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HSA Product

DIANEAL PD-2 PERITONEAL DIALYSIS SOLUTION WITH 2.5% DEXTROSE

Product approved by Health Sciences Authority (SG)

Basic Information

DIANEAL PD-2 PERITONEAL DIALYSIS SOLUTION WITH 2.5% DEXTROSE

SOLUTION, STERILE

Regulatory Information

SIN05748P

April 8, 1991

General Sale List

Therapeutic

INTRAPERITONEAL

August 10, 2023

May 30, 2025

XB05DA

Company Information

BAXTER HEALTHCARE (ASIA) PTE LTD

BAXTER HEALTHCARE (ASIA) PTE LTD

Active Ingredients

MAGNESIUM CHLORIDE HEXAHYDRATE

Strength: 5.08 mg/100 ml

SODIUM CHLORIDE

Strength: 538 mg/100 ml

CALCIUM CHLORIDE DIHYDRATE

Strength: 25.7 mg/100 ml

SODIUM LACTATE

Strength: 448 mg/100 ml

Detailed Information

Contraindications

**Contraindications** DIANEAL is contraindicated in patients with: - pre-existing severe lactic acidosis. - uncorrectable mechanical defects that prevent effective PD or increase the risk of infection. - documented loss of peritoneal function or extensive adhesions that compromise peritoneal function.

Indication Information

**AMBU-FLEX Container For Peritoneal Dialysis** **Indications and Usage** Peritoneal dialysis is indicated for patients in acute or chronic renal failure when nondialytic medical therapy is judged to be inadequate. It may also be indicated in the treatment of certain fluid and electrolyte disturbances, and for patients intoxicated with certain poisons and drugs. However, for many substances other methods of detoxification have been reported to be more effective than peritoneal dialysis. **ULTRABAG System For Continuous Ambulatory Peritoneal Dialysis (CAPD)** **Indications and Usage** Dianeal PD-2 peritoneal dialysis solutions in UltraBag containers are indicated for use in chronic renal failure patients being maintained on continuous ambulatory peritoneal dialysis when nondialytic medical therapy is judged to be inadequate.

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