Octaplus approved for blood coagulation disorders

Thursday, January 17 (HealthDay News)-Octaplas has been approved by the US Food and Drug Administration to enhance insufficient coagulation proteins that can cause excessive bleeding and excessive coagulation.

This product is a sterile frozen solution made from human plasma. A “solvent detergent process” has been applied to minimize the possibility of serious viral infections, the agency said.

To avoid transfusion reactions, OctaPlus should match the recipient’s blood type. According to the FDA, each lot is measured for the presence of required coagulation factors before approval for use.

The current version has been used in Europe and elsewhere since 2006, and the previous prescription was first used in 1992. In total, more than 2 million people have been treated outside the United States with more than 7 million doses.

According to the FDA, OctaPlus clinical trials focus on patients with liver disease, liver transplantation, and heart surgery. The most common side effects were shortness of breath, chest discomfort, itching and rash on the skin, headache and tingling.

Octaplas is manufactured by Octapharma based in Vienna, Austria.

-Scott Roberts

Copyright © 2013 Health Day. all rights reserved.

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Octaplus approved for blood coagulation disorders

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