The Food And Drug Administration (FDA)

The FDA has come a long way since 1906, but in my opinion, I believe that the FDA should do more to protect our health and have stricter laws in place concerning our food and medicines. The FDA allows products to be on the market without prior approval; for the FDA to take action and recall a product something awful like multiple deaths have to happen for them to realize that the product is harmful. Prime example, Red #3 is food coloring that FDA permits in our food to make the food look appealing. However, studies done on animals have proven to show that Red #3 causes cancer. According to an article published in 1990 in the New York Times states that "Red Dye No. 3 still has some approved uses in foods and drugs, but the F.D.A. said it is

The Food and Drug Administration (FDA) is best known for its role on protecting the health of the public by making sure that food, medications are safe and effective. Especially when it comes to the pharmaceutical industry, its mission is to regulate pharmaceutical manufacturers, as well as the drug approval process. However, in the recent years, many arguments and controversy regarding drug development and regulation have risen. Drug advertisements make false and misleading claims, products are being put out on the market without any proof of safety, causing many unwanted incidents such as the Avandia incident and Vioxx incident, which could have been prevented in the first place.

- The FDA is responsible for keeping the public healthy by making sure that the nation’s food supply is clean, clearly and honestly labeled, and healthy for whoever eats it.

The Food and Drug Administration, also known as the FDA or USFDA, is responsible for protecting and advocating public health. They are the official government agency that ensures our drug supply is safe and effective. This is achieved through the regulation and supervision of food safety, dietary supplements, veterinary products, cosmetics, vaccines, biopharmaceuticals, medical devices, prescription and pharmaceutical drugs that can be purchased over- the- counter.

Food and drug administration is a department of U.S health and human services. It’s responsibility is to test the safety and efficacy of new drugs entering the market as well as to make sure that these medicines are quickly accessible to people. The Food, Drug, and Cosmetic Act has been passed in 1938 to ensure that foods other than meat, poultry and fish are clinically hygienic and safe to eat. This act also requires that the food should be labelled according to its content. (FDA.org) Drugs and tobacco are also regulated by FDA and in 1996, FDA strictly regulated the use of tobacco products like nicotine, cigarettes and smokeless tobacco, by children and adolescents because of the increase in diseases prevalence and tobacco addiction. Annually 40000 deaths are attributable to its use and most of them are of premature. Therefore the goal of FDA is to stop the tobacco addiction by minors and prevent the deaths and diseases due to nicotine addiction. (FDA vs Brown, n.d) This essay will cover the food and drug administration’s role in under and over regulating drugs and medicines and how it effects our economy, health care system and patients health and safety.

FDA stands for Food and Drug Administration, it is responsible for protecting the public health by assuring that foods are

Food and Drug administration is a very important agency that has been apart of the government for over a hundred years it was founded in June of 1906.Though FDA can trace its origins back to the creation of the Agricultural Division in the Patent Office in 1848, its origins as a federal consumer protection agency began with the passage of the 1906 Pure Food and Drugs Act.This 1906 act was created because there was along standing abuse in the consumer marketplace.This part of the government was made by Theodore Roosevelt and Harvey Washington Wiley in good faith for the people.

of food, drugs, and cosmetics. The day-to-day operations of the FDA occur within the Office of

The FDA also looks at several products that have chemical implications to them, such as drugs. It looks at drug manufacturing standards, as well as the labels of each drug (both over-the-counter and prescription drugs) and must give its approval on new drugs before they can be sold to the public. The FDA also looks at cosmetics. It must ensure that, like food articles, each product is properly labeled as to what comprises each item. Biological products, such as the nation’s blood supply, are also regulated by the FDA. It does research to improve upon the testing methods of blood, to ensure that the supply in hazard free. It also is in charge of handing out licenses to product and manufacturing establishments.

The United States of America is arguably the greatest country in the history of the world. With this great global influence, one could assume the United States ensures the best for its citizens health and prosperity, to be a role model for the rest of the world. However, you would be greatly surprised. The United States is failing to take action against some of the major immoralities committed by its own bureaucracies, which consistently cause detrimental harm to the well-being of the American public. A significant bureaucracy that is responsible for a great deal of harm to the U.S. is the Food and Drug Administration, or FDA. The FDA is preventing the sustainability of the

FDA is a very important organization to inspect all food additives. FDA stands for Food and Drug Administration. It oversees a variety of products involving food, drugs, cosmetics, animal food, dietary supplements, medical devices, biological goods and blood products. It is the agency in the United States Department of Health and Human Services. Protecting public health is a key priority of the FDA. Safety concerns prompt the FDA to pull one to two drugs and six to eight food and medical devices from the market annually. It is the FDA’s duty to address serious risks that can be avoided and managed. The FDA reviews the safety and effectiveness of food and medical

There was a recent ruling that made the media headlines that shows how important the rulings of the FDA are to the public. On March 18, 2010 new rules were announced that have a strict impact on the way that the tobacco industry can sell and market smokeless products and cigarettes. In particular the advertising that targets the nation’s youth population. That law that takes effect on June 22,

Nevertheless, important amendment in the FDA act in 2007 empowered the body to establish the risk needs and mitigate strategies that included medical testing. In this arrangement, the support staff ensured pharmacies dispensed drug to the disserving patients only. On the contrary, it was argued that given the strict enforcement by the FDA, some patients would be locked out of the arrangement. Nevertheless, this was played down given the need to maintain safety standards by manufacturers who required professionals to adhere to strict standards when collecting vital data to be used in managing the disease (Juusola, Brandeau, Owens & Bendavid,

Tobacco use remains the leading cause of preventable deaths and illnesses. Worldwide, the burden of tobacco exceeds six million deaths and half a trillion in economic loss annually. Tobacco-related deaths are projected to reach 7.4 to 9.7 million by 2030. To combat tobacco-use epidemic, the World Health Organization (WHO) enacted a Framework Convention on Tobacco Control (FCTC) that included six tobacco-control strategies to guard against both demand and supply arms of tobacco use. Abbreviated as “mpower,” these strategies include monitoring tobacco use and prevention strategies; protection against tobacco smoke; offering cessation aid; warnings against tobacco-related risks; enforcing advertising, promotional, and sponsorship bans; and raising taxation on tobacco products. ,

The level of regulation governed by the FDA over drugs, biologics & medical devices is a widely debated topic. In my point of view, the level of regulation on drugs, biologics and medical devices should be strict.