Key points
- We recommend to consult your poison centre with the use of this antidote.
- Activated Charcoal administration is contraindicated for certain toxic agents and not recommended for others which are sparsely or not adsorbed by it.
- The longer the delay after ingestion, the lower the effectiveness of activated charcoal.
- Make sure the patient can protect his/her airway or has a protected airway prior to the administration of activated charcoal.
- Repeated doses of activated charcoal should not be administered if peristalsis is poor or absent.
- Repeated doses may be used to enhance elimination, contact your poison centre for more information.
- The poison centre does not recommend the repeated use of sorbitol activated charcoal suspensions. Only aqueous activated charcoal suspensions is now recommended. The addition of sorbitol to activated charcoal may lead to an increased incidence of adverse effects, especially in children. These include induced vomiting, electrolyte imbalances and dehydration. In the event of a shortage of aqueous activated charcoal suspensions, consult your poison centre before administering subsequent doses of sorbitol activated charcoal suspension
- Note on Shortage of Aqueous Activated Suspensions (French, English).
+ Synonyms and other terms
- Active carbon
- Activated carbon
- Active charcoal
- Charac™
- Charac-tol™
- Charcodote™
+ Indications
Preventing Absorption
- Consider administering a single dose of activated charcoal in these cases:
- Potentially toxic ingestion occurring less than one hour ago*
- If no contraindications are present (e.g., unprotected airway, GCS less than 15, intestinal obstruction, ingestion of a corrosive agent or aliphatic hydrocarbon).
*If the patient has ingested an agent that slows gastric emptying (e.g. anticholinergic, opioid), a salicylate, an extended-release or enteric-coated substance, a significant amount of toxic substance or if there is evidence of bezoars, the administration of activated charcoal could be considered more than one hour post-ingestion and could even be repeated. Consult your poison centre.
+ Dosage
+ Pediatric Dose
- Single dose of activated charcoal
- Aqueous or sorbitol activated charcoal 1 g/kg PO or NG tube for 1 dose (maximum 50 g per dose).
- Considering a 10:1 ratio of activated charcoal: toxic agent, it is possible to administer alternate doses upon consultation with your poison centre. The ideal theoretic dose would then be 10 g of activated charcoal for 1 g of toxic agent, which is not always feasible. If necessary, consult your poison centre.
Repeated doses of activated charcoal: consult your poison centre.
+ Adult Dose
- Single dose of activated charcoal
- Aqueous or sorbitol activated charcoal 1 g/kg PO or NG tube for 1 dose (maximum de 50 g per dose)
- Considering a 10:1 ratio of activated charcoal: toxic agent, it is possible to administer alternate doses upon consultation with your poison centre. The ideal theoretic dose would then be 10 g of activated charcoal for 1 g of toxic agent, which is not always feasible. If necessary, consult your poison centre.
Repeated doses of activated charcoal: consult your poison centre.
+ Renal Impairment
No data suggests that the dose should be modified for short-term use.
+ Hepatic Impairment
No data suggests that the dose should be modified for short-term use.
+ Hemodialysis Patient
No data suggests that the dose should be modified for short-term use.
+ Pregnancy
- Activated charcoal is not absorbed by the gastrointestinal tract.
- No data suggests that the dose should be modified for short-term use.
+ Obese or Overweight Patient
- No data suggests that the dose should be modified for short-term use.
+ Adverse effects
- Gastric distension, constipation, vomiting
- Black stool
- Aspiration that may be complicated by respiration failure
+ Monitoring
- Check regularly that the airway is protected.
- Check regularly on the presence of peristalsis.
+ End of treatment
- After one dose in the majority of cases.
- If onset of contraindication (e.g, impaired peristalsis, unprotected airway).
- If the toxic concentration is no longer worrisome.
- In other situations, if the clinical progression suggests that the poisoning is resolved.
+ Special Notes on Administration
Enteral Route
- Vigorously shake the suspension before administration.
- Administer slowly over a period of 15 minutes to minimize gastric distention and subsequent vomiting.
