Product image of Irinotecan Hcl Aqvida (Irinotecan Hydrochloride) supplied by GNH India

Irinotecan Hcl Aqvida

Active Ingredient:
Irinotecan Hydrochloride
Origin:
EU

Irinotecan Hcl Aqvida (Irinotecan Hydrochloride)

Irinotecan Hydrochloride, the active ingredient in Irinotecan Hcl Aqvida, is a topoisomerase I inhibitor presented as an injectable solution for intravenous use. It is employed to treat colorectal cancer, including metastatic disease, in adult patients.

GNH India supplies Irinotecan Hcl Aqvida as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide.

Manufacturer / TM Owner

Aqvida Gmbh

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Indications & Clinical Uses

  • Irinotecan Hydrochloride is used in oncology to target colorectal cancer and related disease states.
  • Colorectal cancer: improves response rates when combined with other chemotherapeutic agents.
  • Metastatic colorectal cancer: provides therapeutic benefit in first‑line or later‑line regimens.
  • Advanced colorectal cancer: used as part of combination therapy to extend progression‑free survival.

How It Works

  • Irinotecan Hydrochloride is a topoisomerase I inhibitor. After intravenous administration, it is converted to the active metabolite SN‑38, which binds to the DNA‑topoisomerase I complex, preventing the re‑ligation of single‑strand breaks during DNA replication. This inhibition leads to accumulation of DNA damage, triggering apoptosis in rapidly dividing tumor cells.

Side Effects

Irinotecan Hydrochloride may cause a range of adverse reactions, varying in frequency and severity.

Common Side Effects

  • Diarrhea: often severe and may require supportive care.
  • Neutropenia: reduced white blood cell count increasing infection risk.
  • Nausea and vomiting: may be managed with anti‑emetics.
  • Fatigue: general tiredness experienced during treatment.
  • Alopecia: hair loss that is usually reversible.
  • Abdominal pain: discomfort in the stomach area.

Serious or Rare Side Effects

  • Severe neutropenic infection: febrile neutropenia requiring immediate medical attention.
  • Life‑threatening diarrhea: may lead to dehydration and electrolyte imbalance.
  • Hepatotoxicity: elevated liver enzymes indicating liver injury.
  • Hypersensitivity reactions: rash, bronchospasm, or anaphylaxis.
  • Cardiac toxicity: rare cases of arrhythmia or myocardial ischemia.

Precautions & Warnings

  • When using Irinotecan Hydrochloride, clinicians should consider several safety measures.
  • Dose adjustment: modify dose in patients with hepatic impairment.
  • Monitoring: perform regular complete blood counts and liver function tests.
  • Hydration: ensure adequate fluid intake to mitigate diarrhea risk.
  • Drug interactions: avoid concurrent use with strong CYP3A4 inhibitors.
  • Pregnancy and lactation: use only if potential benefit justifies potential risk; data are limited.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze.

Avoid Interactions

Irinotecan Hydrochloride can interact with other medicines, affecting efficacy or safety.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole): increase SN‑38 exposure.
  • UGT1A1 inhibitors (e.g., atazanavir): raise risk of severe neutropenia.
  • High‑dose irinotecan with other topoisomerase I inhibitors: additive toxicity.

Moderate Interactions (Monitor Closely)

  • Anticoagulants (e.g., warfarin): monitor INR for bleeding risk.
  • Antidiarrheal agents (e.g., loperamide): may mask early signs of severe diarrhea.
  • Immunosuppressants (e.g., corticosteroids): increase infection susceptibility.

Frequently Asked Questions

Irinotecan Hcl Aqvida contains irinotecan hydrochloride, a topoisomerase I inhibitor used primarily in the treatment of colorectal cancer, including metastatic disease, as part of combination chemotherapy regimens in adult patients.

After intravenous infusion, irinotecan is metabolized to SN‑38, which binds to the DNA‑topoisomerase I complex, preventing the re‑ligation of single‑strand DNA breaks during replication. This leads to accumulation of DNA damage and triggers apoptosis in rapidly dividing cancer cells.

The specific dose and schedule of Irinotecan Hcl Aqvida are determined by the prescribing oncologist based on the patient’s clinical condition, treatment protocol, and individual factors such as liver function and prior therapy.

Safety data for irinotecan in pregnancy and lactation are limited. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and the decision must be made by a qualified healthcare professional.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain where needed) and necessary import documentation.

Irinotecan belongs to the topoisomerase I inhibitor class, offering a distinct mechanism from fluoropyrimidines (e.g., 5‑FU) and oxaliplatin. It is often combined with these agents to enhance efficacy, and its toxicity profile—particularly diarrhea and neutropenia—differs from other chemotherapeutics, requiring specific monitoring.

Irinotecan Hcl Aqvida should be stored at 2‑8 °C, protected from light, and must not be frozen. Keep the product in its original packaging to maintain stability until it is prepared for intravenous administration.

The medication is supplied as an injectable solution for intravenous infusion. It is administered by a qualified healthcare professional, typically over a set period according to the prescribed chemotherapy protocol.

The most serious risks include severe neutropenia leading to infection, life‑threatening diarrhea that can cause dehydration and electrolyte imbalance, and rare but serious hepatic toxicity. Prompt medical attention is essential if any of these events occur.

Patients with known hypersensitivity to irinotecan or any component of the formulation should avoid its use. Additionally, individuals with severe hepatic impairment or uncontrolled infections may be contraindicated, and the decision should be made by the treating physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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