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1 review pharmacoloy
chapter one review
| Question | Answer |
|---|---|
| The _________blank is the federal agency that enforces the Controlled Substances Act | Drug Enforcement Administration |
| The Food and Drug Administration (FDA) is part of the U.S. Department of Health and Human Services and regulates | drug development, manufacture, and sales to ensure safety and effectiveness. |
| blank is the study of disease processes in the human body, including changes in structure and function. | Pathology |
| The Orphan Drug Act of 1983 is legislation that | provides incentives for manufacturers to speed up the research and development of drugs to treat patients with rare diseases. |
| description | What the drug is made of |
| Action | How the drug works in the body |
| indications | What conditions or diseases the drug is used for |
| interactions | undesirable effects that result if the drug is taken with certain foods or other drugs. |
| contraindications | Conditions under which the drug should not be used |
| precautions | warnings to consider when administering drugs to patients with specific conditions or diseases. |
| hashish | Schedule I |
| amphetamines | Schedule II |
| barbituates | III |
| If you know the generic name for a drug but not the brand names under which it is sold, how would you use the PDR® to find that information? | Look up the generic name in the Brand and Generic Name Index. |
| Drug standards are necessary to | control differences that can occur due to variation in manufacturing methods or locations. |
| Drugs come from three natural sources: plants, animals, and | minerals |
| Which drug reference contains information about products of major pharmaceutical companies, including descriptions and information on actions, indications, adverse reactions, dosage, and administration? | Physician's Desk Reference (PDR®) |
| What is the nonproprietary drug name assigned by the manufacturer with the approval of the United States Adopted Names (USAN) Council? | generic name |
| pharmacokinetics | The absorption, distribution, metabolism, and excretion of drugs |
| pharmacodynamics | The body’s response to a drug |
| Palliative drugs are used for what purpose? | to improve quality of life |
| Drug cards typically contain, at minimum, the | drug name, action, uses, dosage range, side effects, and precautions. |
| he desired or predicted physiologic response to a drug in the body is called its | therapeutic effect. |
| Schedule I | High potential for abuse, produce severe physical and psychological dependence, no accepted medical use, sometimes used for research |
| Schedule II | High potential for abuse, produce severe physical and psychological dependence, acceptable medical uses with restrictions, dispensed by prescription only |
| Schedule III | Moderate potential for abuse, high psychological dependence, low physical dependence, acceptable medical uses, dispensed by prescription only |
| Schedule IV | Lower potential for abuse, limited physical and psychological dependence, acceptable medical uses, dispensed by prescription only |
| Schedule V | Lowest potential for abuse, acceptable medical uses, OTC narcotic drugs, must be sold by registered pharmacists and buyers must be 18 years old and show ID |
| Schedule VI | Some states such as North Carolina have adopted this schedule to place marijuana in a category that allows limited medicinal use in certain situations, requires a prescription |
| Controlled Substances Act of 1990 | The _________blank is legislation that regulates the manufacture and sale of narcotics and dangerous drugs. |
| The four sources of drugs are | plants, animals, minerals, and chemicals |
| The absorption, distribution, metabolism, and excretion of drugs is known as | pharmacokinetics |
| Which drug reference is recognized by the U.S. government as its official list of drug standards? | United States Pharmacopeia/National Formulary |
| Contraception | to prevent pregnancy |