A) "Is this a drug in clinical trials? Those are the only drugs that don't have to have FDA approval."
B) "Is this an over-the-counter drug? Over-the-counter drugs do not need FDA approval."
C) "Your company must be involved in academic research if the drug doesn't need FDA approval."
D) "Any pharmaceutical company must have FDA approval before marketing a drug."
Correct Answer
verified
Multiple Choice
A) This law did not require drug manufacturers to prove that the drug was effective in its claims.
B) This law did not prevent drugs from being marketed for any disease.
C) This law required all drug labels to accurately describe their contents.
D) This law required adequate testing for safety prior to marketing.
E) This law did not encourage the development of drugs for rare or unusual disorders.
Correct Answer
verified
Multiple Choice
A) The clinical trials are continuing to collect new data.
B) Individual client response is compared with the clinical trial data.
C) The efficacy of the drug is determined for new drugs.
D) Harmful effects in the larger population continue to be monitored.
Correct Answer
verified
Multiple Choice
A) Registered nurses
B) Physicians
C) Nurse practitioners
D) Nurse managers
E) Physical therapists
Correct Answer
verified
Multiple Choice
A) "If you continue on this medication for a long time,you will become addicted to it."
B) "You are not an addict,but the Drug Enforcement Agency (DEA) will be watching your prescription drug habits now."
C) "Any drug that has a potential for abuse is considered a controlled substance and is restricted.This does not mean the pharmacist will think you are an addict."
D) "Do you think that you are addicted to your medication?"
Correct Answer
verified
Multiple Choice
A) Strength and purity of products varied from region to region and batch to batch.
B) Strength and purity of products depended on the pharmacist's experience.
C) Strength and purity of products would vary in size,taste,and nutritional value.
D) Strength and purity were mostly guaranteed if products were produced locally,which caused a hardship for those outside the region.
E) Strength and purity could be trusted when the product had gone through extensive local testing.
Correct Answer
verified
Multiple Choice
A) "I should call the office three days before I need a refill called in to the pharmacy."
B) "I will need to see the provider each time for my refill."
C) "This is an addictive drug,so I should try not to take it."
D) "After the first prescription,my doctor will be able to call in my prescription."
Correct Answer
verified
Multiple Choice
A) "The admitting physician needs to know everything you are taking."
B) "You're right.I'm not sure why the admitting paperwork asks for this information.Would you mind listing them anyway?"
C) "The law requires us to keep a list of over-the-counter drugs and supplements that you are taking."
D) "It is true that supplements are not considered drugs; however,some of these products can cause adverse effects with prescribed drugs."
E) "We need to know if you are having an allergic reaction to one of them."
Correct Answer
verified
Multiple Choice
A) Patent medicines contained a brand name that clearly identified the product.
B) Patent medicines claimed to cure just about any disease or condition.
C) Patent medicines were often harmless and ineffective.
D) Many patent medicines contained addictive substances.
E) Patent medicines could not make false therapeutic claims.
Correct Answer
verified
Multiple Choice
A) Biologics
B) Food supplements
C) Herbal preparations
D) Dietary supplements
Correct Answer
verified
Multiple Choice
A) Most drugs do not proceed past the preclinical stage because they are found to be too toxic or just ineffective.
B) At the end of the preclinical research stage,client variability is determined and potential drug-to-drug interactions are examined.
C) The preclinical stage of research involves extensive testing on animals in the laboratory to determine if the drug will cause harm to humans.
D) Preclinical research results are always inconclusive.
E) The Food and Drug Administration (FDA) is responsible for extensive testing for safety before the pharmaceutical company can begin the preclinical research stage of development.
Correct Answer
verified
Multiple Choice
A) It prevented the sale of drugs that had not been tested before marketing.
B) It gave the government the power to change labeling content of medications.
C) It helped to standardize the quality of prepared food,drugs,and cosmetics.
D) It prohibited the sale of drugs labeled with false therapeutic claims to defraud the public.
Correct Answer
verified
Multiple Choice
A) Advertisements are not legally binding and can be misleading.
B) All drugs must be advertised in media to inform the public.
C) Manufacturers have some ability to change things when advertising drugs.
D) False claims of a drug's therapeutic effect are prohibited by law.
Correct Answer
verified
Multiple Choice
A) "Over-the-counter medications are safe,as long as we don't take them at the same time as our prescription medications."
B) "Over-the-counter medications are safe; otherwise,they would require a prescription."
C) "We should not take any over-the-counter medications without first calling our primary health care provider because these medications can interact with other prescriptions or products."
D) "We must read all the label directions before taking any over-the-counter medications."
Correct Answer
verified
Multiple Choice
A) Whether a New Drug Application (NDA) must be filed
B) The marketability of the drug
C) What the cost of the drug should be
D) Whether or not the drug is safe
Correct Answer
verified
Multiple Choice
A) The research drug must be compared to an inert substance to determine effectiveness.
B) The placebo will be given to a control group,and those results will be compared to the group taking the research drug.
C) During the trials,neither group will know if they have the placebo drug or the research drug.
D) The research drug will be considered for a New Drug Application (NDA) if it is found to be effective and safe when compared to the placebo drug.
E) Before the clinical trials,the research drug will be tested on select clients against another standard drug used for the same condition.
Correct Answer
verified
Multiple Choice
A) Diseases that previously were treated with older and less popular drugs
B) Diseases that affect only a small percentage of the population
C) Diseases for which the community raises money for treatment
D) Serious and life-threatening conditions that lack effective treatments
Correct Answer
verified
Multiple Choice
A) "A placebo is a substance that has no therapeutic effect."
B) "A placebo is a similar drug that is safe."
C) "A placebo is a drug that has been tested before."
D) "A placebo is an over-the-counter drug."
Correct Answer
verified
Multiple Choice
A) They were only distributed in elixir formulation.
B) They had dangerous or addictive substances.
C) They smelled like medicine.
D) They could only be made out of natural products.
Correct Answer
verified
Multiple Choice
A) "Drugs with the least amount of side effects can become over-the-counter."
B) "Drugs that have a high safety margin may be reclassified to over-the-counter."
C) "The longer the drug is on the market,the better its chance of going over-the-counter."
D) "If the pharmaceutical company pays the FDA a large amount of money,it can have its drug reclassified."
Correct Answer
verified
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