Product image of Kapecitabin Jgl 500 Mg (Capecitabine) supplied by GNH India

Kapecitabin Jgl 500 Mg

Active Ingredient:
Capecitabine
Origin:
EU

Kapecitabin Jgl 500 Mg (Capecitabine)

Capecitabine, the active ingredient in Kapecitabin Jgl 500 Mg, is an antimetabolite presented as a 500 mg tablet for oral use. It treats certain types of cancer, such as colorectal and breast cancer, in adult patients.

GNH India supplies Kapecitabin Jgl 500 Mg as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres, hospitals and pharmacies worldwide.

Manufacturer / TM Owner

Jadran-Galenski Laboratorij D.D.

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Indications & Clinical Uses

Capecitabine is an oral antimetabolite used in the treatment of solid tumours, particularly those of the colorectal and breast pathways.

  • Colorectal cancer: slows tumour growth and improves survival when combined with other chemotherapy agents.
  • Breast cancer: inhibits tumour progression in HER2‑negative disease as part of combination regimens.
  • Adjuvant therapy for stage III colon cancer: reduces risk of disease recurrence after surgical resection.

How It Works

  • Capecitabine is a pro‑drug that is enzymatically converted to 5‑fluorouracil (5‑FU) preferentially within tumour tissue. The resulting 5‑FU inhibits thymidylate synthase, disrupting DNA synthesis and repair, which leads to selective cytotoxicity in rapidly dividing cancer cells.

Side Effects

Capecitabine may cause a range of adverse reactions, some of which are common and others that are serious or rare.

Common Side Effects

  • Nausea and vomiting: gastrointestinal upset that may require anti‑emetic therapy.
  • Diarrhoea: can be mild to moderate and may need fluid replacement.
  • Hand‑foot syndrome: redness, swelling or pain on the palms and soles.
  • Fatigue: general tiredness affecting daily activities.

Serious or Rare Side Effects

  • Severe neutropenia: marked reduction in white blood cells increasing infection risk.
  • Cardiotoxicity: rare heart-related events such as angina or myocardial infarction.
  • Severe mucositis: painful inflammation of the mouth and gastrointestinal lining.
  • Thromboembolic events: rare blood clots that may be life‑threatening.

Precautions & Warnings

Before initiating therapy, clinicians should assess patient‑specific factors and monitor for potential complications.

  • Renal function: adjust use in patients with impaired kidney function.
  • Hepatic function: evaluate liver enzymes and consider dose modification if needed.
  • Concomitant chemotherapy: monitor for additive toxicities when used with other agents.
  • Pregnancy and lactation: avoid use due to unknown safety profile.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, and protect from moisture.

Avoid Interactions

Capecitabine can interact with several medicines, affecting its efficacy or safety.

Major Interactions (Avoid)

  • Strong CYP2C9 inhibitors (e.g., fluconazole): may increase capecitabine exposure.
  • Anticoagulants (e.g., warfarin): heightened risk of bleeding.
  • Antacids containing magnesium or aluminum: can reduce absorption.

Moderate Interactions (Monitor Closely)

  • Other antimetabolites (e.g., 5‑FU): additive bone‑marrow suppression.
  • Radiation therapy: increased skin toxicity.
  • Herbal supplements (e.g., St. John’s wort): may alter drug metabolism.

Frequently Asked Questions

Kapecitabin Jgl 500 Mg contains capecitabine, an oral antimetabolite indicated for the treatment of colorectal cancer and breast cancer. It is used as part of combination chemotherapy regimens to inhibit tumour growth in adult patients.

Capecitabine is a pro‑drug that is converted to 5‑fluorouracil inside tumour cells. The active metabolite blocks thymidylate synthase, interfering with DNA synthesis and repair, which leads to selective death of rapidly dividing cancer cells.

The dosage of Kapecitabin Jgl 500 Mg is determined by the prescribing physician based on the patient’s cancer type, stage, body surface area and overall health. Only a qualified healthcare professional should set the dosing schedule.

The safety of capecitabine in pregnancy and lactation has not been established. It is generally contraindicated for pregnant or nursing women because potential fetal or infant harm cannot be ruled out.

To request Kapecitabin Jgl, 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 and any necessary import documentation.

Kapecitabin Jgl 500 mg is a generic formulation of capecitabine that offers the same active ingredient, strength and therapeutic profile as other branded or generic versions. Differences may lie in manufacturing standards, regulatory approvals and supply chain reliability, with GNH India emphasizing GDP‑compliant international distribution.

Kapecitabin Jgl tablets should be stored at ambient temperature, below 25 °C, in their original blister pack or container. Protect them from moisture, direct sunlight and excessive heat to maintain potency throughout the shelf life.

Kapecitabin Jgl is taken orally, usually with food to reduce gastrointestinal irritation. The tablets are swallowed whole with water and should be taken exactly as prescribed by the treating oncologist.

Serious risks include severe neutropenia, which can predispose to infections, and rare cardiotoxic events such as angina or myocardial infarction. Patients should be monitored closely for signs of infection, chest pain, or unexplained fatigue.

Kapecitabin Jgl is contraindicated in patients with known hypersensitivity to capecitabine or any component of the formulation, in those with severe renal or hepatic impairment, and in pregnant or breastfeeding women. Clinical judgment should guide use in other special populations.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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