Paracetamol intoxication

From WikiLectures

Paracetamol is one of the most widely used analgesics - antipyretics ( Paralen® ). The acetanilide derivative contained in paracetamol is biotransformed in the liver by cytochrome P450 into highly hepatotoxic N-acetyl-p-benzoquinonimine , which is immediately inactivated by glutathione in therapeutic doses . When glutathione is depleted, hepatocytes are damaged and centrizonal necrosis occurs . A similar biotransformation takes place in the kidneys → also necrosis and kidney damage

Toxicity[edit | edit source]

  • Already a dose higher than 140 mg/kg' (70 kg human − 20 tablets of Paralen 500® = hepatotoxic dose),
  • children are less sensitive (they do not have functional cytochrome P450),
  • more sensitive are alcoholics, patients on antiepileptics.

Clinical picture[edit | edit source]

Treatment[edit | edit source]

  • Administer activated charcoal, suppress vomiting (metoclopramide),
  • 'antidote - N-acetylcysteine initial dose 140-150 mg/kg, continued dose 70 mg/kg, the dosage varies according to the time of intoxication and the method of administration.[1]
  • indication is suspicion of ingestion or paracetamol value in plasma 200 mg/l or more in 2 h after ingestion,
  • hemoperfusion is also effective.


Links[edit | edit source]

Related Articles[edit | edit source]

Source[edit | edit source]

BENEŠ, Jiří. Study materials  [online]. [cit. 24/02/2010].(http://jirben.wz.cz/)

References[edit | edit source]

Used literature[edit | edit source]

  • PELCLOVÁ, Daniela. Nemoci z povolání a intoxikace. 2. vydání. Praha : Karolinum, 2006. 207 s. ISBN 80-246-1183-X.
  1. HODIS, George. New facts about paracetamol, risks of overdose, intoxication and their management. Practical Pharmacy [online]2015, y. 11, vol. 3, p. 90-92, Available from <https://www.praktickelekaranstvi.cz/pdfs/lek/2015/03/03.pdf>. ISSN 1803-5329.