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MEDICINE MONOGRAPH CODE: [12.38] ID: TIP-MED-000270 ⚠️ HIGH-ALERT / SPECIALIST SUPERVISION

Activated Charcoal (Medicinal GI Poison Decontamination Slurry)

Active Ingredient / Scientific Identity: Activated Charcoal • Class: Universal Gastrointestinal Adsorbent Antidote

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1. Clinical & Scientific Overview

Activated Charcoal (Medicinal GI Poison Decontamination Slurry) (TIP-MED-000270, Reference Code [12.38]) is classified under Vaccines, Immunologicals & Emergency Toxicology Antidotes (Ch 12) as a Universal Gastrointestinal Adsorbent Antidote. Within the Indian regulatory and compendial framework, it is governed under Non-Schedule / OTC or Schedule K Permitted Preparation (Medical Supervision Recommended for High-Dose/Therapeutic Regimens).

Verified Indian Market Examples / Compendial Status:
Representative Indian Market Examples (Edition 2.7 Ch 12 [12.38], p. 173): Charcodote, Actidose, Ultra-Carbon — Strengths & Dosage Forms: Powder / Granules for Oral Suspension: 25 g, 50 g bottles/sachets.
Representative Indian Market Examples (Edition 2.7 Ch 12 [12.38], p. 173): Charcodote, Actidose, Ultra-Carbon — Strengths & Dosage Forms: Powder / Granules for Oral Suspension: 25 g, 50 g bottles/sachets.
Dosage Forms & Available Strengths:
Powder / Granules for Oral Suspension: 25 g, 50 g bottles/sachets.
Routes: Oral / Parenteral / Topical as specified by formulation

3. Mechanism of Action & Pharmacodynamics

Pyrolysed carbon matrix with an immense internal pore network (surface area 950–2,000 m2 per gram) adsorbs non-polar organic drug and toxin molecules in the GI lumen via van der Waals forces -> prevents systemic absorption and interrupts enterohepatic/enteroenteric circulation.

4. Therapeutic Indications & Evidence-Supported Uses

  • Acute gastrointestinal decontamination within 1 hour (or longer for modified-release/anticholinergic drugs) of potentially toxic oral ingestion of adsorbable drugs and poisons
  • Multi-Dose Activated Charcoal (MDAC) for 'gut dialysis' of Carbamazepine, Phenobarbitone, Phenytoin, Theophylline, Dapsone, or Quinine

5. Educational Dosage Context, Formulations & Administration

Educational Dosing & Regimen Summary: Adult: Single-Dose GI Decontamination (within 1 hour of ingestion): 50–100 g (or 1 g/kg; 10:1 weight ratio of charcoal to ingested toxin) mixed in 250–400 mL water as an oral slurry or via nasogastric tube. Multi-Dose Activated Charcoal (MDAC for Carbamazepine/Theophylline/Phenobarbitone/Dapsone): 50 g initially, followed by 25 g q2h or 50 g q4h. • Paediatric: Children 1–12 years: 0.5–1 g/kg (typically 10–25 g in <5 yr; 25–50 g in 5–12 yr) mixed in water or fruit juice.

Administration & Meal Timing: See Administration & Counselling below. | Standard clinical schedule per indication.

6. Pharmacokinetics, Metabolism & Renal/Hepatic Adjustment

Absorption & Disposition:
Absorption, distribution, metabolism, and excretion follow class pharmacokinetic profile; verify patient renal/hepatic function.
Metabolism & Biotransformation:
Renal: No adjustment. • Hepatic: No adjustment.
Elimination & Renal Adjustment:
Renal: No adjustment. • Hepatic: No adjustment.
Hepatic Impairment Considerations:
Renal: No adjustment. • Hepatic: No adjustment.

7. Contraindications, Precautions & High-Risk Warnings

Contraindications & Red-Flag Precautions:
  • Contraindications: UNPROTECTED AIRWAY (drowsy, stuporous, comatose, or seizing patient without a cuffed endotracheal tube—aspiration of charcoal causes fatal obliterative bronchiolitis and ARDS!); ingestion of caustics/corrosives (strong acids or alkalis—charcoal is ineffective and obscures urgent diagnostic endoscopy); ingestion of volatile hydrocarbons (kerosene, petrol, turpentine—high aspiration risk); bowel obstruction, ileus, or GI perforation. • Precautions: DOES NOT ADSORB ('PHAILS' Mnemonic): Pesticides (Organophosphates poorly if in hydrocarbon solvent—protect airway first!), Hydrocarbons, Acids/Alkalis/Alcohols (Ethanol, Methanol, Ethylene glycol), Iron salts, Lithium, or Solvents/Heavy Metals (Lead, Mercury, Arsenic, Potassium, Cyanide). Do not use sorbitol-containing charcoal repeatedly in MDAC (causes severe hypernatraemic dehydration in children).

Key Clinical Precautions: Renal: No adjustment. • Hepatic: No adjustment.

8. Adverse Effects Profile

Common & Mechanism-Related Adverse Effects:
  • Black stools, vomiting, constipation, abdominal bloating.
  • Pulmonary aspiration pneumonitis / ARDS (if given without airway protection), bowel obstruction or charcoal bezoar (if given in ileus).
Serious / Dose-Limiting Adverse Effects:
  • Monitor for severe hypersensitivity, organ toxicity, or dose-limiting adverse events.

