GNH USA

Europe — EMA

Irinotecan Eugia

GNH USA supplies Irinotecan Eugia (Irinotecan), a topoisomerase I inhibitor for metastatic colorectal cancer. Request a quote for qualified buyers today.

Irinotecan Hydrochloride Trihydrate

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What is Irinotecan Hydrochloride Trihydrate?

Irinotecan, the active ingredient in Irinotecan Eugia, is a topoisomerase I inhibitor presented as an injectable solution for intravenous use. Originating from the European market, this generic formulation is employed in the treatment of metastatic colorectal cancer in adult patients, often as part of combination chemotherapy regimens.

GNH USA supplies Irinotecan Eugia as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres, hospitals and specialty pharmacies worldwide, ensuring quality and regulatory conformity with reliable cold‑chain logistics where required and timely delivery.

What is Irinotecan Hydrochloride Trihydrate used for?

Irinotecan is used in colorectal cancer therapy, targeting tumor cells that rely on topoisomerase I activity.

- Metastatic colorectal cancer: improves survival when combined with fluoropyrimidine‑based regimens. - Advanced colorectal carcinoma: provides therapeutic benefit after failure of first‑line treatment. - Colorectal adenocarcinoma: used as part of combination chemotherapy protocols.

What are the side effects of Irinotecan Hydrochloride Trihydrate?

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

Common Side Effects: - Nausea: mild to moderate nausea often occurring during infusion. - Diarrhea: acute diarrhea that may require antidiarrheal therapy. - Neutropenia: reduced neutrophil count increasing infection risk. - Fatigue: generalized tiredness affecting daily activities. - Alopecia: hair loss that is usually reversible after treatment.

Serious or Rare Side Effects: - Severe neutropenia with fever: febrile neutropenia requiring hospitalization. - Grade 3–4 diarrhea: may lead to dehydration and colitis. - Hepatic toxicity: elevated liver enzymes or bilirubin. - Allergic reactions: rash, pruritus, or anaphylaxis. - Severe abdominal pain: may indicate intestinal perforation.

What precautions apply to Irinotecan Hydrochloride Trihydrate?

Prior to initiating Irinotecan therapy, several safety considerations should be evaluated.

- Monitor blood counts: perform baseline and periodic CBC to detect neutropenia. - Assess liver function: evaluate hepatic enzymes and bilirubin, adjust dose if impaired. - Ensure adequate hydration: maintain fluid intake to mitigate diarrhea risk. - Review concomitant medications: avoid strong CYP3A4 inhibitors that may increase exposure. - Pregnancy and lactation: use only if potential benefit justifies potential risk to fetus or infant. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze.

What does Irinotecan Hydrochloride Trihydrate interact with?

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

Major Interactions (Avoid): - Ketoconazole: potent CYP3A4 inhibitor that can raise irinotecan plasma levels. - Rifampin: strong CYP3A4 inducer that may reduce therapeutic exposure. - Atazanavir: UGT1A1 inhibitor increasing SN‑38 concentrations and toxicity.

Moderate Interactions (Monitor Closely): - Warfarin: may experience altered anticoagulant effect; monitor INR. - Loperamide: can mask early signs of irinotecan‑induced diarrhea. - Anticholinergic agents: may exacerbate constipation and affect gastrointestinal motility.

Frequently asked questions

What is Irinotecan Eugia used for?+
Irinotecan Eugia is used primarily in the treatment of metastatic colorectal cancer. It is administered as part of combination chemotherapy regimens to help control tumor growth and improve patient outcomes in adult oncology patients.
How does Irinotecan work?+
Irinotecan is a pro‑drug that is metabolized inside cancer cells to SN‑38, which inhibits topoisomerase I. This inhibition prevents the resealing of DNA strands during replication, causing DNA damage and ultimately leading to cell death in rapidly dividing tumor cells.
What determines the dose of Irinotecan Eugia?+
The dose of Irinotecan Eugia is determined by the prescribing physician based on factors such as the patient’s body surface area, overall health, liver function, and the specific chemotherapy protocol being used. No fixed dosing schedule is provided here.
Is Irinotecan safe during pregnancy or breastfeeding?+
Irinotecan is generally contraindicated during pregnancy and lactation unless the potential therapeutic benefit justifies the potential risk to the fetus or infant. Clinicians should discuss risks and alternatives with patients who are pregnant, planning pregnancy, or breastfeeding.
How do I order Irinotecan Eugia from GNH USA?+
To order Irinotecan Eugia, submit an enquiry on the product page at gnh-usa.com specifying the required quantity. GNH USA supplies hospitals, pharmacies and procurement teams across international markets, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain where required) and necessary import documentation.
How does Irinotecan compare with other colorectal cancer drugs?+
Irinotecan belongs to the topoisomerase I inhibitor class, whereas alternatives such as oxaliplatin are platinum‑based agents and fluorouracil is a pyrimidine analogue. Irinotecan is often chosen for patients who have progressed after fluoropyrimidine therapy, offering a different mechanism of action and a distinct side‑effect profile.
What are the storage and handling requirements for Irinotecan Eugia?+
Irinotecan Eugia should be stored at 2‑8 °C in a refrigerator, protected from light, and must not be frozen or shaken. The product should be kept in its original packaging until ready for preparation and administration.
How is Irinotecan administered?+
Irinotecan is given by intravenous infusion under the supervision of a qualified healthcare professional. The infusion rate, duration, and schedule are determined by the treating oncologist and are typically part of a multi‑drug chemotherapy protocol.
What are the most serious risks to watch for with Irinotecan?+
The most serious risks include severe neutropenia with fever (febrile neutropenia), grade 3‑4 diarrhea that can lead to dehydration or colitis, hepatic toxicity, and rare but life‑threatening allergic reactions such as anaphylaxis. Prompt medical attention is required if these occur.
Who should not use Irinotecan?+
Patients with known hypersensitivity to irinotecan or its excipients, those with severe hepatic impairment, or individuals with uncontrolled infections should avoid Irinotecan. The drug should also be used with caution in patients with pre‑existing 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
Eugia Pharma (Malta) Ltd
Origin
EU

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