- U.S. Births Barely Rise in 2024
- U.S. Faces Largest Measles Outbreak Since 2000
- Scoring System Can Avoid Unnecessary Surgery For Clogged Arteries
- Anemia In Pregnancy Increases Risk Of Heart Defects
- Urinary Incontinence Linked To Heart Disease Risk In Women
- Opioids Tough To Prescribe For Legitimate Patients, Doctors Say
- Cancer Prevention Not Yet Recovered From Pandemic-Era Declines, Report Says
- Virtual Singing Programs Boost Mood, Well-Being Of Isolated Seniors
- FDA Approves Dupixent for Chronic Spontaneous Urticaria
- Some OB/GYNS Stay in States With Abortion Bans, Despite Legal Risks
First Treatment Approved for Disease Linked to Stem Cell Transplant

Defitelio (defibrotide sodium) has been approved by the U.S. Food and Drug Administration to treat a rare, but usually fatal liver disease that affects some people who have had a stem cell transplant.
The condition, fatal in as many as 80 percent of cases, is called hepatic veno-occlusive disease (VOD). It affects people who have had a stem cell transplant to treat cancers of the blood or bone marrow.
Hepatic VOD causes blockage of blood vessels in the liver, which could lead to damage of the liver, kidneys and lungs, the FDA said.
Defitelio was investigated in 528 people with hepatic VOD who participated in three clinical studies. The most common side effects included low blood pressure, diarrhea, vomiting, nausea and nosebleed.
More serious side effects could include internal bleeding and allergic reactions, the FDA said.
Defitelio is marketed by Jazz Pharmaceuticals, based in Palo Alto, Calif.
More information
The FDA has more about this approval.
Source: HealthDay
Copyright © 2025 HealthDay. All rights reserved.