GNH USA

Europe — EMA

Irinotecano Azevedos

GNH USA supplies Irinotecano Azevedos (Irinotecan), a topoisomerase I inhibitor for metastatic and advanced colorectal cancer. Get a quote for supply today.

Irinotecan Hydrochloride

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What is Irinotecan Hydrochloride?

Irinotecan, the active ingredient in Irinotecano Azevedos, is a topoisomerase I inhibitor presented as a sterile intravenous solution for infusion use. It is employed in the treatment of metastatic and advanced colorectal cancer in adult patients.

GNH USA supplies Irinotecano Azevedos as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide. The company adheres to stringent quality standards and provides reliable cold‑chain logistics for the product. Clients benefit from consistent batch release, regulatory documentation, and responsive technical support throughout the procurement process.

What is Irinotecan Hydrochloride used for?

Irinotecan is used in colorectal cancer regimens that target tumor cell proliferation.

- Metastatic colorectal cancer: used in combination chemotherapy to improve overall survival and disease control. - Advanced colorectal cancer: administered as part of second‑line therapy to achieve tumor response. - Colorectal cancer (first‑line with FOLFIRI): combined with fluorouracil and leucovorin to enhance treatment efficacy.

What are the side effects of Irinotecan Hydrochloride?

Irinotecan 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. - Neutropenia: reduced white blood cell count increasing infection risk. - Nausea: feeling of sickness often accompanied by vomiting. - Fatigue: persistent tiredness affecting daily activities.

Serious or Rare Side Effects: - Febrile neutropenia: fever with low neutrophils requiring urgent medical care. - Severe colitis: intense inflammation of the colon leading to abdominal pain and blood in stool. - Allergic reaction: rash, itching, swelling, or anaphylaxis. - Hepatic toxicity: elevated liver enzymes or jaundice indicating liver injury.

What precautions apply to Irinotecan Hydrochloride?

Before using Irinotecano Azevedos, several safety considerations should be observed.

- Renal impairment: monitor kidney function and adjust therapy as needed. - Hepatic impairment: assess liver enzymes and consider dose modification. - Pregnancy: avoid use unless benefits outweigh potential fetal risks. - Concomitant radiation therapy: increased risk of gastrointestinal toxicity. - Monitor blood counts: regular CBC testing to detect neutropenia early. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Irinotecan Hydrochloride interact with?

Irinotecan interacts with several medicines that can alter its efficacy or safety profile.

Major Interactions (Avoid): - Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): increase irinotecan exposure and toxicity. - UGT1A1 inhibitors (e.g., atazanavir): raise SN‑38 levels, heightening risk of neutropenia and diarrhea. - Concurrent myelosuppressive agents (e.g., carboplatin, paclitaxel): additive bone‑marrow suppression.

Moderate Interactions (Monitor Closely): - Antiemetics such as ondansetron: may affect metabolism of irinotecan. - Warfarin: monitor INR as irinotecan can influence anticoagulant effect. - Fluoroquinolones (e.g., ciprofloxacin): potential increase in gastrointestinal side effects.

Frequently asked questions

What is Irinotecano Azevedos used for?+
Irinotecano Azevedos contains irinotecan, which is indicated for the treatment of metastatic and advanced colorectal cancer. It is typically used as part of combination chemotherapy regimens to improve survival outcomes and control tumor growth in adult patients.
How does Irinotecan work?+
Irinotecan is a pro‑drug that is metabolised inside cancer cells to SN‑38, a potent topoisomerase I inhibitor. By stabilising the DNA‑topoisomerase I complex, it prevents the re‑ligation of single‑strand DNA breaks, leading to DNA damage, cell‑cycle arrest and ultimately tumour cell death.
What determines the dose of Irinotecano Azevedos?+
The dose of Irinotecano Azevedos is determined by the prescribing oncologist based on the patient’s clinical condition, body surface area, organ function and treatment protocol. Specific dosing regimens are not disclosed publicly and should only be set by a qualified healthcare professional.
Is Irinotecano Azevedos safe during pregnancy or breastfeeding?+
The safety of Irinotecano Azevedos in pregnancy or while breastfeeding has not been established. It is generally contraindicated unless the potential benefit justifies the potential risk to the fetus. Women of child‑bearing potential should use effective contraception during treatment and for a defined period afterward.
How do I order Irinotecano Azevedos from GNH USA?+
To place an order, 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 any necessary import documentation.
How does Irinotecan compare with other colorectal cancer drugs?+
Irinotecan belongs to the topoisomerase I inhibitor class and is often used after or in combination with fluoropyrimidines and oxaliplatin. Compared with agents such as oxaliplatin, irinotecan has a distinct toxicity profile, with higher rates of diarrhea and neutropenia but lower neurotoxicity, making it a valuable option in sequential or combination regimens.
How should Irinotecano Azevedos be stored and handled?+
The product should be stored at 2‑8 °C in a refrigerator, protected from light and moisture. It must not be frozen or shaken. Prior to administration, the solution should be inspected for particulate matter and used within the time frame recommended by the manufacturer.
How is Irinotecano Azevedos administered?+
Irinotecano Azevedos is supplied as a sterile intravenous solution and is administered by a qualified healthcare professional as an infusion. The infusion rate and schedule are defined by the treating oncologist and are usually given on a specific day of a treatment cycle, often every two weeks.
What are the most serious risks to watch for with Irinotecano Azevedos?+
The most serious adverse events include severe neutropenia with fever (febrile neutropenia), life‑threatening diarrhea or colitis, allergic reactions that may progress to anaphylaxis, and hepatic toxicity. Prompt medical attention is required if patients develop fever, persistent diarrhea, jaundice, or signs of an allergic response.
Who should not use Irinotecano Azevedos?+
Patients with known hypersensitivity to irinotecan or any component of the formulation should avoid the product. It is also contraindicated in individuals with severe uncontrolled infections, significant bone‑marrow suppression, or those who are pregnant without a clear therapeutic justification.
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
Laboratórios Azevedos - Indústria Farmacêutica, S.A.
Origin
EU

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