What is Kristalose and how is it used?
Kristalose is a prescription medicine used to treat the symptoms of Constipation and as a prophylaxis to prevent Portal Systemic Encephalopathy. Kristalose may be used alone or with other medications.
Kristalose belongs to a class of drugs called Laxatives, Osmotic; Ammonium Detoxicants.
What are the possible side effects of Kristalose?
Kristalose may cause serious side effects including:
- difficulty breathing,
- swelling of your face, lips, tongue, or throat, and
- severe or ongoing diarrhea
Get medical help right away, if you have any of the symptoms listed above.
The most common side effects of Kristalose include:
- stomach pain,
- nausea, and
Tell the doctor if you have any side effect that bothers you or that does not go away.
These are not all the possible side effects of Kristalose. For more information, ask your doctor or pharmacist.
Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
KRISTALOSE® (Lactulose) is a synthetic disaccharide in the form of crystals for reconstitution prior to use for oral administration. Each 10 g of lactulose contains less than 0.3 g galactose and lactose as a total sum. The pH range is 3.0 to 7.0.
Lactulose is a colonic acidifier which promotes laxation.
The chemical name for lactulose is 4-0- (3-D-Galactopyranosyl-D-fructofuranose. It has the following structural formula:
The molecular formula is C12H22011. The molecular weight is 342.30. It is freely soluble in water.
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KRISTALOSE® (Lactulose) For Oral Solution is indicated for the treatment of constipation. In patients with a history of chronic constipation, lactulose therapy increases the number of bowel movements per day and the number of days on which bowel movements occur.
DOSAGE AND ADMINISTRATION
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 normalbowel movement.
Directions For Preparation
Dissolve contents of packet in half a glass (4 ounces) of water.
When Lactulose For Oral Solution is dissolved in water, the resulting solution may be colorless to a slightly pale yellow color.
KRISTALOSE® (Lactulose) For Oral Solution is available in single dose packets of 10 g (NDC 66220-719-01) and single dose packets of 20 g (NDC 66220-729-01). The packets are supplied as follows:
NDC 66220-719-30 (Carton of thirty 10 g packets)
NDC 66220-729-30 (Carton of thirty 20 g packets)
STORE AT ROOM TEMPERATURE, 15°-30°C (59°-86°F).
To report adverse events associated with this product, please call 1 -877-484-2700.
Distributed by : Cumberland Pharmaceuticals Inc. Nashville,TN37203. Revised: Sep 2012
Precise frequency data are not available.
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.
Nausea and vomiting have been reported.
Results of preliminary studies in humans and rats suggest that nonabsorbable antacids given concurrently with lactulose may inhibit the desired lactulose-induced drop in colonic pH. Therefore, a possible lack of desired effect of treatment should be taken into consideration before such drugs are given concomitantly with lactulose.
A theoretical hazard may exist for patients being treated with lactulose who may be required to undergo electrocautery procedures during proctoscopy or colonoscopy. Accumulation of H2 gas in significant concentration in the presence of an electrical spark may result in an explosive reaction. Although this complication has not been reported with lactulose, patients on lactulose therapy undergoing such procedures should have a thorough bowel cleansing with a non-fermentable solution. Insufflation of C02 as an additional safeguard may be pursued but is considered to be a redundant measure.
Since KRISTALOSE® (Lactulose) For Oral Solution contains galactose and lactose (less than 0.3 g/10 g as a total sum), it should be used with caution in diabetics.
Carcinogenesis, Mutagenesis, Impairment Of Fertility
There are no known human data on long-term potential for carcinogenicity, mutagenicity, or impairment of fertility.
There are no known animal data on long-term potential for mutagenicity.
Administration of lactulose syrup in the diet of mice for 18 months in concentrations of 3 and 10 percent (v/w) did not produce any evidence of carcinogenicity.
Pregnancy Category B
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 wellcontrolled 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.
Safety and effectiveness in pediatric patients have not been established.
Signs and Symptoms
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 LD50 of the drug is 48.8 mL/kg in mice and greater than 30 mL/kg in rats.
Dialysis data are not available for lactulose. Its molecular similarity to sucrose, however, would suggest that it should be dialyzable.
Since KRISTALOSE ® (LACTULOSE) For Oral Solution contains galactose (less than 0.3 g/10 g as a total sum with lactose), it is contraindicated in patients who require a low galactose diet.
KRISTALOSE® (Lactulose) is poorly absorbed from the gastrointestinal tract and no enzyme capable of hydrolysis of this disaccharide is present in human gastrointestinal tissue. As a result, oral doses of lactulose reach the colon virtually unchanged. In the colon, lactulose is broken down primarily to lactic acid, and also to small amounts of formic and acetic acids, by the action of colonic bacteria, which results in an increase in osmotic pressure and slight acidification of the colonic contents. This in turn causes an increase in stool water content and softens the stool.
Since lactulose does not exert its effect until it reaches the colon, and since transit time through the colon may be slow, 24 to 48 hours may be required to produce desired bowel movement.
Lactulose given orally to man and experimental animals resulted in only small amounts reaching the blood. Urinary excretion has been determined to be 3% or less and is essentially complete within 24 hours.
Report Problems to the Food and Drug Administration
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.
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