Senokot
Senokot
Generic Name
Senokot
Mechanism
Senokot contains sennosides A and B, anthraquinone glycosides that are biologically inactive until converted by colonic bacteria into active lactones (rhein and emodin).
• Stimulation of colonic mucosa: The active lactones depolarize the enteric nerve endings, triggering smooth‑muscle contraction.
• Increased colonic fluid secretion: They inhibit sodium‑potassium exchange, enhancing water and electrolyte entry into the lumen.
• Rapid onset (30–90 min) and short duration (≈ 1 day), making it effective for acute constipation or intermittent use.
Pharmacokinetics
| Parameter | Detail |
| Absorption | Minimal systemic absorption; > 95 % remains in the colon. |
| Metabolism | Oral sennosides → hydrolyzed by colonic bacteria to active lactones; subsequent hepatic glucuronidation. |
| Distribution | Little tissue binding; remains in GI tract. |
| Elimination | Renal excretion of glucuronide conjugates; dose‑dependent urinary excretion. |
| Half‑life | Active lactones: ~15 h; overall effect lasts ~24 h. |
| Drug Interactions | May antagonize absorption of oral iron, calcium, and tetracyclines; avoid concurrent use within 1 h. |
Indications
- Acute constipation (e.g., post‑operative, after long travel).
- Chronic constipation (≤ 4 weeks) for symptom relief.
- Intermittent constipation or scheduled bowel preparation.
- Pediatric constipation (≥ 6 yrs) with physician guidance.
Contraindications
- Intestinal obstruction or perforation.
- Inflammatory bowel disease (active ulcerative colitis, Crohn’s disease).
- Severe electrolyte imbalance (hypokalemia, hyponatremia).
- Pregnancy: Category C—use only if benefits outweigh risks; short courses 4 weeks of continuous therapy.
- Pseudomembranous colitis: Contraindicated due to potential exacerbation.
- Allergy to senna or other anthraquinone laxatives.
Dosing
- Adults & Adolescents (≥ 12 yrs): 15 mg (1 tablet) 1–2 times per day, maximum 30 mg/day.
- Children (6–11 yrs): 5 mg (½ tablet) once daily; titrate based on response.
- Geriatric: Start at lower end (≤ 15 mg) to reduce cramping.
- Extended‑Use: Not recommended beyond 4 weeks without medical supervision.
- Administration: Oral, with a full glass of water; can be taken with or without food.
- Missed dose: Take as soon as remembered; skip if later in the day.
Adverse Effects
| Category | Examples |
| Common (≥5 %) | Abdominal cramps, diarrhea, flatulence, nausea, headache. |
| Serious (≤1 %) | Electrolyte disturbances (hypokalemia, hyponatremia), dehydration, severe cramping leading to obstruction. |
| Rare | Rebound constipation, dependency, senna‑induced liver injury (especially in long‑term use). |
Monitoring
- Vital signs: BP, pulse (especially if diarrhea or dehydration suspected).
- Electrolytes: Serum potassium, sodium, chloride every 2–4 weeks in chronic users.
- Renal function: eGFR baseline, particularly in elderly or chronic kidney disease.
- Hydration status: Oral intake, urine output, weight.
- Bowel habits: Document frequency, consistency, and any abdominal discomfort.
Clinical Pearls
- Short‑Term Safeguard: Use Senokot only for ≤ 4 weeks to avoid laxative dependence and colonic mucosal adaptation.
- Pregnancy & Lactation: A lower dose (5–10 mg) is still considered the safest option; always consult obstetrics/radiology for contrast studies.
- Drug‑Drug Synergy: Co‑administer with magnesium hydroxide or aluminium hydroxide *only* if a 1‑h buffer is observed; these antacids can reduce efficacy.
- Tolerance & Break‑In: Take break days 4‑7 of a 2‑week cycle to maintain colonic sensitivity.
- Patient Education: Instruct patients to increase fluid intake (≥ 2 L/day) and incorporate fiber to mitigate cramping and promote stool bulk.
- Differential Tolerance: Elderly or comorbid patients occasionally experience *prolonged* diarrhea (> 30 min); promptly report any extended loose stools.
- Monitoring for Rebound: When discontinuing Senokot, gradually taper by reducing dose by 5 mg every 3–5 days to prevent rebound constipation.
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• Key Terms: *senna*, *anthraquinone*, *lactones*, *intestinal motility*, *electrolyte imbalance*, *short‑term use*.