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Pharm Practice Ch 3
Pharmacy Tech JATC
| Question | Answer |
|---|---|
| When a generic manufacturer files an abbreviated NDA with the FDA, it must prove | Bioequivalence |
| Deceptive advertising by manufacturers of dietary supplements is regulated by the | FTC |
| The FDA monitors the incidence and risk of adverse drug reactions to vaccines on the market with | VAERS |
| Select the TRUE statement regarding an active ingredient | It exerts the desired therapeutic effect |
| What is the function of a vaccine? | to produce Immunity to disease |
| What defines a synthesized drug? | An imitation of naturally occurring substances |
| What is the field of study that examines the relationship between an individual's genes and his or her body's response to a drug? | Pharmacogenomics |
| What is true about an inert ingredient | It has no pharmacological effect |
| What is the purpose of a pharmacodynamic Agent | to alter body functioning |
| The FDA's medical product safety reporting program for the health professions, and patients and consumers | Medwatch |
| What Discovery let to the emphasis on sterility and cleanliness in the practice of medicine and manufacture of pharmaceuticals? | Germ Theory |
| Which of the following would be classified as drugs by the FDA? | homeopathic medications |
| Probiotics are Microorganisms that | promote positive digestive health |
| Which of these is not a Hormone therapy | nitroglycerine |
| Why is the generic drug application submitted to the FDA called abbreviated? | It only need to prove bioequivalence |
| Why does the FDA require OTC product labeling to list active and inactive ingredients? | prevent allergic reactions |
| To fill a prescription and bill insurance for Xanax, a pharmacy technician will need the prescriber's | NPI and DEA number |
| Based on significant incidents of adverse drug reactions, who has the power to recall, or pull drugs off the market? | FDA |
| If a drug have the possibility of an extreme ADR, this information must be included in the | Product package insert's black box and the patient's information printout |
| The discovery of the existence of microbes and their role in causing illness is known as the | germ theory |
| The process by which patients are protected from harmful germs during surgery or medical procedures is called | aseptic technique |
| The hormone insulin was discovered and isolated for the treatment of diabetes due to the difficulties in the functioning of the | pancreas |
| Antineoplastic drugs are classified as | destructive agent |
| When receiving a prescription to fill and talking to a patient, you should get a complete _______________ to prevent the patient form having a bad reaction to the drug | allergy history |
| If a liquid antibiotic had flavoring added to improve the taste what type ingredient would that be? | inert |
| What document signed by a research-study participant states the purpose and the risk o the research in easy to understand terms? | informed consent form |
| If you are helping a patient find a good quality vitamin, what marking on the label identifies the supplement is good quality? | USP verified |
| Which of the following statements about dietary supplements approval process is true? | Supplements are considered to be food, not drugs |
| The FDA monitors the incidence and risk of adverse drug reactions to new drugs on the market with | AERS |
| A medications that targets specific needs in the body is? | Therapeutic |
| What classification of drugs are natural substances combined with laboratory substances? | Semisynthetic drugs |
| Where do would you find the NDC number on a stock bottle | At the top of the bottle or in the bar code |
Created by:
Leo12345
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