Rebutrix 150 mg. 500 mg FILM COATED TABLETS

Rebutrix 150 mg. 500 mg FILM COATED TABLETS

S4
PDF Leaflet Revision Date: 29 July 2025

API: Capecitabine | Company: Aurogen Sa

Clinical Summary

Quick overview from the medicine insert

Indication

Treatment of advanced breast, colorectal, and gastric cancers.

Dosage (summary)

1,250 mg/mu00b2 twice daily for 14 days, followed by a 7-day rest period.

Special Populations

  • Elderly
  • Hepatic impairment
  • Renal impairment

Pregnancy & Breastfeeding

Contraindicated in pregnancy; avoid breastfeeding during treatment and for 2 weeks after.

Key Drug Interactions

  • Warfarin
  • Phenytoin
  • Leucovorin
  • Sorivudine

Contraindications

  • Hypersensitivity to capecitabine
  • Severe renal impairment
  • Severe hepatic impairment
  • Dihydropyrimidine dehydrogenase deficiency

Common side effects

  • Diarrhoea
  • Nausea
  • Fatigue
  • Hand-foot syndrome

Counselling Points

  • Take with water within 30 mins after meals.
  • Report any severe diarrhoea or toxicity.
  • Use effective contraception during treatment.

Serious warnings

  • Monitor INR with anticoagulants
  • Risk of severe mucocutaneous reactions
  • Cardiotoxicity
Important Disclaimer

The Rebutrix 150 mg. 500 mg FILM COATED TABLETS professional information leaflet below is the property of Aurogen Sa and is provided on Medinsert exactly as issued, with no.. alterations or editorial changes. We make every effort to keep content current by updating documents as soon as new versions become available. Medinsert serves as a trusted access point for healthcare professionals, but does not replace official sources or clinical judgement. For more details, please read our full disclaimer. read more>>

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