GNH USA

Europe — EMA

Irinotecan Hcl-3-Water Koanaa

GNH USA supplies Irinotecan Hcl-3-Water Koanaa (Irinotecan Hydrochloride), a topoisomerase I inhibitor for metastatic colorectal cancer and other solid

Irinotecan Hydrochloride

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What is Irinotecan Hydrochloride?

Irinotecan Hydrochloride, the active ingredient in Irinotecan Hcl-3-Water Koanaa, is a topoisomerase I inhibitor presented as an intravenous solution for intravenous use. It treats metastatic colorectal cancer and other solid tumors as part of combination chemotherapy regimens.

GNH USA supplies Irinotecan Hcl-3-Water Koanaa as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide.

What is Irinotecan Hydrochloride used for?

Irinotecan Hydrochloride is used in oncology to target cancers that are treated with topoisomerase I inhibition. - Metastatic colorectal cancer: improves survival when combined with fluoropyrimidine‑based regimens. - Advanced colorectal cancer: provides disease control as part of second‑line therapy. - Other solid tumors: used in combination protocols for gastric, pancreatic, and lung cancers where topoisomerase I inhibition is indicated.

What are the side effects of Irinotecan Hydrochloride?

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

Common Side Effects: - Diarrhea: often severe and may require antidiarrheal therapy. - Nausea: may be managed with anti‑emetics. - Fatigue: general tiredness experienced during treatment. - Neutropenia: reduced white blood cell count increasing infection risk.

Serious or Rare Side Effects: - Severe neutropenic infection: life‑threatening bacterial infection. - Febrile neutropenia: fever with low neutrophil count. - Acute cholinergic syndrome: abdominal cramps, sweating, and bradycardia.

What precautions apply to Irinotecan Hydrochloride?

Before initiating therapy, clinicians should evaluate patient‑specific factors and monitor for known risks. - Monitor blood counts: regular CBC to detect neutropenia. - Assess liver function: dose adjustments may be needed for hepatic impairment. - Evaluate renal function: consider renal status before administration. - Use anti‑diarrheal prophylaxis: loperamide may reduce severity of diarrhea. - Avoid in patients with known hypersensitivity to irinotecan or its excipients. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Irinotecan Hydrochloride interact with?

Irinotecan Hydrochloride interacts with several drug classes; some require avoidance while others need close monitoring.

Major Interactions (Avoid): - Strong CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce irinotecan exposure. - UGT1A1 inhibitors (e.g., atazanavir): increase risk of severe neutropenia and diarrhea. - Concurrent use of other myelosuppressive agents: can exacerbate bone marrow suppression.

Moderate Interactions (Monitor Closely): - Anticoagulants (warfarin, DOACs): increased bleeding risk due to mucosal damage. - Anticholinergic drugs (e.g., atropine): may mask cholinergic syndrome symptoms. - Proton pump inhibitors: possible alteration of drug metabolism, monitor efficacy.

Frequently asked questions

What is Irinotecan Hcl-3-Water Koanaa used for?+
Irinotecan Hcl-3-Water Koanaa contains irinotecan hydrochloride, a topoisomerase I inhibitor used in combination chemotherapy for metastatic colorectal cancer, advanced colorectal cancer, and selected solid tumors such as gastric, pancreatic, and lung cancers.
How does Irinotecan Hydrochloride work?+
After intravenous administration, irinotecan is metabolised to SN‑38, which binds to DNA topoisomerase I and prevents the re‑ligation of single‑strand DNA breaks. This leads to accumulation of DNA damage, inhibition of replication, and ultimately death of rapidly dividing cancer cells.
What is the usual dose of Irinotecan Hcl-3-Water Koanaa?+
The specific dose and schedule are determined by the treating oncologist based on the patient’s cancer type, stage, body surface area, and concurrent therapies. Dosing is individualized and should follow established clinical protocols.
Is Irinotecan safe during pregnancy or breastfeeding?+
Safety data for irinotecan in pregnancy and lactation are limited. It is generally contraindicated in pregnant or nursing patients unless the potential benefit outweighs the risk, and it should be used only under strict medical supervision.
How do I order Irinotecan Hcl-3-Water Koanaa 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 where required), and necessary import documentation.
How does Irinotecan compare with other topoisomerase I inhibitors?+
Irinotecan is the most widely used topoisomerase I inhibitor in colorectal cancer regimens. Compared with newer agents like topotecan, irinotecan generally shows higher activity in colorectal and certain gastrointestinal tumors, but both share similar toxicity profiles such as neutropenia and diarrhea.
What are the storage and handling requirements for Irinotecan Hcl-3-Water Koanaa?+
The product should be stored at 2‑8 °C, protected from light, and must not be frozen or shaken. Before administration, the solution is allowed to reach room temperature and inspected for particulate matter or discoloration.
How is Irinotecan Hcl-3-Water Koanaa administered?+
Irinotecan is given as an intravenous infusion, typically over 30 to 90 minutes depending on the protocol. Administration is performed by qualified healthcare professionals in a clinical setting, with appropriate monitoring for infusion‑related reactions.
What are the most serious risks associated with Irinotecan therapy?+
The most critical risks include severe neutropenia leading to infection, febrile neutropenia, and life‑threatening diarrhea that may cause dehydration and electrolyte imbalance. Prompt recognition and supportive care are essential to mitigate these complications.
Who should not receive Irinotecan Hcl-3-Water Koanaa?+
Patients with known hypersensitivity to irinotecan or any of its excipients, those with uncontrolled infections, or individuals with severe hepatic impairment should avoid this medication. Clinical judgment is required for patients with significant 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
Route
Intravenous Use
Manufacturer
Koanaa Healthcare Spain S.L.
Origin
EU

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