Ch. 4 Review Questions
Order by
24 terms
Terms | Definitions |
|---|---|
 THe law that requires manufacturers to prove that a drug is both safe and effective for condition for which it is marketed is the ____? | Food, Drug and Cosmetic Act |
| There are ___ categories of drug recalls, and the recall class number that is the most serious is ___. | 3 and 1 |
| The prime purpose of phase I clinical trials of an inivestigational drug is to evaluate the _____? | safety |
| THe level of performance expected of a healthcare professional in carrying out his or her profession duties is called what? | standard of care |
| Guiddlines for activities that can be legally performed by a healthcare professional are called what? | scope of practice |
| The expiration date on a manufacturer's bottle of a prescription medication is June 2007. The actual date this product will expire is _____? | the last day of june |
| The form that must be used to order schedule II narcotics is called what? | DEA form 222 |
| Two drugs that are exempt from the Posion Prevention Packaging Act are what and what? | Nitrogloserim and Subliguulin Potasium |
| The middle 4 digits of an NDC number are assigned by the manufactorer identify ________ | specific drug doseage and strength |
| The statement "Caution: federal law prohibits the transfer of this drug to any person other than the patient for whom it was prescribes: is required to be on the container of any _______ drug that is dispensed. | controlled |
| If a DEA Form 222 has an error on one of the lines, the supplier can cross out that line and fill the remainder of the order. | False |
| A physician's assistant will have DEA number that begins with the letter M followed by the first initial of his last name. | True |
| A schedule III, IV, or V controlled-drug presciption may have the physician's name typewritten on the signature line. | false |
| All schedule II drugs must be kept in a locked cabinet in the pharmacy. | False |
| Schedules III, IV, and V drugs may be kept on an open shelf together in one section of the pharmacy as long as they are not in plain view of customers. | false |
| Brand Name | Trade name given to a drug by the manufacturer for marketing purposes |
| Exempt narcotics | Controlled drugs that can be sold in limited quantities without a prescription in some states. |
| Adulterated drugs | Drugs that contain any unclean substance, are prepared in unsanitary conditions or containers, or differ in strength, quality, or purity from the official drug standards. |
| Misbranded | Drugs with a labeling error or any discrepancy between the label and product |
| Tort | A law concerning personal injury. |
| Plaintiff | THe party bringing a complaint against defendant. |
| Malpractice | A form of professional negligence, a careless mistake, or an error in judgement |
| Contributory negligence | An action or inaction on the part of a plaintiff that caused or increased the risk of harm to the patient. |
| Breach of duty | Not providing a reasonable amount of care in performing a duty expected of a health professional. |
First Time Here?
Welcome to Quizlet, a fun, free place to study. Try these flashcards, find others to study, or make your own.