9. Major Drug–Drug, Drug–Food & Drug–Herb Interactions

  • Adsorbs oral antidotes (e
  • , oral Methionine or oral N-Acetylcysteine—use IV N-Acetylcysteine in Paracetamol overdose if Activated Charcoal was given) and stops absorption of all concurrent oral medications

10. Clinical Monitoring, Patient Counselling & Storage

Clinical & Laboratory Monitoring: Monitor clinical response, baseline renal/hepatic parameters, and relevant serum biomarkers.

Pharmacist Patient Counselling Points:

  • Patient Counselling Checklist: Shake slurry thoroughly before drinking through a covered cup and straw (hiding the black appearance improves palatability in children); stools will turn black harmlessly for 2-3 days.
  • Meal & Clock Timing Instruction: See Administration & Counselling below. (Standard clinical schedule per indication.)
  • Missed Dose Protocol: Take as soon as remembered unless close to next scheduled dose; never double the dose.
  • Geriatric Dispensing Pearl: Schedule: OTC / Non-Schedule | NLEM 2022: Yes | Compendia: IP 2026 / NFI 7th Ed 2026 / NLEM 2022 / BNF 90th Ed

Storage, Stability & Dispensing Safeguards: Store below 25°C–30°C in original moisture- and light-resistant packaging out of reach of children. Available forms: Powder / Granules for Oral Suspension: 25 g, 50 g bottles/sachets.

11. Visual Pharmacology & Mechanism Diagram (svg-v339-01-adme-12-step-journey)

THE 12-STEP ORAL DRUG JOURNEY THROUGH THE HUMAN BODY (LADME) Note: IV bolus enters Step 6 directly (F = 100%); Sublingual & Transdermal routes bypass Step 4–5 Portal First-Pass Metabolism 1. Oral Administration • Tablet / Capsule swallowed • Gastric emptying to duodenum pH 1.5–3.5 (Stomach) 2. Disintegration & Dissolution • Tablet breaks into granules • API dissolves in GI fluid Noyes-Whitney Dissolution Rate 3. GI Epithelial Absorption • Crosses intestinal villi • Passive / Active / P-gp efflux Small Intestine (Large Surface Area) 4. Portal Circulation • Mesenteric veins → Portal vein • Delivers blood to liver sinusoids Pre-systemic Venous Conduit 5. First-Pass Metabolism • Gut & hepatic CYP450 extraction • High: GTN, Propranolol, Morphine Determines Bioavailability (F = f_a × (1-E_H)) 6. Systemic Circulation • Hepatic vein → IVC → Heart • Unbound vs Albumin-bound drug Only FREE drug is active 7–8. Tissue Distribution (Vd) • Capillary permeation to organs • Blood-Brain & Placental barriers Vd = Dose / C_0 (L or L/kg) 9. Target Site of Action • Receptors (GPCR, Ion channel) • Enzymes & Carrier Transporters Pharmacodynamic Effect (E_max, EC50) 10. Hepatic Biotransformation • Phase I (CYP450 Oxidation/Hydrolysis) • Phase II (Glucuronidation/Sulfation) Converts lipophilic drug → hydrophilic metabolite 11. Renal & Biliary Elimination • Nephron: Filtration + Secretion − Reabsorption • Biliary excretion & Enterohepatic recycling Total Clearance CL_tot = CL_renal + CL_hepatic 12. Excretion from the Body • Urine (Primary polar metabolite route) • Bile/Faeces, Expired Air, Sweat, Milk Elimination Half-Life t1/2 = (0.693 × Vd) / CL
svg-v339-01-adme-12-step-journey — 8.1 Complete 12-Step Journey of an Orally Administered Drug (ADME): Figure 8.1: The 12-step physiological journey of a typical orally administered solid dosage form through Liberation, Absorption, Distribution, Metabolism, and Excretion (LADME). Note: Parenteral (IV), sublingual, and inhalational routes bypass gastrointestinal absorption and/or hepatic first-pass metabolism.

12. Authoritative References, Regulatory Sources & Editorial Disclaimer

Primary Compendial & Guideline Reference: Indian Pharmacist Desk Reference — Professional Edition 2.7 (2026–27) • Ch 12 [12.38] (p. 173)

Official Verification Portals: Indian Pharmacopoeia Commission (IPC) & National Formulary of India (NFI) • Central Drugs Standard Control Organization (CDSCO) • Ministry of Health & Family Welfare — NLEM 2022 • NCBI Bookshelf / StatPearls Pharmacology Reference • DailyMed (US FDA Official Prescribing Reference)

Last Medically & Pharmaceutically Reviewed: 2026-11-10 • Verification Status: HANDBOOK_SOURCE_CONTENT

Educational & Clinical Disclaimer: This reference profile is published solely for pharmacy education, academic study, and professional clinical reference. It does not substitute for patient-specific clinical judgement, qualified specialist oncology/medical supervision, or official CDSCO/IP prescribing information. Never self-medicate with prescription, Schedule H/H1/X, NDPS, or oncology medicines.