Should Drugs Be Safe For Consumption?

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 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.

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

The Federal Food, Drug Administration is responsible for establishing the Code of Federal Regulations which outlines the rules and regulations governing pharmaceuticals. The rules are divided into sections and include guidance based on drug categories. Due to each person having varying reactions to pharmaceutical products not all side-effects are detected during clinical testing. The Federal Food, Drug Administration is responsible for sharing the information with consumers. However, it seems a bit unethical because the large pharmaceutical companies do not have to share all of side-effect information that may assist consumers in making its choice on whether to try a product or to not try a product. Through various survey’s it was discovered that consumers are under the opinion that pharmaceutical companies need to have improved internal controls to ensure their compliance with regulations. Due to physicians and pharmaceutical companies working together and are dependent on one another there needs to be controls in place that would have an unbiased view of the regulations. The government will need to continue introducing new regulations that will aide in monitoring the relationships.

The Food & Drug Administration became a possibility because of the Pure Food and Drugs Act of 1906. Harvey Washington Wiley was the driving force behind this law and headed its enforcement, which provided basic elements of protection that consumers had never had before (FDA's Origin). The FDA is an agency that works within the US Department of Health and Human Services of the executive branch of government (About FDA). The Food and Drug Administration is responsible for protecting the public health of all Americans by ensuring the safety, efficacy, and security of a large range of products from drugs to cosmetics (What We Do).

The FDA’s regulations would impact the food and drug production industries in multiple ways. Firstly, the regulation decreased the quantity of goods that the companies had available to sell. For example, before the Pure Food and Drug Act, meat-packing companies could pack and sell deceased animal meat, like from dead cattle. The sum of the dead

Everyone in America, is at risk for being diagnosed with a condition that they don't have, and being prescribed medications they do not need. Its, everyday advertisments on TV for clients who may have had a missed diagnosis, and experienced a side effect from a medication they where prescribed, physicians try to follow national standards of care to protect themselves from lawsuit or even losing their licenses.

The Food and Drug Administration (FDA) and United States Department of Agriculture (USDA) are government agencies that coordinate with one another to ensure the safety of our nation’s food supply. For instance, the FDA is responsible for protecting the public health by assuring safety, effectiveness, quality and security of human/veterinary drugs, vaccines, and medical services. In addition, the FDA is also responsible for all cosmetics and dietary supplements, tobacco and products of radiation. There is a law in place, which has been recently signed by President Obama on January 4, 2001 called the Food Safety Modernization Act. This reformed food safety law is over sighted by the FDA agency to ensure that the U.S. food supply is safe, by focusing on ways to prevent contamination from previously reported

There was a time where there was no limits to what substances were in products we humans consume or use everyday. It is alarming to think that there could be items in our food or medicine that are potentially dangerous and deadly. It is for these reasons that the Food and Drug Administration came to be. It all started in a time where companies could say anything they wanted about a product without any scientific validation or proof. The government stepped in and established the Pure Food and Drugs Act of 1906 along with a new agency: the FDA. This act's purpose was to protect the public against dangerous substances in food and from products identified as healthy without scientific support. This law was an accumulation of many bills and ideas that aimed to protect consumers from contaminated products. (The Pure Food and Drug Act) Now, the FDA conducts recalls, market withdraws, and safety alerts in order to protect the citizens.

What is the FDA and what does it do you may ask? The FDA stands for Food and Drug Administration. They are responsible for protecting the public’s health, and ensure the safety and security of human and veterinary dugs. They also regulate the making, selling and distribution of products. The FDA regulates many things including foods, like additives and supplements, drugs, both prescription and non-prescription, biologics, like vaccines and blood products,

Are prescription drugs overprescribed? Are patients being prescribed the correct medications that they actually need? Are generic drugs doing the same for the human body that marked up brand name medications are? These are some of the public’s biggest questions that can be easily answered by research. Everyone is affected by medication and healthcare in general today. Many real life scenarios are offered throughout this writing to support the argument. The following thesis statement is a worldwide problem. Unfortunately, the United States has the largest problem with inflation of drug cost and over-prescription of medications. Many people are to blame: drug manufacturers, insurers, prescribers, educators, and many others. A change is needed.

In the article “The Political Economy of FDA Drug Review: Processing, Politics and Lessons for Policy”, the author Daniel P.Carpenter discusses different aspects of the FDA’s drug processing system and the political effects that can alter the routes and outcomes of that process. The role of the FDA is often thought to be mainly focused on protecting the public from non-efficient drugs and that that is the reason behind its popularity. However, the article points out how this role is actually more focused on protecting the FDA’s own reputation; as a long-time FDA observer said, “The FDA is very responsive to what I would call ‘opinion leaders’ in the scientific and medical communities. It cares very much about what these people think as to how the agency is doing”. It is rather surprising and makes complete sense at the same time. I believe because the public often saw the FDA as a heroic agency that shielded them from harmful drugs with no concern of the outcomes. But this vision would certainly vanish if the

In the article, Does the FDA Adequately Protect the Public? by Marc Ferris, he argues that the drug could pose a serious health threat. Most people take medications when they get sick, but taking medications could make their health worse. Ferris said that “but in recent years, the reputation of the nation's drug-safety system has been especially tarnished after several prescription drugs approved by the U.S. Food and Drug Administration (FDA) were later found to have dangerous side effects for some users, triggering voluntary manufacturer recalls” (par. 3). He claims that the FDA approved prescription drugs, and there were several cases that they recalled the drugs due to dangerous side effects which could lead to deaths. Therefore, he wonders

As the years, products, and medical advancements progress so has regulations, but what surprised me is that these tragedies that had to be the means of creating the FDA to what it is today. The first event that was mentioned was the public outcry regarding the chemical foods and phony medications that were being sold. In discovery of the way these necessities for the population were being handled it made me think that those handling the products were all about the money. I understand that things happen and they were trying to accommodate more people, or better products but of you see a problem address it, it’s disappointing in learning the facts about these issues, and how they were not address until the people demanded a change.