Question

In: Math

The Food and Drug Administration (FDA) is asked to approve a new drug. The new drug...

The Food and Drug Administration (FDA) is asked to approve a new drug. The new drug should contain less than 25mg of the active ingredient “toxin”, which is assumed to have dangerous side effects. The FDA would like to restrict the error of “approving the drug despite its too high content of toxin” to a maximum risk of 5% (α ≤ 0.05). Let Xi : “ The content of toxin in the i-th pill [in mg].” ∼ N(µ, σ2 ) ∼ N(µ, 4). A simple random sample of n = 50 pills ( Xi ∼ i.i.d.) will be used for the test.

7. Given a significance level of α = 5% what is the highest probability of making a type II error?

8. In the sample, x¯ = 24.6. Compute the p-value. What do you conclude? [Write down the probability that you computed.]

9. Has a type I error occurred? Explain your answer.

10. Has a type II error occurred? Explain your answer.

Solutions

Expert Solution

7. Given , is the probability of type 1 error that is error of rejecting a true null hypothesis

Type 2 error is the error of accepting a false null hypothesis

The highest probability of type 2 error = 1- 0.05 = 0.95

Highest probability of type 2 error is 95%

8.The null and alternative hypotheses

Test statistic

= -1.41

P value = P( z < -1.41)

= 0.0787

Since P value > 0.05

We fail to reject H0.

There is not sufficient evidence to conclude that new drug contains less than 25 mg of toxins .

Note : we get the value from z table for area from to -1.41

Or excel formula " =NORM.S.DIST(-1.41,TRUE)"

9. Type 1 error is the error of rejecting a true null hypothesis

Since we fail to reject H0 , type 1 error has not occurred .

10. Since P value > 0.05

We fail to reject H0.

That is we accept H0.

Now if H0 is true , we are correct in our decision

If H0 is false , we commit error

Accepting a null hypothesis , if it is false is type 2 error

So type 2 error has occurred.


Related Solutions

A drug company applied for the approval of the Food and Drug Administration (FDA) to market...
A drug company applied for the approval of the Food and Drug Administration (FDA) to market a miracle drug that the company believed could cure some cancers. During the period that the application was under consideration the company's stock rose to $65 per share. The president of the company learned that the FDA application was about to be denied. You are a personal friend of the president, and he told you that he believed that the stock will start trading...
The U.S. Food and Drug Administration (FDA) recently approved the marketing of a new chemical solution,...
The U.S. Food and Drug Administration (FDA) recently approved the marketing of a new chemical solution, Caridex, which disolves cavities. In a study conducted by dental researchers at Northwestern University, 21 of the 35 patients with cavities preffered treatment with Caridex to drilling (Gainesville Sun, Feb. 11, 1988). Find a 90% confidence interval for the true proportion of dental patients who prefer having cavities dissolved with Caridex rather than drilled. (0.46,0.74) (0.44,0.76) (0.39,0.81)
1. In 1995, the Food and Drug Administration (FDA) published new labeling standards for bottled water....
1. In 1995, the Food and Drug Administration (FDA) published new labeling standards for bottled water. (The full text of the final rule can be found at http://cfr.vlex.com/vid/165-110-bottled-water-19705533.) Prior to that time, bottlers could sell regular tap water under a bottled water label. In fact, the FDA estimated that approximately 25 percent of the supply of bottled water was nothing more than ordinary tap water. (a) Consider how these tougher standards eliminated 25 percent of the supply of bottled water....
The U.S. Food and Drug Administration (FDA) requires nutrition labeling for most foods. Under FDA regulations,...
The U.S. Food and Drug Administration (FDA) requires nutrition labeling for most foods. Under FDA regulations, manufacturers are required to list the amounts of certain nutrients in their foods, such as calories, sugar, fat, and carbohydrates. This nutritional information is displayed on the food’s package. Calories (C) Sugar (S) Fat (F) Carbohydrates (R) 100 12 0.5 25 130 11 1.5 29 100 1 2 20 130 15 2 31 130 13 1.5 29 120 3 0.5 26 100 2 0...
1. The The Food and Drug Administration (FDA) requires which ONE of the following products to...
1. The The Food and Drug Administration (FDA) requires which ONE of the following products to contain specific levels of microbial inhibitors or acidifying agents such as phosphoric or citric acid to prevent production of Clostridium botulinum toxin in the product? (NOTE: An anaerobic environment is present in both bottled and canned products. ) Hint: Look at the lecture slides that discuss how some of these products are made. You can also look up specific information for these items on...
1. The The Food and Drug Administration (FDA) requires which ONE of the following products to...
1. The The Food and Drug Administration (FDA) requires which ONE of the following products to contain specific levels of microbial inhibitors or acidifying agents such as phosphoric or citric acid to prevent production of Clostridium botulinum toxin in the product? (NOTE: An anaerobic environment is present in both bottled and canned products. ) Hint: Look at the lecture slides that discuss how some of these products are made. You can also look up specific information for these items on...
The federal drug and administration will not approve new pharmaceuticals products unless the developer can prove...
The federal drug and administration will not approve new pharmaceuticals products unless the developer can prove that the product is both safe and effective remedy for specified ailments. Do you think the safe and effective criterion would be good for Congress to adopt for the passage of new legislation> Why or Why not? Do you think most government action would meet this criterion? Discuss.
(20pts) The Food and Drug Administration (FDA) has established an upper tolerance of 5 parts per...
(20pts) The Food and Drug Administration (FDA) has established an upper tolerance of 5 parts per billion for the cancer-causing substance nitrosamine in beer. Suppose that Pabst and Miller are identified by the FDA as containing excessive concentrations of nitrosamines and are tested by an independent testing agency with the results shown in the accompanying table (in parts per billion). Also suppose that 36 bottles were randomly selected from each brand.                      Stat.     Pabst    Miller                      --------  -----    ------                      Mean      5.25     5.31                      Std. Dev. 1.20     1.44 Specify the null...
The Federal Drug Administration will not approve new phar- maceutical products unless the developer can prove...
The Federal Drug Administration will not approve new phar- maceutical products unless the developer can prove that its product is both safe and effective as a remedy for specified ailments. Do you think the “safe and effective” criterion would be a good one for Congress to adopt for the passage of new legislation? Why or why not? Do you think most govern- ment action would meet this criterion? Discuss.
The FDA is the administrative agency that oversees the food and drug industry in America. There...
The FDA is the administrative agency that oversees the food and drug industry in America. There are two types of administrative agencies. Identify the two types of administrative agencies, and identify what makes them different. What types of administrative agency is the FDA and what are the functions of the FDA?
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT