Overdose / drug poisoning
A streamlined, differential-led presentation for rapid clinical review.
Twenty-second review
- Drug poisoning may depress or stimulate the nervous system, impair ventilation, alter conduction, disrupt temperature control, or cause delayed organ injury.
- Bradypnea, apnea, shock, seizure, dysrhythmia, hyperthermia, severe agitation, or declining GCS requires immediate supportive care and escalation.
- Keep hypoglycemia or head injury in the differential; overlapping or concurrent illness remains possible.
- For overdose / drug poisoning, trends and combinations of findings are more informative than one isolated vital sign.
Compare the clinical patterns
The repeated material is grouped inside each possibility. Open only the condition you need.
CardiotoxicTime-sensitive high-risk possibility
HPI
Clarify substance(s), amount, route and time; intentional or accidental; co-ingestants.
Signs & symptoms
QRS or QT change, hypotension, seizure, or dysrhythmia.
Focused exam
Assess pupils, skin, bowel sounds, temperature, mental status, respiratory pattern, rhythm, and signs of trauma or concealed co-ingestion; Repeat observations because drug effects may evolve.
Brief pathophysiology
Cardiotoxic may cause overdose / drug poisoning through a time-sensitive process capable of rapid physiological deterioration.
What the trend may show
Toxic effects vary by agent and co-exposure. Ventilation, rate/rhythm, pressure, and temperature are the most useful four observations for recognizing an evolving toxidrome.
Respiratory rate (breaths/min)
May rise or fallVentilation can be depressed or stimulated depending on the agent.
Heart rate (bpm)
Rate / rhythm may changeObtain ECG monitoring when cardiotoxicity is plausible.
Blood pressure (mmHg)
May rise or fallPressure direction depends on agent, dose, and stage.
Temperature (°C)
May rise or fallTemperature disturbance can identify severe stimulant, anticholinergic, sedative, or environmental toxicity.
Front-load in the triage report
- Cardiotoxic: QRS or QT change, hypotension, seizure, or dysrhythmia.
- Substance(s), amount, route and time.
- Intentional or accidental?
Mixed overdoseTime-sensitive high-risk possibility
HPI
Clarify intentional or accidental; co-ingestants; initial loc, rr and spo2.
Signs & symptoms
QRS or QT change, hypotension, seizure, or dysrhythmia.
Focused exam
Repeat observations because drug effects may evolve; Assess pupils, ventilation, skin, temperature, rhythm, trauma, injection sites, pill containers, and co-ingestants.
Brief pathophysiology
Mixed overdose may cause overdose / drug poisoning through a time-sensitive process capable of rapid physiological deterioration.
What the trend may show
Toxic effects vary by agent and co-exposure. Ventilation, rate/rhythm, pressure, and temperature are the most useful four observations for recognizing an evolving toxidrome.
Respiratory rate (breaths/min)
May rise or fallVentilation can be depressed or stimulated depending on the agent.
Heart rate (bpm)
Rate / rhythm may changeObtain ECG monitoring when cardiotoxicity is plausible.
Blood pressure (mmHg)
May rise or fallPressure direction depends on agent, dose, and stage.
Temperature (°C)
May rise or fallTemperature disturbance can identify severe stimulant, anticholinergic, sedative, or environmental toxicity.
Front-load in the triage report
- Mixed overdose: QRS or QT change, hypotension, seizure, or dysrhythmia.
- Intentional or accidental?
- Co-ingestants.
SedativeCommon presentation pattern
HPI
Clarify substance(s), amount, route and time; intentional or accidental; co-ingestants.
Signs & symptoms
Reduced consciousness, bradypnea, shallow breathing, or miosis may predominate.
Focused exam
Assess pupils, skin, bowel sounds, temperature, mental status, respiratory pattern, rhythm, and signs of trauma or concealed co-ingestion; Repeat observations because drug effects may evolve.
Brief pathophysiology
Sedative may explain the presenting symptoms through a common clinical mechanism, while serial assessment checks for complications or an alternate cause.
What the trend may show
Ventilation is the priority in opioid or sedative toxicity. SpO₂ can look acceptable with supplemental oxygen while dangerous hypoventilation persists.
Respiratory rate (breaths/min)
May fallBradypnea, shallow breathing, or apnea indicates ventilatory failure.
Oxygen saturation (SpO₂)
May fallDesaturation can occur, but SpO₂ does not measure ventilation.
Heart rate (bpm)
VariableRate depends on agent, co-ingestants, hypoxia, and baseline.
Blood pressure (mmHg)
May fallHypotension can occur in severe toxicity or mixed overdose.
Front-load in the triage report
- Reduced consciousness, bradypnea, shallow breathing, or miosis may predominate.
- Substance(s), amount, route and time.
- Intentional or accidental?
Opioid toxicityCommon presentation pattern
HPI
Clarify intentional or accidental; co-ingestants; initial loc, rr and spo2.
