MedPath
HSA Product

Renvela ® Tablet 800mg

Product approved by Health Sciences Authority (SG)

Basic Information

Renvela ® Tablet 800mg

TABLET, FILM COATED

Regulatory Information

SIN13725P

November 6, 2009

Prescription Only

Therapeutic

ORAL

August 10, 2023

May 30, 2025

XV03AE02

Company Information

SANOFI-AVENTIS SINGAPORE PTE. LTD.

SANOFI-AVENTIS SINGAPORE PTE. LTD.

Active Ingredients

Detailed Information

Contraindications

**4\. CONTRAINDICATIONS** Renvela is contraindicated in patients with hypophosphatemia or bowel obstruction. Renvela is contraindicated in patients with hypersensitivity to sevelamer carbonate, sevelamer hydrochloride, or to any of the excipients.

Indication Information

**1\. INDICATIONS AND USAGE** Renvela is indicated for the control of hyperphosphataemia in adult patients receiving hemodialysis or peritoneal dialysis. Renvela is also indicated for the control of hyperphosphataemia in adult patients with chronic kidney disease not on dialysis with serum phosphorus ≥ 1.78 mmol/l. Renvela should be used within the context of a multiple therapeutic approach, which could include calcium supplement, 1,25-dihydroxy Vitamin D3 or one of its analogues to control the development of renal bone disease.

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