GNH USA

Europe — EMA

Irinocan

GNH USA supplies Irinocan (Irinotecan), a topoisomerase I inhibitor for metastatic colorectal cancer.

Irinotecan Hydrochloride Trihydrate

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What is Irinotecan Hydrochloride Trihydrate?

Irinotecan, the active ingredient in Irinocan, is a topoisomerase I inhibitor presented as an injectable solution for intravenous use. It is employed in the treatment of metastatic colorectal cancer in adult patients, interfering with DNA replication in rapidly dividing tumor cells and providing a targeted chemotherapeutic approach.

GNH USA supplies Irinocan as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres worldwide.

What is Irinotecan Hydrochloride Trihydrate used for?

Irinocan is used in the management of colorectal cancer, targeting metastatic disease.

Metastatic colorectal cancer: improves survival outcomes when incorporated into combination chemotherapy regimens.

What are the side effects of Irinotecan Hydrochloride Trihydrate?

Irinocan may cause 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 severe and may require supportive care. - Nausea and vomiting: typical chemotherapy‑related symptoms. - Alopecia: hair loss during treatment cycles. - Fatigue: generalized tiredness affecting daily activities. - Anemia: decreased red blood cell levels causing weakness.

Serious or Rare Side Effects: - Febrile neutropenia: fever with low neutrophil count, a medical emergency. - Severe colitis: life‑threatening inflammation of the colon. - Allergic reactions: rash, bronchospasm, or anaphylaxis. - Pulmonary toxicity: interstitial lung disease or pneumonitis. - Hepatic dysfunction: elevated liver enzymes or jaundice. - Hemorrhagic events: bleeding due to thrombocytopenia.

What precautions apply to Irinotecan Hydrochloride Trihydrate?

Before initiating Irinocan therapy, clinicians should assess patient‑specific risk factors and monitor for toxicity throughout treatment. - Monitor blood counts: perform regular complete blood count tests to detect neutropenia. - Assess liver function: check hepatic enzymes and bilirubin before each cycle. - Evaluate renal function: adjust therapy if creatinine clearance is impaired. - Use anti‑emetics prophylactically: reduce nausea and vomiting incidence. - Avoid concurrent strong CYP3A4 inhibitors: these may increase Irinotecan exposure. - Store at ambient temperature: keep in original packaging, protect from moisture and light.

What does Irinotecan Hydrochloride Trihydrate interact with?

Irinocan can interact with several medicines, altering its efficacy or safety profile.

Major Interactions (Avoid): - Strong CYP3A4 inhibitors (e.g., ketoconazole): may raise Irinotecan plasma levels. - UGT1A1 inhibitors (e.g., atazanavir): increase risk of severe neutropenia. - Live vaccines: immunosuppression can reduce vaccine effectiveness.

Moderate Interactions (Monitor Closely): - Moderate CYP3A4 inhibitors (e.g., erythromycin): may modestly increase exposure. - Warfarin: Irinotecan may affect INR, requiring closer monitoring. - NSAIDs: combined use can heighten gastrointestinal toxicity.

Frequently asked questions

What is Irinocan used for?+
Irinocan contains the chemotherapeutic agent Irinotecan and is indicated for the treatment of metastatic colorectal cancer. It is typically administered as part of combination chemotherapy regimens to improve survival outcomes in adult patients with advanced disease.
How does Irinotecan work?+
Irinotecan is a pro‑drug that is converted inside cancer cells to SN‑38, an active metabolite that inhibits topoisomerase I. This inhibition prevents the re‑ligation of single‑strand DNA breaks during replication, leading to DNA damage, cell‑cycle arrest and ultimately tumor cell death.
What is the usual dose of Irinocan?+
The dosing regimen for Irinocan is individualized by the prescribing oncologist based on factors such as patient weight, performance status, prior therapies and laboratory values. The prescriber determines the appropriate dose, schedule and any necessary dose adjustments.
Is Irinocan safe during pregnancy or breastfeeding?+
Safety data for Irinocan in pregnancy and lactation are limited, and the drug may pose risks to the fetus or nursing infant. It is generally contraindicated in pregnant or breastfeeding women unless the potential benefit justifies the potential risk, and a specialist should be consulted.
How do I order Irinocan from GNH USA?+
To request Irinocan, 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 if needed) and import documentation.
How does Irinocan compare with other colorectal cancer drugs?+
Irinocan belongs to the topoisomerase I inhibitor class, whereas alternatives such as oxaliplatin or fluoropyrimidines act on DNA cross‑linking or thymidylate synthase, respectively. Irinocan offers a distinct mechanism that can be synergistic when combined with these agents, but its toxicity profile, especially for neutropenia and diarrhea, differs and requires specific monitoring.
What are the storage and handling requirements for Irinocan?+
Irinocan should be stored at ambient temperature, protected from moisture and light, and kept in its original packaging until use. Once reconstituted for intravenous infusion, it must be used within the time frame specified in the product labeling and discarded if any discoloration or particulate matter is observed.
How is Irinocan administered?+
Irinocan is supplied as an injectable solution for intravenous infusion. It is administered by a qualified healthcare professional, typically over a period of 30 to 90 minutes, depending on the prescribed protocol and patient tolerance. Infusion rates and pre‑medication for anti‑emesis are determined by the treating physician.
What are the most serious risks associated with Irinocan?+
The most serious adverse events include severe neutropenia with fever (febrile neutropenia), life‑threatening diarrhea or colitis, allergic reactions such as anaphylaxis, and hepatic toxicity. Prompt recognition and supportive care are essential, and patients should be educated to report fever, persistent diarrhea, or signs of infection immediately.
Who should not use Irinocan?+
Irinocan is contraindicated in patients with known hypersensitivity to Irinotecan or any of its excipients, in those with severe bone‑marrow suppression, and in individuals receiving concurrent strong CYP3A4 or UGT1A1 inhibitors that cannot be safely managed. Clinicians must assess each patient’s medical history 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
Demo Abee
Origin
EU

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