This Question: 1 pt 6 of 15 (0 complete) This Test: 15 pts possible Many consume
ID: 3268338 • Letter: T
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This Question: 1 pt 6 of 15 (0 complete) This Test: 15 pts possible Many consumer groups feel that the Country A drug approval process is too easy and, as a result, too many drugs are approved that are later found to be unsafe. On the other hand, a number of industry lobbyists have pushed fora more lenient approval process so that pharmaceutical companies can get new drugs approved more easily and quickly. Consider a null hypothesis that a new, unapproved drug is unsafe and an alternative hypothesis that a new, unapproved drug is safe. Complete parts (a) through (c) below. a. Explain the risks of committing a Type l or Type Il error. Choose the correct answer below. A. A Type I error would be incorrectly failing to approve an unsafe drug. A Type Il error would be incorrectly O B. A Type l error would be incorrectly failing to approve a safe drug. A Type II error would be incorrectly ° C. A Type l error would be incorrectly approving a safe drug. A Type II error would be incorrectly failing to D. A Type I error would be incorrectly approving an unsafe drug. A Type II error would be incorrectly failing b. Which type of error are the consumer groups trying to avoid? Explain. Choose the correct answer below. 0 A. The consumer groups are trying to avoid a Type I error because they think that too many safe drugs are O B. The consumer groups are trying to avoid a Type II error because they think that too many unsafe drugs O C. The consumer groups are trying to avoid a Type ll error because they think that too many safe drugs are approving a safe drug. approving an unsafe drug. approve an unsafe drug. to approve a safe drug. unapproved are approved.Explanation / Answer
a. The Type I error refer to the likelihood of incorrectly rejecting a true null hypothesis. Thus, if a researcher rejects that new, unapproved drug is unsafe, when actually it is unsafe, the researcher committs Type I error. Thus if researcher incorrectly approve an unsafe drug, he makes Type I error. Type II error refer to incorrectly retaining a false null hypothesis, that is concluding the new, unapproved drug to be unsafe when it is actually safe. Therefore, going by the analysis, one can discard options A, B and C easily. Option D is correct.
b. Consumer would like to avoid Type I error (incorrect rejection of true null hypothesis), as it would mean that too many unsafe drugs are approved. Thus, one can easily discard options A, B and C. Option D is right.
c. The goal of industrial lobbyists is to release more new drugs, that is to facilate drig approval process. Industrial lobbyists are trying to avoid Type II error (incorrectly retaining a false null hypothesis), as it would mean lesser number of new, unapproved drugs to be declared safe. Options B, C and D are discarded, leaving option A to be correct.
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