Hepatorenal syndrome

Active Ingredient: Terlipressin

Indication for Terlipressin

Population group: only adults (18 years old or older)
Therapeutic intent: Curative procedure

For this indication, competent medicine agencies globally authorize below treatments:

4-12 mg in 4-6 divided doses daily

For:

Route of admnistration

Intravenous

Defined daily dose

4 - 12 mg

Dosage regimen

From 1 To 3 mg 4 time(s) per day every day for 7 day(s)

Detailed description

Treatment in adults is usually started with a dose of 1 mg terlipressin acetate# (5 ml of solution) at 4 to 6-hour intervals. The dose can be increased to a maximum of 2 mg terlipressin acetate# (10 ml of solution) every 4 hours if the serum creatinine does not decrease by at least 25% after 3 days of treatment.

# 1 mg terlipressin acetate corresponding to 0.85 mg terlipressin; 2 mg terlipressin acetate corresponding to 1.7 mg terlipressin

The treatment is continued until the serum creatinine has dropped below 1.5 mg/dl (133 ยตmol/l). In patients with a partial response (serum creatinine does not drop below 133 ยตmol/l) or in patients whose serum creatinine does not decrease, treatment should be stopped within 14 days.

In most clinical studies supporting the use of terlipressin for the treatment of hepatorenal syndrome, human albumin was administered simultaneously at a dosage of 1 g/kg of body weight on the first day and afterwards at a dosage of 20-40 g/day.

The usual duration of treatment of hepatorenal syndrome is 7 days, and the maximum recommended duration is 14 days.

Active ingredient

Terlipressin

Terlipressin inhibits portal hypertension with simultaneous reduction of blood circulation in portal vessels. Terlipressin contracts smooth oesophageal muscle with consecutive compression of oesophageal varices.

Read more about Terlipressin

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