Bulk-Forming Laxatives
Drug class: Antineoplastic Agents
Usage of Bulk-Forming Laxatives
Constipation
Relief of occasional constipation; restore bowel movement regularity.
Initial treatment of choice for simple constipation caused by a low-fiber and/or low-fluid diet.
Bulk-forming laxatives, stool softeners, or mineral oil preferred in conditions in which straining at defecation should be avoided (e.g., MI, vascular diseases, diseases of the anus or rectum, hernias, recent rectal surgery).
Treatment of constipation that occurs following prolonged bed rest or hospitalization.
Treatment of choice for constipation resulting from diminished colonic motor response in geriatric patients; condition is usually due to psychological or physical laxative dependence.
Bulk-forming laxatives or stool softeners are the preferred treatment for constipation occurring during pregnancy or the puerperium.
Not for use when prompt or thorough bowel evacuation is necessary (e.g., poisonings, radiologic examination, bowel surgery).
Diarrhea
Increase the bulk of stools in patients with chronic, watery diarrhea; subjective improvement noted but the total water content of the stool was unchanged.
GI Pain
Reduce intraluminal rectosigmoid pressure and pain in diverticular disease.
Hypercholesterolemia† [off-label]
Psyllium preparations have been used as an adjunct to dietary therapy to reduce elevated serum total cholesterol, LDL cholesterol, apolipoprotein B (apo B) concentrations and the ratio of LDL-cholesterol to HDL-cholesterol in adults with mild to moderate hypercholesterolemia† [off-label].
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How to use Bulk-Forming Laxatives
Administration
Oral Administration
Administer orally, in conjunction with adequate fluid intake.
For treatment of constipation, administer ≥1 full glass (250 mL) of liquid with each dose. Some manufacturers recommend another full glass of liquid after dose.
When used to increase the bulk of stools in chronic, watery diarrhea, one manufacturer suggests administering 1/3 of a glass (80 mL) of liquid with each dose.
Administer as infrequently as possible at the lowest effective dosage level. Do not use for >1 week unless directed by a clinician.
In patients receiving large dosages, administer in divided doses instead of a single daily dose to reduce the risk of esophageal obstruction.
To minimize side effects, initially administer 0.5–1 dose daily; increase as needed up to 3 doses daily.
Methylcellulose PowderFill glass with ≥240 mL (8 ounces) of cold water; level powder and add to water; stir briskly and drink promptly. Chocolate powder may be mixed with milk.
Psyllium PowderPlace dose in empty glass; fill with ≥240 mL of water or other beverage; stir briskly and drink promptly. If mixture thickens, add additional liquid and stir.
Psyllium CapsuleSwallow 1 capsule at a time.
Dosage
Available as calcium polycarbophil; dosage expressed in terms of polycarbophil.
Pediatric Patients
Constipation Oral (Calcium Polycarbophil Caplet)Children ≥12 years of age: Initially, 1 g once daily. May increase gradually as needed up to 4 times daily.
Oral (Methylcellulose Caplet)Children 6–12 years of age: 500 mg (1 caplet) 1–6 times daily.
Children >12 years of age: 1 g (2 caplets) 1–6 times daily.
Oral (Methylcellulose Powder)Children 6–11 years of age: 1 g 1–3 times daily.
Children ≥12 years of age: 2 g 1–3 times daily.
Oral (Malt Soup Extract)Children 2–5 years of age: 3–8 g 1–3 times daily.
Children 6–11 years of age: 3–16 g 1–3 times daily.
Children ≥12 years of age: 3–32 g 1–3 times daily.
Oral (Psyllium Capsule)Children ≥12 years of age: 2.6 g (5 capsules) 1–3 times daily.
Oral (Psyllium Powder)Children 6–11 years of age: Usually, 1.7 g 1–3 times daily.
Children 6–11 years of age (Hydrocil): 3.5 g; maximum 14 g daily in divided doses.
Children 6–11 years of age (Konsyl): 3 g 1–3 times daily.
Children ≥12 years of age: Usually, 3.4 g 1–3 times daily.
Children ≥12 years of age (Hydrocil): 3.5–7 g; maximum 28 g daily in divided doses.
Children ≥12 years of age (Konsyl): 6 g 1–3 times daily.
Oral (Psyllium Wafer)Children 6–11 years of age: 1.7 g (1 wafer) 1–3 times daily.
Children ≥12 years of age: 3.4 g (2 wafers) 1–3 times daily.
Adults
Constipation Oral (Calcium Polycarbophil Caplet)1 g once daily. May increase gradually as needed up to 4 times daily.
Oral (Methylcellulose Caplet)1 g (2 caplets) 1–6 times daily.
Oral (Methylcellulose Powder)2 g 1–3 times daily.
Oral (Malt Soup Extract)3–32 g 1–3 times daily.
