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ALIMENTARY TRACT AND METABOLISM › DRUGS FOR CONSTIPATION › DRUGS FOR CONSTIPATION › Contact laxatives
contact laxatives in combination
A06AB20
Forms & Strengths
- Oral tablets: Senna 8.6 mg + Docusate Sodium 50 mg
- Oral capsules: Bisacodyl 5 mg + Docusate Sodium 100 mg
- Oral liquid: Casanthranol 30 mg/15 mL + Mineral Oil emulsion
Adult Dosing
- Senna/Docusate: 1-2 tablets orally once to twice daily
- Bisacodyl/Docusate: 1-2 capsules orally daily as needed
- Maximum duration of use: 1 week without medical supervision
Pediatric Dosing
- Children < 6 years: Safety and efficacy not established
- Children 6-12 years: Half the adult starting dose, as directed by a physician
- Adolescents >= 12 years: Same as adult dosing
Indications
- Short-term relief of occasional constipation
- Prevention of opioid-induced constipation
- Bowel evacuation prior to diagnostic or surgical procedures
Mechanism of Action
- Stimulant laxative component (e.g., senna, bisacodyl) directly stimulates enteric nerves and colonic mucosa to increase peristalsis
- Stool softener component (e.g., docusate) lowers surface tension, allowing water and fats to penetrate fecal material
- Combined action accelerates intestinal transit and softens stool consistency
Contraindications
- Hypersensitivity to any active ingredient
- Symptoms of appendicitis, acute surgical abdomen, or intestinal obstruction
- Undiagnosed rectal bleeding or severe dehydration
- Children under 6 years of age
Adverse Reactions
- Abdominal cramping and colicky pain
- Nausea and diarrhea
- Electrolyte disturbances with chronic use (hypokalemia)
- Melanosis coli with prolonged anthraquinone (senna) use
Drug Interactions
- Cardiac glycosides (digoxin): Risk of toxicity if laxative-induced hypokalemia occurs
- Diuretics: Increased risk of electrolyte depletion and dehydration
- Oral medications: Decreased absorption due to accelerated gastrointestinal transit
- Mineral oil: Combined use with stool softeners may increase systemic absorption of mineral oil
Curated Content: Needs Vetting Before Put to Clinical Use