Signs & symptoms
Reduced consciousness, bradypnea, shallow breathing, or miosis may predominate.
Focused exam
Repeat observations because drug effects may evolve; Assess pupils, ventilation, skin, temperature, rhythm, trauma, injection sites, pill containers, and co-ingestants.
Brief pathophysiology
Opioid toxicity may explain the presenting symptoms through a common clinical mechanism, while serial assessment checks for complications or an alternate cause.
What the trend may show
Ventilation is the priority in opioid or sedative toxicity. SpO₂ can look acceptable with supplemental oxygen while dangerous hypoventilation persists.
Respiratory rate (breaths/min)
May fallBradypnea, shallow breathing, or apnea indicates ventilatory failure.
Oxygen saturation (SpO₂)
May fallDesaturation can occur, but SpO₂ does not measure ventilation.
Heart rate (bpm)
VariableRate depends on agent, co-ingestants, hypoxia, and baseline.
Blood pressure (mmHg)
May fallHypotension can occur in severe toxicity or mixed overdose.
Front-load in the triage report
- Reduced consciousness, bradypnea, shallow breathing, or miosis may predominate.
- Intentional or accidental?
- Co-ingestants.
HypoglycemiaImportant alternative presentation
HPI
Clarify substance(s), amount, route and time; intentional or accidental; co-ingestants.
Signs & symptoms
Common reversible or traumatic mimics of intoxication.
Focused exam
Assess pupils, skin, bowel sounds, temperature, mental status, respiratory pattern, rhythm, and signs of trauma or concealed co-ingestion; Repeat observations because drug effects may evolve.
Brief pathophysiology
Hypoglycemia can resemble overdose / drug poisoning through overlapping symptoms or referred physiology despite a different primary mechanism.
What the trend may show
Confirm low capillary glucose and reassess after treatment. Adrenergic signs may be absent in recurrent hypoglycemia or blunted by medications.
Blood glucose (mmol/L)
< 4.0 mmol/LBCEHS defines hypoglycemia as blood glucose below 4.0 mmol/L.
Heart rate (bpm)
May riseAdrenergic activation commonly produces tachycardia, but this is not universal.
Blood pressure (mmHg)
Often preservedBlood pressure is not a reliable discriminator; hypotension suggests another or additional process.
Temperature (°C)
May fallHypothermia can accompany prolonged or severe hypoglycemia.
Front-load in the triage report
- Common reversible or traumatic mimics of intoxication.
- Substance(s), amount, route and time.
- Intentional or accidental?
Head injuryImportant alternative presentation
HPI
Clarify intentional or accidental; co-ingestants; initial loc, rr and spo2.
Signs & symptoms
Common reversible or traumatic mimics of intoxication.
Focused exam
Repeat observations because drug effects may evolve; Assess pupils, ventilation, skin, temperature, rhythm, trauma, injection sites, pill containers, and co-ingestants.
Brief pathophysiology
Head injury can resemble overdose / drug poisoning through overlapping symptoms or referred physiology despite a different primary mechanism.
What the trend may show
Toxic effects vary by agent and co-exposure. Ventilation, rate/rhythm, pressure, and temperature are the most useful four observations for recognizing an evolving toxidrome.
Respiratory rate (breaths/min)
May rise or fallVentilation can be depressed or stimulated depending on the agent.
Heart rate (bpm)
Rate / rhythm may changeObtain ECG monitoring when cardiotoxicity is plausible.
Blood pressure (mmHg)
May rise or fallPressure direction depends on agent, dose, and stage.
Temperature (°C)
May rise or fallTemperature disturbance can identify severe stimulant, anticholinergic, sedative, or environmental toxicity.
Front-load in the triage report
- Common reversible or traumatic mimics of intoxication.
- Intentional or accidental?
- Co-ingestants.
Findings that should escalate concern
- Bradypnea, apnea, shock, seizure, dysrhythmia, hyperthermia, severe agitation, or declining GCS requires immediate supportive care and escalation.
- Cardiotoxic or mixed overdose: QRS or QT change, hypotension, seizure, or dysrhythmia.
Medication recognition
Continue the clinical pathway
Clinical and academic sources
Curated clinical guidance and peer-reviewed evidence supporting this presentation. Current BCEHS guidance, medical direction, and local policy remain authoritative for practice.
BCEHS Handbook — specific CPGs
Supporting clinical and academic evidence
- CEDIS Presenting Complaint List updateCanadian Association of Emergency Physicians
Presenting-complaint terminology and categorization context. It does not establish a prehospital “top 100” ranking.
- Guidelines for establishing a poison centreWorld Health Organization
Clinical toxicology context for time-critical poisoning, supportive care, consultation, and poison-centre expertise.
- Adult and Pediatric Special Circumstances of Resuscitation: 2025 AHA GuidelinesCirculation · 2025
Evidence-based resuscitation considerations for poisoning and other reversible special circumstances.