GNH USA

Europe — EMA

Irinotecan Accord

GNH USA supplies Irinotecan Accord (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 Irinotecan Accord, is a topoisomerase I inhibitor presented as an injectable solution for intravenous use. It is used to treat metastatic and advanced colorectal cancer in adult patients.

GNH USA supplies Irinotecan Accord as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres, hospitals and specialty pharmacies worldwide.

What is Irinotecan Hydrochloride Trihydrate used for?

Irinotecan is employed in the management of colorectal cancer and related disease stages.

Metastatic colorectal cancer: helps control tumor growth and prolong survival in patients with metastatic disease. Advanced colorectal cancer: provides disease stabilization and symptom relief in advanced cases. Colorectal cancer (general): used as part of combination chemotherapy regimens to improve treatment outcomes.

What are the side effects of Irinotecan Hydrochloride Trihydrate?

Irinotecan therapy is associated with a range of adverse reactions that vary in frequency and severity.

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

Serious or Rare Side Effects: - Febrile neutropenia: fever with low neutrophils requiring urgent care. - Severe colitis: intense inflammation of the colon. - Cholinergic syndrome: sweating, lacrimation, and bradycardia. - Hepatic toxicity: elevated liver enzymes or jaundice. - Allergic reactions: rash, itching, or anaphylaxis. - Hemorrhagic cystitis: bladder inflammation with bleeding.

What precautions apply to Irinotecan Hydrochloride Trihydrate?

Prior to initiating Irinotecan therapy, clinicians should assess patient-specific risk factors and monitor for potential complications.

Monitor blood counts: perform regular complete blood counts to detect neutropenia. Assess liver function: evaluate hepatic enzymes before and during treatment. Evaluate bowel health: screen for pre‑existing gastrointestinal disorders. Use anti‑emetics: prophylactic medication can reduce nausea and vomiting. Adjust dose in renal/hepatic impairment: modify regimen based on organ function. 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, altering its efficacy or safety profile.

Major Interactions (Avoid): - Strong CYP3A4 inhibitors (e.g., ketoconazole): may increase SN‑38 exposure. - Enzyme inducers (e.g., rifampin): may reduce therapeutic effect. - Concurrent myelosuppressive agents: heightened risk of severe neutropenia.

Moderate Interactions (Monitor Closely): - Anticoagulants (e.g., warfarin): potential for altered bleeding risk. - Other antidiarrheal drugs: may mask early signs of severe diarrhea. - Drugs affecting cholinergic pathways: could exacerbate cholinergic syndrome.

Frequently asked questions

What is Irinotecan Accord used for?+
Irinotecan Accord contains the chemotherapy agent irinotecan, which is used primarily to treat metastatic and advanced colorectal cancer in adult patients. It is administered as part of a systemic chemotherapy regimen to help control tumor growth and improve survival outcomes.
How does Irinotecan work in the body?+
Irinotecan is a prodrug that is converted inside cancer cells to its active metabolite SN‑38. SN‑38 inhibits the enzyme topoisomerase I, preventing the re‑ligation of single‑strand DNA breaks during replication. This leads to accumulation of DNA damage, halting cell division and causing cancer cell death.
What is the usual dose of Irinotecan Accord?+
The specific dose of Irinotecan Accord is determined by the prescribing oncologist based on factors such as the patient’s body surface area, overall health, and treatment protocol. Only a qualified healthcare professional can set the appropriate dosing schedule.
Is Irinotecan safe during pregnancy or breastfeeding?+
The safety of Irinotecan during pregnancy or while breastfeeding has not been established. It is generally contraindicated because of potential risks to the fetus or infant. Women who are pregnant, planning to become pregnant, or nursing should discuss alternative options with their healthcare provider.
How do I order Irinotecan Accord from GNH USA?+
To request Irinotecan Accord, 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 handling if needed), and required import documentation.
How does Irinotecan compare with other colorectal cancer drugs?+
Irinotecan belongs to the topoisomerase I inhibitor class, differing from agents such as oxaliplatin (a platinum‑based drug) or fluoropyrimidines like 5‑fluorouracil. While all are used in colorectal cancer regimens, irinotecan offers a distinct mechanism of action and is often combined with other agents to enhance efficacy and overcome resistance.
What are the storage and handling requirements for Irinotecan Accord?+
Irinotecan Accord should be stored at 2‑8 °C (refrigerated). Keep the product in its original packaging, protect it from light, and avoid freezing or shaking the vial. Follow all local regulations for handling cytotoxic medicines.
How is Irinotecan Accord administered?+
Irinotecan Accord is given by intravenous infusion under the supervision of qualified medical personnel. The infusion rate and duration are determined by the treating oncologist and may be adjusted based on patient tolerance and clinical response.
What are the most serious risks associated with Irinotecan?+
The most serious risks include severe neutropenia (low white blood cells), febrile neutropenia, life‑threatening diarrhea or colitis, cholinergic syndrome, and rare allergic reactions. Prompt medical attention is required if any of these symptoms develop during treatment.
Who should not receive Irinotecan Accord?+
Irinotecan is contraindicated in patients with known hypersensitivity to irinotecan or any of its excipients, those with severe bone‑marrow suppression, uncontrolled infections, or significant hepatic impairment. Clinicians should also exercise caution in patients with pre‑existing gastrointestinal disorders.
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
Accord Healthcare Polska Sp. Z O.O.
Origin
EU

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