Sichuan Yuanda Shuyang Pharmaceutical Co., Ltd.

Sichuan Yuanda Shuyang Pharmaceutical Co., Ltd.

FDA approves treatment to improve kidney function in adults with hepatorenal syndrome

2024 10/17

FDA has approved Terlipressin injection to improve kidney function in adults with hepatorenal syndrome (HRS) with rapid reduction in kidney function. Terlipressin is the first FDA-approved medication for this condition.

 

Disease or Condition

HRS is characterized bya progressive deterioration in kidney functionin people withadvanced liver disease. This is most common in those with advanced cirrhosis (liver scarring) and ascites, an abnormal buildup of fluid in the abdomen that is often related to liver disease. The prognosis is very poor, particularly if patients liver disease is not treated with liver transplantation. Rising levels of serum creatinine (a waste product in the blood) in patients with HRS can indicate worsening kidney function.

Effectiveness

The effectiveness of Terlipressin was assessed in a double-blind study. Participants with HRS with rapid reduction in kidney function were randomly assigned to receive Terlipressin (199 participants) or a placebo (101 participants). Participants received either 0.85 mg of Terlipressin or a placebo every six hours as an injection in the vein for a maximum of 14 days. The dose was adjusted based on changes in kidney function.

The primary effectiveness outcome was the percentage of patients who had kidney function improvement, defined by two consecutive days of serum creatinine levels of 1.5 mg/dL or less, obtained at least two hours apart, by day 14 or the participant’s final day in the study. Twenty-nine percent of participants in the Terlipressin group had kidney function improvement compared to 16 percent of participants in the placebo group.

People with serum creatinine levels of 5 mg/dL or greater should not take Terlipressin because they are unlikely to benefit from treatment.

Safety Information

Terlipressin increases the risk of serious or fatal respiratory (breathing) failure. Patients with low oxygen in their blood should not start the medication. During treatment, patients should be monitored for breathing problems with a pulse oximeter — a tool that measures oxygen levels in the blood.

Side effects of Terlipressin may prevent patients from receiving a liver transplant. Terlipressin can cause ischemic events (that occur when blood does not reach certain parts of the body) that may require pausing or stopping treatment; the medication may also cause fetal harm when used during pregnancy.

The most common side effects include abdominal pain, nausea, diarrhea, respiratory failure, and dyspnea (difficulty breathing).

Our Product

Terlipressin for Injection 1mg

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