Primary Biliary Cholangitis

Primary biliary cholangitis (PBC) is a chronic autoimmune liver disease in which the immune system gradually destroys the small bile ducts inside the liver. Bile backs up, causing inflammation and, over years, scarring. Most people diagnosed are women over 40, and the condition is often found incidentally during routine blood tests before any symptoms appear.

Medicine used to treat Primary Biliary Cholangitis

Urso

Ursodeoxycholic Acid

150 · 300mg

This product is designed to support liver health in primary biliary cholangitis and is indicated to address the presence of specific gallstones.

From $1.07 / tablet View

Slowing the progression of primary biliary cholangitis

There is no cure, but treatment can significantly slow liver damage and reduce symptoms such as fatigue and itching. The mainstay is ursodeoxycholic acid, a naturally occurring bile acid that improves bile flow and reduces the toxic build-up that injures liver cells. When started early and taken consistently, it lowers liver enzyme levels and, in many patients, delays progression to cirrhosis.

PBC sits within the broader field of digestive health care. Regular monitoring through blood tests (liver enzymes, bilirubin) and periodic imaging remains essential, as response to treatment guides long-term management. Anyone experiencing unexplained itching, right-side abdominal discomfort, or persistent fatigue should discuss liver function testing with a doctor.