Drug Information for SUCRAID (sacrosidase) oral solution: (QOL Medical, LLC): ADVERSE REACTIONS

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  • Adverse experiences with SUCRAID in clinical trials were generally minor and were frequently associated with the underlying disease.

    In clinical studies of up to 54 months duration, physicians treated a total of 52 patients with SUCRAID. The adverse experiences and respective number of patients reporting each event (in parenthesis) were as follows: abdominal pain (4), vomiting (3), nausea (2), diarrhea (2), constipation (2), insomnia (1), headache (1), nervousness (1), and dehydration (1).

    Note: diarrhea and abdominal pain can be a part of the clinical presentation of the genetically determined sucrase deficiency, which is part of congenital sucrase-isomaltase deficiency (CSID).

    One asthmatic child experienced a serious hypersensitivity reaction (wheezing) probably related to sacrosidase (see Warnings). The event resulted in withdrawal of the patient from the trial but resolved with no sequelae.

  • Drug Information Provided by National Library of Medicine (NLM).
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