Scope
The Bottom Line
- At every transition, reconcile the most accurate medicine list including non-prescription, complementary, intermittent and recently stopped products.
- Document indication, intended benefit, dose source, duration and monitoring for each medicine and remove duplicate or indication-free therapy collaboratively.
- Use generic and brand names when formulations differ and verify modified-release, patch, inhaler and insulin device details.
- Use shared decision-making that explains alternatives, expected benefit, common and serious harm and what matters to the person, including treatment burden.
Practical clinical workflow
Topic-specific assessment action
Topic-specific diagnostic action
Topic-specific management action
Topic-specific follow-through
Safety boundaries and escalation
- Report suspected adverse reactions and urgently manage overdose, severe interaction, anaphylaxis, bleeding, serotonin toxicity or another serious medicine harm.
- Ask how medicines are actually taken and inspect packs or dispensing history when adherence uncertainty affects safety.
Implementation
Clinical use boundary
This independently written summary is not an official guideline. Check the linked source version, current TGA-approved product information where medicines are involved, and the applicable state, territory and local pathway at the point of care.
Source documents
Use the linked source documents for complete recommendations, evidence grading, exclusions and implementation detail.
- Australian Commission on Safety and Quality in Health CareMedication Safety StandardNSQHS Standards second edition, current page checked 2026-08-20 路 accessed 2026-08-20view source
From guidance to deliberate practice and evidence
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