Toxicology and Drug Overdose

Paracetamol (Acetaminophen) Overdose

•    Toxic dose: >10 g (single) or >150 mg/kg, or staggered ingestion over 24 hours

•    Stages:

o    Early (0–24h): asymptomatic, nausea, vomiting

o    24–72h: ALT/AST, RUQ pain

o    72–96h: hepatic failure, encephalopathy, coagulopathy

•    Investigations: serum paracetamol level + time since ingestion (use Rumack–Matthew nomogram)

•    Antidote: N-acetylcysteine (NAC) – effective even if >8 hrs post-ingestion

•    Staggered dose or unknown time: treat immediately with NAC


Tricyclic Antidepressant (TCAs) Overdose

•    Key signs: anticholinergic (dry mouth, urinary retention), 

                                                cardiotoxicity (prolonged QRS >100 ms, arrhythmias), seizures

•    ECG findings: sinus tachycardia, widened QRS, right axis deviation

•    Antidote: IV sodium bicarbonate (even if normopH) – narrows QRS, reduces arrhythmias

•    Avoid class Ia/III antiarrhythmics


Theophylline Overdose

•    Narrow therapeutic window

•    Toxic signs: nausea, vomiting, tremor, seizures, tachyarrhythmias, hypokalaemia

•    Management: activated charcoal if within 1 hr, consider haemodialysis in severe cases


Iron Overdose

•    Toxic dose: >60 mg/kg elemental iron

•    Four phases:

1.    GI phase (0–6h): vomiting, diarrhoea, abdominal pain

2.    Latent phase (6–24h): apparent recovery

3.    Systemic toxicity (12–96h): shock, metabolic acidosis, hepatic necrosis

4.    Late phase (2–6 weeks): GI strictures

•    Investigations: serum iron (4–6h post-ingestion), metabolic panel

•    Antidote: IV deferoxamine (chelates iron) – urine turns pink ("vin rose")


Salicylate (Aspirin) Overdose

•    Toxic dose: >150 mg/kg

•    Acid-base disturbance:

o    Early: respiratory alkalosis (direct stimulation of respiratory centre)

o    Later: metabolic acidosis with increased anion gap

•    Features: tinnitus, nausea, vomiting, hyperventilation, pyrexia, confusion

•    Management:

o    Activated charcoal if <1 hr

o    IV bicarbonate (alkalinise urine)

o    Haemodialysis if pH <7.3, salicylate >700 mg/L, renal failure, or pulmonary oedema


Ethylene Glycol / Methanol Poisoning 

•    Both cause high anion gap metabolic acidosis

•    Ethylene glycol: renal failure due to calcium oxalate crystals in urine

•    Methanol: visual loss, retinal damage

•    Antidote: fomepizole (1st line) or ethanol (competitive inhibition of alcohol dehydrogenase)

•    Consider haemodialysis in severe cases


Carbon Monoxide (CO) Poisoning

•    Binds haemoglobin carboxyhaemoglobin tissue hypoxia

•    Signs: headache, dizziness, cherry-red lips (rare), confusion

•    Pulse oximetry is falsely normal

•    Diagnosis: elevated carboxyHb on co-oximetry

•    Treatment: high-flow O₂ (100%), consider hyperbaric O₂ if:

o    Neurological symptoms

o    CarboxyHb >25% (or >15% in pregnancy)

o    Loss of consciousness


Elimination Methods in Overdose

•    Activated charcoal:

o    Effective if given within 1 hour of ingestion

o    Not useful for metals, alcohols, or corrosives

•    Haemodialysis: for elimination of:

o    Lithium

o    Salicylates

o    Ethylene glycol

o    Methanol

o    Theophylline (in severe toxicity)

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Author & Educational Disclaimer


Author:

Dr Phillip Cockrell BM FRCP DipClinEd


Dr Phillip Cockrell is a UK Consultant Physician in Internal Medicine, currently working at Queen Alexandra Hospital, Portsmouth University Hospitals NHS Trust. He has previously worked as a registrar across Intensive Care Medicine, Gastroenterology, Cardiology, Stroke Medicine, Acute Medicine, and Respiratory Medicine.


He has held senior leadership roles including Associate Clinical Director of the Acute Medical Unit, Clinical Director of Internal Medicine, and Chief of Medicine. Dr Cockrell has over 15 years’ experience in postgraduate medical education, having lectured extensively across the MRCP syllabus and contributed to MRCP revision teaching and course development.


Dr Cockrell holds a Bachelor of Medicine (BM), Fellowship of the Royal College of Physicians (FRCP), and a Diploma in Clinical Education (DipClinEd). His teaching approach is based on structured consolidation of complex medical topics to support efficient and effective revision for postgraduate examinations.


Purpose of this content:

The material on this page is intended solely for educational purposes to support revision for the MRCP (UK) Part 1 examination. It reflects examination-relevant principles of internal medicine and is designed to aid learning and pattern recognition.


Medical disclaimer:

This content is designed for postgraduate medical examination revision and does not constitute medical advice, diagnosis, or treatment guidance and must not be used as a substitute for professional clinical judgement, local guidelines, or specialist consultation. Clinical decisions should always be made in the context of individual patient circumstances and current national guidance.