GNH USA

Europe — EMA

Irinotecan Kabi

GNH USA supplies Irinotecan Kabi (Irinotecan Hydrochloride), a topoisomerase I inhibitor for metastatic colorectal and small cell lung cancers.

Irinotecan Hydrochloride Trihydrate

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What is Irinotecan Hydrochloride Trihydrate?

Irinotecan Hydrochloride Trihydrate, the active ingredient in Irinotecan Kabi, is a topoisomerase I inhibitor presented as a sterile powder for intravenous use. It treats certain advanced cancers in adult patients, most commonly metastatic colorectal cancer and relapsed small cell lung cancer. GNH USA supplies Irinotecan Kabi as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide.

What is Irinotecan Hydrochloride Trihydrate used for?

Irinotecan Kabi is employed in oncology regimens that target rapidly dividing tumor cells. - Metastatic colorectal cancer: improves survival when used in combination chemotherapy protocols. - Relapsed small cell lung cancer: provides disease control as a second‑line option. - Advanced gastrointestinal cancers: contributes to tumor reduction as part of multi‑agent therapy.

What are the side effects of Irinotecan Hydrochloride Trihydrate?

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

Common Side Effects: - Neutropenia: reduced white blood cell count increasing infection risk. - Diarrhea: often severe and may require supportive care. - Nausea and vomiting: typical chemotherapy‑related symptoms. - Alopecia: temporary hair loss. - Fatigue: generalized tiredness. - Abdominal pain: discomfort in the stomach area.

Serious or Rare Side Effects: - Febrile neutropenia: fever with low neutrophils, a medical emergency. - Severe colitis: life‑threatening inflammation of the colon. - Cholinergic syndrome: sweating, salivation, and bradycardia. - Hypersensitivity reactions: rash, bronchospasm, or anaphylaxis. - Hepatic toxicity: elevated liver enzymes or jaundice. - Thromboembolic events: blood clots in veins or arteries.

What precautions apply to Irinotecan Hydrochloride Trihydrate?

Before initiating therapy with Irinotecan Kabi, several safety considerations are essential. - Dose adjustment: modify dosing in patients with hepatic impairment to avoid excess exposure. - Monitor blood counts: perform regular CBC tests to detect neutropenia early. - Assess renal function: adjust if severe renal dysfunction is present. - Avoid strong CYP3A4 inhibitors: concurrent use may increase drug levels and toxicity. - Pregnancy: prescribe only when potential benefits justify potential fetal risks. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Irinotecan Hydrochloride Trihydrate interact with?

Irinotecan Kabi can interact with other medicines, influencing its efficacy or safety.

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

Moderate Interactions (Monitor Closely): - CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce therapeutic effect. - Warfarin: may enhance anticoagulant effect, requiring INR monitoring.

Frequently asked questions

What is Irinotecan Kabi used for?+
Irinotecan Kabi is a chemotherapy agent indicated for the treatment of metastatic colorectal cancer and relapsed small cell lung cancer in adult patients, typically as part of combination regimens designed to improve survival and disease control.
How does Irinotecan Hydrochloride work?+
Irinotecan Hydrochloride is converted in the body to the active metabolite SN‑38, which inhibits topoisomerase I. This prevents the re‑ligation of single‑strand DNA breaks during replication, leading to DNA damage, cell cycle arrest, and apoptosis of rapidly dividing cancer cells.
What is the usual dose of Irinotecan Kabi?+
The prescribed dose of Irinotecan Kabi is determined by the treating oncologist based on the specific cancer type, patient body surface area, organ function, and prior therapies. Dosing regimens are individualized and should follow the prescriber’s instructions.
Is Irinotecan Kabi safe during pregnancy or breastfeeding?+
Safety of Irinotecan Kabi in pregnancy has not been established; it is generally contraindicated unless the potential benefit justifies the risk to the fetus. Breastfeeding is not recommended because the drug may be excreted in milk and could harm the infant.
How do I order Irinotecan Kabi from GNH USA?+
To order Irinotecan Kabi, 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 and any required import documentation.
How does Irinotecan compare with other chemotherapy agents?+
Compared with other topoisomerase I inhibitors, Irinotecan has a distinct toxicity profile, notably higher rates of severe diarrhea and neutropenia. It is often chosen when fluoropyrimidine‑based regimens are insufficient, while alternatives such as topotecan or newer targeted therapies may be preferred in different clinical contexts.
What are the storage and handling requirements for Irinotecan Kabi?+
Irinotecan Kabi should be stored at 2‑8 °C, protected from light, and kept in its original container. It must not be frozen or shaken. Reconstitution should be performed using aseptic technique immediately before intravenous infusion.
How is Irinotecan Kabi administered?+
Irinotecan Kabi is supplied as a sterile powder for intravenous infusion. After reconstitution with the appropriate diluent, it is administered over 30‑90 minutes under medical supervision, following the dosing schedule prescribed by the oncologist.
What are the most serious risks to watch for with Irinotecan Kabi?+
The most critical risks include severe neutropenia, febrile neutropenia, life‑threatening diarrhea (colitis), cholinergic syndrome, and hypersensitivity reactions. Patients should be monitored closely for signs of infection, dehydration, and allergic responses throughout treatment.
Who should not use Irinotecan Kabi?+
Patients with known hypersensitivity to Irinotecan or its excipients, those with severe hepatic impairment, uncontrolled infections, or a history of severe myelosuppression should avoid the drug. The prescribing physician must evaluate each individual’s suitability 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
Fresenius Kabi Polska Sp. Z O.O.
Origin
EU

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