Which federal action sets the standard for quality and requires proper medication, labeling for preparations containing morphine A. Durham-Humphrey amendments B. Food drug and cosmetic act C. Pure food and drug act. D. Controlled substances act

Drugs that are listed with a C – I Are considered to A. Have a high-abuse potential with no medical use. B. Be appropriate for postoperative pain control. C. Have a low-abuse potential (e.g., steroids) D. Be available over-the-counter.

Which government agency was established to enforce the controlled substances act A. Occupational Safety and Health Administration (OSHA) B. The US food and drug administration (FDA) C. The drug enforcement agency (DEA) D. The joint commission (TJC)

All of the following items are on the <do not use> list of abbreviations except A. U for unit B. The trailing zero. C. QD for once daily. D. Zero before the decimal point.

Nonprescription medication’s are also known as A. Addictive medications B. Over-the-counter Medications C. Controlled substances. D. Schedule C – II Medication

All of the following factors are disadvantages to Pharmacogenetics except A. It’s used to target specific diseases. B. The complexity of its development. C. The cost of genetic research. D. Educating healthcare providers to It’s use

Who assigned a brand name to a new medication? A. The FDA. B. Manufacturer. C. Pharmacist. D. Drug reference publishers.

A medication’s generic name is A. Never capitalized on the label. B. Followed by the registered trademark symbol. C. It’s formula. D. It’s proprietary name.

On some medication labels, the generic name is A. Placed inside parentheses B. Capitalized C. Not required. D. Most prominent.

The full quantity contained in a medication bottle is it’s A. Control number. B. Administration route. C. Total volume. D. Supply dosage.

The organization that intentionally regulates medication is A. The joint commission. (TJC) B. The FDA. C. OSHA. D. The world health organization. (WHO)

The identifying number on every prescription that is required by federal law is called the A. National drug code. B. Label alert. C. Barcode symbol. D. Lot number.

Coordination of research about drug abuse in another country is regulated by the A. CDC. B. WHO. C. FDA. D. DEA.

Which drug law established classifications known as schedules of medication’s that had potential for abuse A. Controlled substances act B. Pure food and drug act. C. Federal food, drug and cosmetic act D. Drug enforcement administration.

Drugs that have an accepted use in the surgical setting are on the _____ schedule A. C-I B. C-II C. C-III D. C-IV

How does a surgical tech technologist know if he or she can handle an administer medication’s in his or her state? A. By asking the surgeon. B. By asking the facilities risk management. C. By researching the states policy online. D. By contacting the AORN.

Which factor is an advantage of pharmacogenomics? A. Complexity of genetic research. B. Cost of genetic research. C. Education and the use of this technology. D. Facilitate the medication approval process.

What should be done to an otic Suspension medication to dilute the particles before it is administered to the patient A. It must be liquefied. B. It must be concentrated. C. It must be shaken. D. It must be sterilized.

How should an outdated multi-use vile of a local anesthetic be handled? A. By finishing the vile. B. By returning it to the pharmacy. C. By giving it to anesthesia team. D. By discarding the vile.

All are found on medication labels except A. Supply dosage. B. Control number. C. Label alert. D. PDR number

Which medication reference is published annually and updated quarterly by the American Society of health system pharmacist A. AHFS. B. USP – NF. C. PDR. D. WHO.

Which source is the most reliable way to check that medication information is accurate online A. Searching the Internet. B. Using a government website. C. Asking a clinical coordinator. D. Calling the FDA.

Which categories of medication’s under the FDA’s pregnancy categories are considered to be within safe limits for use during pregnancy A. Categories B and C. B. Categories A and B. C. Categories C and D. D. Categories A and X.

And the phases of human medication testing what is the last phase? A. Phase 0. B. Clinical investigation. C. Clinical trials. D. Postmarketing study.

Drugs that are used for diseases and disorders that affect fewer than 200,000 people in the United States are considered A. Phase 0 drugs. B. Category A drugs. C. C – III drugs. D. Orphan drugs.