Europe — EMA
Irican
GNH USA supplies Irican (Irinotecan), a topoisomerase I inhibitor for metastatic colorectal cancer, adjuvant colon cancer and small cell lung cancer.
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What is Irinotecan Hydrochloride Trihydrate?
Irinotecan, the active ingredient in Irican, is a topoisomerase I inhibitor presented as an intravenous formulation for use in oncology patients. It is employed in the treatment of certain advanced solid tumours and as adjuvant therapy in colon cancer. GNH USA supplies Irican as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide.
What is Irinotecan Hydrochloride Trihydrate used for?
Irican belongs to the topoisomerase I inhibitor class and is used in cancers that rely on rapid DNA replication. - Metastatic colorectal cancer: improves overall survival when combined with fluoropyrimidine‑based regimens. - Adjuvant treatment of colon cancer: reduces risk of disease recurrence after surgical resection. - Small cell lung cancer: provides therapeutic benefit as part of combination chemotherapy protocols.
What are the side effects of Irinotecan Hydrochloride Trihydrate?
Irinotecan is associated with a range of adverse reactions that vary in frequency and severity.
Common Side Effects: - Diarrhea: often delayed and may be severe. - Nausea and vomiting: typically manageable with anti‑emetics. - Neutropenia: reduced white blood cell count increasing infection risk. - Alopecia: temporary hair loss. - Fatigue: generalized tiredness during treatment cycles.
Serious or Rare Side Effects: - Febrile neutropenia: fever with low neutrophil count requiring urgent care. - Severe colitis or bowel perforation: life‑threatening gastrointestinal complications. - Anaphylactic reactions: rare but may occur during infusion. - Hepatotoxicity: elevated liver enzymes indicating liver injury.
What precautions apply to Irinotecan Hydrochloride Trihydrate?
Before initiating Irican therapy, clinicians should assess patient‑specific factors and monitor for toxicity. - Monitor blood counts: perform regular complete blood count to detect neutropenia. - Assess liver function: adjust dosing in hepatic impairment. - Evaluate bowel status: avoid use in patients with recent abdominal surgery or obstruction. - Use anti‑emetics prophylactically: to reduce nausea and vomiting. - Adjust dose for UGT1A1 polymorphisms: consider genetic testing where available. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze.
What does Irinotecan Hydrochloride Trihydrate interact with?
Irinotecan may interact with other medicines that affect its metabolism or increase toxicity.
Major Interactions (Avoid): - Strong CYP3A4 inducers (e.g., rifampin): may markedly reduce irinotecan exposure. - UGT1A1 inhibitors (e.g., atazanavir): can increase SN‑38 levels and risk of severe neutropenia. - Concurrent myelosuppressive agents: heighten risk of bone‑marrow suppression.
Moderate Interactions (Monitor Closely): - Moderate CYP3A4 inhibitors (e.g., fluconazole): may modestly increase exposure. - Anticoagulants (e.g., warfarin): monitor coagulation parameters due to potential bleeding risk. - NSAIDs or aspirin: may exacerbate gastrointestinal toxicity.
Frequently asked questions
What conditions is Irican used to treat?+
How does irinotecan work in the body?+
What is the usual dose of Irican?+
Is Irican safe to use during pregnancy or breastfeeding?+
How do I order Irican from GNH USA?+
How does Irican compare with other topoisomerase I inhibitors?+
What are the storage requirements for Irican?+
How is Irican administered to patients?+
What are the most serious risks associated with Irican therapy?+
Who should not receive Irican?+
Product details
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