IXCHIQ and Ocaliva withdrawn from the market due to potential safety concerns

Effective immediately, IXCHIQ® and Ocaliva® have been withdrawn from the market by the U.S. Food and Drug Administration (FDA) due to potential safety concerns. 

We're notifying members

Impacted members will receive letters in the mail informing them of the drug changes and encouraging them to discuss concerns or alternative treatment plans with their provider. These changes will only impact a total of 26 members. You can find more information on these changes below.

IXCHIQ®

What it treats

IXCHIQ works to prevent chikungunya virus in individuals 18 years and older who are at an increased risk of exposure.

Reason for withdrawal

The FDA suspended the biologics license for IXCHIQ due to serious safety concerns, including reports of chikungunya-like illness and hospitalizations following vaccination.

Ocaliva®

What it treats

Ocaliva is used to treat biliary cholangitis, a rare liver condition caused by bile build-up.

Reason for withdrawal

Ocaliva is being voluntarily withdrawn from the market by the manufacturer, Intercept Pharmaceuticals, at the request of the FDA due to concerns of potential liver damage.