Sucraid Oral Solution 8500U Drug Medication Dosage Information
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Sucraid: Oral solution (8500U)

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What is this Medicine?

SACROSIDASE is used to treat sucrase deficiency. This is part of a genetic condition known as congenital sucrase-isomaltase deficiency (CSID).

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Sucraid 8500unit/ml Solution

NDC: 621610011
  • Prescription Required
  • Not a Controlled Drug
    (CSA Schedule)
  • FDA Approved




FDA approved for the following conditions:
Congenital Sucrase-isomaltase Deficiency (CSID)

Sucraid 8500unit/ml Solution

Reported Side Effects for Sucraid 8500unit/ml Solution

Dehydration Incidence:
1.9%*
Severity: MODERATE
Onset: DELAYED
Headache Incidence:
1.9%*
Severity: MILD
Onset: EARLY
Inability To Sleep Incidence:
1.9%*
Severity: MILD
Onset: EARLY
Constipation Incidence:
3.8%*
Severity: MODERATE
Onset: DELAYED
Loose Stools Incidence:
3.8%*
Severity: MILD
Onset: EARLY
Upset Stomach Incidence:
3.8%*
Severity: MILD
Onset: EARLY
Vomiting Incidence:
5.8%*
Severity: MILD
Onset: EARLY
Stomach Pain Incidence:
7.7%*
Severity: MILD
Onset: EARLY
*This is an approximate aggregated range of reported side effects from clinical studies performed on this drug. Your experience with this drug may be different.
Daily Life Interactions for Sucraid 8500unit/ml Solution

Elements of your daily lifestyle may have an effect on the medications you are taking. Drug interactions can result in unwanted side effects, reduce the effectiveness of your medicine or possibly increase the action of a particular medicine.

Moderate Lifestyle Interaction
Acidic food and Sucraid 8500unit/ml Solution(Sacrosidase)
Acidic food and Sacrosidase(Sacrosidase)
Do not take Sacrosidase (Sucrase) with acidic foods like fruit juices since these juices could decrease the actions of the Sacrosidase.
Pregnancy & Lactation Information
FIRST Trimester

Class C - Animal studies have shown an adverse effect and there are no adequate and well-controlled studies in pregnant women. OR No animal studies have been conducted and there are no adequate and well-controlled studies in pregnant women.

SECOND Trimester

Class C - Animal studies have shown an adverse effect and there are no adequate and well-controlled studies in pregnant women. OR No animal studies have been conducted and there are no adequate and well-controlled studies in pregnant women.

THIRD Trimester

Class C - Animal studies have shown an adverse effect and there are no adequate and well-controlled studies in pregnant women. OR No animal studies have been conducted and there are no adequate and well-controlled studies in pregnant women.

Lactation

Caution - Not enough information is available to rule out harm to infants when this drug is taken by nursing mothers.


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