In addition to enzyme replacement therapy with Sucraid®, some individuals with Congenital Sucrase-Isomaltase Deficiency (CSID) may require dietary changes.
If you have been diagnosed with CSID, ask your GI doctor if Sucraid® is right for you.
Download the Sucraid® and your diet guide
Infant dietary guide for individuals treated with Sucraid®
Child dietary guide for individuals treated with Sucraid®
Adult dietary guide for individuals treated with Sucraid®
How to read a food label
*You should discuss dietary changes with your physician or a registered dietitian prior to making any changes to your diet.
†Be cautious when adding processed foods and baked goods and read food labels carefully, since many hidden ingredients could trigger GI symptoms.
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.FDA.gov/medwatch or call 1-800-FDA-1088.
Sucraid® (sacrosidase) Oral Solution is an enzyme replacement therapy for the treatment of genetically determined sucrase deficiency, which is part of
Congenital Sucrase-Isomaltase Deficiency (CSID).