What is kristalose

What should I discuss with my healthcare provider before taking lactulose? You should not use lactulose if you are on a special diet low in galactose milk sugar.

Tell your doctor if you have ever had: diabetes; or if you need to have any type of intestinal test using a scope such as a colonoscopy.

Tell your doctor if you are pregnant or breastfeeding. How should I take lactulose? Mix lactulose powder with at least 4 ounces of water, milk, or fruit juice. Measure liquid medicine with the supplied measuring device not a kitchen spoon.

Lactulose should produce a bowel movement within 24 to 48 hours. If you use this medicine long-term, you may need frequent medical tests. Tell your doctor if you have a planned colonoscopy or proctoscopy procedure. Store tightly closed at room temperature, away from moisture and heat. Avoid freezing. What happens if I miss a dose? What happens if I overdose? Seek emergency medical attention or call the Poison Help line at What should I avoid while taking lactulose?

What are the possible side effects of lactulose? This information should not be used to decide whether or not to take Kristalose or any other medicine.

Only the healthcare provider has the knowledge and training to decide which medicines are right for a specific patient. This information does not endorse any medicine as safe, effective, or approved for treating any patient or health condition. This is only a brief summary of general information about this medicine. It does NOT include all information about the possible uses, directions, warnings, precautions, interactions, adverse effects, or risks that may apply to Kristalose.

This information is not specific medical advice and does not replace information you receive from the healthcare provider. You must talk with the healthcare provider for complete information about the risks and benefits of using this medicine. Seasonal affective disorder SAD is a type of depression that usually occurs in winter.

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There are no known human data on long-term potential for carcinogenicity, mutagenicity, or impairment of fertility. Reproduction studies have been performed in mice, rats, and rabbits at doses up to 3 or 6 times the usual human oral dose and have revealed no evidence of impaired fertility or harm to the fetus due to lactulose.

There are, however, no adequate and well-controlled studies in pregnant women. Because animal reproduction studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed. It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when lactulose is administered to a nursing woman. Initial dosing may produce flatulence and intestinal cramps, which are usually transient.

Excessive dosage can lead to diarrhea with potential complications such as loss of fluids, hypokalemia, and hypernatremia. There have been no reports of accidental overdosage. In the event of overdosage, it is expected that diarrhea and abdominal cramps would be the major symptoms. Medication should be terminated. The acute oral LD 50 of the drug is Dialysis data are not available for lactulose. Its molecular similarity to sucrose, however, would suggest that it should be dialyzable.

The usual adult dosage is 10 g to 20 g of lactulose daily. The dose may be increased to 40 g daily if necessary. Twenty-four to 48 hours may be required to produce a normal bowel movement. When Lactulose For Oral Solution is dissolved in water, the resulting solution may be colorless to a slightly pale yellow color.