Question

33 Chapter 7 . Responsibilities and Principles of Drug Administration 8. What actions has the FDA taken in response to the voluntary reports on the MEDWATCH for the MEDWATCH forms from the health care community? A. It has filed a suit against the facility where the patient was receiving treatment. 13. It has set up opposition action toward the individual health care professionals who filled out the reports C. It has issued warnings, made labeling changes, required manufacturers to do postmarketing studies, and ordered the withdrawal of certain products from the market. D. It has worked together with the facility involved to assist the patients who were affected by the prod. ucts in a positive or negative way. 9. While medication errors can and do occur in all health care settings, more errors are reported in which settings A. Acute care B. Outpatient C. Long-term care D. Ambulatory care 10. When a mistake is made in the administration of medication(s), the health care professional should first: A. Report the error immediately to the one in charge so that corrective action can be taken B. Apologize to the nursing staff, the physician, and the other health care professionals C. Complete a written incident report as a legal requirement D. Ask the patient not to file a civil suit against the health care provider Matching A intion in Column R

Answer 1

Answers:

8. C. It has issued warnings,made labeling changes, required manufacturers to do postmarketing studies and ordered the withdrawal of certain products from the market.

Reason: FDA is responsible for monitoring the product safety and take necessary actions to protect the patient and health care professionals.

9. A. Acute care

Reason: Immediate and emergency care settings has high rates of medication errors when compared to others.

10.A. Report the error immediately to the one in charge so that corrective action can be taken.

Reason: First priority is to provide corrective action, otherwise it will leads more complications.