- The dose of activated charcoal can be divided in order to improve its tolerance.
- PO
- Cut the tip of the bottle and insert a straw.
- Palatability: Activated charcoal has a grainy texture that can give it an unpleasant taste and make it difficult to swallow. Adding a flavouring agent (regular cola, cherry syrup) just before administration to patients - particularly pediatric patients - can improve taste and acceptability.
- Volume ratio of activated charcoal: cola of 1:1
- Volume ratio of activated charcoal: cherry syrup of 6:1
- Putting the activated charcoal in an opaque, colourful bottle with a straw may also help improve acceptability in pediatric patients.
- Nasogastric Tube
- Cut the tip of the bottle and insert the end of the probe inside. Gently squeeze the bottle to empty to content into the gastric tube.
- Rinse the content of the tube with 5 to 10 ml of sterile water for injection, then clamp the tube for a period of 1 to 2 hours.
- PO
Reconstitution
- Activated charcoal that is not an oral suspension can be diluted in water or cola to obtain an activated charcoal: fluid ratio of 1:5.
Compatibility
- Activated charcoal may reduce the absorption of many drugs co-administered by enteral or even parenteral route.
Stability
- Store product at room temperature.
+ Available products
- Charac - 25 PED, 222 mg/ml, oral susp.,112.5 ml (25 g), Omega, DIN 02056429,
- Charac - 50, 222 mg/ml, oral susp, 225 ml (50 g), Omega, DIN 00637955,
- Charactol - 25, 200 mg/ml, oral susp, 125ml (25 g), Oméga, DIN 02060205
- Charactol - 50, 200mg/ml, oral susp, 250ml (50g), Oméga, DIN 00649236
- Activated charcoal USP, Pd. (454 g), Galenova.
+ Amount required to treat a person weighting 70kg during 24 hours
- At least 300 g.
+ References
Chan, Betty S. H., Kate Sellors, Angela L. Chiew, and Nicholas A. Buckley. 2015. “Use of Multi-Dose Activated Charcoal in Phenytoin Toxicity Secondary to Genetic Polymorphism.” Clinical Toxicology 53 (2):131–33.
Cheng, Adam, and Savithiri Ratnapalan. 2007. “Improving the Palatability of Activated Charcoal in Pediatric Patients.” Pediatric Emergency Care 23 (6):384–86.
Chyka, P. A., D. Seger, E. P. Krenzelok, J. A. Vale, American Academy of Clinical, Toxicology, European Association of Poisons, Centres, and Clinical, Toxicologists. 2005. “Position Paper: Single-Dose Activated Charcoal.” Clinical Toxicology 43 (2):61–87.
Dagnone, Damon, Doreen Matsui, and Michael J. Rieder. 2002. “Assessment of the Palatability of Vehicles for Activated Charcoal in Pediatric Volunteers.” Pediatric Emergency Care 18 (1):19–21.
Guenther Skokan, E., E. P. Junkins Jr, H. M. Corneli, and J. E. Schunk. 2001. “Taste Test: Children Rate Flavoring Agents Used with Activated Charcoal.” Archives of Pediatrics & Adolescent Medicine 155 (6):683–86.
Juurlink, David N. 2016. “Activated Charcoal for Acute Overdose: A Reappraisal.” British Journal of Clinical Pharmacology 81 (3):482–87.
“Position Statement and Practice Guidelines on the Use of Multi-Dose Activated Charcoal in the Treatment of Acute Poisoning. American Academy of Clinical Toxicology; European Association of Poisons Centres and Clinical Toxicologists.” 1999. Journal of Toxicology. Clinical Toxicology 37 (6):731-51
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ISSN : 2292-230X
Authors: Bailey B, Blais R, Dubé PA, Friesen M, Gaudreault P, Gosselin S, Laliberté M, Larocque A, St-Onge M
Reviewers: Elliott A, Mackenzie C, Murphy N, Letarte A, Pursell R, Thompson M, Yarema M