DH206 Midterm Review Guide EXAM

DH206 Midterm Review Guide 2023 - 2024 EXAM Which type of drug name usually begins with a lowercase letter? Brand name Code name Generic name Trade name Generic name Only assigned once in a lifetime. Trade names of drugs are always__________ and Generic names are always __________ Capitalized, Lowercase Which of the following is true c oncerning generic and trade names of drugs? A drug may only have one generic name and one trade name. A drug may only have one generic name, but it may have several trade names. A drug may have several generic names, but it may only have one trade name. A drug may have several generic names and several trade names. *Two drug formulations that produce similar concentrations in the blood and tissues after drug administration are te rmed _____ equivalent. chemically biologically therapeutically biologically *Two formulations of a drug meet the chemical and physical standards established by regulatory agencies chemically biologically therapeutically Chemically equivalent *Two formulations of a drug have an equal therapeutic effect chemically biologically therapeutically Therapeutically equivalent ***The federal body that determines whether a drug is considered a controlled substance and to which schedule it belongs is the Food and Drug Administration (FDA). Federal Trade Commission (FTC). Drug Enforcemen t Administration (DEA). U.S. Pharmacopeia (USP). Drug Enforcement Administration (DEA). ***Which federal regulatory agency decides which drugs require a prescription and which drugs may be sold over -the-counter (OTC)? FDA (U.S. Food and Drug Administration) OSHA FTC (Federal Trade Commission) DEA (Drug Enforcement Administration) FDA *Whic h federal regulatory body regulates the trade practices of drug companies and prohibits false advertising of foods, nonprescription drugs, and cosmetics? Food and Drug Administration (FDA). Federal Trade Commission (FTC). Drug Enforcement Administration ( DEA). U.S. Pharmacopeia (USP). FTC (Federal Trade Commission) A drug's generic name is selected by the pharmaceutical company manufacturing it. Food and Drug Administration (FDA). U.S. Adopted Name Council. Federal Patent Office. U.S. Adopted Name Counc il. *Phase 1 clinical trials involve all of the following except which one? Safe dose range Toxic effects of the drug Metabolism Effectiveness Effectiveness Phase 1 PHASE 1 OF CLINICAL STUDIES ▪Small and then increasing doses are administered to a limited number of healthy human volunteers ▪Determines biologic effects, metabolism, safe dose range in humans, and toxic effects of the drug *Clinical studies of drugs first involve human voluntee rs during which phase of drug testing? Phase 1 Phase 2 Phase 3 Phase 4 Phase 1