compare with other topoisomerase I inhibitors?+
Irinotecan and topotecan are the two main topoisomerase I inhibitors used in oncology. Irinotecan is typically employed for colorectal and certain solid tumours, while topotecan is more common in ovarian and small‑cell lung cancer. Both share a similar mechanism but differ in pharmacokinetics, toxicity profiles and approved indications.
What are the storage and handling requirements for Irinotekanijev Klorid Kabi?+
The injectable solution should be stored refrigerated at 2‑8 °C, protected from light, and must not be frozen or shaken. Prior to administration, the product should be inspected for particulate matter and used within the time frame specified in the manufacturer’s labeling.
How is Irinotekanijev Klorid Kabi administered?+
Irinotekanijev Klorid Kabi is given by intravenous infusion. The solution is diluted according to the prescribing information and infused over a defined period, usually 30‑90 minutes, under medical supervision. Infusion rates may be adjusted based on patient tolerance and clinical response.
What are the most serious risks associated with Irinotecan therapy?+
The most serious adverse events include severe neutropenia with risk of infection, febrile neutropenia, life‑threatening diarrhoea (including colitis or bowel perforation), hepatic toxicity, and rare allergic reactions such as anaphylaxis. Prompt monitoring and supportive care are essential to manage these risks.
Who should not use Irinotekanijev Klorid Kabi?+
Patients with known hypersensitivity to irinotecan or any component of the formulation should avoid the product. It is also contraindicated in individuals with severe bone‑marrow suppression, uncontrolled infections, or those who are pregnant unless the therapeutic benefit outweighs the risk. Clinical judgment is required for other special populations.
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
Fresenius Kabi Austria Gmbh
Origin
EU

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