Free Online Flashcard Deck

5 Medication Safety Reporting and Response Free Online FlashCards

Study 5 Medication Safety Reporting and Response with 12 free online flashcards. Review key terms, definitions, and concepts with this interactive flashcard deck.

12 cards
01
Front

What is a medication error?

Back

A medication error is a preventable event that may cause harm or be intercepted before reaching the patient.

02
Front

What is a near miss?

Back

A near miss is an error or hazardous condition that did not reach the patient or cause harm.

03
Front

What is the first priority after a medication error?

Back

Protect the patient first: stop or contain the error, assess the patient, and arrange needed care.

04
Front

What assessment is important after a high-alert medication error?

Back

Promptly assess for effects specific to the medication and the dose or administration involved.

05
Front

Should a near miss be reported if no harm occurred?

Back

Report near misses and hazardous conditions through the organization’s event-reporting system, even when no harm occurred.

06
Front

What should disclosure to a patient include?

Back

Explain what is known, acknowledge the event, describe the patient’s condition and care plan, and explain how follow-up will occur.

07
Front

How should uncertainty be handled when disclosing an event?

Back

Be honest about what is uncertain; do not speculate or assign blame before the facts are established.

08
Front

What key details belong in the clinical record after an error?

Back

Record what happened and when, relevant medication details, the patient’s assessment and response, notifications, interventions, monitoring, and communication.

09
Front

Does clinical documentation replace an internal safety report?

Back

The clinical record supports continuity of care; it does not replace the separate internal safety report required by policy.

10
Front

What makes an internal event report useful?

Back

Describe the event sequence and relevant contributing conditions, such as a similar drug name, unclear order, interruption, or technology issue.

11
Front

What does FDA MedWatch accept?

Back

In the United States, FDA MedWatch accepts voluntary reports of medication and product-use errors, including some without patient harm.

12
Front

What is a limitation of event-reporting systems?

Back

Reporting systems do not capture every event and cannot, by themselves, establish how often errors occur.