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Educational draft · awaiting clinical reviewUse Rapid for revision, not patient-care decisions. Check current national and local guidance and the BNF or BNFC before acting.
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Adverse drug reactions

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Adult medicine-triggered anaphylaxis

Sudden airway, breathing or circulation compromise after a medicine requires immediate treatment, even without a rash.

Action: In an adult, stop the trigger, call the emergency team, use ABCDE and give adrenaline 500 micrograms intramuscularly into the anterolateral thigh; repeat after 5 minutes if airway, breathing or circulation problems persist. Do not allow the patient to stand or walk.

Synopsis

Recognise suspected medicine-related harm, distinguish allergic from non-allergic reactions, manage immediate risk and document evidence that prevents re-exposure.

  • A reaction can follow a new medicine, dose increase, interaction or altered clearance of long-established treatment.
  • Severity describes intensity; seriousness describes outcomes such as hospitalisation, disability or threat to life.
  • An adverse drug reaction is not automatically an allergy; record the actual phenotype and its timing.

Key red flags

Painful skin with blistering, mucosal erosions or systemic illness after a new medicine requires immediate withdrawal of suspected culprits and urgent hospital assessment.

Reasoning priorities

01
Exposure timeline

Relate medicine use to the onset and evolution of harm.

Include first and last doses, changes in strength, intermittent products, injections, patches and medicines stopped recently. Plot the symptom onset against each exposure. A plausible sequence supports causality, but temporal association alone is insufficient: the illness prompting treatment may produce the same findings.

Worked reasoning

Worked caseEvaluate a possible pulmonary drug reaction

A 68-year-old taking long-term nitrofurantoin for recurrent urinary infections develops progressive dry cough and breathlessness. Oxygen saturation is 91% on air; there is no recent urinary illness and the repeat medicine has not been reviewed for a year.

  1. Prioritise the respiratory impairment and arrange urgent assessment. Establish observations and examine for infection, heart failure and other causes; do not assume a familiar long-term preventive medicine is irrelevant merely because it predates the symptoms.
  2. Reconstruct the duration of nitrofurantoin exposure and any previous respiratory or hepatic symptoms. The temporal pattern is compatible with a delayed medicine reaction, but alternative pathology remains possible and requires appropriate investigation.
  3. Stop nitrofurantoin when pulmonary toxicity is suspected and document the reason. Assess the ongoing need for urinary prophylaxis separately after the acute problem is addressed; replacing one preventive prescription should not distract from current hypoxaemia.
  4. Arrange focused respiratory evaluation and review any relevant liver abnormalities. Explain the suspected relationship, the uncertainty and what symptoms should prompt immediate help. Record the medicine as a suspected serious reaction with its actual manifestations.
  5. Verify the outcome through follow-up of respiratory findings and investigation results, update the repeat system and communicate with the regular prescriber. Submit a Yellow Card on suspicion; improvement after withdrawal adds evidence without proving that every symptom was drug-induced.
Causality assessmentBuild and revise a defensible explanation

A stable patient develops a new symptom that could plausibly reflect a medicine effect.

Key medicines

Adrenaline for adult anaphylaxisGive 500 micrograms intramuscularly: 0.5 mL of 1 mg/mL adrenaline into the anterolateral thigh; repeat after 5 minutes for persisting airway, breathing or circulation problems.Confirm concentration and intramuscular route; intravenous adrenaline requires experienced specialist management. Antihistamines do not treat airway compromise or shock.
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Sources and review status4 sources · checked 7 Sept 2026 · clinical review pending
Sources

Sources and review status

National guidance is shown before implementation-dependent detail. Typical adult dose examples remain subject to patient factors, contraindications and the live BNF or specialist protocol. Source check completed 7 Sept 2026; clinical approval remains outstanding.

Authoring stateRapid draftClinical stateAwaiting reviewJurisdictionUnited Kingdom