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Alpha-1 Antitrypsin Deficiency as related to Balsalazide


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AAT; alpha-1 proteinase inhibitor; alpha-1 related emphysema; genetic emphysema; hereditary pulmonary emphysema; inherit... 

balsalazide disodium; Colazal 

Alpha-1 is an inherited disorder that may result in you developing a serious lung/ liver disease and passing the defective AAT gene onto your children. An estimated 100,000 people in the U.S. and a similar number in Europe are estimated to have the severe deficiency. In normal individuals large amounts of alpha-1 antitrypsin (AAT) is made in the liver and released into the blood. In AAT deficient individuals, the AAT made in the liver cannot be fully released into the blood.

Colazal is used to treat the signs and symptoms of mild to moderately active ulcerative colitis. The safety and efficacy of Colazal are not known after 12 weeks.


Alpha-1 Antitrypsin Deficiency as related to Balsalazide


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November 23, 2009


Page Updated: January 17, 2009
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