TASK DEFINITION: In this task, you are given a question and a context passage. You have to answer the question based on the given passage.
PROBLEM: What is an opposite result of an idea posted here?, Context: Greek drama exemplifies the earliest form of drama of which we have substantial knowledge. Tragedy, as a dramatic genre, developed as a performance associated with religious and civic festivals, typically enacting or developing upon well-known historical or mythological themes. Tragedies generally presented very serious themes. With the advent of newer technologies, scripts written for non-stage media have been added to this form. War of the Worlds (radio) in 1938 saw the advent of literature written for radio broadcast, and many works of Drama have been adapted for film or television. Conversely, television, film, and radio literature have been adapted to printed or electronic media.

SOLUTION: television, film, and radio literature have been adapted to printed or electronic media

PROBLEM: What is the second largest ocean in the world?, Context: The Philadelphia dialect, which is spread throughout the Delaware Valley and South Jersey, is part of Mid-Atlantic American English, and as such it is identical in many ways to the Baltimore dialect. Unlike the Baltimore dialect, however, the Philadelphia accent also shares many similarities with the New York accent. Thanks to over a century of linguistics data collected by researchers at the University of Pennsylvania, the Philadelphia dialect under sociolinguist William Labov has been one of the best-studied forms of American English.[f]

SOLUTION: Atlantic

PROBLEM: What does the FDA oversee?, Context: In the United States, new pharmaceutical products must be approved by the Food and Drug Administration (FDA) as being both safe and effective. This process generally involves submission of an Investigational New Drug filing with sufficient pre-clinical data to support proceeding with human trials. Following IND approval, three phases of progressively larger human clinical trials may be conducted. Phase I generally studies toxicity using healthy volunteers. Phase II can include pharmacokinetics and dosing in patients, and Phase III is a very large study of efficacy in the intended patient population. Following the successful completion of phase III testing, a New Drug Application is submitted to the FDA. The FDA review the data and if the product is seen as having a positive benefit-risk assessment, approval to market the product in the US is granted.

SOLUTION:
new pharmaceutical products

