GNH USA

Europe — EMA

Kapecitabin Sandoz

GNH USA supplies Kapecitabin Sandoz (Capecitabine), an antimetabolite for colorectal, breast and gastric cancers. Request a quote for global supply today.

Capecitabine

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What is Capecitabine?

Capecitabine, the active ingredient in Kapecitabin Sandoz, is an antimetabolite presented as an oral tablet for oral use. It treats colorectal, breast and gastric cancers in adult patients.

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

What is Capecitabine used for?

Kapecitabin Sandoz (capecitabine) is employed in the treatment of solid tumours that are responsive to antimetabolite chemotherapy.

- Colorectal cancer: used as part of combination regimens to inhibit tumour growth and improve survival. - Breast cancer: administered to patients with advanced or metastatic disease to slow disease progression. - Gastric cancer: incorporated into first‑line therapy to enhance response rates in eligible adults.

What are the side effects of Capecitabine?

Capecitabine may cause a range of adverse reactions that vary in frequency and severity.

Common Side Effects: - Nausea and vomiting: mild to moderate gastrointestinal upset. - Diarrhoea: watery stools that may require hydration. - Hand‑foot syndrome: redness, swelling or pain on palms and soles. - Fatigue: persistent tiredness affecting daily activities. - Alopecia: thinning or loss of hair.

Serious or Rare Side Effects: - Severe neutropenia: markedly reduced white blood cells increasing infection risk. - Thromboembolic events: blood clots that can affect lungs or deep veins. - Cardiotoxicity: chest pain or arrhythmias requiring immediate attention. - Severe mucositis: painful inflammation of the mouth and gastrointestinal lining.

What precautions apply to Capecitabine?

Before initiating therapy with Kapecitabin Sandoz, several safety considerations should be reviewed.

- Pregnancy: avoid use; classified as Category D due to fetal risk. - Breastfeeding: discontinue if nursing, as drug may be excreted in milk. - Renal impairment: dose adjustment may be required; monitor kidney function. - Hepatic dysfunction: assess liver enzymes and consider dose modification. - Concomitant anticoagulants: increased risk of bleeding; monitor coagulation parameters. - Store at ambient temperature: keep below 25 °C, in the original container, protected from moisture and light.

What does Capecitabine interact with?

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

Major Interactions (Avoid): - Strong CYP2C9 inhibitors (e.g., fluconazole): may increase capecitabine exposure. - Warfarin: heightened anticoagulant effect, raising bleeding risk.

Moderate Interactions (Monitor Closely): - Antacids containing magnesium or aluminum: may reduce absorption; separate dosing by at least 2 hours. - 5‑FU‑based regimens: additive toxicity, especially myelosuppression. - Herbal supplements (e.g., St. John’s wort): potential induction of metabolic pathways, lowering drug levels.

Frequently asked questions

What conditions is Kapecitabin Sandoz used for?+
Kapecitabin Sandoz, containing capecitabine, is indicated for the treatment of adult patients with colorectal cancer, breast cancer and gastric cancer. It is typically used as part of combination chemotherapy regimens to help control tumour growth and improve clinical outcomes.
How does capecitabine work in the body?+
Capecitabine is a prodrug that is converted inside tumour cells to 5‑fluorouracil (5‑FU). The active 5‑FU inhibits thymidylate synthase, disrupting DNA synthesis, and becomes incorporated into RNA and DNA, leading to impaired nucleic acid function and ultimately causing cancer cell death.
What is the usual dose of Kapecitabin Sandoz?+
The specific dose of Kapecitabin Sandoz is determined by the prescribing oncologist based on the patient’s cancer type, stage, body surface area and overall health. Only a qualified healthcare professional should set the dosing schedule and any adjustments.
Is Kapecitabin Sandoz safe during pregnancy or breastfeeding?+
Capecitabine is classified as Pregnancy Category D, indicating evidence of fetal risk. It should not be used during pregnancy, and breastfeeding is contraindicated because the drug can be excreted in milk and may harm the infant.
How do I order Kapecitabin Sandoz from GNH USA?+
To place an order, submit an enquiry on the product page at gnh-usa.com specifying the required quantity. GNH USA supplies hospitals, pharmacies and procurement teams worldwide, and will request trade or institutional credentials before providing pricing, availability, shipping details and any necessary import documentation.
How does Kapecitabin Sandoz compare with other antimetabolites?+
Kapecitabin Sandoz (capecitabine) offers oral administration, which can be more convenient than intravenous agents such as 5‑fluorouracil. Both deliver 5‑FU systemically, but capecitabine’s tumor‑targeted activation may reduce systemic exposure, though safety profiles are broadly similar.
What are the recommended storage conditions for Kapecitabin Sandoz?+
Store Kapecitabin Sandoz at ambient temperature, preferably below 25 °C. Keep the tablets in their original packaging, protect them from moisture, heat and direct sunlight to maintain stability throughout their shelf life.
How is Kapecitabin Sandoz administered?+
Kapecitabin Sandoz is taken orally, usually with water, and may be prescribed to be taken with food to reduce gastrointestinal discomfort. The exact schedule—such as daily dosing cycles—must be followed as directed by the treating physician.
What are the most serious risks associated with Kapecitabin Sandoz?+
Serious risks include severe neutropenia, which can predispose to infections; thromboembolic events such as deep‑vein thrombosis; and cardiotoxicity presenting as chest pain or arrhythmias. Patients should be monitored closely for signs of infection, clotting or cardiac symptoms.
Who should not use Kapecitabin Sandoz?+
Kapecitabin Sandoz should be avoided in patients with known hypersensitivity to capecitabine or other fluoropyrimidines, in pregnant women, and in individuals with severe renal or hepatic impairment unless dose adjustments are made. It is also contraindicated for patients receiving certain strong CYP2C9 inhibitors.
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
Capecitabine
Route
Oral Use
Manufacturer
Sandoz D.O.O.
Origin
EU

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