GNH USA

Europe — EMA

Irinotecan Eugia

GNH USA supplies Irinotecan Eugia (Irinotecan), a topoisomerase I inhibitor for colorectal cancer treatment. Request a quote for reliable supply.

Irinotecan Hydrochloride Trihydrate

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What is Irinotecan Hydrochloride Trihydrate?

Irinotecan Hydrochloride Trihydrate, the active ingredient in Irinotecan Eugia, is a topoisomerase I inhibitor presented as a sterile injectable solution for intravenous use. It is employed in the treatment of colorectal cancer, primarily in adult patients requiring systemic chemotherapy, and is commonly used within combination regimens such as FOLFIRI under the supervision of qualified healthcare professionals.

GNH USA supplies Irinotecan Eugia as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and procurement teams worldwide, ensuring quality‑assured product availability and regulatory compliance.

What is Irinotecan Hydrochloride Trihydrate used for?

Irinotecan Eugia is a topoisomerase I inhibitor used in colorectal cancer chemotherapy.

Colorectal cancer (adjuvant setting): improves disease‑free survival when added to postoperative chemotherapy. Metastatic colorectal cancer (first‑line): forms part of combination regimens to reduce tumor burden. Metastatic colorectal cancer (second‑line): provides an alternative after progression on oxaliplatin‑based therapy.

What are the side effects of Irinotecan Hydrochloride Trihydrate?

Irinotecan Eugia may cause a range of adverse reactions, varying from mild to severe.

Common Side Effects: - Diarrhea: often delayed and may be severe. - Neutropenia: reduced white blood cell count. - Nausea and vomiting. - Fatigue: general tiredness.

Serious or Rare Side Effects: - Febrile neutropenia: fever with low neutrophils. - Life‑threatening diarrhea (colitis) leading to dehydration. - Cholinergic syndrome: sweating, bradycardia, bronchospasm. - Hypersensitivity reactions: rash, anaphylaxis.

What precautions apply to Irinotecan Hydrochloride Trihydrate?

When using Irinotecan Eugia, several precautions should be observed to minimize risks and ensure safe administration.

- Monitor blood counts: perform regular CBC to detect neutropenia. - Assess liver function: adjust dose in hepatic impairment. - Maintain hydration: adequate fluids reduce severity of diarrhea. - Avoid strong UGT1A1 inhibitors: drugs like atazanavir may increase toxicity. - Pregnancy and lactation: use only if potential benefit justifies risk. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Irinotecan Hydrochloride Trihydrate interact with?

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

Major Interactions (Avoid): - Strong UGT1A1 inhibitors (e.g., atazanavir, indinavir): increase SN‑38 exposure. - CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): raise plasma levels. - Concurrent myelosuppressive agents: heightened risk of severe neutropenia. - Anticholinergic drugs: may exacerbate cholinergic syndrome.

Moderate Interactions (Monitor Closely): - CYP3A4 inducers (e.g., rifampin, St. John’s wort): may reduce effectiveness. - Warfarin: monitor INR as irinotecan may affect coagulation. - NSAIDs: increase risk of gastrointestinal toxicity.

Frequently asked questions

What is Irinotecan Eugia used for?+
Irinotecan Eugia contains the cytotoxic agent irinotecan hydrochloride tri­hydrate and is used in oncology as part of chemotherapy regimens for patients with colorectal cancer, including both adjuvant and metastatic settings. It works by interfering with DNA replication in rapidly dividing tumor cells.
How does Irinotecan work?+
The drug is converted inside cells to the active metabolite SN‑38, which binds to the DNA‑topoisomerase I complex and prevents the re‑ligation of single‑strand DNA breaks during replication. This leads to accumulation of DNA damage and triggers apoptosis of cancer cells.
What is the usual dose of Irinotecan Eugia?+
The prescribed dose of Irinotecan Eugia is determined by the treating oncologist based on factors such as the patient’s body surface area, disease stage, prior therapies and organ function. The healthcare professional sets the exact dosing schedule and infusion rate.
Is Irinotecan safe during pregnancy or breastfeeding?+
Safety data for Irinotecan in pregnancy and lactation are limited. It should only be used when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and breastfeeding is generally discouraged during treatment.
How do I order Irinotecan Eugia from GNH USA?+
To place an order, submit an enquiry on the Irinotecan Eugia 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 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. Both are used in combination regimens, but they differ in toxicity profiles; irinotecan is more associated with diarrhea and neutropenia, while oxaliplatin commonly causes peripheral neuropathy.
What are the storage and handling requirements for Irinotecan Eugia?+
Irinotecan Eugia should be stored refrigerated at 2 °C to 8 °C, 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 Eugia administered?+
The medication is supplied as a sterile injectable solution for intravenous infusion. It is administered by a qualified healthcare professional, typically as an infusion over 30 to 90 minutes, according to the dosing schedule prescribed by the oncologist.
What are the most serious risks associated with Irinotecan Eugia?+
The most severe adverse events include febrile neutropenia, life‑threatening delayed diarrhea (colitis), cholinergic syndrome, and severe hypersensitivity reactions. Prompt recognition and supportive care are essential to manage these risks.
Who should not receive Irinotecan Eugia?+
Patients with known hypersensitivity to irinotecan or any of its excipients, those with severe hepatic impairment, and individuals with uncontrolled infections or active bowel obstruction should avoid Irinotecan Eugia. The prescribing clinician must evaluate each patient’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
Eugia Pharma (Malta) Ltd
Origin
EU

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