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The content outline, domain by domain

Types of errors

Compiled by the Sitonce editorial team from PTCB's own published outline, the federal regulations named below and US Bureau of Labor Statistics dataUpdated 2 min readFacts verified 5 September 2026
The short answer

Errors are categorized by what went wrong: wrong drug, wrong dose, wrong patient, wrong form or route, wrong quantity, wrong label, or an omission.

A named knowledge area, and the categories matter because each one has a different control.

The categories

  • Wrong drug, often a look-alike sound-alike selection
  • Wrong dose or strength
  • Wrong patient
  • Wrong dosage form or route
  • Wrong quantity
  • Wrong or incomplete labeling, including directions
  • Omission, where something that should have been dispensed was not
  • Wrong time, where timing matters clinically

Why naming it matters

The category points at the control

A wrong-drug error caused by similar names is addressed by tall man lettering and separation. A wrong-dose error is addressed by standardized concentrations and double checks. A wrong-patient error is addressed by identity verification. Questions asking what should be done are frequently answerable only once you have named what went wrong.

Where in the process

Errors are also classified by stage: prescribing, transcribing or order entry, dispensing, and administration.

A technician's exposure is concentrated in order entry and dispensing, which is where most exam scenarios sit.

Near misses

An error caught before it reaches the patient. It should still be reported, because it reveals the same system weakness as one that got through.

A question about whether to report a near miss resolves to yes, and the reasoning is that next time the same weakness may not be caught.

Errors that reach the patient without harm

Also reportable. The absence of harm was often luck rather than design, and the reporting system exists to find the design problem.

What a technician does

Report it, accurately and promptly, and do not attempt to resolve the clinical consequence. That is the pharmacist's.

Common questions

What are the types of prescription errors?

Wrong drug, dose, patient, form or route, quantity, label, timing, and omissions.

Why does the category matter?

Each category points at a different control, and questions often require naming the error first.

What is a near miss?

An error caught before reaching the patient. It should still be reported.

Should a no-harm error be reported?

Yes. The absence of harm is often luck rather than design.

What does a technician do?

Report accurately and promptly, and refer the clinical consequence to the pharmacist.