Chapter 7 Responsbinies and Principles of Drug Adminstration 33 8. What actions

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Chapter 7 Responsbinies and Principles of Drug Adminstration 33 8. What actions has the FDA taken in response to the voluntary reports on th e MEDWATCH forms from the health care community? A. It has filed a suit against the facility where the patient was receiving treatment B. It has set up opposition action toward the individual health care pro ofe essionals who f lled out the reports C. It has issued warnings, made labeling changes, required I manufacturers to do postmarketing studies, and ordered the withdrawal of certain products from t 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 tion 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. Complet D. Ask e a written incident report as a legal requirement the patient not to file a civil suit against the health care provider Matching A Match the "right" medication administration in Column A with the description in Column B. COLUMN A COLUMN B 1, Right medication 2. Right amount 3. Right time 4. Right route 5. Right patient 6. Right documentation F. Recording the time the pain medication was given, along with the A. Checking the patient's identification band and then asking the patient B. Number of times per day the medicine is to be administered C. Drug dosage ordered compared very carefully with dose listed on label D. Important because of its effect on degree of absorption, speed of E. Carefully comparing the name or the drug prescribed with the label to state his or her name (e.g, bid, or twice a day) of package, bottle, or unit-dose packet drug action, and side effects on the package, bottle, or unit-dose pack dosage, route, and location if an injection Matching B Match the action of the administering health care professional in Column A with the corresponding responsibility in Column B. Note that the terms in Column B can be used more than once. COLUMN A COLUMN B 1. Observing the patient's vital signs before administering a medication 2. Writing the results of a medication on the patient's record 3. Taking steps to counteract an adverse reaction 4. Taking a complete history, including all medical conditions 5. Asking the patient if the medication has relieved his or her pain A. Assessment B. Intervention C. Evaluation ocumentation 2019 Cengage Learning, Enc. May not be scanned, c pied or duplicated or posted to a pullely accessible website, in whole or in part.

Explanation / Answer

Ans 1: ( C ) The Agency uses this information to update drug labeling, and, on rare occasions, to reevaluate the approval or marketing decision.

Ans 2: (B) Out patient

Ans 3: (A) Report the error immidiately to the one incharge so that corrective mesures should be taken.

* Match The following:

1) Right medication - (E ) carefully comparing the name of the drug prescribed with the label of package.

2) Right amount     - (C) Drug dosage ordered compared carefullywith dose listed on the label of package.

3) Right time   - (B) number of times per day medicine to be administered.

4) Right route - ( D) Important becauseits effect on degree of absorption, speed of drug action and side effects.

5) Right patient - (A) Checking the patient's identification band and the asking the patient to state his name.

Ans 6: Right documentation - (F) Recording the time the pain medication was given, along with the dose, route and location of injection.

* Match the following:

1. (C) Evaluation

2.(D) Documentation

3.(B) Intervention

4.(A) Assesment

5. (C) Evaluation

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