Oral (Psyllium Capsule)2.6 g (5 capsules) 1–3 times daily.
Oral (Psyllium Powder)Usually, 3.4 g 1–3 times daily.
Hydrocil: 3.5–7 g; maximum 28 g daily in divided doses.
Konsyl: 6 g 1–3 times daily.
Oral (Psyllium Wafer)3.4 g (2 wafers) 1–3 times daily.
Hypercholesterolemia† [off-label] Oral (Psyllium Capsule)3.2 g (6 capsules) 3 times daily.
Oral (Sugar-Free Psyllium Powder)3.4 g 3 times daily before meals.
Prescribing Limits
Pediatric Patients
Constipation Oral (Calcium Polycarbophil Caplet)Children ≥12 years of age, as self-medication: Maximum 4 g (8 caplets) daily; maximum of 7 days.
Oral (Malt Soup Extract)Children 2–5 years of age: Maximum 16 g daily.
Children 6–11 years of age: Maximum 32 g daily.
Children ≥12 years of age: Maximum 64 g daily.
Oral (Psyllium Powder)Children 6–11 years of age (Hydrocil): Maximum 14 g daily.
Children ≥12 years of age (Hydrocil): Maximum 28 g daily.
Adults
Constipation Oral (Calcium Polycarbophil Caplet)Self-medication: Maximum 4 g (8 caplets) daily; maximum of 7 days.
Oral (Malt Soup Extract)Maximum 64 g daily.
Oral (Psyllium Powder)Hydrocil: Maximum 28 g daily.
Special Populations
No special population dosage recommendations at this time.
Warnings
Contraindications
Warnings/Precautions
Warnings
ObstructionBowel and/or esophageal obstruction, swelling or blockage of the throat, choking, or asphyxiation reported when insufficient liquid (e.g., <250 mL) administered with some bulk-forming laxatives. Administer each dose with ≥1 full glass (250 mL) of liquid. (See Administration under Dosage and Administration and also see Contraindications under Cautions.)
Sensitivity Reactions
Psyllium HypersensitivitySerious hypersensitivity reactions possible to inhaled or ingested psyllium.
Do not inhale psyllium hydrophilic mucilloid particles. Severe hypersensitivity reactions (e.g., rhinoconjunctivitis, acute bronchospasm, anaphylaxis) may occur in susceptible individuals (e.g., those with psyllium sensitivity or suffering from respiratory disorders) following inhalation of psyllium dust particles.
One manufacturer suggests that health-care personnel dispense powdered psyllium preparations with a spoon instead of pouring them directly from the container to minimize exposure and sensitization to airborne particles of psyllium.
Milk HypersensitivityCitrucel Fiber Shake, Chocolate Flavor, contains dry milk powder; hypersensitivity reactions possible in patients sensitive to milk.
PhenylketonuriaMetamucil Smooth Texture Sugar Free Orange Flavor contains aspartame (NutraSweet), which is metabolized in the GI tract to provide 25 mg phenylalanine per 3.4 g dose.
Metamucil Sugar Free Berry Burst Flavor contains aspartame (NutraSweet), which is metabolized in the GI tract to provide16 mg phenylalanine per 3.4 g dose.
Citrucel Sugar Free Orange Flavor contains aspartame (NutraSweet), which is metabolized in the GI tract to provide 52 mg per 10.2 g dose.
Citrucel Fiber Shake, Chocolate Flavor contains aspartame (NutraSweet), which is metabolized in the GI tract to provide 49 mg per 10.7 g dose.
Specific Populations
PregnancyPsyllium: Category B.
Pediatric UseSafety and efficacy of methylcellulose not established in children <6 years of age.
Safety and efficacy of malt soup extract not established in children <2 years of age.
Safety and efficacy of psyllium powders and wafers not established in children <6 years of age.
Safety and efficacy of calcium polycarbophil and psyllium capsules not established in children <12 years of age.
Avoid use of laxatives in infants and children.
Renal ImpairmentUse with caution and monitor electrolytes (e.g., magnesium, potassium) in patients with impaired renal function.
Common Adverse Effects
Psyllium: Changes in bowel habits, minor bloating.
What other drugs will affect Bulk-Forming Laxatives
GI Absorption of Other Drugs
By increasing intestinal motility, can potentially decrease transit time of concomitantly administered oral drugs and thereby decrease their absorption.
Administer ≥2–3 hours before or after other medications.
Specific Drugs
Drug
Interaction
Comments
Digitalis
May bind digitalis in the GI tract and decrease absorption
Administer laxative at least 3 hours before or after digitalis
Nitrofurantoin
May bind nitrofurantoin in the GI tract and decrease absorption
Administer laxative at least 3 hours before or after nitrofurantoin
Salicylates
May bind salicylate in the GI tract and decrease absorption
Administer laxative at least 3 hours before or after salicylate
Disclaimer
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