- T-Day Dinner, Post-Election: Experts Offer Tips to Keep Things Calm
- Stroke Guidelines Updated, With Focus on Women and GLP-1s
- Vaping Immediately Changes Your Blood Flow
- Yoga Helps Women Deal With the Mental Stress of Cancer
- Illinois Study Finds Steep Rise in Serious Complications of Pregnancy
- Reaching Age at Which a Parent Died by Suicide Raises Risk in Adult Child
- Could a Common Thyroid Medicine Weaken Bones?
- Long COVID Hits the Young Harder Than the Old, Study Finds
- For Some, ‘Tis the Season for Loneliness. Experts Offer Tips to Stay Connected
- Taking a GLP-1 Medication? Here’s Tips to Holiday Eating
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 © 2024 HealthDay. All rights reserved.