GNH USA

Europe — EMA

Irinotecán Tarbis

GNH USA supplies Irinotecán Tarbis (Irinotecan), a Topoisomerase I inhibitor for metastatic and advanced colorectal cancer. Request a quote for global supply.

Irinotecan Hydrochloride Trihydrate

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What is Irinotecan Hydrochloride Trihydrate?

Irinotecan, the active ingredient in Irinotecán Tarbis, is a Topoisomerase I inhibitor presented as a sterile solution for intravenous use. It is employed in the treatment of metastatic and advanced colorectal cancer in adult patients. GNH USA supplies Irinotecán Tarbis as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres worldwide.

What is Irinotecan Hydrochloride Trihydrate used for?

Irinotecan is used in oncology to target colorectal cancer pathways.

Metastatic colorectal cancer: improves overall survival when combined with standard chemotherapy regimens. Advanced colorectal cancer: reduces tumor progression and may downstage disease. Colorectal cancer (first‑line setting): used as part of combination therapy to enhance response rates.

What are the side effects of Irinotecan Hydrochloride Trihydrate?

Irinotecan therapy is associated with a range of adverse reactions.

Common Side Effects: - Diarrhea: often delayed and may be severe. - Nausea and vomiting: typical chemotherapy‑related symptoms. - Neutropenia: reduced white blood cell count increasing infection risk. - Fatigue: generalized tiredness during treatment cycles. - Alopecia: hair loss that may be temporary. - Abdominal pain: discomfort in the gastrointestinal tract.

Serious or Rare Side Effects: - Severe neutropenic infection: febrile neutropenia requiring urgent care. - Acute cholinergic syndrome: sweating, salivation, and bronchospasm. - Severe diarrhea leading to dehydration and electrolyte imbalance. - Hepatotoxicity: elevated liver enzymes indicating liver injury. - Allergic reactions: rash, urticaria, or anaphylaxis in rare cases.

What precautions apply to Irinotecan Hydrochloride Trihydrate?

When using Irinotecán Tarbis, clinicians should observe several safety measures.

Dose adjustment: modify dose in patients with hepatic impairment. Monitoring: perform regular complete blood counts to detect neutropenia. Hydration: ensure adequate fluid intake to mitigate diarrhea‑related dehydration. Drug interactions: avoid concurrent use of strong CYP3A4 inhibitors without dose reduction. Pregnancy and lactation: contraindicated unless benefits outweigh potential fetal risks. Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake the product.

What does Irinotecan Hydrochloride Trihydrate interact with?

Irinotecan may interact with several drug classes, requiring careful management.

Major Interactions (Avoid): - Strong CYP3A4 inhibitors (e.g., ketoconazole): can increase SN‑38 exposure and toxicity. - CYP3A4 inducers (e.g., rifampin): may reduce efficacy by lowering drug levels. - Anticholinergic agents: may exacerbate cholinergic syndrome.

Moderate Interactions (Monitor Closely): - Anticoagulants (e.g., warfarin): monitor INR due to potential bleeding risk. - Other myelosuppressive agents: increase risk of severe neutropenia. - Proton pump inhibitors: may affect gastric pH and drug absorption.

Frequently asked questions

What is Irinotecán Tarbis used for?+
Irinotecán Tarbis contains irinotecan, a chemotherapy agent indicated for the treatment of metastatic and advanced colorectal cancer in adult patients. It is typically administered as part of combination regimens to improve survival and control tumor growth.
How does irinotecan work in cancer therapy?+
Irinotecan is a prodrug that is metabolized to SN‑38, which inhibits topoisomerase I. This inhibition prevents the re‑ligation of single‑strand DNA breaks during replication, leading to DNA damage, halted cell division, and ultimately cancer cell death.
What is the usual dose of Irinotecán Tarbis?+
The specific dose and schedule of Irinotecán Tarbis are determined by the prescribing oncologist based on the patient’s condition, body surface area, and treatment protocol. Only a qualified healthcare professional should set the dosing regimen.
Is Irinotecán Tarbis safe during pregnancy or breastfeeding?+
Irinotecan is classified as contraindicated in pregnancy and breastfeeding unless the potential benefit justifies the risk. It can cross the placenta and may be excreted in breast milk, potentially harming the fetus or infant.
How do I order Irinotecán Tarbis from GNH USA?+
To request Irinotecán Tarbis, submit an enquiry on the product page at gnh-usa.com with 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 necessary import documentation.
How does Irinotecán Tarbis compare with other colorectal cancer drugs?+
Irinotecán Tarbis belongs to the topoisomerase I inhibitor class, differing from agents such as oxaliplatin (a platinum compound) or fluoropyrimidines. It offers a distinct mechanism of DNA damage and is often combined with these agents to achieve synergistic anti‑tumor effects.
What are the storage requirements for Irinotecán Tarbis?+
Irinotecán Tarbis should be stored at 2‑8 °C in a refrigerator, protected from light, and must not be frozen or shaken. Maintaining the cold chain preserves drug stability and efficacy.
How is Irinotecán Tarbis administered?+
The product is supplied as a sterile solution for intravenous infusion. Administration is performed by qualified healthcare personnel, typically over a set period according to the treatment protocol, and may require pre‑hydration to reduce gastrointestinal toxicity.
What are the most serious risks associated with Irinotecán Tarbis?+
Serious risks include severe neutropenia leading to infection, delayed diarrhea that can cause dehydration and electrolyte imbalance, and rare but life‑threatening cholinergic syndrome. Prompt monitoring and supportive care are essential to manage these complications.
Who should not receive Irinotecán Tarbis?+
Patients with known hypersensitivity to irinotecan or its excipients, those with severe hepatic impairment, or individuals with uncontrolled infections should not receive Irinotecán Tarbis. Additionally, it is contraindicated in pregnant or breastfeeding women unless absolutely necessary.
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
Tarbis Farma, S.L.
Origin
EU

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