Many consumer groups feel that the U.S. Food and Drug Administration (FDA) 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 for a more lenient approval process so that pharmaceutical companies can get new drugs approved more easily and quickly. The FDA wants to set up a hypothesis test to show that the new drug is safe before approving it by assuming it to be unsafe. Suppose the p-value for the evidence is 0.07. Your decision on the test using a 0.10 level of significance should be to
a. reject null hypothesis
b. not reject null hypothesis
c. accept the null hypothesis
d. reject the alternative hypothesis
since p value of 0.07 is less than 0.10 level , correct option is"A
a. reject the null hypothesis
Many consumer groups feel that the U.S. Food and Drug Administration (FDA) drug approval process is...
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 for a 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...
What incentives does the FDA have regarding drug approvals, according to some FDA critics? The FDA is more concerned with preventing approval of a drug that results in people dying than it is with approving a drug that benefits unidentifiable patients whose lives might be saved if the drug is approved earlier. The FDA is more concerned with preventing statistical deaths than with “visible” or “identifiable” lives. The FDA is too quick to approve new drugs because of pressure from...
The Food and Drug Administration (FDA) is a U.S. government agency that regulates (you guessed it) food and drugs for consumer safety. One thing the FDA regulates is the allowable insect parts in various foods. You may be surprised to know that much of the processed food we eat contains insect parts. An example is flour. When wheat is ground into flour, insects that were in the wheat are ground up as well. The mean number of insect parts allowed...
Question 6 Select one answer. The Food and Drug Administration (FDA) is a U.S. government agency that regulates (you guessed it) food and drugs for consumer safety. One thing the 10 points FDA regulates is the allowable insect parts in various foods. You may be surprised to know that much of the processed food we eat contains insect parts. An example is flour. When wheat is ground into flour, insects that were in the wheat are ground up as well....
Question 6 Select one answer The Food and Drug Administration (FDA) is a U.S. government agency that 10 points regulates (you guessed it) food and drugs for consumer safety. One thing the FDA regulates is the allowable insect parts in various foods. You may be surprised to know that much of the processed food we eat contains insect parts. An example is flour. When wheat is ground into flour, insects that were in the wheat are ground up as well....
Question2 (A) The US Federal Drugs Administration (FDA) recently approved a drug for a rare fatal genetic disease that had only been trialled on 12 patients, without a placebo. One condition of the approval is that the company must carry out a more complete trial, even though sufferers can receive the drug because it is approved. Why will it be difficult to carry out such a trial? (B) A recent study reported that upper class people spent less time than...
2. The FDA approves drugs when the drug has a beneficial effect in a controlled experi- ment, based on a one-sided 5% level test with Ho the drug has no effect. A drug company has developed a new painkiller for chronic pains, although it is doubtful whether the new drug actually has any effect. The company conducts a double-blind ex periment with n = 298 randomly chosen chronic pain patients over a 6 months period. All patients receive the drug...
part b please
2. The FDA approves drugs when the drug has a beneficial effect in a controlled experi ment, based on a one-sided 5% level test with Ho, the drug has no effect. A drug company has developed a new painkiller for chronic pains, although it is doubtful whether the new drug actually has any effect. The company conducts a double-blind ex- periment with n-298 randomly chosen chronic pain patients over a 6 months period. All patients receive the...
Please read the following article: Your Google Searches Could Help the FDA Find Drug Side Effects The Food and Drug Administration is talking to Google about how the search engine could help the agency identify previously unknown side effects of medications. Agency officials held a conference call on June 9 with a senior Google researcher who co-wrote a 2013 paper about using search query data to identify adverse drug reactions, according to a record of the meeting posted to the...
Clinical trials are usually conducted in phases that build on one another. Each phase is designed to answer certain questions. Knowing the phase of the clinical trial is important because it can give you some idea about how much is known about the treatment being studied. There are pros and cons to taking part in each phase of a clinical trial. Phase I clinical trials: Is the treatment safe? Phase I studies of a new drug are usually the first...